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2019-06:
01 민유정   J.Club
01 유경훈 Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program     J.Club
03 한봄   TopicSem
03 김기태   TopicSem
06 ... 휴일  TopicSem
06 ... 휴일  TopicSem
08 김주연   J.Club
08 민병주   J.Club
10 국수경   TopicSem
10 윤선민   TopicSem
13 박유미   TopicSem
13 김효정   TopicSem
15 김기태   J.Club
15 유승원   J.Club
17 김주연   TopicSem
17 민병주   TopicSem
20 유경훈   TopicSem
20 유승원   TopicSem
22 서명의   J.Club
22 채정환   J.Club
24 안세환   TopicSem
24 권호식   TopicSem
27 채정환   TopicSem
27 최선   TopicSem
29 한봄   J.Club
29 국수경   J.Club

2019-05:
02 최선 Dimension calculation in CNN  MAInfo
02 김주연 Synthetic association analysis of PGx variants extracted from GWAS  TopicSem
02 김효정 Clinical Genome Data Model (CGDM) provides Interactive Clinical Decision Support for Precision Medicine; review   TopicSem
02 권호식 MTX Genomic markers from literatures  xMutant
04 김재환 Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterion     J.Club
04 부은경 Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma     J.Club
06 ... 휴일  TopicSem
06 ... 휴일  TopicSem
09 김기태 GSDBA: Computational approach for Gene Set wise Deleterious Burden Analysis   TopicSem
09 민병주 Application of next‑generation sequencing to analyze drug response in human leukemia  TopicSem
09 박유미 Whole-genome reference panel of 1781 Northeast Asians improves imputation accuracy of rare and low-frequency variants  xMutant
09 임영균 Cancer Dependency Map  MAInfo
11 안세환 New drug candidates for treatment of atypical meningiomas: An integrated approach using gene expression signatures for drug repurposing     J.Club
11 김효정 Pharmacogenomic clinical decision support design and multi-site process outcomes analysis in the eMERGE Network     J.Club
13 유경훈 Comparative study of escitalopram according to CPIC guideline (CYP2C19/CYP2D6 Metabolizer Status)  TopicSem
13 유승원 6MP analysis - Candidate analysis based on new criteria(ANC<500 relative frequency)  TopicSem
13 박유미 Evaluating potential drug targets through human loss-of- function genetic variation  SysBiol
13 안세환 Clinical data for each project in GDM  BioEMR
16 안세환 The issues of importing gdm into cbioportal  TopicSem
16 채정환 further study of taxol related ADR  TopicSem
16 윤선민 The Medical Genome Reference Bank: a whole-genome data resource of 4000 healthy elderly individuals. Rationale and cohort design  xMutant
16 윤선민 Case-control analysis identifies shared properties of rare germline variation in cancer predisposing genes   MAInfo
18 권호식 The germline genetic component of drug sensitivity in cancer cell lines     J.Club
18 이우승 Somatic_Mutations_increase_Hepatic_Clonal_Fitness_and_Regeneration_in_Chronic_Liver_Disease     J.Club
20 국수경   TopicSem
20 최선 Drug classification  TopicSem
20 한봄 The IMGT/HLA Database  BioEMR
20 김기태 Parallel processing in R   SysBiol
23 이우승 The Progsotic Potential of Loss of Heterozygosity in Cancer  TopicSem
23 김재환 Current status of Precision Medicine Assistant Tool development  TopicSem
23 김기태 Parallel processing in R   MAInfo
25 임영균 Prioritization of cancer therapeutic targets using CRISPR–Cas9 screens     J.Club
25 윤선민 Interpreting the clinical significance of combined variants in multiple recessive disease genes: systematic investigation of Joubert syndrome yields little support for oligogenicity.     J.Club
27 권호식   TopicSem
27 서명의   TopicSem
30 임영균   TopicSem
30 부은경   TopicSem

2019-04:
01 김주연 Star allele determination overview and exploration of methods  TopicSem
01 유승원 apoptosis,DNA repair-related candidate burden and 6MP dose percentage  TopicSem
04 유경훈 Comparative study of escitalopram according to CPIC guideline (CYP2C19 Metabolizer Status)  TopicSem
04 민병주 SNVs of multidrug efflux pump transporter genes in antibiotic-resistant H. pylori strains  TopicSem
04 김기태 GS-DBA: Gene Set Deleterious Burden Analysis  MAInfo
06 채정환 A joint study of whole exome sequencing and structural MRI analysis in major depressive disorder     J.Club
06 서명의 Variants of unknown significance in genes associated with heritable thoracic aortic disease can be low penetrant ‘‘risk variants’’     J.Club
08 안세환 File Formats of cBioPortal  TopicSem
08 채정환 taxol further study  TopicSem
08 김주연 A disease-drug database to support drug prescribing based on patient pharmacogenomics test results  SysBiol
08 한봄 A review on a project about the benefit of mobile technology for clinical care.  BioEMR
11 권호식 Clinical data of HD-MTX ALL samples and the progress  TopicSem
11 최선 TSA on renal disease  TopicSem
11 이우승 The Progsotic Potential of Loss of Heterozygosity   MAInfo
12 이우승 Copy Number Variation Algorithm  xMutant
13 김주연 Analysis of comprehensive pharmacogenomic profiling to impact in-hospital prescribing     J.Club
13 유승원 Discovering the ‘Dark matters’ in expression data of miRNA based on the miRNA-mRNA and miRNA-lncRNA networks     J.Club
15 민유정 Introduction to GDM Portal  TopicSem
15 김재환 Development of RarePedia knowledge base and SAG  TopicSem
15 김주연 CYP2D6 star allele calling with Stargazer  BioEMR
15 안세환 Select available columns in cBioPortal mutation file  SysBiol
18 이우승 The Progsotic Potential of Loss of Heterozygosity   TopicSem
18 서명의 Candidate variants in 12 genes for systematic mutagenesis  TopicSem
18 유승원 miRNA Databases discussion  xMutant
18 유승원 Intersect and combine approach for alginers,variant callers - based on NA12878 gold standard WES data  MAInfo
18 유승원 review of miRNA, lncRNA databases  xMutant
18 유승원 review of miRNA, lncRNA databases  xMutant
20 한봄 Cross-ethnicity tagging SNPs for HLA alleles associated with adverse drug reaction     J.Club
20 국수경 Whole-exome sequencing and clinical interpretation of FFPE tumor samples to guide precision cancer medicine     J.Club
22 박유미 Gene-wise variant burden (GVB) score: implications for characteristics of genetic features   TopicSem
22 부은경 Parkinson's Disease NGS Data  TopicSem
22 김효정 [Review] From Big Data to Precision Medicine.     BioEMR
22 한봄 Definitions of HLA typing terms  SysBiol
22 한봄 Definitions of HLA typing terms  SysBiol
24 유경훈 VIVA (VIsualization of VAriants): A VCF file visualization tool  xMutant
25 한봄 Steroid-induced Hyperglycemia  TopicSem
25 임영균 somatic mutation filtering in tumor-only sequencing data  TopicSem
25 권호식 Considerations in Assigning Star Alleles to 1KGP  MAInfo
27 최선 Using RNN to predict heart failure     J.Club
27 박유미 Whole exome sequencing and characterization of coding variation in 49,960 individuals in the UK Biobank     J.Club
29 최선 Case series Report  BioEMR
29 민유정 GDM Portal Development  TopicSem
29 윤선민 Analysis of candidate variants in patients with side effects of L-asparaginase  TopicSem
30 유경훈 Clinical use of current polygenic risk scores may exacerbate health disparities  SysBiol

2019-03:
02 박유미 Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder     J.Club
02 김효정 Toward a normalized clinical drug knowledge base in China—applying the RxNorm model to Chinese clinical drugs     J.Club
04 김효정 Assessment of Diagnostic Usefulness of Liver Fibrosis Predictive Markers   BioEMR
04 최선 K-CDM analysis on renal disease  TopicSem
04 유승원 6MP analysis : novel candidate variants and IL6-related variants  TopicSem
07 안세환 Importing sample data into cBioPortal  TopicSem
07 채정환 taxol analysis : further study  TopicSem
07 안세환 File Formats for cBioPortal  SysBiol
09 권호식 Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions     J.Club
09 이우승 Re-identification of individuals in genomic data-sharing beacons via allele inference     J.Club
11 서명의 Candidate variant selection for systematic mutagenesis and suitable activity assay  TopicSem
11 유경훈 Pharmacogenetics of escitalopram response: a candidate gene analysis�  TopicSem
11 한봄 Wellcome Trust Protocol about QC  BioEMR
14 이우승 Inhouse CNV Algorithm  TopicSem
14 권호식 Variants of Star Allele Wild Type samples from 1KGP  TopicSem
14 국수경 Advantages and disadvantages of the Foundation-Medicine cancer panel in head and neck adenocarcinoma  MAInfo
14 권호식 Clinical data of HD-MTX samples   xMutant
16 최선 Risk prediction for chronic kidney disease progression using heterogeneous electronic health record data and time series analysis     J.Club
16 윤선민 Rapid and accurate interpretation of clinical exomes using Phenoxome: a computational phenotype-driven approach     J.Club
18 임영균 Pancreatic cancer FNA 2번째 sample 분석  TopicSem
18 정문경   TopicSem
18 김효정 Assessment of serologic markers on liver fibrosis: descriptive statistics  SysBiol
21 한봄 Steroid-induced Hyperglycemia  TopicSem
21 김기태 GS-DBA: Gene Set Deleterious Burden Analysis  TopicSem
21 채정환 taxol study_tcga data  xMutant
21 임영균 Installation and Run of Neopepsee   MAInfo
23 임영균 Widespread Selection for Oncogenic Mutant Allele Imbalance in Cancer     J.Club
23 유경훈 Improved Pathogenic Variant Localization via a Hierarchical Model of Sub-regional Intolerance     J.Club
25 국수경 Prognostic factor analyses for head and neck adenocarcinomas using gene expression profiles  TopicSem
25 윤선민 Analysis of candidate variants in patients with side effects of L-asparaginase  TopicSem
25 박유미 An open resource of structural variation for medical and population genetics  SysBiol
25 유경훈 DGIdb 3.0: a redesign and expansion of the drug-gene interaction database  SysBiol
25 안세환 About cBioPortal on GDPortal  BioEMR
28 박유미 Gene-wise variant burden(GVB) score: additional things required to be developed  TopicSem
28 김효정 Establishment of Integrated Drug Database based on National Standards in Korea  TopicSem
28 박유미 Difference of genetic architectures in men and women with depression  xMutant
28 윤선민 Settling the score  MAInfo
30 김기태 Pathway Based Analysis of Mutation Data Is Efficient for Scoring Target Cancer Drugs     J.Club
30 민병주 An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders     J.Club

2019-02:
02 김주연 Projected impact of a multigene pharmacogenetic test to optimize medication prescribing in cardiovascular patients     J.Club
02 서명의 The malaria-protective human glycophorin structural variant DUP4 shows somatic mosaicism and association with hemoglobin levels     J.Club
04 ... 설날  TopicSem
04 ... 설날  TopicSem
07 최선 NSAIDs induced ADRs _Comorbidity analysis  TopicSem
07 권호식 HD-MTX induced renal toxicity In Pediatric Patients with ALL  TopicSem
07 김기태 Consensus Path DB  SysBiol
07 권호식 star allele assignment and annotation  MAInfo
09 유승원 Predicting protein-protein interactions using high-quality non-interacting pairs  J.Club
09 정문경   J.Club
11 김기태 Analysis of Age at onset in MDD : Optimizing the cut-off   TopicSem
11 윤선민 Analysis of candidate variants in patients with side effects of L-asparaginase  TopicSem
11 김주연 Progress in troubleshooting of LSPE study error  BioEMR
12 유승원 discussion : strategies for identification of read errors during Ion Proton based sequencing file calling workflow  xMutant
14 박유미 Evidence of indirect associations between MDD and FBF1  TopicSem
14 김주연 Synthetic association analysis with significant variants from PGx GWAS studies  TopicSem
14 김재환 Development of knowledge base (RarePedia) and software platform (VAAT & PMAT) for NGS study result based genetic counseling  MAInfo
14 김주연 Evaluation of synthetic association detection using gene deleteriousness scores in hearing loss case  SysBiol
16 정문경 Patients Know Best: Qualitative Study on How Families Use Patient-Controlled Personal Health Records     J.Club
16 유경훈 Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data     J.Club
18 ... GDA  TopicSem
18 ... GDA  TopicSem
21 ... GDA  TopicSem
21 ... GDA  TopicSem
23 채정환 Nonsynonymous Variants in PAX4 and GLP1R Are Associated With Type 2 Diabetes in an East Asian Population     J.Club
23 안세환 GenIO: a phenotype-genotype analysis web server for clinical genomics of rare diseases     J.Club
25 ... GDA  TopicSem
25 ... GDA  TopicSem
28 김효정 간섬유화 지표의 유용성 평가_연구대상 정의를 위한 탐색적분석  TopicSem
28 민병주 Determinants and prediction of antibiotic resistance genotypes of host and &H.pylori  TopicSem
28 채정환 WES seq analysis  MAInfo
28 한봄 Marker selection for genetic case-control association studies  SysBiol

2019-01:
02 권호식 discussion about HD-MTX analysis  xMutant
03 김기태 Analysis of early response in MDD: Additional variant level analysis   TopicSem
03 윤선민 Analysis of candidate variants in patients with side effects of L-asparaginase  TopicSem
03 한봄 Data quality control in genetic association studies  SysBiol
03 임영균 HCMDB data curation  MAInfo
05 권호식 ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants     J.Club
05 이우승 Forward and reverse mutations in stages of cancer development     J.Club
07 정문경 Practice webpage plan for CKD Nutrition  TopicSem
07 박유미 Finding indirect associations of tagging SNPs with MDD  TopicSem
07 김효정 Assessment of Diagnostic Usefulness of Liver Fibrosis Predictive Markers  BioEMR
08 채정환 .  xMutant
10 김효정 Genome data model for clinical utilization; review  TopicSem
10 김주연 Evaluation of gene deleteriousness scores in the confirmation synthetic association signals  TopicSem
10 윤선민 Analysis of candidate variants in patients with side effects of L-asparaginase  MAInfo
10 유경훈 Drug Targetor: a web interface to investigate the human druggome for over 500 phenotypes  SysBiol
12 최선 Active Disease Surveillance in an Electronic Health Database Using a Common Data Model Based Tool      J.Club
12 윤선민 High Yield of Pathogenic Germline Mutations Causative or Likely Causative of the Cancer Phenotype in Selected Children with Cancer     J.Club
14 최선 Forest plot  BioEMR
14 이정훈 Prediction censored data  TopicSem
14 민병주 Combined analysis of Helicobacter pylori and host cytochrome p450 system  TopicSem
15 박유미 Why do polygenic risk scores get so much hype?   xMutant
17 유경훈 Pharmacogenetics of escitalopram response: a candidate gene analysis   TopicSem
17 유승원 6MP analysis : IL6 and novel candidate variants  TopicSem
17 이정훈 Combination chemotherapy in advanced gastric cancer  SysBiol
17 김기태 Analysis of age at onset in depression  MAInfo
19 임영균 A map of constrained coding regions in the human genome     J.Club
19 한봄 Functional annotation of genomic variants in studies of late-onset Alzheimer     J.Club
21 안세환 The Mutation Significance Cutoff(MSC)  TopicSem
21 채정환 taxol_data analysis  TopicSem
21 안세환 How to use cBioPortal in GDPortal  BioEMR
22 윤선민 WES analysis of AML samples according to neutropenia duration   xMutant
24 한봄 Steroid-Induced Hyperglycemia in ALL patients  TopicSem
24 서명의 Protein domain structure and star alleles of candidate proteins for mutagenesis  TopicSem
24 김효정 Assessment of Diagnostic Usefulness of Liver Fibrosis Predictive Markers   SysBiol
25 이우승 Comparison of Inhouse CNV Algorithms and Ioncopy with Microarray CNV Data  MAInfo
26 김기태 Efficiient Parameter Estimation Enables the Prediction of Drug Response Using a Mechanistic Pan-Cancer Pathway Model     J.Club
26 민병주 Genetic Determinants and Prediction of Antibiotic Resistance Phenotypes in Helicobacter pylori     J.Club
28 이우승 Comparison of Inhouse CNV Algorithms and Ioncopy with Microarray CNV Data  TopicSem
28 최선 NSAIDs induced ADRs_additional analysis  TopicSem
29 이우승 Comparison of three variant callers(DeepVariant, GATK 4 and SpeedSeq) for WGS  xMutant
31 임영균 Distribution of population frequency and SIFT/Gene Score in in SCS genes  TopicSem
31 정문경 Avatar Beans: Summarizing Test Results - data review and ideas  TopicSem
31 박유미 Difference of genetic architectures in men and women with depression  SysBiol
31 유승원 Homopolymer error types from Ion Proton sequencer  MAInfo

