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팀:   발표자:    제목/키워드:    날짜:   

2021-12:
02 최선   TopicSem
02 윤미선   TopicSem
04 김나영   J.Club
04 임영균   J.Club

2021-11:
01 윤미선   TopicSem
01 이우승   TopicSem
04 홍진희   TopicSem
04 서명의   TopicSem
06 조원일   J.Club
06 안세환   J.Club
08 ... GDA  TopicSem
08 ... GDA  TopicSem
11 ... GDA  TopicSem
11 ... GDA  TopicSem
13 홍진희   J.Club
13 이시은   J.Club
15 조민아   TopicSem
15 유준기   TopicSem
18 정문경   TopicSem
18 부은경   TopicSem
20 이우승   J.Club
20 권호식   J.Club
22 김나영   TopicSem
22 임영균   TopicSem
25 이시은   TopicSem
25 안세환   TopicSem
27 유준기   J.Club
27 최선   J.Club
29 조원일   TopicSem
29 권호식   TopicSem

2021-10:
02 최선 The measurement of Cobb angle based on spine X ray     J.Club
02 임영균 Rare variant contribution to human disease in 281,104 UK Biobank exomes     J.Club
04 ... 대체공휴일  TopicSem
04 ... 대체공휴일  TopicSem
05 조원일 genetic correlation  SysBiol
07 서명의 NGS platform for Helicobacter pylori ampliseq panel  TopicSem
07 조민아 The results of association study in IBD discovery and replication  TopicSem
07 임영균 Cancer register in UKB  MAInfo
09 ... 한글날  J.Club
09 ... 한글날  J.Club
11 ... 대체공휴일  TopicSem
11 ... 대체공휴일  TopicSem
12 안세환 Segmented haplotype estimation and imputation tools (SHAPEIT4)  SysBiol
12 안세환 Segmented haplotype estimation and imputation tools (SHAPEIT4)  SysBiol
14 유준기 Rare variant analysis incorporating functional annotations  TopicSem
14 임영균 Case reconstruction by candidate variants for PEP patients  TopicSem
14 이우승 Aggregate Trend of LOH by eQTL method  MAInfo
16 윤미선 A RELATIONAL-LEARNING PERSPECTIVE TO MULTI-LABEL CHEST X-RAY CLASSIFICATION      J.Club
16 김나영 Pragmatic MDR: a metadata repository with bottom up standardization of medical metadata through reuse     J.Club
18 김나영 CHMR curation tool improvement ideas  TopicSem
18 이시은 Ontology and Heterogeneous Lifelong Mining  TopicSem
20 정문경 Google AppSheet  BioEMR
20 정문경 Google AppSheet  BioEMR
20 정문경 Google AppSheet  BioEMR
21 정문경 만성콩팥병 맞춤식이 연구 프로세스  TopicSem
21 부은경 Evaluation of association between genetic variants and TIL in 3 IBD datasets  TopicSem
21 권호식 Sequencing and Imputation  MAInfo
23 조민아 Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes     J.Club
23 서명의 Position effects at the FGF8 locus are associated with femoral hypoplasia     J.Club
25 안세환 Phylogenetic clustering results of T1GP  TopicSem
25 조원일 The relationship between Type 2 Diabetes patients & polyneuropathy(DPN) in UKBB [sampling]  TopicSem
26 조민아 Liftover using r package, rtracklayer  SysBiol
27 김나영 SMART Markers: Framework for Capturing Patient Generated Digital Endpoints  BioEMR
28 권호식 Adverse effects of Contrast Media  TopicSem
28 최선 Spine Segmentation for Automatic Diagnosis of Scoliosis     TopicSem
30 정문경 A simulation-based evaluation of machine learning models for clinical decision support: application and analysis using hospital readmission     J.Club
30 부은경 Polygenic basis and biomedical consequences of telomere length variation     J.Club

2021-09:
02 서명의 Comparison with AML H. pylori antibiotic resistance NGS panel  TopicSem
02 조민아 The results of association study in IBD discovery and replication  TopicSem
02 서명의 Comparison with AML H. pylori antibiotic resistance NGS panel  TopicSem
02 조민아 The results of association study in IBD discovery and replication  TopicSem
04 조원일 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases     J.Club
04 이시은 Deep-learning-based automated terminology mapping in OMOP-CDM      J.Club
06 유준기 Autoimmune disease single tissue eQTL analysis in UK Biobank  TopicSem
06 임영균 Polymorphism affecting Tacrolimus flat peak  TopicSem
08 정문경 CKD cohort in UKBB : CKD diagnosis  BioEMR
09 부은경 Association between genetic variants and thiopurine-induced leukopenia in IBD patients  TopicSem
09 이시은 Analysis of brain cognitive function using fNIRS  TopicSem
09 최선 Research idea challenge using cancer big data  MAInfo
11 홍진희 scRNA-seq technologies and related computational data analysis  J.Club
11 조동영 Prioritization of candidate causal genes for asthma in susceptibility loci derived from UK Biobank     J.Club
13 정문경 Developing Digital Literacy Instrument for IBD Care Mobile App  TopicSem
13 김나영 Numbers of DEs extracted from five clinical documents  TopicSem
15 김나영 HL7 FHIR standard-based resource modeling  BioEMR
15 최선 Public Cancer Bigdata  MAInfo
16 안세환 Results of matching Health Showcase data with T1GP haplogroups  TopicSem
16 조원일 diabetes and polyneuropathy gwas study in UKBB  TopicSem
18 권호식 Copy number variation profiling in pharmacogenes using panel-based exome resequencing and correlation to human liver expression     J.Club
18 이우승 Synthetic lethality mediated precision oncology via the tumor transcriptome     J.Club
20 ... 추석  TopicSem
20 ... 추석  TopicSem
23 권호식 Association between Traits in UK Biobank and Potential variant related with Methotrexate-induced nephrotoxicity  TopicSem
23 최선 Pill_classification_service  TopicSem
24 최선 Cancer idea challenge_0924  MAInfo
25 유준기 Set based rare variant expression quantitative trait loci in blood and brain from Alzheimer Disease study participants     J.Club
25 안세환 High coverage whole genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios     J.Club
27 윤미선 Study Idea using Cancer Big Data   TopicSem
27 이우승 Prognostic Potential of Loss of Heterozygosity in Triple Negative Breast Cancer  TopicSem
28 부은경 Comparison of TIL incidence rate in combined IBD dataset  SysBiol
29 이시은 BIg Query Architecture  BioEMR
30 홍진희 Genetic association of ibd in 20K WES ukbiobank and classification of ibd  TopicSem
30 조동영   TopicSem
30 유준기 Comparing Rare Variant Association Tests  MAInfo

2021-08:
02 유준기 Comparative analysis integrating UK Biobank and eQTL data  TopicSem
02 임영균 Polymorphism affecting Tacrolimus flat peak  TopicSem
02 임영균 Molecular Features for subgrouping cancer patients혻  MAInfo
03 조민아 The CCGWAS R package : a tool for case-case association testing of two different disorders based on their respective case-control GWAS results  SysBiol
04 김형준 Digital signature and blockchain  BioEMR
05 부은경 Genetic variants that increase susceptibility to thiopurine-induced leukopenia in IBD patients  TopicSem
05 이시은 Lung Segmentation of Health BigData Showcase images using U-Net  TopicSem
07 김나영 Towards achieving semantic interoperability of clinical study data with FHIR     J.Club
07 임영균 Pathogenic missense protein variants affect different functional pathways and proteomic features than healthy population variants     J.Club
09 김형준 Decentralized ID and Zero-Knowledge proof  TopicSem
09 정문경 Ideation of Meal Recommender for CKD patients  TopicSem
09 이우승 AlphaFold : Highly Accurate Protein Structure Prediction  MAInfo
10 부은경 Survival Analysis Using Frailty Models  SysBiol
11 정문경 Exploring CKD cohort in UKBB: Social factors  BioEMR
12 김나영 DE review on DNet and Avatar Beans  TopicSem
12 김주연 Replicating Parkinsons disease genetic analysis with UK Biobank  TopicSem
13 Intern (heeseung) parsing HISAT2 result to sql file format   Seminar
13 Intern (heeseung) Web structure of Healthcare Showcase demo version  Seminar
14 윤미선 Encoding CT Anatomy Knowledge for Unpaired Chest X-ray Image Decomposition     J.Club
14 서명의 Comparison of culture with antibiogram to NGS using bacterial isolates and formalin fixed paraffin embedded gastric biopsies     J.Club
16 ...   TopicSem
16 ...   TopicSem
17 조원일 genetic correlations of polygenic disease traits  SysBiol
18 김나영 Merging two ontologies_MELLO and PACO  BioEMR
19 안세환 Hierarchical clustering of TPMT haplgroups  TopicSem
19 조원일 the relationship between diabetes and polyneuropathy in UKBB  TopicSem
21 김주연 Utilising large electronic medical record datasets to identify novel drug-gene interactions for commonly used drugs     J.Club
21 정문경 Development of a Spanish food exchange list: application of statistical criteria to a rationale procedure     J.Club
23 권호식 Identification of potential variants related with Methotrexate-induced nephrotoxicity  TopicSem
23 최선 Pill classification  TopicSem
24 안세환 TPMT star-alleles and haplogroups of Health Showcase data  SysBiol
26 윤미선 Image generation of chest x-ray  TopicSem
26 이우승 Prognostic Potential of Loss of Heterozygosity in TNBC  TopicSem
28 조민아 The molecular basis, genetic control and pleiotropic effects of local gene co-expression     J.Club
28 부은경 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses     J.Club
30 홍진희 gene variants association with ibd in ukbb  TopicSem
30 조동영 Improving Genomic Discovery with Machine Learning Based Phenotyping  TopicSem
30 권호식 Genebass  MAInfo

2021-07:
01 ... .  TopicSem
01 정문경 Ideation of Meal Recommender for HD patients  TopicSem
03 조민아 A framework to decipher the genetic architecture of combinations of complex diseases: Applications in cardiovascular medicine     J.Club
03 이시은 A Transparent and Privacy-Preserving Healthcare Platform With Novel Smart Contract for Smart Cities     J.Club
05 최선 Review: Multi-omics approaches to disease     MAInfo
05 김형준 Healthavatar API and data granularity  TopicSem
05 김나영 5 intragrated clinical documents and KNet issues  TopicSem
06 안세환 Querying against cell viability data(PRISM) in CMap LINCS website  SysBiol
07 김나영 Transformation rules to import MELLO on Protege using Cellfie plugin  BioEMR
08 김주연 Parkinson disease genetic analysis with UK Biobank  TopicSem
08 안세환 Compare star-alleles and haplogroups in TPMT  TopicSem
08 김형준 HAP blockchain  Seminar
10 홍진희 Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood     J.Club
10 조동영 Genome-wide study identifies association between HLA-B*55:01 and penicillin allergy     J.Club
12 Intern cGDM Schema Design of HLA data  TopicSem
12 Intern Storing and analyzing a data on a blockchain  TopicSem
12 Intern Determining what makes SARS-CoV-2 B.1.617.2 variant highly contagious  TopicSem
12 윤미선 A Nextflow Genome-Wide Association Study Pipeline  MAInfo
12 윤미선 A Nextflow Genome-Wide Association Study Pipeline  MAInfo
14 이시은 Introduction to MIMIC dataset  BioEMR
15 안선주   TopicSem
15 조원일 .The relationship between Diabetes patients prescribed DPP-4 inhibitor and pancreatitis in UKbiobank      TopicSem
17 유준기 Association between major depressive disorder and multiple disease outcomes: a phenome-wide Mendelian randomisation study in the UK Biobank     J.Club
17 권호식 Systematic single-variant and gene-based association testing of 3,700 phenotypes in 281,850 UK Biobank exomes     J.Club
19 권호식 Interpretation and literature review for the results of HD-MTX induced nephrotoxicity analysis  TopicSem
19 최선 Time series analysis of renal disease patient records  TopicSem
19 최선 Traces_Python library for unevenly-spaced time series analysis  MAInfo
20 윤미선 Group-based pharmacogenetic prediction  SysBiol
21 조원일 Individual patients analysis(UKBB database)   BioEMR
22 윤미선 Class Activation Map in Chest X-ray  TopicSem
22 이우승 Prognostic Potential of Loss of Heterozygosity in Triple Negative Breast Cancer  TopicSem
24 김형준 Combining Ontologies and Open Standards to Derive a Middle Layer Information Model for Interoperability of Personal and Electronic Health Records     J.Club
24 안세환 Haplotype-resolved diverse human genomes and integrated analysis of structural variation     J.Club
26 홍진희 Gene associated with inflammatory bowel disease and further study  TopicSem
26 조동영 Storing Healthcare Big Data Showcase PGx data using cGDM  TopicSem
26 유준기 Combining UKB dataset with eQTL data  MAInfo
27 김주연 Comparing distribution of variants in PD genes among 1KGP3 populations  SysBiol
28 김주연 Evaluating candidate Parkinson disease genes with UK biobank  BioEMR
28 김주연 Evaluating candidate Parkinson disease genes with UK biobank  BioEMR
29 서명의 Scale down the target ampliseq panel of host whole exome plus H.pylori genes for clinical application  TopicSem
29 조민아 The results of association study in IBD and IBD2  TopicSem
31 최선 Medical Transformer: Gated Axial-Attention for Medical Image Segmentation     J.Club
31 이우승 The tumor therapy landscape of synthetic lethality     J.Club

