팀:AllSeminarBioEMRxMutantSysBiolMAInfoJ.ClubTopicSemBookReading   발표자: All국수경권호식김민정김재환김지헌민유정부은경안세환유경훈유승원유승원정문경채정환최선최선한봄...AlexanderDesok KimHJInternJee-Young ChoiJee-Young ChoiJee-Young ChoiJee-Young ChoiJee-Young ChoiJee-Young Jasmine CHOIJee-Young Jasmine CHOIJee-Young Jasmine CHOIJee-Young Jasmine Choi KelseyKwangsung AhnMike JacksonNULLNULLNULLNULLNULLNULLNULLNULLPPPrabinRockyabe torkeltonbenhjkyutest강기원강병희강병희강병희강석훈강소영고인석김경화김경화김기태김도균김동호김민구김보성김승빈김승호김영성김영훈김주연김주한김준호김지미김지훈김지희김진환김현대김형준김혜현김효정김효진나영지류영재민병주박원준박유랑박유미박은영박이영박정수박지연박지혜박찬희박호경백수연서명의서희원손경아송영수심재현심재현심혜진안빈안선주양웅철엄세인오가희우정훈윤선민윤영조이계화이수연이수연S이수현이우승이정우이정훈이현임영균임재현임준호전은주정상원정승원정용정태수정해원정희준조성범조용래주경민초빙강연최광윤최윤영최준영한미령한지예한현욱홍승권홍주영황동현源����������臾닿�����理���ㅼ��김기원김미현김세영김예진김옥구김윤희김지훈(H)박지연박지연변상재서화정신용준신현정온정헌윤혜성이석호이영주이정애이혜원임수아안성준권혜진유방암센터유수영유의혁(세종대)이권무황기태unknown세종대외부특강전체정혜림팀원권창혁송유림윤준희정제균   제목/키워드:    날짜:   

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			TopicSem
14	윤선민			TopicSem
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			TopicSem
18	김효정			TopicSem
21	김주연			TopicSem
21	유경훈			TopicSem
23	채정환			J.Club
23	국수경			J.Club
25	유승원			TopicSem
25	안세환			TopicSem
28	채정환			TopicSem
28	권호식			TopicSem
30	부은경			J.Club
30	김재환			J.Club

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 inpediatric 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

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

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 Heterozygosityin 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

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

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

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

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

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

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

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

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