2018-12:
01 서명의 Homozygous mutations in WEE2 cause fertilization failure and female infertility      J.Club
01 유승원 In silico profiling of systemic effects of drugs to predict unexpected interactions     J.Club
03 박유미 Summary of replication study gene-level results for patients with variant angina  TopicSem
03 안세환 VVA Plots include Protein domains  TopicSem
04 유승원 Questions about SKAT test  xMutant
06 이정훈 TP53 mutation with SYNE2 or SON mutation had Synergistic effect for paclitaxel, and predictive for prognosis in urogenital cancer  TopicSem
06 김주연 Evaluation of candidate SAGs with focus on drug-gene interactions  TopicSem
06 김기태 Analysis of Early response in depression  SysBiol
06 채정환 practice:understanding of TCGA data compared with taxol seq-data  MAInfo
06 채정환 practice:understanding of TCGA data compared with taxol seq-data  MAInfo
08 채정환 Germline Genetic IKZF1 Variation and Predisposition to Childhood Acute Lymphoblastic Leukemia     J.Club
08 한봄 Evaluating Variant Calling Tools for Non-Matched Next-Generation Sequencing Data.     J.Club
10 민병주 Application of next‑generation sequencing to analyze H pylori and host interactions  TopicSem
10 유경훈 Pharmacogenetics of escitalopram response: a candidate gene analysis   TopicSem
10 안세환 VVA background data of protein domians  BioEMR
11 유경훈 FLASK micro web framework in python  xMutant
11 이정훈 FLASK micro web framework in python  xMutant
13 유승원 6MP analysis from two perspectives  TopicSem
13 김효정 Construction of HLA Database (GDM)  TopicSem
13 최선 Comorbidity adjustment in clinical data  MAInfo
13 최선 Comorbidity adjustment in clinical data  MAInfo
13 김주연 ITPA gene variants protecting against anemia as a case of synthetic association  SysBiol
15 정문경 Advancing Models and Theories for Digital Behavior Change Interventions     J.Club
15 이정훈 Pathway-Based Drug Repositioning for Cancers: Computational Prediction and Experimental Validation     J.Club
17 채정환 taxol-ADR  TopicSem
17 권호식 HD-MTX induced renal toxicity in pediatric ALL  TopicSem
17 정문경 Defining a staged-based process for economic and financial evaluations of mHealth programs  BioEMR
17 정문경 Defining a staged-based process for economic and financial evaluations of mHealth programs  BioEMR
18 유경훈 Rare variants in drug target genes contributing to complex diseases, phenome-wide  xMutant
20 최선 NSAIDs induced ADRs detected by K-CDM_additional analysis  TopicSem
20 이우승 The Progsotic Potential of Loss of Heterozygosity in Breast Invasive Carcinoma   TopicSem
20 안세환 Protein domain layer in VVA Plot  SysBiol
22 박유미 Estimating the selective effects of heterozygous protein-truncating variants from human exome data     J.Club
22 안세환 PopViz: a webserver for visualizing minor allele frequencies and damage prediction scores of human genetic variations     J.Club
24 서명의 Protein domain structure of activity assay candidate proteins  TopicSem
24 임영균 Relation between SCS and metastasis  TopicSem
26 임영균 Identification of Synthetic Cancer Survival and Synthetic Cancer Survival Burden in Lung Adenocarcinoma  Seminar
26 김기태 Dopaminergic and noradrenergic system, Neurotransmission and Brain-related genes are associated with treatment response in 1,000 Korean patients with Major Depressive Disorder.   Seminar
26 이우승 The Progsotic Potential of Loss of Heterozygosity in Breast Invasive Carcinoma  Seminar
26 박유미 Evaluating the utility of PGS as a predictor for 6-mercaptopurine intolerance in pediatric ALL patients  Seminar
26 김형준 Healthavatar platform for conserving originality and secure exchange of personal health record with consortium blockchain  Seminar
26 윤선민 L-asparaginase induced acute pancreatitis in pediatric ALL patients  Seminar
26 김주연 Variants contributing to adverse drug reactions through synthetic association  Seminar
26 김효정 Constructing an Integrated Drug Database for Utilization of Public Data in Korea  Seminar
26 이정훈 TP53 synthetic cytotoxic network for paclitaxel is a biomarker for chemotherapeutic response and prognosis of urogenital cancer  Seminar
27 ... 리트릿  TopicSem
27 ... 리트릿  TopicSem
27 유경훈 Pharmacogenetics of escitalopram response: a candidate gene analysis  Seminar
27 유승원 6MP-related side effect analysis with normal NUDT15,TPMT phenotype   Seminar
27 권호식 High dose MTX induced renal toxicity in pediatric acute lymphoblastic leukemia   Seminar
27 안세환 Gene-centered Visualization and Annotation for Exome Variant Analysis(VVA) using GDM  Seminar
27 한봄 Steroid-Induced Hyperglycemia in ALL patients  Seminar
27 김재환 RarePedia: A knowledge base for biomedically coherent query result  Seminar
27 채정환 Taxol induced adverse drug reaction in patient with various types of cancer  Seminar
27 정문경 A study protocol to examine the effect of a smartphone-based self-management support system for hemodialysis patients.  Seminar
27 최선 Evaluating the severity of NSAIDs induced adverse effects by K-CDM in nine institutes  Seminar
29 김효정 Accuracy of an automated knowledge base for identifying drug adverse reactions     J.Club
29 권호식 ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants     J.Club
31 한봄 Carbamazepine-induced SCAR  TopicSem
31 김효정 Accuracy of an automated knowledge base for identifying drug adverse reactions  TopicSem
31 김주연 Addressing issues of applying the Large-Scale Population-Level Evidence Generation study in K-CDM  BioEMR

2018-11:
01 박유미 Understanding the sex bias in major depressive disorder : The male protective effect model  TopicSem
01 김주연 Progress in validation of synthetic association between candidate SAG and PGx variants  TopicSem
03 임영균 Network Propagation Predicts Drug Synergy in Cancers     J.Club
03 이우승 The chromatin accessibility landscape of primary human cancers     J.Club
05 안세환 How to visualize protein domain in VVA  TopicSem
05 김효정 .Genome Data Model for Clinical Utilization   TopicSem
05 정문경 Avatar Beans: UI for the elderly  BioEMR
05 김기태 er  Seminar
06 채정환 variant study of taxol-ADR analysis  xMutant
06 채정환 variant study of taxol-ADR analysis  xMutant
08 민병주 Detection of CYP2C19 Gene Polymorphisms in host and 16S/23S rRNA gene Polymorphisms in H.pylori  TopicSem
08 유경훈 Subgroup analysis based on antidepressant prescription information of 1000 MDD patients   TopicSem
08 유경훈 Analysis of population-specific pharmacogenomic variants using next-generation sequencing data  SysBiol
10 최선 MedEx: a medication information extraction system for clinical narratives     J.Club
10 권호식 Intersect-then-combine approach: improving the performance of somatic variant calling in whole exome sequencing data using multiple aligners and callers     J.Club
12 채정환 taxol-ADR analysis study  TopicSem
12 이정훈 Linking the Regulatory Network of Gene Modules to Drug Sensitivity Reveals that Docetaxel and 5-FU Have a Synergistic Effect in Advanced Gastric Cancer  TopicSem
13 박유미 Genome-wide meta-analysis of depression in 807,553 individuals identifies 102 independent variants with replication in a further 1,507,153 individuals  xMutant
15 유승원 6MP analysis with normal NUDT15,TPMT phenotype   TopicSem
15 권호식 preliminary investigation : Variants and Genes related with adverse effects of MTX  TopicSem
15 이정훈 ConnectivityMAP database in CLUE portal  SysBiol
15 유승원 discussions : rare variant tests(burden test)  MAInfo
17 민병주 Application of next-generation sequencing to characterize novel mutations in clarithromycin-susceptible Helicobacter pylori strains with A2143G of 23S rRNA gene     J.Club
17 김주연 Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes     J.Club
19 최선 NSAIDs adverse effects detected by K-CDM  TopicSem
19 이우승 Analysis of LOH Affecting Breast Cancer Survival   TopicSem
19 김주연 Application of the Large-Scale Population-Level Evidence Generation R package in K-CDM  BioEMR
20 윤선민 WES analysis of AML samples according to neutropenia duration   xMutant
22 서명의 Chromogenic activity evaluation in catalytic domain of FX  TopicSem
22 임영균 Identification of Synthetic Cancer Survival and Synthetic Cancer Survival Burden in Lung Adenocarcinoma  TopicSem
22 김효정 Query design strategy for detecting NSAIDs induced ADRs   SysBiol
22 권호식 Variants related with MTX-induced renal toxicity or HDMTX from research papers  MAInfo
24 유경훈 An optimized prediction framework to assess the functional impact of pharmacogenetic variants     J.Club
24 김기태 Pathway-structured predictive modeling for multi-level drug response in multiple myeloma     J.Club
26 정문경 Avatar Beans - Symptom Survey  TopicSem
26 한봄 Steroid-Induced Hyperglycemia  TopicSem
26 김효정 Basic exploratory analysis strategies using SQL   BioEMR
27 이우승 PEPTATAC : A robust ATAC-seq pipeline  xMutant
29 김기태 Analysis of early response in depression  TopicSem
29 윤선민 L-asparaginase induced acute pancreatitis in 26 pediatric ALL patients  TopicSem
29 박유미 Descriptive data analysis: in vitro functionality of 337 PGx variants  SysBiol
29 김재환 Rarepedia & Genetic variant annotation assistant tool (VAAT) at Laboratory Medicine Annual Meeting 2018  MAInfo

2018-10:
01 이수현   TopicSem
01 유경훈 Subgroup analysis based on antidepressant prescription information of 1000 MDD patients   TopicSem
01 안세환 Changed result table of VVA using GDM  BioEMR
01 이우승 Accurate genotyping across variant classes and length using variant graphs  xMutant
04 권호식 GDM visualization on the web  TopicSem
04 민병주 Optimal design of Helicobacter Pylori amplicon panel target region  TopicSem
04 박유미 Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions  SysBiol
04 최선 Introduction to clinicaltrials.gov DB  MAInfo
06 유승원 Mapping biological process relationships and disease     J.Club
06 채정환 ANGPTL3 Deficiency and Protection Against Coronary Artery Disease     J.Club
08 김주연 Evaluation of the candidate genes in synthetic association to tacrolimus ADR biomarkers  TopicSem
08 안세환 Upgraded VVA Table using GDM  TopicSem
08 최선 Korea public health big data status  BioEMR
08 이정훈 skin classification  xMutant
11 채정환 revision of taxol-ADR project analysis  TopicSem
11 유승원   TopicSem
11 임영균 Variants calling workflow with GATK4   MAInfo
11 김기태 Geneset Deleterious Burden Analysis (GS-DBA)  SysBiol
13 박유미 Trans effects on gene expression can drive omnigenic inheritance     J.Club
13 정문경 THE IMPACT OF INTERPERSONAL CLOSENESS CUES IN TEXT-BASED HEALTHCARE CHATBOTS ON ATTACHMENT BOND AND THE DESIRE TO CONTINUE INTERACTING: AN EXPERIMENTAL DESIGN       J.Club
15 ... 개교기념일  TopicSem
15 ... 개교기념일  TopicSem
15 김주연 Evaluating relation between isoniazid and liver injury using KCDM  BioEMR
15 김주연 Evaluating association between isoniazid and liver injury using KCDM  BioEMR
16 유승원 discussion : workflow for 6MP analysis  xMutant
18 최선 AvatarBeans_Initial draft and considering issues  TopicSem
18 Kelsey Self-Introduction and summary of past research (Genome sequencing and protein domain annotations of Korean Hanwoo cattle identify Hanwoo-specific immunity-related and other genes)  TopicSem
18 김주연 Characteristics of candidate SAGs with regard to ethnicity  SysBiol
18 김기태 Analysis of onset age in depression  MAInfo
20 이정훈 Synthetic Lethality-based Identifcation of Targets for Anticancer Drugs in the Human Signaling Network     J.Club
20 한봄 MediSyn: uncertainty-aware visualization of multiple biomedical datasets to support drug treatment selection     J.Club
22 이우승 Analysis of LOH Affecting Cancer Survival  TopicSem
22 서명의 Chromogenic activity of FX protein with variants and related protein structure  TopicSem
22 김효정 Query design for NSAIDs induced adverse drug reactions  BioEMR
23 유경훈 ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants  xMutant
23 김기태 AOS in MDD  Seminar
23 유경훈 depression  Seminar
23 김기태 EarlyResponse  Seminar
25 임영균 Identification of SCS pairs in public pancreatic cancer data  TopicSem
25 한봄 Steroid-induced Hyperglycemia  TopicSem
25 안세환 The Cochran-Armitage Trend Test(CATT) in result table of VVA  SysBiol
25 이우승 TNBC Analysis of LOH Affecting Cancer Survival  MAInfo
27 안세환 VarCards: an integrated genetic and clinical database for coding variants in the human genome     J.Club
27 김효정 Towards Implementation of OMOP in a German University Hospital Consortium     J.Club
29 정문경 Avatar Beans: Test Result UI update/Visualization  TopicSem
29 김기태 Analysis of Early response in depression  TopicSem
29 안세환 Re-Calculate Allele Frequency of VVA result Table  BioEMR
30 권호식 HGVS nomenclature  xMutant