2021-06:
01 윤미선 Stargazer genotyping  SysBiol
02 이시은 FHIR and blockchain  BioEMR
03 김주연 Genomic variant analysis and interpretation for Parkinson’s disease  TopicSem
03 유경훈   TopicSem
03 김주연 Genomic variant analysis and interpretation for Parkinson’s disease  TopicSem
03 유경훈   TopicSem
05 유준기 Transcript expression-aware annotation improves rare variant interpretation     J.Club
05 김형준 SMART Markers_ collecting patient-generated health data as a standardized property of health information technology     J.Club
07 안세환 Haplogroupswith hierarchical clustering  TopicSem
07 조원일 polygenic risk score (PRS) – Drug relationship : study design  TopicSem
08 김주연 Revised association between PGx haplotype frequency and drug use in the UKBB population  SysBiol
09 조원일 the model method of PRS scoring     BioEMR
09 조원일 the model method of PRS scoring   BioEMR
10 권호식 Adverse Effects of Contrast Media  TopicSem
10 최선 Gene network analysis using TCGA RNA-Seq  TopicSem
12 서명의 High-throughput reclassification of SCN5A variant     J.Club
12 부은경 Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson’s disease     J.Club
14 김형준 Adoption of blockchain technology   Seminar
14 윤미선 Big Data in Healthcare and "Healthcare Big Data Showcase"  TopicSem
14 이우승 Systemic Discovery Prognostic Potential Loss of Heterozygosity IL9 Expression Analysis  TopicSem
15 조민아 Review: Benchmarking the Human Leukocyte Antigen Typing Performance of Three Assays and Seven Next-Generation Sequencing-Based Algorithms  SysBiol
16 김주연 Examining polypharmacy in the Korean elderly  BioEMR
17 홍진희 IBD GWAS in ukbb  TopicSem
17 조동영 HLA Typing using hisat-genotype  TopicSem
19 김주연 Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations     J.Club
19 정문경 Genome-wide gene-diet interaction analysis in the UK Biobank identifies novel effects on Hemoglobin A1c     J.Club
21 서명의 Comparison of Helicobacter pylori ampliseq panel and DPO-PCR method   TopicSem
21 이시은 Lifelog Data Collection with Shoe Insole and Data Integration  TopicSem
21 이우승 GTEX eQTL data   MAInfo
23 김형준 Health systems with document- or data-element-level data handling  BioEMR
24 유준기 GWAS study design using UK Biobank  TopicSem
24 조민아 Association Study between CD and UC   TopicSem
26 조원일 Genome-wide association study of medication-use and associated disease in the UK Biobank     J.Club
26 김나영 One Step Away from Technology but One Step Towards Domain Experts-MDRBridge: A Template-Based ISO 11179-Compliant Metadata Processing Pipeline     J.Club
28 부은경 Association between genetic variants and Thiopurine-induced leukopenia in IBD patients  TopicSem
28 임영균 WES analysis of post-ERCP pancreatitis patients  TopicSem
28 권호식 Filtering out false positive variants  MAInfo
29 조원일 Cyrius: accurate CYP2D6 genotyping using whole-genome sequencing data  SysBiol
30 정문경 CKD cohort in UKBB  BioEMR

2021-05:
01 이시은 An automatic method for lung segmentation and reconstruction in chest X-ray using deep neural networks     J.Club
01 부은경 Genetics of 35 blood and urine biomarkers in the UK Biobank     J.Club
03 이우승 Systemic Discovery Prognostic Potential Loss of Heterozygosity  TopicSem
03 홍진희 IBD GWAS in ukbb   TopicSem
03 최선 cancer subtype classification and modeling by pathway attention and propagation  MAInfo
04 조동영 Pharmacogenomics Application and Challenges  SysBiol
04 조동영 Pharmacogenomics Application and Challenges  SysBiol
06 조동영 Genome Analysis Protocol using Rarepedia  TopicSem
06 서명의 Individual antibiotics resistance profiles for antibiotics used in H.pylori therapy  TopicSem
08 안세환 Genetic ancestry plays a central role in population pharmacogenomics     J.Club
08 최선 Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk     J.Club
10 조민아 Association study in IBD patients with depression called by GATK4  TopicSem
10 유준기 Rarepedia analysis of an individual  TopicSem
10 윤미선 Generative Adversarial Nets and its Application in Biomedical Informatics  MAInfo
11 유경훈 Opportunities and challenges for the computational interpretation of rare variation in clinically important genes  SysBiol
12 김나영 Creation of eCRF questionnaire  BioEMR
12 임영균 Association IRF2BP1 gene and Pancreatitis  MAInfo
13 임영균 WES analysis of post-ERCP pancreatitis patients   TopicSem
13 부은경 Association between genetic variants and Thiopurine-induced adverse reactions in IBD patients  TopicSem
15 윤미선 Differential Gene Set Enrichment Analysis: a statistical approach to quantify the relative enrichment of two gene sets     J.Club
15 권호식 A comparison of tools for copy-number variation detection in germline whole exome and whole genome sequencing data     J.Club
17 ... GDA  TopicSem
17 ... GDA  TopicSem
20 이시은 Healthcare Network Services and PGHD DB Building  TopicSem
20 김형준 Implementation of HAP blockchain and selection of PHR validation mode in Agent apps  TopicSem
22 이우승 Exploiting loss of heterozygosity for allele-selective colorectal cancer chemotherapy     J.Club
22 유경훈 Genetic analyses identify widespread sex-differential participation bias     J.Club
24 ... GDA  TopicSem
24 ... GDA  TopicSem
27 ... GDA  TopicSem
27 ... GDA  TopicSem
29 조동영 Whole genome sequencing delineates regulatory and novel genic variants in childhood cardiomyopathy     J.Club
29 임영균 Evaluating the molecular diagnostic yield of joint genotyping–based approach for detecting rare germline pathogenic and putative loss-of-function variants  J.Club
31 정문경 Interactive Web for CKD Patients  TopicSem
31 김나영 KNet Screen Prototype and data display method  TopicSem

2021-04:
01 이우승 Systemic Discovery of Prognosis Potential in Loss of Heterozygosity  TopicSem
01 홍진희 IBD gwas in ukbb  TopicSem
01 이우승 LOH of Korean TNBC  MAInfo
01 이우승 CovCopCan : An efficient tool to detect Copy Number Variation from amplicon sequencing data in inherited diseases and cancel  xMutant
03 임영균 Genome Sequencing as an Alternative to Cytogenetic Analysis in Myeloid Cancers     J.Club
03 유경훈 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS     J.Club
05 조동영 Genome Analysis Protocol using Rarepedia  TopicSem
05 서명의 Helicobacter pylori panel validation result  TopicSem
08 조민아 Association study in IBD patients with depression called by GATK4  TopicSem
08 유준기 Rarepedia analysis of an individual  TopicSem
08 조민아 Review: Transfer learning enables prediction of CYP2D6 haplotype function  SysBiol
08 권호식 review : Contrast media  MAInfo
10 김나영 QL4MDR: a GraphQL query language for ISO 11179-based metadata repositories     J.Club
10 정문경 DIETOS: A dietary recommender system for chronic diseases monitoring and management     J.Club
12 임영균 WES analysis of post-ERCP pancreatitis patients   TopicSem
12 부은경 PGx of inflammatory bowel disease  TopicSem
13 부은경 A systematic comparison of pharmacogene star allele calling bioinformatics algorithms: a focus on CYP2D6 genotyping  SysBiol
14 김주연 Evaluating risk of problems from Beers Criteria medication combinations  BioEMR
15 이시은 PGHD file format transformation into GDF format     TopicSem
15 김형준 Implementation of HAP blockchain with Avatar app and account management  TopicSem
15 임영균 MSI analysis in Cancer.   MAInfo
17 서명의 Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance     J.Club
17 조원일 Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study     J.Club
19 정문경 Investigation on Digital Health Equity  TopicSem
19 김나영 Clinical Document Integration using metadata from CHMR  TopicSem
20 조원일 Review: Pharmacogenimics_lancet  SysBiol
20 조원일 Review: Pharmacogenimics_lancet  SysBiol
20 조원일 Review: pharmacogenomics_lancet  SysBiol
21 김형준 Distributed Ledger Technology(DLT) and blockchain  BioEMR
22 유경훈 Whole Exome Sequencing & PGx for Major Depression  TopicSem
22 안세환 Deleterious TPMT haplogroups in T1GP  TopicSem
22 이우승 Review of Prognosis Potential Loss of Heterozygosity in TNBC  MAInfo
24 홍진희 Analysis of error profiles in deep next generation sequencing data     J.Club
24 조민아 Cytokines mapping for tissue-specific expression, eQTLs and GWAS traits     J.Club
26 조원일 pg_watch_CPIP guideline_G6PD     TopicSem
26 권호식 Candidate variants related with Methotrexate-induced nephrotoxicity  TopicSem
26 유경훈 ATAV - a comprehensive platform for population-scale genomic analyses  xMutant
27 안세환 Calling star-alleles from NGS data  SysBiol
28 정문경 Investigation on Digital Literacy (for Healthcare)  BioEMR
29 최선 Image segmentation of chest X-ray  TopicSem
29 윤미선 Comparison of Machine learning and Deep learning in prediction of PGx variants  TopicSem
29 권호식 Adverse Effects of Contrast Media  MAInfo

2021-03:
01 ... 삼일절  TopicSem
01 ... 삼일절  TopicSem
04 안세환 Star-allele based phenotypes and haplogroups  TopicSem
04 권호식 Clinical characteristics according to the presence or absence of candidate variants in UK Biobank  TopicSem
04 이우승 OncoKB Annotator  MAInfo
04 이우승 Process of Register Sequence data in Public Repository  xMutant
06 홍진희 Imputing Amino acid polymorphisms in human leukocyte antigens     J.Club
06 조민아 The 1000IBD project: multi-omics data of 1000 inflammatory bowel disease patients; data release 1     J.Club
08 최선 Cohort analysis for the retinal detachment research using UKB  TopicSem
08 이우승 Korean TNBC Kinome data Analysis  TopicSem
11 홍진희   TopicSem
11 서명의 Deleterious variants identified in normal cohort and its metabolic enzyme activity distance from normal function CYP2C19  TopicSem
11 권호식 Charlson comorbidity index  MAInfo
13 부은경 Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture     J.Club
13 안세환 Systems Pharmacogenomic Landscape of Drug Similarities from LINCS data: Drug Association Networks     J.Club
15 조민아 Results of matching depression data with IBD data by several folds   TopicSem
15 임영균 WES analysis of post-ERCP pancreatitis patients  TopicSem
15 권호식 Propensity score analysis and R packages  xMutant
18 부은경 Additional data for interpreting thiopurine intolerance in patients with IBD  TopicSem
18 김형준 Update process for HashSeq management in Avatar DB  TopicSem
20 권호식 Analysis of Drug Metabolizing Gene Panel in Osteosarcoma Patients Identifies Association Between Variants in SULT1E1, CYP2B6 and CYP4F8 and Methotrexate Levels and Toxicities     J.Club
20 최선 Learning Transferable Visual Models From Natural Language Supervision     J.Club
22 정문경 Meal Recommendation Method for CKD patients  TopicSem
22 유경훈 Effect of cytochrome CYP2C19 metabolizing status on antidepressant response and side effects  TopicSem
23 김주연 Parkinsons disease Genomic Analysis  Seminar
23 김형준 Health Avatar Project for Dialysis- and RehabilitationNet  Seminar
23 임영균 Synthetic Cancer Survival  Seminar
23 서명의 PGx of Host and Pathogen in Helicobacter Pylori Infection  Seminar
23 이우승 Loss of Heterozygosity  Seminar
23 유경훈 Whole Exome Sequencing & PGx for Major Depression  Seminar
23 안세환 Factor-specific Pattern Mining of Gene Expression  Seminar
23 최선 Automatic acupoint prescription model  Seminar
23 권호식 MTX-induced Nephrotoxicity in ALL  Seminar
23 정문경 Dietary Intervention using ChatBot for Chronically Ill  Seminar
23 부은경 PGx of Inflammatory Bowel Disease  Seminar
23 조민아 Whole Exome Sequencing for Inflammatory Bowel Disease  Seminar
25 안세환 Diplogroups and star-allele based phenotypes  TopicSem
25 권호식 Methotrexate induced renal toxicity  TopicSem
27 이우승 Machine Learning of Patient Characteristics to Predict Admission Outcomes in the Undiagnosed Diseases Network     J.Club
27 김형준 The HealthChain Blockchain for Electronic Health Records_Development Study     J.Club
29 최선 Cohort analysis for the retinal detachment research using UKB  TopicSem
29 윤미선 Common treatment, common variant: evolutionary prediction of functional pharmacogenomic variants  TopicSem
29 김형준 PHR backup in Healthavatar  Seminar