2018-09:
01 권호식 The landscape of genomic alterations across childhood cancers     J.Club
01 이우승 Evaluation of in silico algorithms for use with ACMG/AMP clinical variant interpretation guidelines     J.Club
03 유경훈 Subgroup analysis based on antidepressant prescription information of 1000 MDD patients   TopicSem
03 유승원 6MP sensitivity analysis  TopicSem
03 유경훈 depression  Seminar
04 권호식 KOVA : Korean Variant Archive  xMutant
06 안세환 Add VEP data to VVA  TopicSem
06 채정환 drug reaction analysis in cancer patient  TopicSem
06 한봄 Study of Glucocorticoid-Induced Diabetes Mellitus  SysBiol
08 임영균 Tumor Mutational Burden and Efficacy of Nivolumab Monotherapy and in Combination with Ipilimumab in Small-Cell Lung Cancer     J.Club
08 김기태 Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines     J.Club
10 서명의 Measuring activity of chromogenic FX protein with target variant  TopicSem
10 이우승 Analysis of LOH Affecting Cancer Survival  TopicSem
10 한봄 Analysis design considering clinical information  BioEMR
11 채정환 taxol-ADR data analysis(FDR/OR statistics)  xMutant
12 김기태 depression  Seminar
12 유경훈 depression  Seminar
13 권호식 GDM conversion and visualization  TopicSem
13 임영균 Features associated immune checkpoint inhibitor  TopicSem
13 이정훈 TP53 Paclitaxel SC Network is Prognostic Factor on Urogenital Cancers  SysBiol
13 유승원 study : exploration of non-linear method(Random Forest) for 6MP dose prediction(  MAInfo
15 유경훈 Covariate selection for association screening in multiphenotype genetic studies     J.Club
15 민병주 Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term Outcomes     J.Club
17 정문경 Avatar Beans - Test Result Page & UI flow revision  TopicSem
17 한봄 Steroid-Induced Hyperglycemia  TopicSem
17 정문경 Avatar Beans Nutrition - questionnaire design  BioEMR
17 정문경 Avatar Beans Nutrition - questionnaire design  BioEMR
18 박유미 Reviewing the clinical utility of polygenic risk score  xMutant
20 김기태 Analysis of Early response in depression  TopicSem
20 박유미 Summary of replication study results for patients with variant angina  TopicSem
20 유경훈 Integrating rare genetic variants into pharmacogenetic drug response predictions  SysBiol
20 김기태 우울증회의자료  Seminar
20 권호식 Study : Leukemia and Anticancer drugs  MAInfo
22 ... 추석     J.Club
22 ... 추석     J.Club
24 ... 추석  TopicSem
24 ... 추석  TopicSem
27 김효정 GDM; operational manager menu design   TopicSem
27 이정훈 NGS Sequencing to Detect Genetic Biomarker of Busulfan Induced Hepatotoxicity  TopicSem
27 김효정 GDM DB migration to NGS server  SysBiol
27 김효정 GDM DB migration to NGS server  SysBiol
27 채정환 Myocardial infarction based study  MAInfo
29 김주연 Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum     J.Club
29 서명의 A dominantly inherited 5` UTR variant causing methylation-associated silencing of BRCA1 as a cause of breast and ovarian cancer      J.Club

2018-08:
02 이우승 Analysis of LOH Affecting Cancer Survival  TopicSem
02 채정환 Breast cancer patient analysis using TCGA database   TopicSem
02 박유미 Worldwide Distribution of Cytochrome P450 Alleles  SysBiol
02 한봄 DrugWatch: Drugs and Defective Medical Devices  BioEMR
04 정문경 Histidine catabolism is a major determinant of methotrexate sensitivity       J.Club
04 한봄 Applications of pharmacogenomics in regulatory science: a product life cycle review     J.Club
06 서명의 Overexpression of FX protein with target variant  TopicSem
06 임영균 SCS analysis in Pancreatic cancer  TopicSem
06 김재환 유전체기반 정밀의료를 위한 진료업무흐름 제안 및 소프트웨어 개발  MAInfo
07 이우승 Preprocessing Pipelines of PacBio and Nanopore Sequencing Data  xMutant
09 김형준 Updated process of HealthAvatar Agent API  TopicSem
09 정문경 Avatar Beans Nutrition - progress & more UX/UI ideas  TopicSem
09 김주연 Using TCGA for validation of synthetic association   SysBiol
09 김주연 Progress in evaluating relation between isoniazid and liver injury  BioEMR
11 유승원 In silico Pathway Activation Network Decomposition Analysis (iPANDA) as a method for biomarker development     J.Club
11 이정훈 Classifying tumors by supervised network propagation     J.Club
13 박유미 Deriving the contribution of NUDT15 variants to enzymatic activity using a functional gene-level score  TopicSem
13 김기태 Analysis of Early response in depression  TopicSem
14 이정훈 Basal like triple negative breast cancer is susceptible to drugs targeting cell cycle and histone acetylation.  xMutant
14 이정훈 Basal like triple negative breast cancer is susceptible to drugs targeting cell cycle and histone acetylation.  xMutant
14 이정훈 Basal like triple negative breast cancer is susceptible to drugs targeting cell cycle and histone acetylation.  xMutant
14 이정훈 Basal like triple negative breast cancer is susceptible to drugs targeting cell cycle and histone acetylation.  xMutant
14 이정훈 Basal like triple negative breast cancer is susceptible to drugs targeting cell cycle and histone acetylation.  xMutant
16 한봄 Drug induced hyperglycemia  TopicSem
16 김효정 Constructing an Integrated National Standard Drug Database for Utilization of Public Data in Korea  TopicSem
16 김형준 Process for patient data storage in Healthavatar Platform  BioEMR
16 김기태 Age of onset in MDD  SysBiol
18 박유미 Loose ends: almost one in five human genes still have unresolved coding status     J.Club
18 이수현 Analysis of safety reporting requirements during medical device clinical trials in Japan.     J.Club
20 이정훈 Synthetic Cytotoxic Network based Supervised Network Propagation Approach Can Identify Paclitaxel Response of Cell Lines  TopicSem
20 김주연 Trial of validating genes with variants in synthetic association to PGx biomarkers using TCGA  TopicSem
20 김기태 [Review]Variant caller  MAInfo
21 유승원 Introduction to COXPRES db  xMutant
23 이수현 K-CDM & K-Sentinel: Progression of active pharmacovigilance system in Korea  TopicSem
23 민병주 Application of custom oligo to analyze 16S, 23S rRNA in Helicobacter Pylori  TopicSem
23 안세환 Add knowledge bases to VVA plot  SysBiol
23 유경훈 depression  Seminar
24 김효정 GDM Update notes  BioEMR
25 안세환 Gene Graphics: a genomic neighborhood data visualization web application     J.Club
25 김효정 Genomic decision support needs in pediatric primary care     J.Club
27 ... GDA  TopicSem
27 ... GDA  TopicSem
28 유경훈 SEQSpark: A Complete Analysis Tool for Large-ScaleRare Variant Association Studies  xMutant
30 ... GDA  TopicSem
30 ... GDA  TopicSem
30 김기태 회의자료  Seminar

2018-07:
02 안세환 VVA plot using GDM  TopicSem
02 채정환 Current work and future plan  TopicSem
02 유승원 circRNA : potential therapeutic target  MAInfo
02 송유림 석사학위논문  Seminar
02 유경훈 depression  Seminar
03 유승원 6MP analysis : questions, discussions  xMutant
05 임영균 Characteristics of germline SCS pair   TopicSem
05 서명의 DNA transfection to 293 cell line for overexpression of FX with the variants  TopicSem
05 유경훈 Interpretation of genes related to early response by antidepressant group  SysBiol
05 김주연 Evaluation of ADR signal detected using K-CDM and KAERS reports  BioEMR
05 김주연 Evaluation of ADR signal detected using K-CDM and KAERS reports  BioEMR
07 김효정 Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings     J.Club
07 임영균 Systematic analysis of complex genetic interactions     J.Club
09 이우승 Survival Analysis- Cox Proportional Hazard of TNBC Analysis   TopicSem
09 정문경 Nutrition in Avatar Beans - Protein and Iron  TopicSem
09 이우승 Copy Number Alteration Visualization  MAInfo
12 김형준 Process of uploading data in GDM and Web portal   TopicSem
12 한봄 Drug-induced Hyperglycemia  TopicSem
12 김효정 Comparing Attributes of GDM and Variant File Format     BioEMR
12 이정훈 NGS biomarker for busulfan ADR  SysBiol
12 이정훈 NGS biomarker for busulfan ADR  SysBiol
14 안세환 Genome U-Plot:a whole genome visualization     J.Club
14 김주연 Impact of germline and somatic missense variations on drug binding sites     J.Club
15 김기태 임시파일  Seminar
16 김기태 Analysis of Early response in depression  TopicSem
16 박유미 Identifying potential major depressive disorder associated genes  TopicSem
16 권호식 Mutational Signatures of COSMIC  MAInfo
17 권호식 GDM Visualization using maftools  xMutant
19 김효정 Genomic Data Model for Clinical Utilization   TopicSem
19 이정훈 Bipartite approach for Metalab DRUG-ADR network  TopicSem
19 한봄 Steroid Induced Hyperglycemia  SysBiol
19 안세환 Modify VVA part interface of GDM portal  BioEMR
21 김기태 Relationship between Deleterious Variation, Genomic Autozygosity, and Disease Risk: Insights from The 1000 Genomes Project     J.Club
21 민병주 Germline de novo mutation clusters arise during oocyte aging in genomic regions with high double-strand-break incidence     J.Club
23 이수현 Warfarin and NOAC (Novel Oral AntiCoagulants) analysis using K-CDM PV  TopicSem
23 김주연 Statistics and interpretation of genes with variants in synthetic association to PGx variants  TopicSem
23 채정환 breast cancer patient RNA-seq data analysis  MAInfo
24 채정환 breast cancer patient SNV analysis  xMutant
24 채정환 breast cancer patient SNV analysis  xMutant
24 채정환 breast cancer patient SNV analysis  xMutant
24 유경훈 The VAAST Variant Prioritizer (VVP)  xMutant
26 유경훈 Subgroup analysis based on antidepressant prescription information of 1000 MDD patients   TopicSem
26 유승원 6MP side effect analysis : pediatric ALL patients  TopicSem
26 김효정 [review] A standard database for drug repositioning  SysBiol
26 정문경 Getting updated FoodDB - web scraping & cleaning data  BioEMR
28 서명의 Functional assays are essential for interpretation of missense variants associated with variable expressivity     J.Club
28 채정환 Association Between SLC16A5 Genetic Variation and Cisplatin Induced Ototoxic Effects in Adult Patients With Testicular Cancer     J.Club
30 민병주 Application of NGS to characterize genetic variants in Helicobacter pylori strains and host genome  TopicSem
30 안세환 Modified VVA Interface  TopicSem
31 박유미 Common Disease Is More Complex Than Implied by the Core Gene Omnigenic Model  xMutant

2018-06:
02 한봄 Cost-effectiveness of HLA-DQB1/HLA-B pharmacogenetic-guided treatment and blood monitoring in US patients taking clozapine     J.Club
02 정문경 First-Stage Development and Validation of a Web-Based Automated Dietary Modeling Tool: Using Constraint Optimization Techniques to Streamline Food Group and Macronutrient Focused Dietary Prescriptions     J.Club
04 이우승 Progress in SNUH TNBC Survival Analysis   TopicSem
04 정문경 Avatar Beans - planning additional function re nutrition  TopicSem
04 권호식 Leukemia WXS Conversion  MAInfo
05 박유미 Potentially susceptible genes to major depressive disorder  xMutant
07 임영균 TMB and Tumor immune in SCS  TopicSem
07 김형준 Current process of uploading data in GDM  TopicSem
07 박유미 Current progress and future prospects in organoid research  SysBiol
07 안세환 GDM and VVA  BioEMR
09 채정환 methylation of l1re1, rarb, and rassf1 function as possible biomarkers for the differential diagnosis of lung cancer.     J.Club
09 박유미 Whole Exome Sequencing in 20,197 Persons for Rare Variants in Alzheimer Disease     J.Club
11 서명의 1000 genome variants in CYP2C19 gene  TopicSem
11 한봄 Tumor-only analysis on rare cancer samples  TopicSem
11 채정환 Tumor microenvironment  MAInfo
12 윤선민 WES analysis of AML samples according to neutropenia duration   xMutant
14 윤선민 L-asparaginase associated acute pancreatitis in pediatric ALL patients  TopicSem
14 김효정 GDM: Progress on operational level   TopicSem
14 정문경 Research & problems of mHealth technology for CKD  BioEMR
16 이정훈 Individual specific edge-network analysis for disease prediction     J.Club
16 이수현 Large-scale adverse effects related to treatment evidence standardization (LAERTES): an open scalable system for linking pharmacovigilance evidence sources with clinical data     J.Club
18 김기태 Analysis of Early response in depression  TopicSem
18 박유미 Identifying potential major depressive disorder associated genes  TopicSem
18 임영균 pVACseq:A cancer immunotherapy pipeline for identifying and prioritizing neoantigens from a list of tumor mutations  MAInfo
19 이우승 Survival Analysis-Cox Proportional-Hazards of TNBC Analysis   xMutant
21 김주연 Interpretation of genes with variants in synthetic association to ADR biomarkers  TopicSem
21 민병주 Ampliseq based ADR(+ PGx SNP) targeted panel  TopicSem
21 김주연 Signatures and examples of synthetic association  SysBiol
21 한봄 Choosing Wisely  BioEMR
21 김주연 Signatures and examples of synthetic association  SysBiol
23 유경훈 Identification of Misclassified ClinVar Variants via Disease Population Prevalence     J.Club
23 김형준 Secure and Trustable Electronic Medical Records Sharing using Blockchain     J.Club
25 이정훈 Link regulatory networks of gene modules to drug sensitivity reveals that Docetaxel and 5-FU have combined effects in advanced stage gastric cancer  TopicSem
25 이수현 K-CDM Pharmacovigilance (K-CDM PV)  TopicSem
25 김기태 UCSC Xena:Analysis tools for cancer   MAInfo
26 이정훈 Radiogenomics for TNBC: Relationship between Microarray profile and radiomics texture data  xMutant
28 유경훈 Subgroup analysis based on antidepressant prescription information of 1000 MDD patients  TopicSem
28 유승원 6MP project analysis : candidate genes and variants  TopicSem
28 안세환 Apply VVA to GDM  SysBiol
28 김형준 GDM database and web  BioEMR
30 권호식 Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes     J.Club
30 이우승 Negative selection in tumor genome evolution acts on essential cellular functions and the immunopeptidome     J.Club

2018-05:
01 이정훈 WXS for leukemia busulfan-VOD  xMutant
03 김형준 Healthavatar and Agents with Blockchain  TopicSem
03 정문경 Ideas for project: connecting nutrition data with clinical information  TopicSem
03 한봄 Tumor-only analysis on rare cancer samples  SysBiol
03 안세환 clinical data for VVA  BioEMR
05 ... 공휴일  J.Club
05 ... 공휴일  J.Club
07 ... 공휴일  TopicSem
07 ... 공휴일  TopicSem
07 윤선민 WES analysis of AML samples according to prolonged neutropenia duration  MAInfo
08 유승원 Work flow discussion  xMutant
10 한봄 Tumor-only Analysis on Rare Cancer Samples  TopicSem
10 김기태 Analysis of response in depression : EN-RN vs. EY-RY  TopicSem
10 안세환 Knowledge Bases for VVA  SysBiol
10 한봄 Leukemia WXS data annotation  BioEMR
12 유경훈 Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression     J.Club
12 민병주 Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy     J.Club
14 윤선민 WES analysis of AML samples according to neutropenia duration   TopicSem
14 박유미 Deriving the contribution of TPMT variants to enzymatic activity using a functional gene-level score  TopicSem
15 유경훈 Patients subgrouping by antidepressant prescription  xMutant
16 김기태 EN-RNvs.EY-RYanalysis in depression  MAInfo
16 김기태 ENvs.EYanalysis in depression  MAInfo
16 김기태 summary  MAInfo
17 김효정 Standard Query Design for an Active ADR Signal Detection Knowledge Pipeline  TopicSem
17 이정훈 Link regulatory networks of gene modules to drug sensitivity reveals that Docetaxel and 5-FU have opposite effects in advanced stage gastric cancer  TopicSem
17 유경훈 Review: Ki Database  SysBiol
17 김형준 GA4GH and Google genomics  BioEMR
19 서명의 Antisense therapy for a common corneal dystrophy ameliorates TCF4 repeat expansion-mediated toxicity     J.Club
19 박지연 Machine Learning Identifies Stemness Features Associated with Oncogenic Dedifferentiation     J.Club
21 유승원 6MP-related neutropenia analysis2  TopicSem
21 이수현 RS-ADR: A reference standard for detection of adverse drug reaction signals using electronic health records database and web site demo   TopicSem
21 이우승 Clinical Feature Selection for Cox Proportional-Hazards Mode in SNUH TNBC Analysis  MAInfo
24 민병주 Somatic second hit mutation candidates in CNV-PTC patients  TopicSem
24 유경훈 Subgroup analysis based on antidepressant prescription information of 1000 MDD patients  TopicSem
24 이정훈 A Next Generation Connectivity-Map L1000 for drug treatment profiles  SysBiol
24 김주연 Use of K-CDM and KAERS report for proactive surveillance of ADRs  BioEMR
26 김주연 Patient-Centered Precision Health In A Learning Health Care System: Geisinger’s Genomic Medicine Experience     J.Club
26 유승원 Systematic identification of feature combinations for predicting drug response with Bayesian multi-view task linear regression     J.Club
28 박지연 mRNA processing analysis in thyroid cancer  TopicSem
28 김주연 Characteristics of genes synthetically associated to ADR biomarkers   TopicSem
28 유승원 introduction : A pathway-centric approach to rare variant association analysis  MAInfo
29 채정환 review; Introduction to bioinformatics algorithms  xMutant
31 안세환 Add knowledge bases to VVA  TopicSem
31 채정환 ongoing project and paper review  TopicSem
31 김효정 TCGA Clinical Data Structure Review   SysBiol
31 김효정 GDM Engine; operational manager menu design  BioEMR

2018-04:
02 한봄 Tumor-only analysis on rare cancer samples  TopicSem
02 김기태 Prediction of response in depression  TopicSem
02 정문경 PRISMA: guidlines for systematic reviews  MAInfo
02 정문경 Leukemia QC and Annotation  MAInfo
02 권호식 Leukemia QC and Annotation  MAInfo
03 채정환 network analysis tools review(cytoscape)  xMutant
05 임영균 GDM analytics  TopicSem
05 박유미 Assessment of Ergonovine-Induced drug hypersensitivity reactions in the diagnosis of Coronary Artery Spasm using resampling validation method  TopicSem
05 박유미 Functionalization of Variants in Clinically Actionable Pharmacogenes (F-CAP)  SysBiol
05 김형준 Python script for uploading data in GDM  BioEMR
07 윤선민 Lessons learned from additional research analyses of unsolved clinical exome cases     J.Club
07 권호식 Analysis of a gene panel for targeted sequencing of colorectal cancer samples     J.Club
09 김효정 Genome data model for clinical use   TopicSem
09 이정훈 Inference of Digenic Disruption Networks for Synthetic Cytotoxicity  TopicSem
09 정문경 Research Interest & Exploring TCGA data  MAInfo
10 박유미 Evaluation of drug scores in antidepressants  xMutant
12 김민정 Extreme cases of CD - risc patients analysis   TopicSem
12 이수현 Review of previous studies for ADR reference and RS-ADR web page design  TopicSem
12 김효정 Exploratory analysis: KAERS dataset   SysBiol
12 김주연 Generating evidence for the comparative effectiveness of treatment pairs using the LargeScalePopEst R package  BioEMR
12 김주연 Generating evidence for the comparative effectiveness of treatment pairs using the LargeScalePopEst R package  BioEMR
12 김주연 Generating evidence for the comparative effectiveness of treatment pairs using the LargeScalePopEst R package  BioEMR
14 이우승 Pan-cancer analysis reveals technical artifacts in TCGA germline variant calls     J.Club
14 김형준 MedRec Using Blockchain for Medical Data Access and Permission Management     J.Club
16 박지연 Update of alternative splicing analysis using RNA-seq data  TopicSem
16 김주연 Extracting genes with variants in synthetic association to PGx variants  TopicSem
16 채정환 coding and non-coding gene variants associated with gene expression and outcome in breast cancer subtypes  MAInfo
17 윤선민 WES analysis of AML samples according to prolonged neutropenia duration  xMutant
19 민병주 CNV-PTC in a family with compound heterozygous APC gene mutations  TopicSem
19 유경훈 1T Depression Analysis: Patients characterization and subgrouping by prescribed drugs   TopicSem
19 김기태 Analysis of onset age in depression  SysBiol
19 김기태 Analysis of onset age in depression_meet  SysBiol
19 김효정 Schema matching & comparison of completeness; between KIDS-KD and generated KAERS report  BioEMR
21 이수현 Medication class enrichment analysis: a novel algorithm to analyze multiple pharmacologic exposures simultaneously using electronic health record data     J.Club
21 임영균 Perspective on Oncogenic Processes at the End of the Beginning of Cancer Genomics      J.Club
22 임영균 Moonlight: a tool for biological interpretation and driver genes discovery  MAInfo
23 유승원 6MP-related neutropenia of pediatric ALL patients  TopicSem
23 안세환 Add advanced features to VVA  TopicSem
24 이우승 Ewing Sarcoma Diagnostic Analysis   xMutant
26 채정환 current interesting issue and overall survival analysis  TopicSem
26 이우승 Comprehensive genetic alteration profiling for Triple-negative Breast Cancer patients by targeted kinome sequencing  TopicSem
26 김주연 Evaluation of extracting genes with variants in synthetic association to ADR biomarkers  SysBiol
26 정문경 PRISMA: guideline for systematic research  BioEMR
28 김기태 An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome Analytics     J.Club
28 김민정 Pan-cancer analysis of bi-allelic alterations in homologous recombination DNA repair genes     J.Club
30 서명의 Mutagenesis and transformation for FX chromogenic activity assay  TopicSem
30 임영균 GDM Analytics Annotation DB  TopicSem
30 박지연 Bioinformatic tools for transcript quantification and alternative splicing  MAInfo

2018-03:
01 ... 공휴일  TopicSem
01 ... 공휴일  TopicSem
03 서명의 Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium     J.Club
03 박지연 Identification of protein features encoded by alternative exons using Exon Ontology     J.Club
05 류영재 Allele matcher scoring scheme alterations  TopicSem
05 김주연 Interpretation of PGx variant candidate SAGs  TopicSem
05 이우승 oncopy: a novel method for calling copy number alterations in amplicon sequencing data including significance assessment  MAInfo
06 유승원 VarDrugPub : Deep learning of mutation-gene-drug relations from the literature  xMutant
08 김민정 annotating and using SIFT scores for analyzing depressive patients  TopicSem
08 이수현 Data-driven knowledgebase for pharmacovigilance using electronic health records database  TopicSem
08 안세환 VVA review and future work  SysBiol
08 안세환 VVA review and future work  SysBiol
08 안세환 VVA review and future work  SysBiol
08 김효정 K-CDM Genome Data Model Fine Tuning   BioEMR
10 유승원 A framework for the detection of de novo mutations in family-based sequencing data     J.Club
10 채정환 Deep learning improves prediction of CRISPR-Cpf1 guide RNA activity     J.Club
12 박지연 Alternative mRNA processing in Thyroid cancer  TopicSem
12 이정훈 Inference of Digenic Disruption Networks for Synthetic Cytotoxicity  TopicSem
12 유승원 Computing tumor trees from single cells-oncoNEM  MAInfo
13 김민정 intra-individual correlation and inter individual correlation using ANCOVA  xMutant
13 김형준 GDM process of importing data  BioEMR
15 민병주 Maternal Insertion of APC gene in female CMV-PTC patients  TopicSem
15 유경훈 1T Depression Analysis: Patients characterization and subgrouping by prescribed drugs  TopicSem
15 한봄 Tumor-only analysis on rare cancer samples  SysBiol
15 안세환 How to trasfer blood dialyzer data to patients using OCR  BioEMR
17 한봄 Evaluating somatic tumor mutation detection without matched normal samples     J.Club
17 정문경 Genomic Landscape of Cell-Free DNA in Patients with Colorectal Cancer       J.Club
19 유승원 6MP-related neutropenia of pediatric ALL patients  TopicSem
19 안세환 Future works of VVA  TopicSem
19 김형준 GDM process of importing data  BioEMR
20 유경훈 KRGdb database overview  xMutant
22 채정환 My current work and future plan  TopicSem
22 이우승 Comparing Genotyping Method with BLAST aligned bam on Sangerseq data  TopicSem
22 유경훈 Sub-group of SIOH patient groups according to drug response record.  SysBiol
22 정문경 Review of BloodPAC Database Structure  BioEMR
22 정문경 Review of BloodPAC data dictionary  BioEMR
24 이정훈 Link synthetic lethality to drug sensitivity of cancer cells     J.Club
24 박유미 The Medical Genome Reference Bank: a whole genome data resource of 4,000 healthy elderly individuals. Rationale and cohort design     J.Club
26 서명의 Additional variant selection for FX chromogenic activity assay  TopicSem
26 윤선민 Modified workflow and statistical methods for AAP analysis  TopicSem
27 권호식 xCell : cell types enrichment analysis  xMutant
28 김기태 iCAGES:integrated Cancer GEnome Score for comprehensively prioritizing driver genes in personal cancer genomes  MAInfo
29 김형준 Smart contract and Dapp in Healthavatar platform  TopicSem
29 정문경 Concepts on Visual Display of Quantitative Information by Edward Tufte  TopicSem
29 이정훈 RS-ADR data portal development, Firebase & vue.js  SysBiol
31 김효정 Drug knowledge bases and their applications in biomedical informatics research     J.Club
31 안세환 Visualization portal for genetic variation(VizGVar): a tool for interactive visualization of SNPs and somatic mutations in exons, genes and protein domains     J.Club

2018-02:
01 이정훈   xMutant
01 김민정 menopausal women with stage 2 and stage 4 depression   TopicSem
01 이우승 The Prognostic Potential of Loss of Heterozygosity in Breast Invasive Carcinoma   TopicSem
01 김기태 Prediction model of treatment response in depression   MAInfo
01 이정훈 STRING NETWORK for Graph-CNN  xMutant
03 김형준 Building a semantic web based metadata repository for facilitating detailed clinical modeling in cacer genome studies     J.Club
03 김기태 A Next Generation Connectivity Map: L1000 Platform and the First 1,000,000 Profiles     J.Club
05 서명의 Site-direct mutagenesis for FX protein activity assay  TopicSem
05 임영균 Drug sensitivity and SCS   TopicSem
08 김형준 Private Ethereum and Healthavatar  TopicSem
08 권호식   TopicSem
08 박유미 Are preprints the future of biology?  xMutant
08 임영균 팀OT & CTRP(Cancer Therapeutics Response Portal) review  MAInfo
08 김형준 Data importing process of KCDM genome   BioEMR
08 이정훈 The comparative analysis of the gene regulatory network according to the pathological stages reveals the characteristics of metastasis in gastric cancer  SysBiol
10 류영재 Reversal of cancer gene expression correlates with drug efficacy and reveals therapeutic targets     J.Club
10 민병주 Reccurrent F8 Intronic Deletion Found in Mild Hemophilia A Causes Alu Exonization     J.Club
12 김기태 Prediction model for response in depression  TopicSem
12 윤선민 L-asparaginase associated acute pancreatitis in pediatric ALL patients  TopicSem
14 류영재 PharmVar database overview  SysBiol
14 박지연 Similarity of alternative polyadenylation in thyroid with kidney and liver cancers  MAInfo
14 김주연 Linking K-CDM to KAERS for active ADE signal detection  BioEMR
14 류영재 PharmVar database overview  SysBiol
14 류영재 PharmVar database overview  SysBiol
14 윤선민 Analysis of AML exome sequencing   xMutant
15 ... 공휴일  TopicSem
15 ... 공휴일  TopicSem
17 ... 공휴일  J.Club
17 ... 공휴일  J.Club
19 ... GDA  TopicSem
19 ... GDA  TopicSem
22 ... GDA  TopicSem
22 ... GDA  TopicSem
22 이우승 Cochle araplasia trio family analysis  xMutant
24 김민정 Integrative analysis of genome-wide gene copy number changes and gene expression in non-small cell lung cancer     J.Club
24 김주연 Multisite Investigation of Outcomes With Implementation of CYP2C19 Genotype-Guided Antiplatelet Therapy After Percutaneous Coronary Intervention     J.Club
26 박유미 The characteristics of singleton variants in Autism Spectrum Disorder  TopicSem
26 김효정 Genome Data Model  TopicSem
28 김주연 Interpretation of genes in synthetic association to PGx variants: a case study  SysBiol
28 윤선민 Modified workflow and statistical methods for AAP analysis  MAInfo
28 이정훈 WEX for Hepatic VOD and Network propagation  xMutant

2018-01:
01 ... 공휴일  TopicSem
01 ... 공휴일  TopicSem
02 김주연 Gene set annotation of genes synthetically associated with PGx variants in GWAS  TopicSem
02 민병주 Compound hetero truncation mutations in APC Reveal CMV-PTC as a Familial Adenomatous Polyposis Variant  TopicSem
03 김효정 K-CDM Genome; panel information  BioEMR
04 유경훈 1T Depression Analysis-Patients characterization and subgrouping by prescribed drugs  TopicSem
04 이우승 The Prognostic Potential of Loss of Heterozygosity in Breast Invasive Carcinoma  TopicSem
04 윤선민 Data integration patient clinical information with medication history   xMutant
04 ... Data integration patient clinical information with medication history  MAInfo
06 이정훈 Hybrid Approach of Relation Network and Localized Graph Convolutional Filtering for Breast Cancer Subtype Classification     J.Club
06 박유미 Pharmacogenomics of GPCR Drug Targets     J.Club
08 서명의 Reinforcement for low coverage regions in DRP290 SNP Panel and LT Ampliseq WES  TopicSem
08 임영균 SCS analysis in MSI colon cancer  TopicSem
11 김형준 Updating mobile eCRF for DNet and ANet and Avatar  TopicSem
11 권호식 Exercise for Visualizing TCGA data   TopicSem
11 박지연 TCGA Pan-Cancer analysis for alternative polyadenylation  xMutant
11 김주연 Pathway annotation of genes synthetically associated to GWAS PGx variants  SysBiol
11 류영재 Problems with allele matcher switching from VCF to GVCF  MAInfo
13 김효정 A Realism-Based View on Counts in OMOP\'s Common Data Model     J.Club
13 이우승 Network dynamics-based cancer panel stratification for systemic prediction of anticancer drug response     J.Club
15 윤선민 Asparaginase-associated pancreatitis in pediatric ALL patients  TopicSem
15 김기태 Prediction model for 12 week remission in depression  TopicSem
18 박유미 The characteristics of singleton variants in neuropsychiatric disorders  TopicSem
18 김효정 K-CDM Genome progress   TopicSem
18 이우승 CNV algorithm for KPCDx Panel   xMutant
18 박지연 Alternative splicing in thyroid cancer  MAInfo
18 이우승 CNV algorithm for KPCDx Panel  xMutant
18 이우승 CNV algorithm for KPCDx Panel  xMutant
18 이우승 CNV algorithm for KPCDx Panel  xMutant
18 이정훈 Synthetic Dosage Cytotoxicity for prioritization of chemotherapy  SysBiol
20 권호식 Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma     J.Club
20 유경훈 Using reference-free compressed data structures to analyze sequencing reads from thousands of human genomes     J.Club
22 류영재 Allele matcher fine-tuning and scoring scheme alterations  TopicSem
22 이정훈 Inference of Digenic Disruption Networks for Synthetic Cytotoxicity  TopicSem
23 김형준 KCDM genome and FHIR genomics  BioEMR
25 유경훈 1T Depression Analysis: Patients characterization and subgrouping by prescribed drugs  TopicSem
25 박지연 Pan-cancer analysis of alternative polyadenylation  TopicSem
25 임영균 The most studies genes of all time and of any time  xMutant
25 이우승 Analysis of Tumor Mutational Burden (TMB) Workflow  MAInfo
27 윤선민 Using ALoFT to determine the impact of putative loss-of-function variants in protein-coding genes     J.Club
27 임영균 Combination Cancer Therapy Can Confer Benefit via Patient-to-Patient Variability without Drug Additivity or Synergy     J.Club
29 김주연 Interpretation of the relation between SAGs of PGx variants and ADEs  TopicSem
29 민병주 Disease mechanism prediction for female specific CMV-PTC  TopicSem
31 ...   TopicSem
31 ...   TopicSem
31 김주연 Pathway enrichment analysis for FDA and GWAS PGx variants  SysBiol