2021-02:
01 부은경 Comparison of clinical outcomes according to pharmacogenetic information   TopicSem
01 김형준 Transaction management of HAP with synchronous and asynchrous blockchain  TopicSem
04 유경훈 Genome-wide association studies of antidepressant response  TopicSem
04 안세환 Introduction of Hail  TopicSem
06 이우승 Comprehensive Analysis of Genetic Ancestry and ItsMolecular Correlates in Cancer     J.Club
06 정문경 Statistical Issues in Analyzing 24-Hour Dietary Recall and 24-Hour Urine Collection Data for Sodium and Potassium Intakes     J.Club
08 권호식 Clinical characteristics according to the presence or absence of candidate variant in UK Biobank  TopicSem
08 최선 Cohort analysis for the retinal detachment research using UKB  TopicSem
11 ... 설날 연휴  TopicSem
11 ... 설날 연휴  TopicSem
13 ... 설날 연휴  J.Club
13 ... 설날 연휴  J.Club
15 서명의 Metabolic activity of mutant CYP2C19 with two types of substrates  TopicSem
15 홍진희 update Fitbit lifelog  TopicSem
18 이우승 Korean TNBC Kinome Data Analysis  TopicSem
18 조민아 Quality control and association study in IBD patients  TopicSem
18 홍진희 ukbb genotype  SysBiol
18 홍진희 ukbb genotype  SysBiol
18 홍진희 ukbb genotype  SysBiol
20 김형준 Article Implement an International Interoperable PHR by FHIR—A Taiwan Innovative Application     J.Club
20 유경훈 The mutational constraint spectrum quantified from variation in 141,456 humans     J.Club
22 임영균 WES analysis of post-ERCP pancreatitis patients  TopicSem
22 부은경 Comparison of clinical outcomes according to pharmacogenetic information   TopicSem
25 김형준 Implementation of Healthavatar blockchain  TopicSem
25 유경훈 Comprehensive analysis to discover the genomic background of antidepressant drug response  TopicSem
25 임영균 metmap  MAInfo
27 최선 Insights into the genetic basis of retinal detachment     J.Club
27 서명의 De novo and bi-allelic pathogenic variants in NARS1 cause neurodevelopmental delay due to toxic gain-of-function and partial loss-of-function effects     J.Club

2021-01:
02 임영균 Comprehensive characterization of amino acid positions in protein structures reveals molecular effect of missense variants     J.Club
02 서명의 Genomic sequencing for newborn screening: results of the NC NEXUS project     J.Club
04 이우승 Korean TNBC Kinome Analysis  TopicSem
04 홍진희 plan of study design in ukbiobank  TopicSem
07 서명의 Variants associated with antibiotics in 23S ribosomal RNA gene of H.pylori  TopicSem
07 조민아 Association study of IBD patients  TopicSem
07 유경훈 Global distribution of CYP2C19 risk phenotypes affecting safety and effectiveness of medications  SysBiol
09 유경훈 Pharmacogenetic information in Swiss drug labels – a systematic analysis     J.Club
09 정문경 When Chatbots Meet Patients: One-Year Prospective Study of Conversations Between Patients With Breast Cancer and a Chatbot     J.Club
11 임영균 Polymorphism affecting Tacrolimus flat peak  TopicSem
11 부은경 Comparison of clinical outcomes according to pharmacogenetic information  TopicSem
14 김형준 Revision comments and response of Healthavatar blockchain  TopicSem
14 유경훈 Genome-wide association studies of antidepressant response  TopicSem
14 홍진희 manual of using GP dataset in ukbb  SysBiol
16 홍진희 HLA typing from RNA-Seq sequence reads     J.Club
16 안세환 A systematic comparison of pharmacogene star allele calling bioinformatics algorithm: a focus on CYP2D6 genotyping     J.Club
18 권호식 Candidate variant as a biomarker for MTX-Induced nephrotoxicity in UK Biobank  TopicSem
18 최선 Cohort design for the retinal detachment research using UKB  TopicSem
21 안세환 Functional or Deleterious variants in each haplogroup  TopicSem
21 이우승 Korean TNBC Kinome data Survival Analysis  TopicSem
23 부은경 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals     J.Club
23 조민아 Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7     J.Club
25 홍진희 Azathioprine side effects among IBD in UKBB  TopicSem
25 서명의 Known mutations in ribosomal binding site of rRNA genes of H.pylori  TopicSem
28 조민아 Association study in IBD patients after NOD2 conditioning  TopicSem
28 임영균 Variants comparison with two calling methods in tacrolimus samples  TopicSem
28 이우승 TNBC Survival Analysis   MAInfo
30 권호식 Real world scenarios in rare variant association analysis: the impact of imbalance and sample size on the power in silico     J.Club
30 임영균 e-MutPath: computational modeling reveals the functional landscape of genetic mutations rewiring interactome networks     J.Club

2020-12:
03 김형준 PHR backup storage based on IPFS  TopicSem
03 김주연 Evaluating PGx molecular phenotype or haplotype frequency association with drug exposure using UK Biobank  TopicSem
03 김형준 PHR backup storage based on IPFS  TopicSem
03 김주연 Evaluating PGx molecular phenotype or haplotype frequency association with drug exposure using UK Biobank  TopicSem
03 이우승 Korean Uveal Melanoma Exome Analysis Figure  MAInfo
03 김주연 Refining the clinical definition of clopidogrel adverse events  SysBiol
05 안세환 A Proteotranscriptomic-Based Computational Drug-Repositioning Method for Alzheimer’s Disease     J.Club
05 김지헌 Genome analysis and knowledge-driven variant interpretation with TGex     J.Club
07 유경훈 Genome-wide association studies of antidepressant response  TopicSem
07 권호식 Candidate variants related with HD-MTX Induced Toxicity in Pediatric ALL  TopicSem
07 안세환 Compare TPMT haplogroup clusterings  BioEMR
07 이우승 Triple Negative Breast Cancer TMB Analysis  xMutant
10 안세환 Discovering three-dimensional FSGPs  TopicSem
10 최선 Relation extraction from clinical articles  TopicSem
12 조민아 Imaging genomics discovery of a new risk variant for Alzheimer     J.Club
12 홍진희 Association between Busulfan Exposure and Outcome in Children Receiving Intravenous Busulfan before Hematologic Stem Cell Transplantation     J.Club
14 김지헌 RarePedia analysis of RP patients  TopicSem
14 이우승 Korean Uveal Melanoma Whole Exome Analysis  TopicSem
14 김주연 PhaCT: a novel approach for preemptive PGx testing and medication therapy optimization  BioEMR
17 홍진희 Upload information of Busulfan patient  TopicSem
17 서명의 Sequencing result of NUDT15 and TPMT gene in 150 leukemia patients by using next-generation sequencing panel  TopicSem
17 최선 Training Keras Models Using the Genetic Algorithm with PyGAD  MAInfo
17 조민아 PHASE: A program for reconstructing haplotypes from population data  SysBiol
19 권호식 Combining clinical and candidate gene data into a risk score for azathioprine-associated leukopenia in routine clinical practice     J.Club
19 김형준 Blockchain for Secure EHRs Sharing of Mobile Cloud based E health Systems     J.Club
21 조민아 Discovery variants associated with IBD(Inflammatory Bowel Disease)  TopicSem
21 임영균 Synthetic Association with ERCC6-rs2228528 in Pancreatic Cancer   TopicSem
24 부은경 Comparison of clinical outcomes between non-WT and WT in IBD  TopicSem
24 김형준 Data communication between XNet and Agent  TopicSem
24 임영균 Comparison deleteriousness between germline and somatic variants in cancer   MAInfo
26 최선 Comparison of laboratory threshold criteria in drug-induced liver injury detection algorithms for use in pharmacovigilance     J.Club
26 이우승 Advances in germline predisposition to acute leukaemias and myeloid neoplasms     J.Club
28 유경훈 Genome-wide association studies of antidepressant response  TopicSem
28 안세환 TPMT haplogroup construction  TopicSem
31 권호식 Candidate variant in UK Biobank  TopicSem
31 최선 Applying the ADR template for retinal detachment used in K-CDM to UKB  TopicSem

2020-11:
02 홍진희 Result if ukbb replicate study and lifelog data format  TopicSem
02 서명의 Measuring enzyme activity of mutant CYP2C19 by using mephenytoin  TopicSem
02 김주연 Selecting ancestry informative markers and random variants for synthetic association analysis  BioEMR
02 최선 Handling temporality of clinical events with application to Adverse Drug Event detection in Electronic Health Records: A scoping review  xMutant
05 조민아 Searching literature regarding candidate variants associated with EOAD(Early onset Alzheimer  TopicSem
05 임영균 Germline variants associated with prognosis and drug response in pancreatic cancer patients  TopicSem
05 조민아 Introduction of Taiwan biobank database  SysBiol
05 이우승 Recent LOH algorithm review  MAInfo
05 조민아 Introduction of Taiwan biobank database  SysBiol
07 최선 Detecting drug-drug interactions using artificial neural networks and classic graph similarity measures     J.Club
07 임영균 Phase and context shape the function of composite oncogenic mutations       J.Club
09 부은경 Variant-level explanation for gender difference in PD  TopicSem
09 김형준 Figures and tables of Healthavatar blockchain  TopicSem
12 김주연 Evaluating CPIC PGx variant associated ADE risks with UK Biobank  TopicSem
12 유경훈 PGx phenotype association with dose and side effects of ADs in 1TD patients.   TopicSem
12 부은경 FastTargetPred: a program enabling the fast prediction of putative protein targets for input chemical databases  SysBiol
14 유경훈 Drug Response Pharmacogenetics for 200,000 UK Biobank Participants     J.Club
14 이우승 Loss of heterozygosity of essential genes represents a widespread class of potential cancer vulnerabilities     J.Club
14 조민아 Review: Neutrophil-to-lymphocyte ratio in inflammatory bowel disease - as a new predictor of disease severity  SysBiol
16 안세환 FSGPs with LINCS L1000 data  TopicSem
16 권호식 Analysis of renal toxicity induced by MTX in Korean pediatric ALL and UKB  TopicSem
19 최선 Algorithm application for clinical information extraction  TopicSem
19 김지헌 Rarepedia analysis of healthy individuals  TopicSem
21 서명의 Germline and mosaic variants in PRKACA and PRKACB cause a multiple congenital malformation syndrome     J.Club
21 부은경 Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy     J.Club
23 이우승 CNV Benchmark Results with Validation data  TopicSem
23 홍진희 Genetic Biomarker of Busulfan induced Hepatotoxicity  TopicSem
23 김주연 Comparing CPIC star allele phenotype or genotype frequencies between the 1000 Genomes and UKBB population  BioEMR
26 서명의 Enzymatic activity of mutant CYP2C19 and variant impact prediction scores  TopicSem
26 조민아 Subsetting LOAD(Late-onset Alzheimer’s disease) from ADSP data and compared to EOAD(Early-onset Alzheimer’s disease) data  TopicSem
26 임영균 pancreatic cancer WES analysis  MAInfo
28 정문경 Designing for Health Chatbots     J.Club
28 김주연 Population structure and pharmacogenomic risk stratification in the United States     J.Club
30 임영균 DNA Damaging Repair (DDR) gene Enrichment and Synthetic Association in Pancreatic Cancer   TopicSem
30 부은경 Classification of IBD subjects into three types of drug metabolizers  TopicSem
9 이우승 Result of BRCA2 CNV qPCR Validation  xMutant

2020-10:
01 ... 추석  TopicSem
01 ... 추석  TopicSem
03 ... 개천절  J.Club
03 ... 개천절  J.Club
05 이우승 Korean TNBC Kinome Analysis   TopicSem
05 홍진희 vitD and inflammatory bowel disease association study in ukbb   TopicSem
08 서명의 Mutant CYP2C19 overexpression by using human cell system  TopicSem
08 조민아 Analysis EOAD using matched depression data and 1000 genome data as control  TopicSem
10 김주연 Polygenic architecture informs potential vulnerability to drug-induced liver injury     J.Club
10 조민아 PCSK5 mutation in a patient with the VACTERL association     J.Club
12 임영균 Identifying genetic variants that affect pancreatic cancer patients survival  TopicSem
12 부은경 Validation of PD-associated Variants Using UKBB data  TopicSem
12 김주연 Progress in star allele calling for UKBB  BioEMR
15 ... 개교기념일  TopicSem
15 ... 개교기념일  TopicSem
17 안세환 Drug-induced adverse events prediction with the LINCS L1000 data     J.Club
17 홍진희 Vitamin D and IBD: Mendelian randomization analyses in the Copenhagen studies and ukbb     J.Club
19 김형준 Healthavatar blockchain with added process of sending data by POST API  TopicSem
19 최선 chart review for kcdm analysis  TopicSem
22 유경훈 Comparative Analysis results of a subgroup filtered with 12-week Escitalopram dose   TopicSem
22 권호식 Analysis of renal toxicity induced by MTX based on fold Cr in Korean pediatric ALL and UKB  TopicSem
22 김주연 Primary care prescription drug use and related actionable drug-gene interactions in the Danish population  SysBiol
22 최선 Pytorch tutorial  MAInfo
24 부은경 Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale     J.Club
24 김지헌 Precision medicine integrating whole-genome sequencing, comprehensive metabolomics, and advanced imaging     J.Club
26 안세환 Discovering cell- and drug-specific patterns with the LINCS L1000 data  TopicSem
26 김주연 Examining the impact of pharmacogenomics testing with UK Biobank and its use for ADR risk comparisons  TopicSem
26 안세환 Introduction of Phylip  BioEMR
29 김지헌 RarePedia analysis of healthy individuals  TopicSem
29 이우승 Triple Negative Breast Cancer Genome Analysis  TopicSem
29 임영균 Summary of Pancreatic cancer data analysis   MAInfo
31 권호식 A novel statistical method for interpreting the pathogenicity of rare variants     J.Club
31 김형준 Using HL7 FHIR to achieve interoperability in patient health record     J.Club

2020-09:
03 안세환 Enrichment Test of drug-specific genes  TopicSem
03 최선 Additional analysis for K-CDM research (2217 kb)  TopicSem
03 안세환 Enrichment Test of drug-specific genes  TopicSem
03 최선   TopicSem
05 김지헌 SWEDEGENE—a Swedish nation-wide DNA sample collection for pharmacogenomic studies of serious adverse drug reactions       J.Club
05 이우승 The repertoire of mutational signatures in human cancer     J.Club
07 홍진희 Candidate of SAG and UKBB  TopicSem
07 서명의 Known mutations in H.pylori genome associated with Amoxicillin resistance and Metronidazole resistance phenotype  TopicSem
07 최선 Chart review to confirm the results of CDM analysis  BioEMR
07 최선 Chart review to confirm the results of CDM analysis  BioEMR
10 김지헌 RarePedia analysis of healthy individuals  TopicSem
10 이우승 Korean Uveal Melanoma Exome Analysis  TopicSem
10 최선 propensity score matching  MAInfo
12 임영균 A cancer drug atlas enables synergistic targeting of independent drug vulnerabilities     J.Club
12 김형준 An Architecture and Management Platform for Blockchain-Based Personal Health Record Exchange: Development and Usability Study      J.Club
14 조민아 Association study using EOAD (Early Onset Alzheimer's Disease) data  TopicSem
14 임영균 Identifying genetic variants that affect pancreatic cancer patients’ survival  TopicSem
14 최선 Basic operation of Flask  xMutant
14 안세환 The PRISM drug repurposing dataset  BioEMR
17 부은경 Validation of PD associated variants using UKBB data  TopicSem
17 김형준 Process for PHR data in Healthavatar blockchain architecture  TopicSem
17 이우승 Triple Negative Breast Cancer Analysis  xMutant
17 임영균 Identifying genetic variant associated FOLFIRINOX regimen  MAInfo
19 정문경 Transparent sharing of digital health data: A call to action     J.Club
19 유경훈 Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population     J.Club
21 김주연 Applying modified method of candidate SAG extraction  TopicSem
21 안세환 Discovering significant and interpretable patterns with LINCS L1000 data  TopicSem
21 김주연 Star allele calling for UKBB  BioEMR
24 유경훈 Comparative Analysis results of a subgroup filtered with 12-week Escitalopram dose   TopicSem
24 권호식 Candidates related with Methotrexate induced acute kidney injury  TopicSem
24 이우승 BLAST Result of UVM for Sanger Validation  MAInfo
26 최선 Scalable and accurate deep learning with electronic health records     J.Club
26 서명의 Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes     J.Club
28 최선 K-CDM analysis_2020mfds  TopicSem
28 김지헌 RarePedia analysis of healthy individuals  TopicSem
28 권호식 review : Oligonucleotide microarray  xMutant

2020-08:
01 정문경 Interaction of DRD2/ANKK1 Taq1A Genotype with in-Store Retail Food Environment Exposures on Diet Quality in a Cohort of Quebec Adults       J.Club
01 서명의 De novo variants in SPOP cause two clinically distinct neurodevelopmental disorders     J.Club
03 최선   TopicSem
03 권호식 MTX and AKI in UK Biobank   TopicSem
06 안세환 Interpretation significant cell- and drug-specific FSGPs  TopicSem
06 김지헌 RarePedia analysis of helathy individuals  TopicSem
06 권호식 Sex chromosomes and genetic association studies   MAInfo
08 채정환 Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses     J.Club
08 부은경 High-definition likelihood inference of genetic correlations across human complex traits     J.Club
10 이우승 Korean Uveal Melanoma Analysis  TopicSem
10 홍진희 synthetic association & UK biobank study guidline  TopicSem
10 이우승 NGS CheckMate : Validating sample identity in NGS studies  xMutant
13 임영균 Pancreatic Cancer with New-onset Diabetes Mellitus  TopicSem
13 조민아 Association study using EOAD (Early Onset Alzheimer's Disease) data  TopicSem
13 임영균 Affecting FOLFIRINOX sensitivity(CAP grade) variants  MAInfo
15 ... 광복절  J.Club
15 ... 광복절  J.Club
17 ... 임시공휴일  TopicSem
17 ... 임시공휴일  TopicSem
20 서명의 CYP2C19 star allele for PPI treatment in Helicobacter pylori eradication therapy  TopicSem
20 부은경 Summary of Candidate PD-associated Variants and Plan for Validation  TopicSem
22 조민아 Germline variant burden in cancer genes correlates with age at diagnosis and somatic mutation burden     J.Club
22 안세환 Improving cell-specific drug connectivity mapping with collaborative filtering     J.Club
24 김형준 Facilitating traceability of PHR data by blockchain  TopicSem
24 윤선민   TopicSem
27 김효정 PGx CDS: modular implementation of CPIC guideline  TopicSem
27 김주연 Updates of process and criteria for candidate SAG extraction  TopicSem
27 이우승 CNV Validation Candidate Selection  MAInfo
29 홍진희 .6mp metabolite profiles provide a biochemical explanation for 6mp resistance in patients with inflammatory bowel disease     J.Club
29 권호식 A functional polymorphism in the ATP-Binding Cassette B1 transporter predicts pharmacologic response to combination of nortriptyline and morphine in neuropathic pain patients     J.Club
31 유경훈 Comparative Analysis results of a subgroup filtered with 12-week Escitalopram dose   TopicSem
31 권호식 Candidate variants related with HD-MTX Induced Toxicity in Pediatric ALL  TopicSem
31 김주연 Identifying populations likely to benefit from pharmacogenomic testing  SysBiol
31 김주연 Implementation of pharmacogenomics via a research biobank  BioEMR

2020-07:
02 최선 Drug side effects detection using K-CDM data for new scenarios  TopicSem
02 안세환 Interpretation FSGPs in activator group  TopicSem
02 최선 Drug side effects detection using K-CDM data for new scenarios  TopicSem
02 안세환 Interpretation FSGPs in activator group  TopicSem
04 권호식 Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes     J.Club
04 이우승 Korean Genome Project: 1094 Korean personal genomes with clinical information     J.Club
04 최선 Sklearn.preprocessing package for preprocessing data   MAInfo
06 김지헌 RarePedia analysis of healthy individuals  TopicSem
06 유경훈 Comparative analysis of 12w Escitalopram/SSRI dose conditioning effects  TopicSem
06 안세환 Significant FSGPs estimating FDR  BioEMR
06 박유미 Genotype Data in UKBiobank  SysBiol
06 이우승 Somatic Mutation Filtering Result with Korea1KG  xMutant
09 권호식 Adverse Effects of Contrast Media   TopicSem
09 이우승 Uveal Melanoma Analysis  TopicSem
09 임영균 CAP grade analysis  MAInfo
11 윤선민 De novo variants in exomes of congenital heart disease patients identify risk genes and pathways     J.Club
11 김형준 Development of Comprehensive Personal Health Records Integrating Patient-Generated Health Data Directly From Samsung S-Health and Apple Health Apps     J.Club
13 홍진희 FSIP2/INSR bam&fasta level read check  TopicSem
13 임영균 Genetic polymorphism affecting FOLFIRINOX response in pancreatic cancer patients  TopicSem
13 김주연 The implementation of pharmacogenomics for older adults  SysBiol
15 이우승 UVM Copy Number Analysis   MAInfo
16 조민아 Replicating prior research using EOAD(Early Onset Alzheimer Disease) data  TopicSem
16 서명의 Mutations associated with Tetracycline and Levofloxacin resistance phenotype in H.pylori  TopicSem
18 최선 Comprehensive comparative effectiveness and safety of first-line antihypertensive drug classes: a systematic, multinational, large-scale analysis     J.Club
18 유경훈 Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts     J.Club
20 부은경 Analysis to explain difference in genetic burden between males and females in PD  TopicSem
20 김형준 Review of MyHealthData Platform and Interoperability  TopicSem
20 김주연 Properties of the imputed genotype data format BGEN  BioEMR
20 권호식 Error and Trouble shooting In TVC and GATK  xMutant
20 유경훈 Perturbation robustness analyses reveal parameters in variant interpretation pipelines  xMutant
23 한봄 CBZ-induced SCAR  TopicSem
23 윤선민   TopicSem
23 홍진희 synthetic association study  SysBiol
23 홍진희 synthetic association study  SysBiol
23 홍진희 synthetic association study  SysBiol
23 홍진희 synthetic association study  SysBiol
23 홍진희 synthetic association study  SysBiol
23 홍진희 synthetic association study  SysBiol
23 홍진희 synthetic association study  SysBiol
23 홍진희 synthetic association study  SysBiol
23 홍진희 synthetic association study  SysBiol
23 홍진희 synthetic association study  SysBiol
25 임영균 A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer     J.Club
25 김주연 Projected impact of pharmacogenomic testing on medications beyond antiplatelet therapy in percutaneous coronary intervention patients     J.Club
27 박유미 Haplogroup construction for CRIM1 and IL6  TopicSem
27 김효정 Clinical genome data model further discussion  TopicSem
27 조민아 Gene set enrichment analysis tools  SysBiol
30 김주연 Frequency of ADR genotypes in UK Biobank  TopicSem
30 유경훈 Comparative analysis of 12w Escitalopram/SSRI dose adjustment effects  TopicSem