2017-12:
02 박호경 Risk factors of isoniazid-induced hepatotoxicity in Tunisian tuberculosis patients     J.Club
02 김기태 Discovering novel pharmacogenomic biomarkers by imputing drug response in cancer patients from large genomics studies     J.Club
04 이우승 The Prognostic Potential of Loss of Heterozygosity in Breast Invasive Carcinoma  TopicSem
04 서명의 Experimental modification of Exome + DRP290 SNP Panel and 2nd test result  TopicSem
06 임영균 Re-analysis of SCS in colon cancer  TopicSem
06 김형준 Secure interconnection between XNet and BioEMR with JSON Web Token.  TopicSem
06 박호경 CPTAC and TCGA Breast Cancer samples, data  MAInfo
06 김효정 Design of K-CDM genome  BioEMR
07 이정훈 Non-linear model to predict cytotoxic drug response  SysBiol
07 이우승 Comparing Gene Fusion Detection Algorithm with WGS  xMutant
07 이우승 Comparing Gene Fusion Detection Algorithm with WGS  xMutant
09 류영재 Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension     J.Club
09 민병주 Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder     J.Club
11 권호식 Plan for my Study Using TCGA data   TopicSem
11 김기태 Analysis of depression between early and later onset  TopicSem
13 윤선민 L-asparaginase associated pancreatitis in pediatric ALL patients   TopicSem
13 박유미 Association of genetic variants with variant angina in 80 case-control individuals  TopicSem
13 이우승 TNBC and Non-TNBC Kinome NGS data  MAInfo
14 김주연 Gene set annotation for genes synthetically associated with PGx variants  SysBiol
14 임영균 Project DRIVE: deep RNAi interrogation of viability effects in cancer  xMutant
16 김민정 Changes in gene expression variability reveal a stable synthetic lethal interaction network in BRCA2- ovarian cancers     J.Club
16 김주연 Pharmacogenomics-Based Point-of-Care Clinical Decision Support Significantly Alters Drug Prescribing     J.Club
18 김효정 Establishment of Integrated Drug Database based on National Standards  TopicSem
18 류영재 NamedAlleleMatcher101 replication  TopicSem
20 이정훈 Microarray data analysis of multi-center breast cancer patients with distant metastasis  TopicSem
20 김민정 Analysis of stage 2 vs stage 4 depression patients   TopicSem
20 김효정 [Review] A Realism-Based View on Counts in OMOP  BioEMR
20 김효정 [Review] A Realism-Based View on Counts in OMOP  BioEMR
20 김기태 Analysis of depression with cut-off in age of onset   MAInfo
21 이정훈 Inference of candidate Synthetic Cytotoxic Drug (Pyrimethamine, Paclitaxel)  xMutant
23 서명의 PGBD5 promotes site-specific oncogenic mutations in human tumors     J.Club
23 박지연 Annotation-free quantification of RNA splicing using LeafCutter     J.Club
25 ... 공휴일  TopicSem
25 ... 공휴일  TopicSem
27 박호경 Drug adverse effects analysis with gene Expression  TopicSem
27 박지연 Statistical models using alternative polyadenylation data  TopicSem
27 김형준 DNet data import to BioEMR  BioEMR
27 임영균 Network of Cancer genes 5.0   MAInfo
28 박유미 The charactericstics of singleton variants in neuropsychiatric disorders  xMutant
28 박호경 1265 Potential drug targets gene  SysBiol
30 ...      J.Club
30 ...      J.Club

2017-11:
01 이우승 The Prognostic Potential of Loss of Heterozygosity in Breast Invasive Carcinoma   TopicSem
01 서명의 Design of Exome + DRP290 SNP Panel and experimental modification  TopicSem
01 김형준 Whan NoSQL makes better sense than RDBS  BioEMR
01 김형준 Whan NoSQL makes better sense than RDBS  BioEMR
01 김기태 Ependymal tumor analysis  MAInfo
02 임영균 Graphtyper: enables population-scale genotyping using pangenome graphs  xMutant
02 박호경 SSRIs drugs with Pharmacogenomic snp and adr  SysBiol
04 박유미 Variant Interpretation: Functional Assays to the Rescue     J.Club
04 김효정 Reverse translation of adverse event reports paves the way for de-risking preclinical off-targets     J.Club
06 권호식 Alamut Visual: Visualization engine for NGS analysis  TopicSem
06 서희원 Drug score distributions for the ten most-prescribed drugs in the 1000 Depressives.  TopicSem
08 김형준 Agent contraction with personal resource authorization list and storing CCR document type data in Avatar DB   TopicSem
08 임영균 SCS analysis in TCGA coad and cell lines data  TopicSem
08 김효정 Semi-automantic KAERS report generation on K-CDM structure   BioEMR
08 임영균 tcga followup clinical data   MAInfo
09 이정훈 K-CDM: Conversion of EMR data to OMOP format  SysBiol
09 이정훈 Regularization Techniques to Detect Biomarker for Cytotoxic Anticancer Drugs  xMutant
11 윤선민 Genetic variation in human drug-related genes      J.Club
11 이우승 Overexpressed Somatic Alleles are Enriched in Functional Elements in Breast Cancer     J.Club
13 김기태 Analysis of 1000 depressive  TopicSem
13 박유미 Category-dependent score adjustment schemes using genetic algorithm  TopicSem
15 김효정 Active ADR surveillance pipeline based on K-CDM   TopicSem
15 류영재 Identifying Splicing Synthetic Cancer Survival in Lung Adenocarcinoma using pooled isoform-based method   TopicSem
15 윤선민 Preprocessing results of 26 AML exome sequencing  MAInfo
15 김형준 OpenEHR archetype structure and REST API  BioEMR
15 김형준 OpenEHR archetype structure and REST API  BioEMR
16 박유미 Comparing protein evolution based score with molecular function score in PPARG  xMutant
16 김주연 Using standard queries to analyze ADR risks across multiple institutions  SysBiol
16 김주연 Using standard queries to analyze ADR risks across multiple institutions  SysBiol
18 김형준 Comparing the Performance of NoSQL Approaches for Managing Archetype Based Electronic Health Record Data     J.Club
18 권호식 Multiregion Whole-Exome Sequencing Uncovers the Genetic Evolution and Mutational Heterogeneity of Early-Stage Metastatic Melanoma     J.Club
20 이정훈 Synthetic Genetic Targeting in Cancer Cell Vulnerability  TopicSem
20 윤선민 Analysis of 26 AML exome sequencing  TopicSem
22 김민정 List of genes associated with Major Depression   TopicSem
22 박호경 Drug adverse effects analysis with gene and protein Expression  TopicSem
22 김효정 OMOP CDM review  BioEMR
22 류영재 Significantly regulated multi-isoform genes  MAInfo
23 윤선민 Data integration patient sample information with medical record  xMutant
23 류영재 PharmCAT review  SysBiol
25 임영균 Comprehensive Analysis of Hypermutation in Human Cancer     J.Club
25 유경훈 A method to decipher pleiotropy by detecting underlying heterogeneity driven by hidden subgroups applied to autoimmune and neuropsychiatric diseases     J.Club
27 박지연 Identification of a new subgroup characterized by long 3UTR in papillary thyroid cancer  TopicSem
27 김주연 Finding genes synthetically associated with PGx variants of GWAS  TopicSem
29 민병주 Allele specific analysis of APC gene exonic region in the CMV-PTC affected sibling pair  TopicSem
29 유경훈 1T Depression Analysis: Patients characterization and subgrouping  TopicSem
29 박지연 Comparison of DaPars and RUD method in alternative polyadenylation study  MAInfo
30 박지연 Identification of molecular classifiers in thyroid neoplasm  xMutant
30 박호경 druggable proteome classification and examples  SysBiol

2017-10:
02 ... TBC  TopicSem
02 ... TBC  TopicSem
04 ... 추석  TopicSem
04 ... 추석  TopicSem
07 ... 연휴  J.Club
07 ... 연휴  J.Club
09 ... 한글날  TopicSem
09 ... 한글날  TopicSem
09 이정훈 Korean Clinical Imaging Guidelines and clinical decision support system  SysBiol
11 권호식 Alamut-Focus : interactive variant filtration application for NGS analysis.  TopicSem
11 윤선민 Analysis of previously reported variants in pediatric ALL patients  TopicSem
11 박지연 Research plan for follicular thyroid neoplasm  MAInfo
12 서희원 SATIE: a web tool to predict sequential treatments in cancer.  xMutant
14 박호경 Sparse whole genome sequencing identifies two loci for major depressive disorder     J.Club
14 김주연 Multidisciplinary model to implement pharmacogenomics at the point of care     J.Club
16 박유미 Finding indirect associations of tagging SNPs with variant angina  TopicSem
16 박지연 Alternative polyadenylation in papillary thyroid cancer (PTC): Comparison of TCGA and SNUH data  TopicSem
16 김주연 Variant level analysis of genes in synthetic association to PGx variants: case for rs4646244 TA, AA  SysBiol
16 김주연 Variant level analysis of genes in synthetic association to PGx variants: case for rs4646244 TA, AA  SysBiol
18 류영재 Identifying Splicing Synthetic Cancer Survival in Lung Adenocarcinoma using isoform-based method  TopicSem
18 이정훈 Analysis of samples according to the number of SDCS pairs  TopicSem
18 박호경 Depression phenotype and gwas studys  MAInfo
18 김형준 New API standard GraphQL   BioEMR
19 박지연 Prognostic power of RUD (relative usage of distal poly(A) sites)   xMutant
21 서명의 Loss-of-function and gain-of-function mutations in KCNQ5 cause intellectual disability or epileptic encephalopathy     J.Club
21 박지연 Interaction Landscape of Inherited Polymorphisms with Somatic Events in Cancer     J.Club
23 김민정 skin cutaneous melanoma: primary vs. metastasis   TopicSem
23 박호경 Drug adverse effects analysis with gene and protein Expression  TopicSem
25 김주연 Finding genes synthetically associated to PGx variants in GWAS  TopicSem
25 민병주 Validation of disease related variants by using brain cancer panel  TopicSem
25 이우승 Somatic Mutation Analysis with WGS of Small Round Cell Tumor in Brain  MAInfo
26 류영재 Extracting information from PharmGKB  SysBiol
26 이우승 Comparison of Adapter Trimmers for Illumina Miseq Data   xMutant
28 서희원 Profiling and leveraging relatedness in a precision medicine cohort of 92,455 exomes     J.Club
28 이정훈 MR Imaging Radiomics Signatures for Predicting the Risk of Breast Cancer Recurrence as Given by Research Versions of MammaPrint, Oncotype DX, and PAM50 Gene Assays     J.Club
30 김효정 Standard Query Design for ADR Signal Detection on K-CDM structure  TopicSem
30 유경훈 1T Depression Analysis: Patients characterization and subgrouping  TopicSem

2017-09:
02 김형준 Opening the Duke electronic health record to apps: ImplementingSMART on FHIR     J.Club
02 윤선민 Common sequence variants affect molecular function more than rare variants?     J.Club
04 김기태 Analysis of Ependymal tumor  TopicSem
04 권호식 Alamut-Batch : annotation engine for NGS analysis  TopicSem
05 임영균 The Mutational Spectrum of MSI Events and MMR Genes in previous studies  xMutant
06 류영재 Additional Methods of Identifying Splicing Synthetic Cancer Survival in Lung Adenocarcinoma  TopicSem
06 이정훈 SDL gene target drugs and drug sensitivity  TopicSem
06 김기태 Analysis of microarray using the GEO data   MAInfo
07 김효정 [Review] Enoxaparin-Induced Liver Injury: Case Report and Review of the Literature and FDA Adverse Event Reporting System (FAERS)  BioEMR
09 임영균 Integrative clinical genomics of metastatic cancer     J.Club
09 유경훈 The druggable genome and support for target identification and validation in drug development     J.Club
11 김민정 Primary versus Metastatic Cancer  TopicSem
11 박호경 Drug adverse effects analysis with gene and protein Expression  TopicSem
11 김주연 Extracting variants associated to drug response from the NHGRI GWAS Catalog  SysBiol
13 박지연 Identification of alternative splicing events associated with pathological phenotypes of papillary thyroid carcinoma  TopicSem
13 김주연 Analysis of synthetically associated genes to PGx variants  TopicSem
13 김형준 NoSQL databases Casssandra for real time ETL of data warehouse  BioEMR
13 임영균 Public Cell lines databases  MAInfo
14 이정훈 miRNA analysis pipeline and report format  xMutant
16 김민정 Identification of prognostic genes through expression differentiation during metastatic process in lung adenocarcinoma     J.Club
16 김기태 Using Clinical Characteristics to Identify Which Patients With Major Depressive Disorder Have a Higher Genetic Load for Three Psychiatric Disorders     J.Club
18 민병주 Germline and somatic APC variants in the CMV-PTC affected sibling pair  TopicSem
18 이우승 CNV analysis of Cancer Panel 2.0 Data  TopicSem
18 류영재 DMET data processing protocol  SysBiol
19 윤선민 Visualization web application for interaction   MAInfo
20 유경훈 WXS analysis in 999 Depression patients with Baseline Information  TopicSem
20 서명의 Whole size FX cDNA library synthesis for cloning and activity assay data analysis plan  TopicSem
20 김효정 Dynamic query function in postgreSQL  BioEMR
21 박유미 Trans-Omics for Precision Medicine (TOPMed) program and Bravo browser  xMutant
23 류영재 Global profiling of alternative RNA splicing events provides insights into molecular differences between various types of HCC     J.Club
23 민병주 Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer- Associated Genes in Families Affected by Breast Cancer     J.Club
25 임영균 Drug sensitivity in SCS genes  TopicSem
25 서희원 Variants associated with an increased risk for severe neutropenia in patients receiving 6MP.  TopicSem
25 박호경 SNRIs Antidepressants and Pharmacogenomic information  SysBiol
25 박호경 SNRIs Antidepressants and Pharmacogenomic information  SysBiol
26 윤선민 The comparison the feature of groups in biological network   xMutant
27 김형준 Agent matching and installation with personal resource authorization list  TopicSem
27 김기태 Analysis with pathway score in 999 Depressive patients  TopicSem
27 류영재 Significantly regulated multi-isoform genes  MAInfo
30 ... TBC  J.Club
30 ... TBC  J.Club

2017-08:
01 박유미 Association of a genetic variant in TSHR with variant angina  xMutant
02 박지혜 Figures and tables for PharmSafe and Enzyme kinetic weighted drug score  TopicSem
02 박호경 Drug adverse effects analysis using GTex and ABCB1 gene Interaction  TopicSem
03 김형준 HealthKit apps with Apples compliance and HIPAA rules  BioEMR
05 서희원 Genetic diagnosis of Mendelian disorders via RNA sequencing     J.Club
05 박지연 RNA splicing is a primary link between genetic variation and disease     J.Club
07 김주연 Extraction and analysis of genes synthetically associated with PGx alleles  TopicSem
07 민병주 Validation of SNVs detected from Molecular pathology test by using KPCDx   TopicSem
07 김주연 Results of predominant and synthetically associated genes to PGx alleles  SysBiol
08 서희원 PanDrugs: Identifying actionable molecular alterations and prioritize drugs  xMutant
09 유경훈 WXS analysis in 999 Depression patients with Baseline Information  TopicSem
09 이우승 Further analysis with Results of LOH Analysis  TopicSem
09 박지연 The effect of BRAF and RAS mRNA expression on posttranscriptional regulation  MAInfo
10 김효정 [Review] Therapeutic indications and other use- case-driven updates in the drug ontology  BioEMR
10 김효정 bioEMR 개선안  BioEMR
10 김효정 bioEMR 개선안  BioEMR
12 서명의 Evaluating the clinical validity of gene-disease associations an evidence-based framework developed by the clinical genome resource     J.Club
12 이정훈 Measuring intratumor heterogeneity by network entropy using RNA-seq data     J.Club
14 류영재 Identification of Synthetic Splicing Cancer Survival in Lung Adenocarcinoma  TopicSem
14 서명의 Synthesis cDNA library of FX gene from lymphoblast cell line  TopicSem
16 임영균 SCS analysis in Colon cancer cell lines   TopicSem
16 김형준 HealthAvatar API based on CCR+ and Composite DataElement  TopicSem
16 박지연 Identification of alternative splicing events associated with pathological phenotypes of papillary thyroid carcinoma (PTC)  xMutant
16 박호경 1000 Depression data and non-baseline clinical variants  MAInfo
17 김형준 Data Element API in FHIR(DSTU2, 3)  BioEMR
19 이우승 A Zoom Focus algorithm to locate the optimal testing region for rare variant association tests     J.Club
19 김효정 Signal Detection of Imipenem Compared to Other Drugs from Korea Adverse Event Reporting System Database     J.Club
21 ... GDA  TopicSem
21 ... GDA  TopicSem
22 박지혜   xMutant
23 ... GDA  TopicSem
23 ... GDA  TopicSem
26 박유미 Gene family information facilitates variant interpretation and identification of disease associated genes     J.Club
26 권호식 Burden of Nonsynonymous Mutations among TCGA Cancers and Candidate Immune Checkpoint Inhibitor Responses     J.Club
28 김효정 Query strategy for KAERS report generation on K-CDM structure  TopicSem
28 서희원 Analysis of previously reported variants associated with MP-induced neutropenia in ALL  TopicSem
28 박호경 Most-Prescribed Antidepressants - Mental Health Daily report  SysBiol
29 이우승 CNV analysis of Cancer Panel 2_0 Data from Pathology Department  xMutant
30 박유미 Selecting appropriate cell lines for evaluating the utility of personalized gene-level scoring (PGS) system  TopicSem
30 윤선민 Asparaginase-associated pancreatitis in pediatric ALL patients  TopicSem
30 이우승 Package of Cancer Panel for Pathology Department  MAInfo
31 김형준 Agent matching process by user authorization list  BioEMR

2017-07:
01 박유미 An Expanded View of Complex Traits: From Polygenic to Omnigenic     J.Club
01 김기태 AACR Project GENIE: Powering Precision Medicine Through An International Consortium     J.Club
03 김효정 Data processing for integrated drug database  TopicSem
03 박호경 Drug adverse effects analysis using GTex and ABCB1 gene Interaction  TopicSem
03 김주연 Updated statistics for determining ADR risk according to PGx variant status using synthetic association  SysBiol
05 박지혜 Analysis of drug characteristics according to half-life class  TopicSem
05 김주연 Variant level analysis of genes synthetically associated with PGx alleles  TopicSem
05 김기태 GENIE : Basic characteristics of clinical and genomic data across the various cancer type  MAInfo
05 이우승 Comparison Results of vcf Normalization  xMutant
06 김효정 Eval SQL.NET: User-Defined Function for Regular Expression in T-SQL  BioEMR
08 유경훈 Semantic prioritization of novel causative genomic variants     J.Club
08 임영균 A global genetic interaction network maps a wiring diagram of cellular function     J.Club
10 민병주 Sequencing uniformity and genotype validation of KPCDx ver 2  TopicSem
10 송유림 RarePedia using Depression WXS data  TopicSem
10 류영재 Chemotherapy and adverse drug reactions in Acute Myeloid Leukemia   SysBiol
12 이우승 Loss of Heterozygosity Analysis in Breast Invasive Carcinoma   TopicSem
12 서명의 Preparing cDNA library of FX gene by using lymphoblast cell lines  TopicSem
12 임영균 SAFE: Spatial Analysis of Functional Enrichment  xMutant
12 Intern Identification of driver mutations in breast cancer  Seminar
12 Intern The correlation of allele frequency and the degree of effect in ADR in population  Seminar
12 송유림 Introduction to ANNOVAR Update  MAInfo
13 김형준 (team_20170713)GluVue_clinical support tool for interpreting blood glucose data  BioEMR
15 윤선민 Using large sequencing data sets to refine intragenic disease regions and prioritize clinical variant interpretation     J.Club
15 김형준 Automated integration of continuous glucose monitor data in the electronic health record using consumer technology     J.Club
17 임영균 Aggregate DNAmethylation to gene scale  TopicSem
17 서희원 Identification of variants with a significantly lower frequency in cases than in controls  TopicSem
17 박지혜 SCAN and PACdb : pharmacogenomics databases  SysBiol
17 박지혜 SCAN and PACdb : pharmacogenomics databases  SysBiol
18 이정훈 SDL pairs validation from cancer cell line data  xMutant
19 유경훈 Analysis for identifying genes and variants  associated with SIOH in 20 patients.  TopicSem
19 김형준 RESTful API with updated authentication and aurhorization in H.A.P  TopicSem
19 임영균 methHC: A database of DNA Methylation and gene expression in Human Cancer  MAInfo
22 김주연 Preemptive Pharmacogenomic Testing for Precision Medicine: A Comprehensive Analysis of Five Actionable Pharmacogenomic Genes Using Next-Generation DNA Sequencing and a Customized CYP2D6 Genotyping Cas     J.Club
22 박호경 Meta-analysis of effects of ABCB1 polymorphisms on clopidogrel response among patients with coronary artery disease     J.Club
24 김기태  Pathway score for survival analysis in HNSC   TopicSem
24 윤선민 Asparaginase-associated pancreatitis in pediatric ALL patients  TopicSem
24 박호경 Tricyclic antidepressants and similarity of interacting genes  SysBiol
25 윤선민 Asparaginase-associated pancreatitis in pediatric ALL patients  xMutant
26 이정훈 Validation a Synthetic Dosage Cancer Survival Pairs using a Genomics of Drug Sensitivity in Cancer database  TopicSem
26 김효정 Query strategy for signal detection from clinical dataset  TopicSem
26 윤선민 Survival analysis of pancreatitis patients using clinical information   MAInfo
27 김효정 Programming functions in PostgreSQL server  BioEMR
29 민병주 Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibility     J.Club
29 류영재 Disease variants alter transcription factor levels and methylation of their binding sites     J.Club
31 박지연 Alternative polyadenylation contributes to an indolent phenotype of RAS mutation in papillary thyroid cancer  TopicSem
31 박유미 Analysis for identifying genes associated with Variant Angina  TopicSem
31 이정훈 Finding genes targeted by GDSC drugs  SysBiol

2017-06:
01 김효정 Problems- drug master data structure conversion  BioEMR
03 박지연 Dissecting the multicellular ecosystem of metastatic melanoma by single-cell RNA-seq     J.Club
03 송유림 A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK     J.Club
05 김주연 ADR risk determination according to PGx variant status쟵sing synthetic association  TopicSem
05 민병주 Optimal design of target sequencing experiment by using KPCDx ver 2.0  TopicSem
05 박지혜 Repositories where researchers can download or upload genomic data  SysBiol
07 유경훈 Analysis for identifying genes and variants  associated with SIOH in 20 patients.  TopicSem
07 이우승 The Prognostic Potential of Loss of Heterozygosity in Breast Invasive Carcinoma   TopicSem
07 윤선민 Asparaginase-associated Pancreatitis in pediatric ALL patients  MAInfo
07 윤선민 Asparaginase-associated Pancreatitis in pediatric ALL patients   xMutant
10 김혜현 Back on Track: A Mobile App Observational Study Using Apple ResearchKit Framework     J.Club
10 서희원 Pharmacogenomic variants have larger effect sizes than genetic variants associated with other dichotomous complex traits.     J.Club
12 서명의 FX cDNA library preparation by using lymphoblast cell lines  TopicSem
12 임영균 Synthetic Cancer Survival relationship between DNA methylation and mutation  TopicSem
12 류영재 Roles of Solute Carriers and the functional consequences of polymorphism  SysBiol
14 송유림 rarePedia filtering strategy  TopicSem
14 김형준 Creating the userdefined CDE through question items in Formbuilder  TopicSem
14 서희원 The analysis of continuous variables in ALL samples.  xMutant
14 류영재 Calculating ERK score of THCA samples  MAInfo
15 김형준 Open source search engines in CDE search  BioEMR
17 이정훈 Supporting precision medicine by data mining across multi-disciplines: an integrative approach for generating comprehensive linkages between single nucleotide variants (SNVs) and drug-binding sites     J.Club
17 이우승 Mutational landscape of matastatic cancer revealed from prospective clinical sequencing of 10,000 patients     J.Club
19 서희원 Mercaptopurine induced neutropenia in ALL   TopicSem
19 김기태 Survival analysis in HNSC with metabolism pathway - Interpretation of the result  TopicSem
19 박호경 Tricyclic antidepressants physiologic action and ADR  SysBiol
21 윤선민 Asparaginase-associated pancreatitis in pediatric ALL patients  TopicSem
21 박유미 Establishing genetic model with consideration of gene-specific characteristics using a distance-based approach  TopicSem
21 박호경 Genome Analysis Toolkit 4 (GATK4) alpha review  MAInfo
21 박지연 Changes in alternative polyadenylation analysis from standard RNA-seq  xMutant
22 김효정 K-CDM ETL Workflow and DB structure review  BioEMR
24 박지혜 Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing      J.Club
24 김효정 The Drug Data to Knowledge Pipeline: Large-Scale Claims Data Classification for Pharmacologic Insight     J.Club
26 이정훈 Data preprocessing for Gene Score, Overexpression and Methylation  TopicSem
26 박지연 Alternative Polyadenylation (APA) changes in Papillary Thyroid Cancer  TopicSem
26 이정훈 A tool for discovering drug sensitivity and gene expression associations in cancer cells  SysBiol
28 류영재 Preliminary miRNA analysis on THCA samples  TopicSem
28 김혜현 Renewal Design of Avatar Beans  TopicSem
28 박지혜 Repositories where researchers can download or upload genomic data   xMutant
28 이우승 OncoKB: A Precision Oncology Knowledge Base  MAInfo
29 김혜현 Renewal of Data Workflow from EMR/OCS to XNetHub  BioEMR

2017-05:
01 서명의 Treatment of lymphoblastoid cell line containing FX variants  TopicSem
01 이우승 The Prognostic Potential of Loss of Heterozygosity in Breast Invasive Carcinoma  TopicSem
01 류영재 Roles of ATP-Binding Cassette transporters and the functional consequences of polymorphism  SysBiol
03 이우승 Improved VCF Nomralization  xMutant
03 unknown   TopicSem
03 unknown   TopicSem
04 김형준 Resource authorization in Apple ResearchKit  BioEMR
06 unknown   J.Club
06 unknown   J.Club
08 unknown   TopicSem
08 unknown   TopicSem
10 유경훈 Analysis for identifying genes and variants associated with SIOH in 20 patients.  TopicSem
10 송유림 RarePedia 관련 정리 상황  TopicSem
10 임영균 PARP inhibitors: Synthetic lethality in the clinic  xMutant
13 박호경 Genetic Polymorphisms Contribute to the Individual Variations of Imatinib Plasma Levels and ADR in Chinese GIST     J.Club
13 김기태 Pathway-Structured Predictive Model for Cancer Survival Prediction: A Two-Stage Approach     J.Club
15 서희원 VVA: Gene-centered Visualization and Annotation for Exome Variant Analysis  TopicSem
15 박호경 P-glycoprotein polymorphism and drug adverse response  SysBiol
15 임영균 Never-smoker LUAD analysis  TopicSem
17 김형준 Resource Authorization and data access control by HealthAvatar platform  TopicSem
17 김기태 Survival analysis with pathway score in metabolism pathways  TopicSem
17 이정훈 Classification and segmentation in convolutional neural network   xMutant
18 김혜현 Representation of cCDE and constraints in CHMR   BioEMR
20 류영재 RNA sequence context effects measured in vitro predict in vivo protein binding and regulation     J.Club
20 민병주 Tumor-suppressor genes that escape from X-inactivation contribute to cancer sex bias     J.Club
22 윤선민 WXS to detect genes causing Asparaginase-associated pancreatitis   TopicSem
22 박유미 Identification of individual-level deleterious genes using a distance-based approach  TopicSem
24 김효정 Constructing an integrated drug database for utilization of public data in Korea  TopicSem
24 류영재 Further investigation on Synthetic Splicing Cancer Survival pairs in Lung Adenocarcinoma  TopicSem
24 박지연 Analysis of posttranscriptional regulation using public data in thyroid cancer  MAInfo
25 김형준 Role + Attribute based Access Control in H.A.P  BioEMR
27 김주연 Creating a scalable clinical pharmacogenomics service with automated interpretation and medical record result integration-experience from a pediatric tertiary care facility     J.Club
27 서명의 A common variant at the 14q32 endometrial cancer risk locus activates AKT1 through YY1 binding     J.Club
29 이정훈 Synthetic dosage cancer survival analysis: Methylation and Under-expression  TopicSem
29 김혜현 Progress of DNet CDE FINAL version  TopicSem
29 김주연 ADR risk according to 8 PGx variant statuses using synthetic association  SysBiol
31 박지혜 Analysis of drug characteristics according to half-life class  TopicSem
31 박호경 Drug adverse effects analysis using GTex and ABCB1 gene interaction  TopicSem
31 박유미 Identifying personalized candidate genes using case-control score distribution dissimilarity  xMutant
31 임영균 somatic mutation aggregation workflow used to generate both the public and protected MAFs in the GDC DNA-Seq pipelines.   MAInfo

2017-04:
01 김혜현 Successful weight reduction and maintenance by using a smartphone application in those with overweight and obesity     J.Club
01 이정훈 Network perturbation by recurrent regulatory variants in cancer     J.Club
03 송유림 RarePedia 2017  TopicSem
03 이계화   TopicSem
03 박지혜 ePGA: AWeb-Based Information System for Translational Pharmacogenomics  SysBiol
05 서희원 Comparison of significant variants in two Ritodrine induced-side effect cohorts  TopicSem
05 김형준 Updated database table of resource permission in Healthavatar platform.   TopicSem
05 박유미 The genome Aggregation Database (gnomAD) : An overview of data properties  xMutant
05 류영재 Isoform fraction analysis methodology  MAInfo
08 서희원 Rare and low-frequency coding variants alter human adult height     J.Club
08 이계화 A systematic approach to the reporting of medically relevant findings from whole genome sequencing     J.Club
10 김기태 Pathway score based on the gene damaging score  TopicSem
10 윤선민 WXS to detect genes causing Asparaginase-associated pancreatitis in 13 SNUH patients  TopicSem
10 박호경 Pharmacogenetics of Membrane Transporters ABCB1  SysBiol
12 박유미 Analysis for identifying genes associated with Variant Angina  TopicSem
12 김효정 Development of Algorithm for minimizing cost of drug combination with same therapeutic effect  TopicSem
12 박지연 Further AS and APA analysis in TCGA THCA data  MAInfo
12 윤선민 a significant variant of NEU4 gene   xMutant
13 김형준 Structured input,output data through CHMR Sphinx search engine  BioEMR
15 김효정 The other side of the coin: Harm due to the non-use of health-related data     J.Club
15 이우승 Fast, scalable prediction of deleterious noncoding variants from functional and population genomic data     J.Club
17 류영재 Isoform fraction analysis in THCA  TopicSem
17 이정훈 Genetic programming to infer the optimal gene scoring method to classify genes  TopicSem
17 이정훈 Gastric cancer metastasis network analysis  SysBiol
19 김혜현 Comparison derived DE to composite DE in discussion  TopicSem
19 박지혜 Pharmacokinetic effects of inter-individual variability in drug response  TopicSem
19 서희원 Three datasets from gnomAD database and their statistics  xMutant
19 박호경 NCBI EST ABCB1 information summary  MAInfo
22 윤선민 SPATIAL: A System-level PAThway Impact AnaLysis approach     J.Club
22 김형준 C3-PRO. Connecting ResearchKit to the Health System Using i2b2 and FHIR     J.Club
24 박호경 Drug adverse effects analysis using GTex tissue specific gene expression dataset  TopicSem
24 박지연 The effect of BRAF and RAS mutations on posttranscriptional regulation in Papillary Thyroid Cancer  TopicSem
24 김주연 Statistics of updated PGx variants for synthetic association analysis  SysBiol
26 김주연 ADR risk determination according to PGx variant status using synthetic association  TopicSem
26 민병주 NGS based cancer panel ver 2 design for actual target regions  TopicSem
26 이우승 How to get controlled access data from ICGC data portal.  MAInfo
26 박지연 Further analysis of alternative polyadenylation in TCGA THCA data  xMutant
29 유경훈 Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites     J.Club
29 임영균 Reassessment of Genomic Sequence Variation to Harmonize Interpretation for Personalized Medicine     J.Club