2020-06:
01 권호식 Candidate variants related with HD-MTX Induced Toxicity in Pediatric ALL  TopicSem
01 유경훈 Genomic variant analysis using thiopurine target panel including 4 genes  TopicSem
01 안세환 Integrative web platform for analysis of LINCS data (iLINCS)  BioEMR
01 부은경 Additional analysis to identify candidate variants associated with PD  SysBiol
04 안세환 Discovering FSGPs using small molecules classified by Moa  TopicSem
04 김주연 Estimating occurrence of South Koreans with ADR-associated genotypes  TopicSem
04 이우승 Uveal Melanoma Analysis: Somatic Mutation   MAInfo
06 ... 현충일  J.Club
06 ... 현충일  J.Club
08 최선 Evaluation of LDL-C target achievement according to age after statin prescription  TopicSem
08 김지헌 Genomic variant analysis of healthy individuals   TopicSem
08 최선 Reflection of expert advice on K-CDM scenario_Psychiatry  BioEMR
08 유경훈 VEF: a variant filtering tool based on ensemble methods  xMutant
08 권호식 Difference in clinical information according to candidate variants in HD-MTX Study  xMutant
08 안세환 Mechanism of action lists in L1000 data  SysBiol
11 이우승 Analysis of Uveal Melanoma Genome  TopicSem
11 홍진희 .연세대 111 patients WXS  TopicSem
11 임영균 Variant Analysis with Pancreatic cancer FNA sample  MAInfo
13 박유미 Pharmacogenetics at scale: An analysis of the UK Biobank     J.Club
13 안세환 Evaluation of Connectivity Map shows limited reproducibility in drug repositioning     J.Club
15 서명의 Variants in H.pylori associated with Clarithromycin resistance phenotype  TopicSem
15 조민아 Exploration and preprocessing of EOAD​ (Early Onset of Alzheimer  TopicSem
15 김주연 Estimating occurrence of adverse drug event risk genotypes with UK Biobank: data exploration  BioEMR
15 한봄 Assessment of case-control studies  SysBiol
18 부은경 Additional analyses to explain gender difference in Parkinson’s Disease  TopicSem
18 한봄 Updates of CBZ-SCAR project  TopicSem
18 권호식 Variants related to MTX efficacy or toxicity reported in PharmGKB and Clinical significance in ClinVar   MAInfo
20 홍진희 wgs is more poweful than wes for detecting exome variants     J.Club
20 김효정 An ancillary genomics system to support the return of pharmacogenomic results     J.Club
22 김형준 HealthAvatar blockchain and PHR type  TopicSem
22 임영균 Concentration ratio of tacrolimus as indicator in follow-up of patients received transplant   TopicSem
22 김효정 Query design for K-CDM ADR studies  BioEMR
22 박유미 GVB score optimization to reduce neutral variant effects  xMutant
25 윤선민 WES analysis of 25 patients with post ERCP pancreatitis  TopicSem
25 박유미 Comparing characteristics between statistical tests and scoring methods  TopicSem
25 임영균 Drug response & Prognosis measurement in Cancer Research   MAInfo
27 조민아 Allele Frequency of Pathogenic Variants Related to Adult-Onset Mendelian Diseases     J.Club
27 김지헌 The emerging landscape of health research based on biobanks linked to electronic health records: Existing resources, statistical challenges, and potential opportunities     J.Club
29 김효정 Appendix for Clinical Genome Data Model towards Precision Medicine  TopicSem
29 김주연 Estimating occurrence of ADR genotypes in UK Biobank: obtaining prescription counts  TopicSem

2020-05:
02 최선 DeepTox_Toxicity Prediction using Deep Learning     J.Club
02 김형준 Toward a Model for Personal Health Record Interoperability     J.Club
04 박유미 Defining anticoagulant-induced adverse reaction  TopicSem
04 김효정 Pharmacogenomic Clinical Decision Support: Modular Implementation of CPIC Guideline   TopicSem
04 박유미 COVID-19 data in the UK Biobank  SysBiol
04 최선 Reflection of expert advice on K-CDM scenario_1  BioEMR
04 최선 Consideration on study subjects utilizing UKbiobank  xMutant
07 김주연 Synthetic association study for 6-mercaptopurine intolerance  TopicSem
07 유경훈   TopicSem
07 권호식 HD-MTX : BUN & Candidates from Fold-Cr  MAInfo
09 윤선민 Blacklisting variants common in private cohorts but not in public databases optimizes human exome analysis     J.Club
09 임영균 A reference map of the human binary protein interactome     J.Club
11 안세환 Discovering FSGP using gene expression signature and fold change  TopicSem
11 권호식 TM7SF3 induced Renal Toxicity in ALL administered with MTX  TopicSem
11 박유미 Update in UK Biobank data table  xMutant
11 김주연 Immune response in Parkinson’s disease driven by HLA display of α-synuclein peptides  BioEMR
11 김주연 Immune response in Parkinson’s disease driven by HLA display of α-synuclein peptides  BioEMR
11 김주연 Contribution of genetic variation in drug-drug-gene-interactions  SysBiol
11 김주연 Contribution of genetic variation in drug–drug–gene interactions  SysBiol
14 최선 EMR Study to verify the efficacy of lipilou  TopicSem
14 이우승 Genome Analysis of Uveal Melanoma   TopicSem
14 임영균 Progression of tacrolimus study  MAInfo
16 정문경 Aggregating multiple real-world data sources using a patient-centered health-data-sharing platform     J.Club
16 김주연 Pharmacogenomic-Based Decision-Support to Predict Adherence to Medications     J.Club
18 서명의 F10 amino acid changes identified from symptomatic subjects of Factor X deficiency  TopicSem
18 임영균 Cpeak/C0 as indicator in follow-up of patients received transplant  TopicSem
18 홍진희 illumina sequencing WES 111 samples  SysBiol
18 윤선민 Tables and figures of AAP data analysis results using the modified workflow  xMutant
18 김효정 Code system review in UKBB:Read Codes and CTV3  BioEMR
21 부은경 Comparison of genetic loads between males and females with PD  TopicSem
21 김형준 Client-side request for PHR validation in Healthavatar blockchain  TopicSem
21 윤선민 Retrieval of AAP patients with acute pancreatitis caused by drugs in UK Biobank data  MAInfo
23 채정환 Development of CRISPR as an Antiviral Strategy to Combat SARS-CoV-2 and Influenza     J.Club
23 한봄 Predicted efficacy of a pharmacogenetic passport for inflammatory bowel disease     J.Club
25 한봄 Whole-exome sequencing identifies genetic risk factors associated with carbamazepine-induced SCAR  TopicSem
25 윤선민 Whole exome sequencing analysis of asparaginase-associated pancreatitis in Korean pediatric patients  TopicSem
25 한봄 Assessment of pharmacogenetic tests  BioEMR
25 조민아 Association analysis-Plink and Snpsift  SysBiol
25 이우승 Uveal melanoma germline analysis   xMutant
28 박유미 Distribution of 1KGP subjects with unclear molecular phenotypes for 17 genes with published CPIC guidelines  TopicSem
28 김효정 Pharmacogenomic Clinical Decision Support: Modular Implementation of CPIC Guideline   TopicSem
29 최선 Research design for TEA  MAInfo
30 서명의 SYCP2 translocation-mediated dysregulation and frameshift variants cause human male infertility     J.Club
30 부은경 Complementary genes contribute sex-biased vulnerability in diverse disorders     J.Club

2020-04:
02 윤선민 Modified figures and tables of WES analysis of AAP in Korean pediatric patients  TopicSem
02 박유미 Protective effect of F10 variants against coronary artery disease in the UK Biobank data  TopicSem
02 윤선민 Modified figures and tables of WES analysis of AAP in Korean pediatric patients  TopicSem
02 박유미 Protective effect of F10 variants against coronary artery disease in the UK Biobank data  TopicSem
02 최선 Rethinking drug design in the artificial intelligence era  MAInfo
04 서명의 Opposite modulation of RAC1 by mutations in TRIO is associated with distinct, domain-specific neurodevelopmental disorders     J.Club
04 부은경 Excess of singleton loss-of-function variants in Parkinson’s disease contributes to genetic risk     J.Club
06 김효정 Pharmacogenomic Clinical Decision Support: Modular Implementation of CPIC Guideline   TopicSem
06 김주연 Synthetic association analysis for tacrolimus response  TopicSem
06 김주연 SWEDEGENE-a Swedish nation-wide DNA sample collection for pharmacogenomic studies of serious adverse drug reactions  BioEMR
06 안세환 The Comparative Toxicogenomics Database  SysBiol
06 윤선민 Candidate variants list by differential cut-off in Asparaginase associated pancreatitis   xMutant
09 유경훈   TopicSem
09 안세환 Top 50 FSGPs in LINCS L1000 data  TopicSem
09 임영균 Comparison variants between TSVC and GATK pipeline  MAInfo
11 한봄 Whole genome sequencing to identify predictive markers for the risk of drug-induced interstitial lung disease     J.Club
11 박유미 Minimal phenotyping yields genome-wide association signals of low specificity for major depression     J.Club
13 채정환   TopicSem
13 권호식 TM7SF3 in UK Biobank  TopicSem
13 한봄 The utility of surrogate markers in predicting HLA alleles associated with adverse drug reactions in Vietnamese  SysBiol
13 이우승 GATK - Germline copy number variant discovery (CNVs)  xMutant
16 최선 Evaluating the efficacy of lipilou using EMR  TopicSem
16 이우승 Genome Analysis of Uveal Melanoma   TopicSem
18 안세환 Predict New Therapeutic Drugs for Hepatocellular Carcinoma Based on Gene Mutation and Expression     J.Club
18 김효정 Concepts Driving Pharmacogenomics Implementation Into Everyday Healthcare     J.Club
20 서명의 FX activity evaluation by using recombinant FX mutant protein  TopicSem
20 임영균 Pancreatic cancer sample with FNA WXS Analysis  TopicSem
20 최선 Database for screening the toxicity of peptides  SysBiol
23 부은경   TopicSem
23 김형준 Healthavatar Blockchain_updated research scope and figures   TopicSem
23 이우승 TNBC survival analysis  MAInfo
25 권호식 Genetic and clinical prediction models for the efficacy and hepatotoxicity of methotrexate in patients with rheumatoid arthritis: a multicenter cohort study     J.Club
25 이우승 Interplay between whole-genome doubling and the accumulation of deleterious alterations in cancer evolution      J.Club
27 한봄 Whole exome sequencing identifies genetic risk factors associated with Carbamazepine induced Severe Cutaneous Adverse drug Reaction  TopicSem
27 윤선민 WES Analysis to search the risk factor of anthracycline-induced prolonged neutropenia  TopicSem
27 안세환 Fold changes of LINCS L1000 data  BioEMR
27 김효정 [review] Development of a Genomic Data Flow Framework: Results of a Survey Administered to NIH-NHGRI IGNITE and eMERGE Consortia Participants  SysBiol
27 권호식 Study of contrast agent to side effects from additional samples  xMutant
30 ... 석가탄신일  TopicSem
30 ... 석가탄신일  TopicSem