2017-03:
01 박지연 Experimental validation and further analysis of alternative splicing and polyadenylation in response to Csnk2b deletion   xMutant
02 이우승 COSMIC v80 Update : Introduction of COSMIC-3D  MAInfo
04 류영재 WT U2AF1 Antagonizes the Splicing Program Characteristic of U2AF1 mutant tumors     J.Club
04 민병주 InterVar: Clinical Interpretation of Genetic Variants by the 2015 ACMG-AMP Guidelines     J.Club
06 김기태 Pathway score based on the gene damaging score  TopicSem
06 김혜현 Applying composite CDEs in eCRFs of Pharmacogenetic study  TopicSem
06 이정훈 Weakly supervised learning  SysBiol
08 박지혜 Review of ePGA   xMutant
08 박유미 Translating phenotype into a functional gene-level score  TopicSem
08 김효정 DB normalization and tuning for calculatable drug master  TopicSem
08 김기태 MEREDITH:Clustering and Visualization tools for TCGA PAN-CANCER with multiplatform genomic data  MAInfo
11 김주연 Clinical impact of pharmacogenetic profiling with a clinical decision support tool in polypharmacy home health patients: A prospective pilot randomized controlled trial     J.Club
11 서명의 Mutations in three genes encoding proteins involved in hair shaft formation cause uncombable hair syndrome     J.Club
13 류영재 Identification of synthetic aberrant splicing event pairs using pairwise survival analysis in colorectal cancer  TopicSem
13 이정훈 Genetic programming to infer the optimal gene scoring method to classify gene  TopicSem
13 김주연 Visualization of variants grouped by genes in synthetic association with PGx variants  SysBiol
15 윤선민 WXS to detect genes causing AAP in 13 SNUH patients   TopicSem
15 박지혜   TopicSem
15 송유림 RarePedia protocol 정리 현황  MAInfo
15 이우승 Result : CNV Detection Algorithm for Cancer Samples  xMutant
16 김효정 Computer-aided diagnosis: A survey with bibliometric analysis  BioEMR
18 박지연 Comprehensive analyses of tumor immunity: implications for cancer immunotherapy     J.Club
18 송유림 Mutation Detection of Fibroblast Growth Factor Receptor 3 for Infiltrative Hepatocellular Carcinoma by Whole-Exome Sequencing     J.Club
20 박호경 Drug adverse effects analysis using GTex tissue specific gene expression dataset  TopicSem
20 박지연 Analysis of BRAF and RAS mRNA expression in SKCM and THCA  TopicSem
20 이계화 Review Cases of Genomic Data Warehouse   SysBiol
22 김주연 ADR risk determination according to PGx variant status using synthetic association  TopicSem
22 민병주 NGS cancer panel design and experimental modification  TopicSem
23 김형준 Database table of resource permission in Healthavatar platform.  BioEMR
25 박지혜 Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network     J.Club
25 박유미 Characterization of ADME gene variation in 21 populations by exome sequencing     J.Club
27 이우승 The prognostic potential of loss of heterozygosity in breast invasive carcinoma   TopicSem
27 임영균 TCGA never smoker LUAD mutation profile  TopicSem
27 류영재 Effects of variants in transporter genes on drug efficacy and toxicity   SysBiol
29 서명의 Validation for candidate genes in familial-NMTC cases  TopicSem
29 이수현 K-CDM scenario of vancomycin associated acute kidney Injury  TopicSem
29 이정훈 Classification and segmentation in convolutional neural network  xMutant
29 윤선민 WXS to detect genes causing AAP in 13 SNUH patients  MAInfo

2017-02:
01 박지연 Posttranscriptional regulation in skin cutaneous melanoma  TopicSem
01 김주연 ADR risk determination according to FDA or PREDICT SNP genotype using synthetic association  TopicSem
01 윤선민 Clinical information of pancreatitis patients  MAInfo
01 이정훈 GeneScore calculation strategy  xMutant
01 홍주영 Healthcare Service  BioEMR
04 이수현 Evaluating common data models for use with a longitudinal community registry     J.Club
04 이우승 Massive interstitial copy-neutral loss of heterozygosity as evidence for cancer being a disease of the DNA-damage response     J.Club
06 민병주 NGS Technology base Pan-cancer diagnostic panel  TopicSem
06 이우승 The prognostic potential of reversal loss of heterozygosity in breast invasive carcinoma  TopicSem
06 홍주영 Transporter-madiated drug-drug interactions  SysBiol
08 서명의 Comparison of manual and semi-automatic NGS result  TopicSem
08 임영균 SMC lung cancer data analysis result  TopicSem
08 김효정 Current US EMR implementation status review  BioEMR
08 박유미 Translating phenotype into a functional gene-level score using Corriell samples Pharmacogenomic genotypes  xMutant
08 류영재 Converting GDC UUID to TCGA barcode  MAInfo
11 김효정 Patients, care partners, and shared access to the patient portal: online practices at an integrated health system     J.Club
11 김형준 Metadata Repository for Improved Data Sharing and Reuse Based on HL7 FHIR     J.Club
13 이수현 K-CDM Allopurinol Scenario  TopicSem
13 서희원 Association of ADRA1A polymorphism with Ritodrine-induced Pulmonary Edema in 13 pregnant women.  TopicSem
15 이계화 The Doctor’s Seq Project:   TopicSem
15 송유림 Association between ApoE variants and Alzheimer’s disease  TopicSem
15 윤선민 Modification of workflow and statistical methods for AAP analysis  xMutant
15 박지연 The effect of BRAF and RAS mRNA expression on alternative polyadenylation in TCGA SKCM and PTC  MAInfo
15 Intern Analysis of 2504 genome vcf files of 26 countries, focusing on Vitamin D Receptor  Seminar
15 Intern Normal Karyotype AML  Seminar
18 윤선민 Controllability analysis of the directed human protein interaction network identifies disease genes and drug targets     J.Club
18 임영균 Somatic Mutation Patterns in Hemizygous Genomic Regions Unveil Purifying Selection during Tumor Evolution     J.Club
22 박호경 Workflow of Single-Cell DNA Sequencing and case example  MAInfo
22 서희원 Preprocessing and QC results of 119 ALL WXSs.   xMutant
23 류영재 Effects of variants in transporter genes on drug efficacy and toxicity  SysBiol
23 김혜현 TTA monthly meeting   BioEMR
25 김기태 Pathway-based gene signatures predicting clinical outcome of lung adenocarcinoma     J.Club
25 박호경 Circular RNAs and their associations with breast cancer subtypes     J.Club
27 홍주영 The Individual Drug-Fit Report  TopicSem
27 김형준 POST API(data creation) in HealthAvatar platform.  TopicSem
27 박호경 Detecting Antibiotic Resistance Genes  SysBiol
28 김혜현 소아암 연구 관련 eCRF 진행상황  BioEMR

2017-01:
02 임영균 Analysis plan of SMC lung cancer data.  TopicSem
02 이수현 K-CDM Structure and Future Works for Drug Safety   TopicSem
02 박지혜 The Use of Gene Ontology Term and KEGG Pathway Enrichment for Analysis of Drug Half Life  SysBiol
02 박지혜 The Use of Gene Ontology Term and KEGG Pathway Enrichment for Analysis of Drug Half Life  SysBiol
04 송유림 Identifying the new susceptibility loci of Alzheimer’s Disease by WXS  TopicSem
04 이계화 Patient-centered reconstruction of candiate genes associated with MRONJ event time   TopicSem
04 박지연 The Effect of MITF abundance on posttranscriptional regulation in skin melanoma  xMutant
04 이우승 Transcript-level expression analysis of RNA-seq experiments with HISAT, StringTie and Ballgown.  MAInfo
04 김효정 [review] Data mining differential clinical outcomes associated with drug regimens using adverse event reporting data  BioEMR
04 김형준 API 개발진행상황  BioEMR
07 김혜현 Opening the Duke electronic health record to apps: Implementing SMART on FHIR     J.Club
07 이계화 Comparison of Approaches for Heart Failure Case Identification From Electronic Health Record Data     J.Club
09 서희원 WXS to Identify Cancer Clearing Genotypes from Matched Donor-recipient Pairs.  TopicSem
09 이정훈 Inference of Gene Scoring Method for Disease Gene Prediction using optimization  TopicSem
09 박호경 PharmGKB Clinical annotation search  SysBiol
11 김형준 Cordination of value domain of user-defined DE with recommended CDE in Easyformbuilder.  TopicSem
11 김기태 Pathway damaging score based on the gene score in the Head and Neck squamous cell carcinomas   TopicSem
11 박지혜 Review of variant annotation tools, genome browsers and biological network analysis tools  xMutant
11 김기태 [Review]Pathway based gene signature predicting clinical outcome in cancer  MAInfo
11 박지혜 Review of Glints  xMutant
11 김기태 [Review]Pathway based gene signature predicting clinical outcome in cancer  MAInfo
14 박유미 The intolerance to functional genetic variation of protein domains predicts the localization of pathogenic mutations within genes     J.Club
14 이정훈 Molecular analysis of urothelial cancer cell lines for modeling tumor biology and drug response     J.Club
16 윤선민 WXS to detect genes causing AAP in 13 SNUH patients  TopicSem
16 박유미 Translating CYP2D6 enzyme activity into a functional gene-level score  TopicSem
16 이정훈 Inference cancer drug prognosis via cell line model  SysBiol
18 김효정 Internet of Avatars, Agents, and Apps; Flexible On-demand Healthcare Information System Architecture  TopicSem
18 류영재 Identification of alternative splicing event pairs and their effects on survival using pairwise survival analysis  TopicSem
18 송유림 Association between ApoE genotype and AD  MAInfo
18 김혜현 CDE template forms status in NIH CDE Browser  BioEMR
18 이우승 Survival analysis of Loss of Heterozygosity in triple-negative breast cancer  xMutant
21 서희원 Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study     J.Club
21 홍주영 A novel algorithm for analyzing drug-drug interactions from MEDLINE literature     J.Club
23 홍주영 Drug Interaction Score  TopicSem
23 김혜현 Development and validation of Dictionary cCDE  TopicSem
23 김주연 Chromosomal distribution of variants synthetically associated with pharmacogenomic SNPs  SysBiol
25 박지혜 Calculating weighted drug score using drug half-life parameters  TopicSem
25 박호경 Drug adverse effects analysis using GTex tissue specific gene expression dataset  TopicSem
25 이수현 K-CDM scenario and review of standardized large-scale analytics tools under development within OHDSI.   BioEMR
25 Intern (Replication) Genomic and Epigenomic Landscapes of Adult De Novo AML     Seminar
25 Intern Analysis of 2504 human genomes from 26 populations, using Python and R  Seminar
25 임영균 Influence of Co-occurring Mutations on Clinical Outcomes in leukemia  MAInfo
25 임영균 SMC lung cancer data 분석경과  xMutant

2016-12:
03 이수현 Electronic Health Record Based Algorithm to Identify Patients with Autism Spectrum Disorder     J.Club
03 류영재 Cancer associated SF3B1 mutatnts recognize otherwise inaccessible cryptic 3 splice sites within RNA secondary structures     J.Club
05 홍주영 PharmGene Platform  TopicSem
05 김형준 Design of HealthAvatar API and current status of API implementation.  TopicSem
05 이정훈 Integrative analysis for identifying the best anticancer therapy based on genomic features  SysBiol
07 김기태 Pathway damaging score based on the gene score in the Head and Neck squamous cell carcinomas   TopicSem
07 윤선민 WXS to detect genes causing L-asparaginase-associated pancreatitis in ALL patients  TopicSem
07 윤선민 Patient Information on L-asparaginase associated Pancreatitis  MAInfo
07 이정훈 Genetic Programming Based Gene Scoring Method for Common-Complex disease Prediction  xMutant
07 김혜현 BMESH browser 진행상황  BioEMR
08 김혜현 표준회의 12월 월례회의 발표자료  BioEMR
10 민병주 Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant     J.Club
10 김주연 Identification of causal genes for complex traits     J.Club
12 서희원 WXS to Identify Cancer Clearing Genotypes from Matched Donor-recipient Pairs  TopicSem
12 김효정 HIRA 처방 공개 데이터 탐색적 분석  TopicSem
12 김주연 Determining adverse drug event risk according to FDA SNP genotype  SysBiol
12 김주연 Determining adverse drug event risk according to FDA SNP genotype  SysBiol
12 김주연 Determining adverse drug event risk according to FDA SNP genotype  SysBiol
12 김주연 Determining adverse drug event risk according to FDA SNP genotype using synthetic association  SysBiol
14 류영재 Methodology for identifying the effects of alternative splicing events on survival using pairwise survival analysiso  TopicSem
14 이정훈 Synthetic dosage cancer survival: pan-cancer analysis for systematic inference of negative genetic interaction  TopicSem
14 박유미 Evaluating the intolerance of genic sub-regions     xMutant
14 김형준 Current process of API implementation  BioEMR
14 김형준 Current process of API implementation  BioEMR
14 류영재 Comparing SURVIV results with results from paper  MAInfo
17 서명의 Sequencing the GRHL3 coding region reveals rare truncating mutations and a common susceptibility variant for nonsyndromic cleft palate     J.Club
17 박지연 The prognostic potential of alternative transcript isoforms across human tumors      J.Club
19 김혜현 Revised figures of cCDE types  TopicSem
19 박지혜 Pharmacokinetic effects of inter-individual variability in drug response  TopicSem
19 홍주영 [DDGI DB] TRANSFORMER  SysBiol
21 박호경 drug adverse effects analysis using GTex tissue specific gene expression  TopicSem
21 박지연 Posttranscriptional analysis of public melanoma RNA-seq data  TopicSem
21 박지연 Experimental validation of alternative splicing and polyadenylation in mouse model for Csnk2b deletion   MAInfo
21 윤선민 Patient Information on L-asparaginase associated Pancreatitis   xMutant
24 송유림 Increased burden of deleterious variants in essential genes in autism spectrum disorder     J.Club
24 박지혜 The global spectrum of protein-coding pharmacogenomic diversity     J.Club
26 김주연 Determining ADR risk according to FDA & PREDICT SNP genotype  TopicSem
26 민병주 Changes in coagulation factor activity induced by F10 inhibitor  TopicSem
26 류영재 SFINX database  SysBiol
27 이수현 K-CDM ETL  BioEMR
28 이우승 The prognostic potential of loss of heterozygosity in breast invasive carcinoma  TopicSem
28 서명의 FNMTC candidate gene shared between two ns-FNMTC families  TopicSem
28 서희원 Recommended Coverage and Read Depth for NGS Applications.  xMutant
28 박호경 SNP and gene name search  MAInfo
30 박유미 A Personalized Gene-level Scoring System for Exome Variants: Comprehensive Evaluation in Multiple Genetic Conditions.  Seminar
30 김기태 Pathway damaging score based on the gene score in the Head and Neck squamous cell carcinomas   Seminar
30 윤선민 Whole-exome sequencing to detect genes causing L-asparaginase-associated pancreatitis in 13 ALL patients  Seminar
30 박호경 Drug adverse effects analysis using GTex tissue specific gene expression dataset  Seminar
30 박지혜 Pharmacokinetic effects of inter-individual variability in drug response  Seminar
30 서희원 Association of ATP8B4 polymorphism with Ritodrine induced side effects in 13 pregnant women  Seminar
30 김주연 Determining ADR risk according to FDA & PREDICT SNP genotypes  Seminar
30 류영재 Identification of prognostic aberrant splicing event pairs using pairwise survival analysis in invasive breast cancer patients  Seminar
30 이수현 Development of Controlled Vocabulary-Based Drug Safety(CDS) Model to Utilize Laboratory and Descriptive Data in Pharmacovigilance   Seminar
30 홍주영 Modeling and Usage of PharmacoGene Pathway Database(PG-path)  Seminar
30 김형준 EasyFormBuilder- Semi-automatic form building tool based on standardized metadata repository for semantic interoperability.  Seminar
30 송유림 Identifying the new susceptibility loci of Alzheimer’s Disease by whole exome sequencing   Seminar
31 전체 리트릿  J.Club
31 전체 리트릿  J.Club