2020-03:
02 부은경 Gender Differences in Parkinson’s Disease   TopicSem
02 한봄 HISAT2 HLA typing  TopicSem
02 김효정 [Review] Precision Medicine Is Not Just Genomics: The Right Dose for Every Patient  BioEMR
02 박유미 Comparing polygenic risk scores between male and female depressive patients  SysBiol
05 김형준 Implementation of Healthavatar blockchain  TopicSem
05 윤선민 Figures and tables of WES analysis of AAP in Korean pediatric patients  TopicSem
05 이우승 PRISM Drug Repurposing Resource  xMutant
05 임영균 Pan-Cancer Analysis of Whole Genomes (PCAWG) project.   MAInfo
07 윤선민 Time to Rethink the Genetic Architecture of Long QT Syndrome      J.Club
07 유경훈 A genetics-led approach defines the drug target landscape of 30 immune-related traits     J.Club
09 박유미 A complementary strategy to the current patient drug intolerance classification system using massively parallel sequencing results  TopicSem
09 김효정 Toward systematic integration of CPIC guideline into clinical practice   TopicSem
09 김주연 Review of PGx-Passport: a DPWG-based preemptive pharmacogenetic testing panel  BioEMR
09 김주연 The design and implementation strategy of European pharmacogenomics through the U-PGx consortium  SysBiol
09 김주연 The design and implementation strategy of European pharmacogenomics through the U-PGx consortium  SysBiol
12 김주연 Gene-wise analysis of Parkinsons disease candidate SAGs  TopicSem
12 유경훈 Star allele phenotype distribution over the 50 pgx genes in 1TD patients  TopicSem
12 이우승 Access and Download the EGA European Genome-Phenome Archive  MAInfo
12 유경훈 Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations  xMutant
14 임영균 Identification of cancer driver genes based on nucleotide context     J.Club
14 최선 A Hybrid Health Journey Recommender System using Electronic Medical Record     J.Club
16 안세환 Determining significant FSGP using permutation  TopicSem
16 권호식 TM7SF3 candidate variant : Renal Toxicity in Pediatric ALL patients administered with HD-MTX  TopicSem
16 최선 Consideration of new scenario for detecting ADR in K-CDM  BioEMR
19 채정환   TopicSem
19 최선 Automated systematic review     TopicSem
19 권호식 Discussion for defining phenotypes from UKB  xMutant
19 홍진희 Whole exome seuqence varinat calling in 2 ALL patient     SysBiol
19 홍진희 Whole exome seuqence varinat calling in 2 ALL patient  SysBiol
19 홍진희 Whole exome seuqence varinat calling in 2 ALL patient  SysBiol
19 윤선민 Figures and tables of WES analysis of AAP in Korean pediatric patients   MAInfo
21 정문경 The mechanisms of pharmacokinetic food_drug interactions_A perspective from the UNGAP group     J.Club
21 김주연 Estimated nationwide impact of implementing a preemptive pharmacogenetic panel approach to guide drug prescribing in primary care in The Netherlands     J.Club
23 이우승 Genome Analysis of Asian Uveal Melanoma  TopicSem
23 서명의 Chromogenic activity evaluation of FX protein with mutant catalytic domain  TopicSem
23 안세환 Discovering FSGP for UKBiobank  BioEMR
23 조민아 Preprocessing WES data of EOAD (Early Onset Alzheimer’s Disease)  SysBiol
23 조민아 Preprocessing WES data of EOAD (Early Onset Alzheimer’s Disease)  SysBiol
23 조민아 Preprocessing WES data of EOAD (Early Onset Alzheimer’s Disease)  SysBiol
26 임영균 Variant analysis in tacrolimus PK genes  TopicSem
26 부은경 Identification of Candidate Variants in Parkinson’s Disease   TopicSem
26 최선 Drug classification-ATC code, RXnorm  xMutant
26 최선 Drug classification-ATC code, RXnorm  xMutant
26 권호식 TM7SF3 variant in UKB  MAInfo
28 국수경 Integrative analysis of multi-omics data identified EGFR and PTGS2 as key nodes in a gene regulatory network related to immune phenotypes in head and neck cancer     J.Club
28 채정환 The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants     J.Club
30 김형준 Healthavatar Blockchain_update figures and supplementary data  TopicSem
30 한봄 CBZ-induced SCAR  TopicSem
30 부은경 Variants associated with PD  SysBiol
30 박유미 Ischemic heart disease group extraction from UK Biobank patients  xMutant

2020-02:
01 채정환 Hyperactivation of TORC1 Drives Resistance to the Pan-HER Tyrosine Kina  J.Club
01 한봄 The GenomeAsia 100K Project enables genetic discoveries across Asia     J.Club
03 김주연 Detection of variants contributing to synthetic association in Parkinson’s disease  TopicSem
03 유경훈 HLA Association with Antidepressant- Induced Adverse Reactions and Response  TopicSem
03 안세환 Permutation testing for the distance measures  BioEMR
06 김재환 Development and demonstration of RarePedia (through web service and Python3 API) and Retinitis pigmentosa analysis platform  TopicSem
06 안세환 Interpretable patterns from LINCS-L1000 data  TopicSem
06 최선 Query design for emr study&  xMutant
06 최선 Query design for emr study&  xMutant
06 유승원 mercaptopurine study - discussion issues  MAInfo
08 국수경 Shared genetic and epigenetic mechanisms between chronic periodontitis     J.Club
08 김효정 Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network      J.Club
10 ... GDA  TopicSem
10 ... GDA  TopicSem
13 ... GDA  TopicSem
13 ... GDA  TopicSem
15 박유미 GeVIR is a continuous gene-level metric that uses variant distribution patterns to prioritize disease candidate genes      J.Club
15 안세환 eVIP2: Expression-based variant impact phenotypic to predict the function of gene variants     J.Club
17 ... GDA  TopicSem
17 ... GDA  TopicSem
17 김재환 Development and demonstration of RarePedia and Retinitis pigmentosa analysis platform  Seminar
20 채정환 taxol further study  TopicSem
20 최선 Study on non-inferiority of lipilou  TopicSem
20 박유미 Helix UK Biobank browser  xMutant
20 권호식 BiobankRead  MAInfo
22 부은경 Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts     J.Club
22 이우승 Discovering the anticancer potential of nononcology drugs by systematic viability profiling     J.Club
24 권호식 Clinical Data in UK Biobank   TopicSem
24 서명의 Chromogenic activity of overexpressed F10 protein with mutant catalytic domain  TopicSem
24 김효정 [Review] Personalized Medicine and the Power of Electronic Health Records  SysBiol
24 김효정 [Review] Personalized Medicine and the Power of Electronic Health Records  SysBiol
27 이우승   TopicSem
27 임영균 Identification of genomic markers affecting sentivity of tacrolimus   TopicSem
27 윤선민 Study overview of post ERCP pancreatitis  xMutant
27 최선 Advanced SQL query using sub query, CTE  MAInfo
29 권호식 Identification of pathogenic variant enriched regions across genes and gene families     J.Club
29 김형준 OmniPHR: A distributed architecture model to integrate personal health records     J.Club

2020-01:
02 윤선민 WES Analysis to search the risk factor of anthracycline-induced prolonged neutropenia  TopicSem
02 권호식 HD-MTX induced Renal Toxicity in Pediatric ALL  TopicSem
02 윤선민 WES Analysis to search the risk factor of anthracycline-induced prolonged neutropenia  TopicSem
02 권호식 HD-MTX induced Renal Toxicity in Pediatric ALL  TopicSem
02 윤선민 Therapeutic index measured on FDA approved drugs for population comparison  xMutant
02 최선 유방암과 위암의 항암치료원칙  MAInfo
04 임영균 The mutational footprints of cancer therapies     J.Club
04 권호식 Evaluating potential drug targets through human loss-of function genetic variation     J.Club
06 최선 Automated systematic review_sampling  TopicSem
06 김재환 Migration and upgrade of RarePedia, GVAT, and GIAT with Retinitis pigmentosa pipline development  TopicSem
06 김주연 Clinical Utility of Pharmacogene Panel-Based Testing in Patients Undergoing Percutaneous Coronary Intervention (PCI)  BioEMR
06 부은경 Synergyfinder: Calculate and Visualize Synergy Scores for Drug Combinations  SysBiol
09 이우승 SCV:Statistical algorithm to detect gene-wide Copy number Variant  TopicSem
09 서명의 Application of next‑generation sequencing to analyze drug response in human leukemia by using the panel including 11 genes  TopicSem
09 이우승 Docker Pusing for release and PyQT for GUI programming  xMutant
09 이우승 Docker Pusing for release and PyQT for GUI programming  xMutant
09 임영균 Genetic polymorphism influences the pharmacokinetics of tacrolimus  MAInfo
11 정문경 Multi-trait genome-wide association meta-analysis of dietary intake identifies new loci and genetic and functional links with metabolic traits     J.Club
11 유승원 Inverse similarity and reliable negative samples for drug side-effect prediction     J.Club
13 임영균 Genetic polymorphism influences the pharmacokinetics of tacrolimus  TopicSem
13 부은경 Variants associated with PD  TopicSem
13 김효정 FAIR data principle  BioEMR
13 안세환 Visualize interpretable pattern from LINCS-L1000  SysBiol
16 김형준 Secure patient-centered health data management and exchange in Healthavatar Blockchain.  TopicSem
16 한봄 CBZ-induced SCAR  TopicSem
16 윤선민 WES Analysis to search the risk factor of anthracycline-induced prolonged neutropenia  MAInfo
16 유승원 scientific data collection-multi-omics data sharing(from 2019.10)  xMutant
18 서명의 Gain-of-function MN1 truncation variants cause a recognizable syndrome with craniofacial and brain abnormalities     J.Club
18 김주연 Economic burden of adverse drug reactions and potential for pharmacogenomic testing in Singaporean adults     J.Club
20 ... 인턴  TopicSem
20 ... 인턴  TopicSem
20 최선 Query design for EMR study  BioEMR
20 한봄 HLA*IMP  SysBiol
23 김기태 Identifying genes related to age of onset in Major Depressive Disorder (MDD) patients (Additional analysis of suicide attempt)  TopicSem
23 윤선민 WES Analysis to search the risk factor of anthracycline-induced prolonged neutropenia   TopicSem
23 유경훈 Identifying cross-disease components of genetic risk across hospital data in the UK Biobank  xMutant
23 김기태 A brief history of human disease genetics  MAInfo
25 ... 설날  J.Club
25 ... 설날  J.Club
27 ... 대체휴일  TopicSem
27 ... 대체휴일  TopicSem
30 박유미 Stratification of ALL patients at risk for thiopurine-induced toxicity using GVB  TopicSem
30 김효정 Toward systematic integration of CPIC guideline into clinical practice   TopicSem
30 권호식 GeneHancer: genome-wide integration of enhancers and target genes in GeneCards  xMutant

2019-12:
02 최선 Automated systematic review  TopicSem
02 이우승 Novel Gene-Wide Copy Number Variation Detection algorithm  TopicSem
02 김주연 Pathway-based analysis for cSAGs of Parkinson’s disease  BioEMR
02 김효정 [Review] The Role of Modeling in Clinical Information System Development Life Cycle  SysBiol
05 김재환 Current status of RarePedia & SAG migration and API development  TopicSem
05 서명의 Antibiotics resistance variants in Helicobacter pylori sequence identified from H.plyori panel sequencing  TopicSem
05 유승원 Updates in TCGAbiolinks R package  xMutant
05 김기태 Identifying genes related to age of onset in Major Depressive Disorder (MDD) patients  MAInfo
07 박유미 Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations     J.Club
07 안세환 .     J.Club
09 임영균 Genetic polymorphism influences the pharmacokinetics of tacrolimus  TopicSem
09 부은경 Variant-level Analysis for Parkinson's Disease  TopicSem
09 박유미 The GenomeAsia 100K Project enables genetic discoveries across Asia  SysBiol
09 김효정 Warfarin dosing guideline review  BioEMR
09 김효정 Warfarin dosing guideline review  BioEMR
12 김형준 PHR validation and PHR data segments in Healthavatar blockchain  TopicSem
12 한봄 CBZ-induced SCAR  TopicSem
12 권호식 MAC: identifying and correcting annotation for multi-nucleotide variations  xMutant
12 이우승 Packaging Novel Gene-Wide Copy Number Variation Detection Algorithm  MAInfo
14 김효정 Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics Network     J.Club
14 최선 Medical device surveillance with electronic health records     J.Club
16 김기태 Analysis of Ossification of posterior longitudinal ligament study  TopicSem
16 국수경   TopicSem
16 김기태 Identifying genes related to age of onset in Major Depressive Disorder (MDD) patients  SysBiol
18 김기태 Identifying genes related to age of onset in Major Depressive Disorder (MDD) patients  Seminar
19 윤선민 WES Analysis to search the risk factor of anthracycline-induced prolonged neutropenia  TopicSem
19 박유미 Improved stratification of ALL patients at risk for thiopurine-related toxicity using GVB  TopicSem
19 유승원 Gene ontology 분석 툴 정보 공유 : FunSet(an open-source software and web server for performing and displaying Gene Ontology enrichment analysis)  MAInfo
19 최선 Imbalanced data processing  xMutant
21 이우승 UK-Biobank Whole Exome Sequence Binary Phenome Analysis with Robust Region-based Rare Variant Test      J.Club
21 유경훈 Towards precision medicine: interrogating the human genome to identify drug pathways associated with potentially functional, population-differentiated polymorphisms     J.Club
23 김효정 Clinical genome data model provides interactive clinical decision support for precision medicine  TopicSem
23 김주연 Evaluation of cSAGs in Parkinson’s disease based on association analysis   TopicSem
23 이우승 Introduction to Biobank  Seminar
23 안세환 Streamlined analysis of LINCS L1000 data with the slinky package for R  BioEMR
23 김주연 Examination of Parkinson’s disease cSAG deleteriousness using GVB score and pathway analysis  SysBiol
26 유경훈 HLA Association with Antidepressant-Induced Adverse Reactions and Response  TopicSem
26 유승원 Mercaptopurine adverse effect research : sample expansion, multi-gene effect issues  TopicSem
26 박유미 Review of clinical coding classification systems: Read, BNF, and dm d  xMutant
26 권호식 The genome Aggregation Database  MAInfo
28 김형준 Secure and Scalable mHealth Data Management Using Blockchain Combined With Client Hashchain: System Design and Validation     J.Club
28 윤선민 Determining the balance between drug efficacy and safety by the network and biological system profile of its therapeutic target     J.Club
30 안세환 Discovering interpretable pattern from LINCS-L1000 data  TopicSem
30 채정환 taxol study  TopicSem
30 한봄 Heart failure and healthcare informatics  BioEMR