2016-11:
02 윤선민 Whole-exome sequencing to detect genes causing L-asparaginase-associated pancreatitis in 12 ALL patients  TopicSem
02 서희원 Variant Visualization and Annotation Tool Available Online  TopicSem
02 서희원 Public genome databases: GnomDB, ExAC and ESP6500.  xMutant
02 박호경 single-cell RNA-seq data analysis workflow  MAInfo
02 김형준 XNet, Avatar 소개 및 시연 동영상 제작 (APAMI2016)  BioEMR
05 김효정 Clinical reasoning in the context of active decision support during medication prescribing      J.Club
05 이계화 Development of clinical decision support alerts for pharmacogenomic incidental findings from exome sequencing      J.Club
07 김효정 IoA3 Homepage for Developer  TopicSem
07 류영재 Survival analysis of mNA isoform variation using TCGA datai  TopicSem
07 홍주영 Human BioPathway Databases  SysBiol
07 홍주영 Results of predominant and synthetically associated genes to PGx alleles  SysBiol
09 김주연 Gene score distribution of genes including or proximate to pharmacogenomic SNPs  TopicSem
09 김혜현 Developing Xnet CDE Browser  TopicSem
09 박지연 Overview of Analysis method and Database for genome-wide CLIP experiments  xMutant
09 이우승 Genotype-Tissue Expression(GTEx) Portal  MAInfo
09 이수현 K-CDM 충북대데이터 ETL 결과  BioEMR
12 이우승 Genome-wide significance testing of variation from single case exomes     J.Club
12 윤선민 A pathway-centric approach to rare variant association analysis     J.Club
14 박지혜 PharmSafe - Personalized Prevention of Adverse Drug Reaction   TopicSem
14 박호경 Replication of Characterizing perturbation sensitivity of genes   TopicSem
14 류영재 DMET data processing protocol  SysBiol
16 박지연 Validation of TCGA SKCM analysis using public data   TopicSem
16 이정훈 Synthetic dosage cancer survival gene pairs  TopicSem
16 김기태 [Review] Filtering variant and Direction of effect in SKAT-O test  MAInfo
16 박지혜 Variant damaging score algorithm list  xMutant
19 김형준 SMART on FHIR implemented over i2b2     J.Club
19 박호경 Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study     J.Club
21 이우승 Loss of Heterozygosity Analysis across 4 Cancer Types  TopicSem
21 임영균 Identification of Synthetic Cancer Survival and Synthetic Cancer Survival Burden   TopicSem
21 박지혜 Review of BRENDA database  SysBiol
23 민병주 Genetic characteristic of factor X variants in human populations  TopicSem
23 이수현 Summary of Sentinel Operations Center meeting and K-CDM elaboration plan   TopicSem
23 김효정 HIRA 처방 공개 데이터 탐색적 분석  BioEMR
23 이우승 Characters of Singletones in 1KGenome  xMutant
26 임영균 Exploring genetic suppression interactions on a global scale     J.Club
26 김기태 A new correlation clustering method for cancer mutation analysis     J.Club
27 박호경 drug side effects information – ex Metformin  SysBiol
28 서명의 FNMTC candidate gene validation using Sanger sequencing and THCA data  TopicSem
28 이계화 Doctor’s Seq Project:   TopicSem
30 송유림 Analysis of ADSP WXS data  TopicSem
30 박유미 Comprehensive Evaluation of Gene-level Scoring Systems for Deleterious Exome Variants: Score Normalization issues  TopicSem
30 홍주영 PathVisio Review  BioEMR
30 임영균 overview of gain of function studies  MAInfo
30 임영균 Loss-of-function genetic tools for animal models: cross-species and cross-platform differences  xMutant

2016-10:
01 박지연 Direct Transcriptional Consequences of Somatic Mutation in Breast Cancer      J.Club
01 송유림 Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer     J.Club
03 unknown 개천절  TopicSem
03 unknown 개천절  TopicSem
03 김형준 Specification of source codes in Healthavatar platform server   BioEMR
03 류영재 SFINX database  SysBiol
05 김현대 UCSD에서 참여했던 여러 연구들과 data validation 적용 방안  TopicSem
05 박지혜 PharmSafe - Personalized Prevention of Adverse Drug Reaction  TopicSem
05 임영균 Pembrolizumab MSKCC data analysis  MAInfo
05 임영균 LUAD acs-mutation/expression analysis  xMutant
08 박지혜 REVEL: an Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants     J.Club
08 홍주영 How Informative Are Drug-Drug Interactions of Gene-Drug Interactions?     J.Club
10 김주연 South Korean geriatrics on Beers Criteria medications at risk of adverse drug events  TopicSem
10 민병주 Molecular defects in the factor X gene caused by heterozygous variant in EGF2 domain  TopicSem
10 박지혜 validation result of PharmSafe by variant score filter  SysBiol
12 이우승 Loss of heterozygosity as prognostic marker in Breast invasive carcinoma  TopicSem
12 서명의 Experimental validation for candidate variants of FNMTC family  TopicSem
12 윤선민 Localization of TCGA clinical data from GDC Data Portal  MAInfo
12 이수현 K-CDM 과제 진행 사항  BioEMR
15 이정훈 Mutual exclusive network and inference target from drug sensitivity  xMutant
17 전체 TBC 2016  TopicSem
17 전체 TBC 2016  TopicSem
17 박호경 Bina - develops next-generation genomic management   SysBiol
19 임영균 Differential characteristics among SCS burden groups   TopicSem
19 송유림 Identification of disease-specific variants in Alzheimer’s Disease  TopicSem
19 박유미 Functional similarity of genes by CDS length  xMutant
19 류영재 Taking rMATS output files and plotting aligned exon read densities using Sashimi plot  MAInfo
19 홍주영 Standard Format of Bio-Pathway Information  BioEMR
19 박호경 Mutual exclusive network and inference target from drug sensitivity  SysBiol
19 박호경 Mutual exclusive network and inference target from drug sensitivity  SysBiol
19 박호경 Mutual exclusive network and inference target from drug sensitivity   SysBiol
22 서희원 Genetic Variation Among 82 Pharmacogenes: The PGRNseq Data From the eMERGE Network      J.Club
22 김혜현 Detecting Unplanned Care From Clinician Notes in Electronic Health Records     J.Club
24 김형준 Current status of HAP server.  TopicSem
24 이계화 Doctor’s Seq Project - Basic Statistics and Incidental Findings  TopicSem
25 김혜현 Preparation of APAMI 2016  BioEMR
26 이수현 K-CDM ETL test result using SNUH data  TopicSem
26 홍주영 Pharmsafe Platform  TopicSem
26 윤선민 WXS to detect genes causing L-asparaginase induced pancreatitis  xMutant
26 박지연 Updated splicing analysis of papillary thyroid cancer  MAInfo
26 김효정 Health Avatar Webpage: for developer  BioEMR
27 김혜현 Preparation of APAMI 2016 2  BioEMR
29 이정훈 ENCAPP: elastic-net-based prognosis prediction and biomarker discovery for human cancers     J.Club
29 박유미 The whole genome sequences and experimentally phased haplotypes of over 100 personal genomes      J.Club
31 박유미 Comprehensive Evaluation of Gene-level Scoring Systems for Deleterious Exome Variants: GDI, RVIS, and PGDS  TopicSem
31 김기태 WXS analysis in COPD patients with LABA/LAMA treatment  TopicSem
31 김주연 Results of variant-centric approach for MRONJ  SysBiol
31 김주연 Human BioPathway Databases  SysBiol

2016-09:
03 임영균 A Network of Conserved Synthetic Lethal Interactions for Exploration of Precision Cancer Therapy     J.Club
03 김형준 ODMedit_ uniform semantic annotation for data integration in medicine based on a public metadata repository     J.Club
05 홍주영 Knowledge based Pharmsafe Database  TopicSem
05 이계화 Gender difference of drugscore  TopicSem
05 서희원 CRAM format - An efficiently compressed BAM file  xMutant
05 김형준 Updated processes of agent registration for API  BioEMR
05 이수현 K-CDM specification version 1.0  BioEMR
07 서희원 Depression WXS QC - 10 samples of FASTQ from Illumina HiSeq 2500  TopicSem
07 송유림 Descriptive statistics about distribution of variants in Alzheimer’s Disease group  TopicSem
07 박호경 SEVEN BRIDGES - The Biomedical Data Analysis Platform  MAInfo
10 윤선민 Analysis of protein-coding genetic variation in 60,706 humans     J.Club
10 민병주 Determinants of Power in Gene-Based Burden Testing for Monogenic Disorders     J.Club
12 김형준 Process of Agent registration for HealthAvatar API   TopicSem
12 김기태 WXS analysis in COPD patients with LABA/LAMA treatment  TopicSem
12 박지연 Analysis of splicing and polyadenylation in mouse model with MEK deletion   xMutant
12 이계화 Gender Difference in ADR - Review of Article (Systematic Analysis of Adverse Event Reports for Sex Differences in Adverse Drug Events, 2015, Scientific Report)   SysBiol
14 unknown 추석  TopicSem
14 unknown 추석  TopicSem
14 이우승 Review_ Epigenome-wide Association Studies and the Interpretation of Disease -Omics  MAInfo
14 홍주영 YouScript Personalized Prescribing Software  BioEMR
19 윤선민 The human diseases network using genomic information  TopicSem
19 박유미 Evaluation of gene-wise scores; Personalized Gene Deleteriousness Score (PGDS)  TopicSem
19 김주연 Risk for ADEs in South Korean geriatrics from Beers Criteria medications  SysBiol
21 김효정 Health Avatar Platform: Component Description  TopicSem
21 류영재 Methods for assessing effects of variants on alternative splicing and disease  TopicSem
21 김기태 [Review]Towards precision medicine   MAInfo
21 박지혜 [REVIEW] Mutations and Drugs Portal(MDP) : A database linking drug response data and genomic information   xMutant
21 김효정 [Review] The impact of real-time alerting on appropriate prescribing in kidney disease  BioEMR
24 김주연 The effect of pharmacogenetic profiling with a clinical decision support tool on healthcare resource utilization and estimated costs in the elderly exposed to polypharmacy     J.Club
24 서명의 Parent-of-origin-specific signatures of de novo mutations     J.Club
26 이정훈 Synthetic dosage cancer survival  TopicSem
26 김혜현 MDR기반 PHR 운용을 위한 참조모델  TopicSem
26 홍주영 Physiologically Based Pharmacokinetic Modeling  SysBiol
28 박지연 Identification of clinically relevant genes from mRNA and splicing changes of skin cutaneous melanoma   TopicSem
28 박호경 Replication of Characterizing perturbation sensitivity of genes  TopicSem
28 김혜현 Panel based new design of BMESH browser  BioEMR
28 송유림 Download TCGA clinical data from GDC data portal   MAInfo
28 이우승 Cancer Panel - Comparing 4 different callers on KRAS region  xMutant
28 이우승 Cancer Panel - Comparing 4 different callers on KRAS region  xMutant
28 이우승 Cancer Panel - Comparing 4 different callers on KRAS region  xMutant
9 이정훈 WGCNA Network analysis of Microarray data  SysBiol

2016-08:
01 박유미 Comparing gene scoring methods: RVIS, GDI, and Personalized Gene Damaging Score (PGDS)  TopicSem
01 김효정 DB construction for minimizing cost of drug combination with same therapeutic effect   TopicSem
01 김혜현 MDR 기반 개인건강기록 운용을 위한 참조모델의 이해  BioEMR
01 임영균 Analysis colon cancer in ICGC data  xMutant
01 김주연 Distribution of F10 mutations in the 1000 Genomes phase 3 population  SysBiol
03 류영재 Motif analysis of RNA-binding proteins in papillary thyroid carcinoma samples  TopicSem
03 이정훈 Network Analysis of Dysfunctional Genes in Endodermal Cancers  TopicSem
03 임영균 Types of measures of prognosis  MAInfo
06 김혜현 Developing a data element repository to support EHR-driven phenotype algorithm authoring and execution     J.Club
06 이정훈 A Landscape of Pharmacogenomic Interactions in Cancer     J.Club
08 박호경 Replication of Characterizing perturbation sensitivity of genes  TopicSem
08 박지연 Identification of survival-associated genes in cutaneous melanoma  TopicSem
08 홍주영 Developing the Rivaroxaban Surveillance Plan through Mini-Sentinel  BioEMR
08 이우승 KRAS Depth Status of Cancer Panel  xMutant
08 이우승 KRAS Depth Status of Cancer Panel  xMutant
08 홍주영 Knowledge based Pharmsafe Database  SysBiol
10 김혜현 Revised evaluation results for semantic relationships of CDEs  TopicSem
10 김주연 Finding genomic features that affect drug response  TopicSem
10 김기태 [review]Personalized pathway enrichment map   MAInfo
13 김효정 User-driven prioritization of features for a prospective InterPersonal Health Record: Perceptions from the Italian context     J.Club
13 이우승 Protein-structure-guided discovery of functional mutations across 19 cancer types     J.Club
15 unknown 광복절  TopicSem
15 unknown 광복절  TopicSem
15 unknown 광복절  BioEMR
15 unknown 광복절  SysBiol
15 이정훈 Microarray analysis for stem cell differentication  xMutant
15 류영재 Exome Sequencing Project  SysBiol
17 박지혜 Calculating drug score by ATC class with multiple variant scores   TopicSem
17 민병주 Heterozygous variant in EGF2 domain of coagulation Factor X  TopicSem
17 윤선민 The summary of TCGA clinical data  MAInfo
19 이계화 Exome sequencing identifies new candidate mutations for susceptibility to MRONJ   Seminar
19 김기태 Identifying the functional target using the combination of genes across the multiple carcinomas  Seminar
19 임영균 Identification of combinatory mutational effect between genes for patient survival in colon cancer     Seminar
19 이정훈 Synthetic Dosage Cancer Survival:a computational approach for identification of negative genetic interaction  Seminar
19 서희원 Whole-exome sequencing to detect significantly altered genes causing Ritodrine induced side effects in 13 pregnant women.  Seminar
19 박유미 ReAlCap (Reads Alignment Capture) : A fast and handy tool for capturing genomic reads  Seminar
19 이수현 RS-ADR: A reference standard for detection of adverse drug reaction signals using electronic health records database   Seminar
19 박지혜 PharmSafe_Personalized Prevention of Adverse Drug Reactions  Seminar
19 김형준 Form building tool based on standardized metadata repository for semi-automatic semantic annotation  Seminar
19 이우승 Finding Loss of heterozygosity as prognostic marker in Breast invasive carcinoma  Seminar
19 류영재 PharmPortal_A Personal Pharmacogenomics Knowledgebase  Seminar