2019-11:
02 유경훈 Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network     J.Club
02 김기태 Ancestry-Dependent Enrichment of Deleterious Homozygotes in Runs of Homozygosity     J.Club
04 서명의 Target sequencing panel for Helicobacter pylori and host DNA  TopicSem
04 임영균 tacrolimus sensitivity analysis with clinical variables  TopicSem
04 김효정 [Review] Implementation and obstacles of pharmacogenetics in clinical practice: An international survey  BioEMR
07 부은경 Gender Differences in Parkinson’s Disease  TopicSem
07 이우승 Copy Number Alteration Algorithms for Amplicon-based Targeted Sequencing Panel data  TopicSem
07 박유미 Variant-level comparison between in silico prediction scores and VAMP-seq scores  xMutant
07 권호식 Analysis of HD-MTX induced renal toxicity In Pediatric Patients with ALL   MAInfo
09 임영균 Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype     J.Club
09 한봄 HLA and non-HLA genes and familial predisposition to autoimmune diseases in families with a child affected by type 1 diabetes     J.Club
11 국수경   TopicSem
11 김기태 Comprehensive genomic analysis for identifying genes related to age of onset in Major Depressive Disorder (MDD) patients  TopicSem
11 최선 Device Surveillance-CDM   BioEMR
11 최선 Device Surveillance-CDM   BioEMR
11 안세환 Introduction to Genetic Algorithm  SysBiol
14 한봄 Carbamazepine-induced SCAR  TopicSem
14 윤선민 WES Analysis to search the risk factor of anthracycline-induced prolonged neutropenia  TopicSem
14 윤선민 A coding variant in FTO related to thiopurine-induced leukopenia in East Asian  xMutant
15 최선 항암치료원칙  MAInfo
16 유승원 prioritizing target-disease associations with novel safety and efficacy scoring methods     J.Club
16 서명의 Diagnostic utility of Next-Generation Sequencing for Disorders of Somatic Mosaicism-a five-year cumulative cohort     J.Club
18 박유미 Improved stratification of subjects at high-risk of thiopurine-related toxicity using gene-wise variant burden score (TPMT and NUDT15)   TopicSem
18 김효정 Toward systematic integration of CPIC guideline into clinical practice: development of PGx CDS pipeline   TopicSem
18 안세환 Breast cancer(adenocarcinoma) data in L1000  BioEMR
21 김주연 Evaluation of candidate SAGs contributing to Parkinson’s disease  TopicSem
21 유경훈 Analysis of CYP2C19 association with efficacy and side effects of escitalopram using 1000 MDD WES data.  TopicSem
21 이우승 Visualization of Copy Number Variation  xMutant
23 채정환 Low Dose of Paclitaxel Combined with XAV939 Attenuates Metastasis, Angiogenesis and Growth in Breast Cancer by Suppressing Wnt Signaling.     J.Club
23 국수경 A three-gene expression signature associated with positive surgical margins in tongue squamous cell carcinomas: Predicting surgical resectability from tumour biology?     J.Club
25 유승원 NUDT15와 TPMT가 모두 normal metabolizer인 급성림프구성 백혈병 환자의 IL6 변이와 치오퓨린(thiopurine) 독성  TopicSem
25 안세환 Discovering significant and interpretable pattern from L1000 data  TopicSem
25 한봄 Genomics and electronic health record systems  BioEMR
25 김기태 major result of AOS in depression  Seminar
25 유경훈 Towards precision medicine: interrogating the human genome to identify drug pathways associated with potentially functional, population-differentiated polymorphisms  SysBiol
28 채정환 taxol related project review  TopicSem
28 권호식 HD-MTX induced renal toxicity in pediatric ALL  TopicSem
28 Genomic analysis of L-asparaginase-induced pancreatitis in 25 Korean pediatric ALL patients.  MAInfo
28 유경훈 A Genocentric Approach to Discovery of Mendelian Disorders  xMutant
30 부은경 Discovering personalized driver mutation profiles of single samples in cancer by network control strategy     J.Club
30 김재환 Recommendations for Clinical CYP2C9 Genotyping Allele Selection     J.Club

2019-10:
03 ... 개천절  TopicSem
03 ... 개천절  TopicSem
03 ... 개천절  TopicSem
03 ... 개천절  TopicSem
05 안세환 Drug Gene Budger (DGB): an application for ranking drugs to modulate a specific gene based on transcriptomic signatures.     J.Club
05 권호식 Exome-wide assessment of the functional impact and pathogenicity of multinucleotide mutations     J.Club
07 한봄 Carbamazepine-induced SCAR  TopicSem
07 김기태 Comprehensive genomic analysis for identifying genes related to age of onset in Major Depressive Disorder (MDD) patients  TopicSem
07 안세환 Use of Sharesource in Remote Patient Management in Peritoneal Dialysis: A UK Nurse  BioEMR
08 최선 KCDM WORK  BioEMR
10 국수경 Head and neck squamous cell carcinoma of the cancer genome atlas (TCGA) and Somatic calling  TopicSem
10 윤선민 Characteristic of pathogenic genes in ALL childhood patients with adverse reaction in L-asparaginase  TopicSem
10 유승원 ProteinPaint : Exploring genomic alteration in pediatric cancer using ProteinPaint  xMutant
10 김기태 Analysis of OPLL  MAInfo
10 윤선민 WES analysis of AML samples according to neutropenia duration   MAInfo
12 이우승 How good are pathogenicity predictors in detecting benign variants?     J.Club
12 최선 BioBERT: a pre-trained biomedical language representation model for biomedical text mining     J.Club
14 박유미 Improved stratification of subjects at high-risk of thiopurine-related toxicity using gene-wise variant burden score  TopicSem
14 김효정 Systematic integration of CPIC guideline into clinical practice: development of PGx CDS pipeline based on the cGDM   TopicSem
14 박유미 Distribution of in silico prediction scores for NUDT15 variants identified in gnomAD database  SysBiol
17 김주연 Evaluation of candidate genes contributing to synthetic association  TopicSem
17 유경훈 Influence of CYP2C19 Metabolizer Status on Escitalopram Tolerability and Response in Depressive Disorders  TopicSem
17 이우승 Performance Comparison of Ampicon Based Sequencing Conpy Number Detection Tools  MAInfo
19 김형준 Tamper Resistant Mobile Health Using Blockchain Technology     J.Club
19 윤선민 Genotype-based Treatment With Thiopurine Reduces Incidence of Myelosuppression in Patients With Inflammatory Bowel Diseases     J.Club
21 ... 리트릿  TopicSem
21 ... 리트릿  TopicSem
21 김기태 Comprehensive genomic analysis for identifying genes related to age of onset in Major Depressive Disorder (MDD) patients  Seminar
21 김형준 Healthavatar Platform_Mobile Healthcare Platform Facilitating Secure Exchange and Management of Personal Health Record With Permissioned Blockchain  Seminar
21 박유미 Comprehensive genomic characterization of pharmacogenetic, common-disease, and Mendelian-disease genes facilitates the risk gene prioritization.  Seminar
21 윤선민 Genomic analysis of L-asparaginase-induced pancreatitis in 25 Korean pediatric ALL patients.  Seminar
21 임영균 Identification of genomic markers affecting sentivity of tacrolimus  Seminar
21 김주연 Evaluation of systematic synthetic association-contributing variant detection  Seminar
21 유승원 ROC curve analysis of 6MP drug adverse effect  Seminar
21 권호식 Identification of potential genomic markers related with adverse effects of Contrast Media  Seminar
21 한봄 Carbamazepine-induced Severe Cutaneous Adverse Reactions  Seminar
21 김기태 Analysis of OPLL  SysBiol
22 유경훈 Influence of CYP2C19 Metabolizer Status on Escitalopram Tolerability and Response in Depressive Disorders  Seminar
22 부은경 Gender Differences in Parkinson’s Disease  Seminar
22 김효정 Systematic integration of CPIC guideline into clinical practice: development of PGx CDS pipeline based on the cGDM   Seminar
24 유승원 Star allele and GVB(bPGS) relationship in 6MP analysis : sample expansion  TopicSem
24 안세환 FSGP for L1000 breast carcinoma cancer cell lines   TopicSem
24 권호식 Impact of outdated gene annotation on Enrichment analysis  xMutant
24 유경훈 Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statistics  xMutant
26 윤선민 Genotype-based Treatment With Thiopurine Reduces Incidence of Myelosuppression in Patients With Inflammatory Bowel Diseases      J.Club
26 김주연 Analyzing the Clinical Actionability of Germline Pharmacogenomic Findings in Oncology     J.Club
28 권호식 Identification of potential genomic variants related with adverse effects of Contrast Media  TopicSem
28 최선 K-CDM research for 2019 mfds  TopicSem
28 김주연 Examination of variants potentially contributing to synthetic association in Parkinson's disease  BioEMR
28 김주연 Evaluation of candidate SAGs using tacrolimus sample WXS data  SysBiol
31 김재환 Development of Genomic variant Interpretation Assistant Tool (GI-AT)  TopicSem
31 김형준 Mobile Healthcare Platform Facilitating Secure Exchange and Management of Personal Health Record With Permissioned Blockchain  TopicSem
31 최선 Device Surveillance-CDM  xMutant
31 유승원 Introduction : GO-CAM(Gene Ontology Causal Activity Modeling)  MAInfo

2019-09:
02 한봄 Carbamazepine-induced SCAR  TopicSem
02 김효정 Systematic integration of CPIC guideline into clinical practice: development of PGx CDS pipeline based on the cGDM   TopicSem
02 안세환 L1000 data overview  BioEMR
02 김기태 OPLL analysis   SysBiol
05 김주연 Candidate SAG extraction and evaluation using tacrolimus sample data  TopicSem
05 유경훈 Influence of CYP2C19 Metabolizer Status on Escitalopram Tolerability and Response in Depressive Disorders  TopicSem
05 박유미 The all of us research program  xMutant
05 임영균 Networks of Cancer Gene 6.0  MAInfo
07 한봄 Understanding HLA associations from SNP summary association statistics     J.Club
07 국수경 Immune profiles in primary squamous cell carcinoma of the head and neck     J.Club
09 유승원 Study design-Whole exome sequencing analysis (variant caller comparison)  TopicSem
09 안세환 Overview of L1000 data  TopicSem
09 김주연 Candidate SAG evaluation using tacrolimus sample data  SysBiol
12 ... 추석  TopicSem
12 ... 추석  TopicSem
14 ...   J.Club
14 ...   J.Club
16 채정환   TopicSem
16 권호식 Adverse Effects of Contrast Media  TopicSem
16 김주연 Examination of Stargazer through application to 1000 Genomes Project data  BioEMR
16 안세환 Subtype of Cell Lines in L1000 data  SysBiol
19 최선 Research plan for automatic systematic review  TopicSem
19 김재환 Pilot phase of GV-AT SNUBI development (naive user interface with a sample protocol)  TopicSem
19 윤선민 Analysis of genetic and clinical data in AML patients with prolonged neutropenia   xMutant
19 최선 google cloud platform  MAInfo
21 김재환 Multi-Gene Panel Testing of 23,179 Individuals for Hereditary Cancer Risk Identifies Pathogenic Variant Carriers Missed by Current Genetic Testing Guidelines     J.Club
21 박유미 Massive parallel variant characterization identifies NUDT15 alleles associated with thiopurine toxicity     J.Club
23 이우승 Copy number detection in amplicon based targeted sequencing  TopicSem
23 서명의 Deleterious variants in CYP2C19 Rapid metabolizer  TopicSem
23 한봄 Biomarkers of adverse drug reactions  SysBiol
23 한봄 Biomarkers of adverse drug reactions  SysBiol
26 임영균 Tacrolimus high peaks variant analysis  TopicSem
26 부은경 Identifying Gender-Specific Variants in Parkinson  TopicSem
26 Characteristics of candidate genes that cause side effects of L-asparaginase  MAInfo
26 이우승 GDC Tumor Only Variant Calling Pipeline with Uveal Melanoma  xMutant
28 부은경 Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing     J.Club
28 김효정 The Coriell personalized medicine collaborative pharmacogenomics appraisal, evidence scoring and interpretation system     J.Club
30 김형준 Reviews of other medical blockchain systems  TopicSem
30 김지헌 Rare-Variant Association Testing  TopicSem
30 유경훈 Pharmacogenomic genotypes define genetic ancestry in patients and enable population-specific genomic implementation  SysBiol

2019-08:
01 권호식 Adverse Effects of Contrast Media  TopicSem
01 최선 Comparative study of statin drugs�  TopicSem
01 유경훈 A robust benchmark for germline structural variant detection  xMutant
01 권호식 Rare-Variant Association  MAInfo
03 임영균 RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues     J.Club
03 윤선민 Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation     J.Club
05 서명의 Comparison between full matrix and sparse matrix in CYP2C19 gene  TopicSem
05 이우승 Prognostic Potential Loss of Heterozygosity in TNBC  TopicSem
05 김주연 Utility of extended Stargazer for calling star alleles with WGS data  BioEMR
08 김재환 Design and development of GV-AT SNUBI with Module functionality extension  TopicSem
08 부은경 Gender Differences in Parkinson’s Disease  TopicSem
08 유승원 Whole Exome Sequencing : germline variant caller comparison  MAInfo
08 권호식 Markers related with Iopromide from Literatures  xMutant
10 김기태 Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genome     J.Club
10 유경훈 Impact of pharmacogenomics on clinical outcomes in major depressive disorder in the GUIDED trial: A large, patient- and rater-blinded, randomized, controlled study     J.Club
12 임영균 FNA 3번째 실험 분석  TopicSem
12 박유미 Comprehensive genomic characterization of pharmacogenetic, common-disease, and Mendelian-disease genes and its applications to gene prioritization.  TopicSem
12 박유미 Whole-genome sequencing of rare disease patients in a national healthcare system - Genomics England 100,000 genomes project  SysBiol
12 김효정 analysis of cpic knowledge resource to build machine readable knowledgebase   BioEMR
12 유경훈 Standardized Biogeographic Grouping System for Annotating Populations in Pharmacogenetic Research     SysBiol
15 ... 휴일  TopicSem
15 ... 휴일  TopicSem
17 이우승 A longtudinal big data approach for precision health     J.Club
17 민병주 Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease     J.Club
19 ... GDA  TopicSem
19 ... GDA  TopicSem
22 ... GDA  TopicSem
22 ... GDA  TopicSem
24 김주연 Characterizing pharmacogenomic-guided medication use with a clinical data repository     J.Club
24 서명의 Paralog studies augment gene discovery:DDX and DHX genes     J.Club
26 김형준 Healthavatar platform for conserving originality and secure exchange of personal health record with permissioned blockchain  TopicSem
26 김기태 Analysis of age at onset in depression  TopicSem
26 최선 Discussion of Rehabilitation-CDM  BioEMR
26 김효정 [review] Genomic information for clinicians in the EHR: lessons learns from clinGen and eMerge  SysBiol
29 국수경 Subtypes of Head and Neck Squamous Cell Carcinoma  TopicSem
29 윤선민 Characteristic of pathogenic genes in ALL childhood patients with adverse effect in L-asparaginase  TopicSem
31 유승원 Drug combination sensitivity scoring facilitates the discovery of synergistic and efficacious drug combinations in cancer     J.Club
31 채정환 PPM1D Mutations Drive Clonal Hematopoiesis in Response to Cytotoxic Chemotherapy     J.Club

2019-07:
01 한봄 Carbamazepine-induced SCAR  TopicSem
01 김재환 Current status of Genomic Variant analysis Assistant Tool (GV-AT) SNUBI development  TopicSem
01 김주연 A clinical trial testing the effects of CYP2D6-guided versus usual opioid prescribing on pain control  BioEMR
01 박유미 Association of CRIM1 variant and 6-mercaptopurine-induced adverse effects in childhood acute lymphoblastic leukemia  SysBiol
01 유경훈 Hubble2D6: A deep learning approach for predicting drug metabolic activity  SysBiol
04 이우승 Systematic discovery of Prognostic Potential Loss of Heterozygosity  TopicSem
04 서명의 Systematic mutagenesis and enzymatic activity assay for CYP2C19 gene  TopicSem
04 박유미 Mutagenesis-based protein structure determination   xMutant
04 임영균 National Omics Data Encyclopedia (NODE) review   MAInfo
06 민유정 TogoGenome/TogoStanza: modularized Semantic Web genome database     J.Club
06 부은경 Expanding Parkinson’s disease genetics: novel risk loci, genomic context, causal insights and heritable risk     J.Club
08 임영균 Tacrolimus sample sequencing summary  TopicSem
08 민유정   TopicSem
08 김기태 Analysis of age at onset in depression  SysBiol
11 부은경 PPMI WES Data Overview and Analysis Plan  TopicSem
11 윤선민 WES Analysis using multiple samples with side effects of L-asparaginase  TopicSem
11 윤선민 Candidate variants of regression analysis in AML patients with prolonged neutropenia  xMutant
11 윤선민 MetaDome: Pathogenicity analysis of genetic variants through aggregation of homologous human protein domains  MAInfo
13 김재환 A Model Information Management Plan for Molecular Pathology Sequence Data Using Standards     J.Club
13 박유미 Evolutionary coupling analysis identifies the impact ofdisease-associated variants at less-conserved sites     J.Club
15 국수경 WHO Classification of Salivary Gland Tumours  TopicSem
15 김기태 Analysis of age at onset in 1000 Korean MDD patients  TopicSem
15 김주연 ADR related synthetic association study: data processing flow and statistics  SysBiol
15 김효정 [Review] Implementing Genomic Clinical Decision Support for Drug-Based Precision Medicine  BioEMR
15 김효정 [Review] Implementing Genomic Clinical Decision Support for Drug-Based Precision Medicine  BioEMR
18 박유미 Developing modifications for gene-wise variant burden score  TopicSem
18 김효정 Systematic integration of CPIC guideline into clinical practice: development of PGx CDS pipeline based on the cGDM   TopicSem
18 김기태 Workflow and Kaplan-Meier estimation for MDD   MAInfo
18 이우승 Caveats and pitfalls of ROC analysis in clinical microarray research  xMutant
20 안세환 L1000 Viewer: A Search Engine and Web Interface for the LINCS Data Repository     J.Club
20 권호식 Pathogenic Germline Variants in 10,389 Adult Cancers     J.Club
22 김주연 Refining method of candidate SAG extraction   TopicSem
22 민병주 Development of NGS panel to analyze the effect of bacterial and host factors on Helicobacter pylori eradication therapy  TopicSem
22 안세환 294 Hugo gene symbols not in cBioPortal  BioEMR
22 안세환 The GCTx format and cmap{Py, R, M, J} packages: resources for optimized storage and integrated traversal of annotated dense matrices  SysBiol
25 안세환 A system that measures the weight of a peritoneal dialysis fluid in real time  TopicSem
25 유승원 6MP analysis-AUC analysis, drugscore analysis of 6MP metabolism related genes  TopicSem
25 이우승 Funcotator : FUNCtional annOTATOR  MAInfo
25 유승원 R package for BAM file read visualiztion : BBCAnalyzer  xMutant
27 김효정 A Pharmacogenomics Clinical Decision Support Service Based on FHIR and CDS Hooks      J.Club
27 최선 Cardiologist-level arrhythmia detection and classification in ambulatory electrocardiograms using a deep neural network     J.Club
29 유경훈 Influence of CYP2C19 Metabolizer Status on Escitalopram Tolerability and Response in Depressive Disorders  TopicSem
29 채정환 6MP leukemia experimental designs  TopicSem

2019-06:
01 민유정 .Genomic Common Data Model for Seamless Interoperation of Biomedical Data in Clinical Practice: Retrospective Study     J.Club
01 유경훈 Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program     J.Club
03 한봄 Carbamazepine-induced SCAR  TopicSem
03 김기태 GSDBA - A computational approach for Gene Set wise Deleterious Burden Analysis  TopicSem
03 김효정 Genome data model engine   BioEMR
03 안세환 Errors in importing Leukemia Data  SysBiol
06 ... 휴일  TopicSem
06 ... 휴일  TopicSem
08 김주연 Network, transcriptomic and genomic features differentiate genes relevant for drug response     J.Club
08 민병주 Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia     J.Club
10 국수경 Somatic Calling in Salivary Gland Tumors  TopicSem
10 윤선민 Analysis of candidate variants in patients with side effects of L-asparaginase  TopicSem
10 최선 Handling missing value in medical dataset  BioEMR
10 한봄 Read quality check using CaReal  SysBiol
13 박유미 Data overview for Parkinsons Progression Markers Initiative (PPMI) project  TopicSem
13 김효정 CGDM database: current datasets and status  TopicSem
13 유경훈 A benchmark study of scoring methods for non-coding mutations.  xMutant
13 유승원 discussion : application of drug score, pathway score to 6MP analysis  MAInfo
15 김기태 Conditional and interaction gene-set analysis reveals novel functional pathways for blood pressure     J.Club
15 유승원 Systematic discovery of germline cancer predisposition genes through the identification of somatic second hits     J.Club
17 김주연 Candidate SAG characteristic examination based on drug-gene interaction status  TopicSem
17 민병주 Genomic variant analysis using leukemia target panel including 11 genes  TopicSem
17 안세환 Datasets in cBioPortal  BioEMR
20 유경훈 Comparative study of escitalopram according to CPIC guideline (CYP2C19/CYP2D6 Metabolizer Status)  TopicSem
20 유승원 6MP analysis(Drug score & gene-wise approach)  TopicSem
20 권호식 Review : Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls  xMutant
20 권호식 List of public primary datasets and discussion  MAInfo
22 서명의 Length of uninterrupted CAG, independent of polyglutamine size, results in increased somatic instability, hastening onset of Huntington Disease     J.Club
22 채정환 Genomic and Transcriptomic Landscape of Triple-Negative Breast Cancers: Subtypes and Treatment Strategies     J.Club
24 안세환 Importing Leukemia Dataset into cBioPortal  TopicSem
24 권호식 Adverse effects of Contrast media  TopicSem
24 김효정 [Review] Standardizing terms for clinical pharmacogenetic test results: consensus terms from the CPIC  SysBiol
27 채정환 taxol ADR related candidate genes; review  TopicSem
27 최선 Practice of text analysis for medical record  TopicSem
27 최선 rehab-CDM  xMutant
27 최선 Consideraton for development of rehabilitation-CDM  MAInfo
27 최선 Consideraton for development of rehabilitation-CDM  MAInfo
29 한봄 Immune diversity sheds light on missing variation in worldwide genetic diversity panels     J.Club
29 국수경 Tracing Oncogene Rearrangements in the Mutational History of Lung Adenocarcinoma.     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
23 이우승 Deep-coverage whole genome sequences and blood lipids among 16,324 individuals  xMutant
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 The List of Public Databases and Discussion  TopicSem
27 서명의 Work flow for systematic mutagenesis candidate selection  TopicSem
27 김주연 Linkage disequilibrium between PGx GWAS and candidate SAG variants  BioEMR
27 김주연 Candidate SAG interpretation based on inter-ethnic variability  SysBiol
30 임영균 SCS in public cellline data   TopicSem
30 부은경 Multiple Myeloma: Data Preprocessing  TopicSem
30 이우승 Optimization Filtering for Detecting Putative Tumor Mutations with Know Cancer Mutations  MAInfo
30 유승원 Introduction of ontology analysis tool : GOnet  xMutant

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