팀:AllSeminarBioEMRxMutantSysBiolMAInfoJ.ClubTopicSemBookReading   발표자: All국수경권호식김나영김민정김재환김지헌민유정배소정부은경안선주안세환유경훈유승원유승원유준기윤미선이시은인턴임성수전예진정문경조동영조민아조원일차재현채정환최선최선한봄홍진희...AlexanderBaby Anusha SatravadaBaby Anusha SatravadaBaby Anusha SatravadaDesok KimHJInternJee-Young ChoiJee-Young ChoiJee-Young ChoiJee-Young ChoiJee-Young ChoiJee-Young Jasmine CHOIJee-Young Jasmine CHOIJee-Young Jasmine CHOIJee-Young Jasmine Choi KelseyKwangsung AhnLiliaMike JacksonNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLPPPrabinRockySo Jeongabe torkeltonbenhjkyutest강기원강병희강병희강병희강석훈강소영고인석김경화김경화김기태김도균김동호김민구김보성김승빈김승호김영성김영훈김주연김주한김준호김지미김지훈김지희김진환김현대김형준김혜현김효정김효진나영지류영재민병주박원준박유랑박유미박은영박이영박정수박지연박지혜박찬희박호경백수연서명의서희원손경아송영수심재현심재현심혜진안빈안선주양웅철엄세인오가희우정훈윤선민윤영조이계화이수연이수연S이수현이우승이정우이정훈이현임영균임재현임준호전은주정상원정승원정용정태수정해원정희준조성범조용래주경민초빙강연최광윤최윤영최준영한미령한지예한현욱홍승권홍주영황동현源����������臾닿�����理���ㅼ��김기원김미현김세영김예진김옥구김윤희김지훈(H)박지연박지연변상재서화정신용준신현정온정헌윤혜성이석호이영주이정애이혜원임수아안성준권혜진유방암센터유수영유의혁(세종대)이권무황기태unknown세종대외부특강전체정혜림팀원권창혁송유림윤준희정제균   제목/키워드:    날짜:   

02	최선	PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning framework		J.Club
02	차재현	Large mosaic cnv confer autism risk		J.Club
04	조민아	Network properties and community analysis of Ulcerative colitis extension		TopicSem
04	유준기	Synthetic rescue analysis using TCGA and ADSP data		TopicSem
06	유준기	TCGA PanCanAtlas data		MAInfo
07	부은경	Variant- and gene-wise analyses of Parkinson’s disease		TopicSem
07	임성수	Identifying synthetic anti-metastasis pairs from TCGA COAD and READ		TopicSem
09	윤미선	Assessment of clinically actionable pharmacogenetic markers to stratify anti-seizure medications		J.Club
09	배소정	Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression		J.Club
11	박유미	Preprocessing of PacBio whole genome sequencing data		TopicSem
11	차재현	.Replication : Clustering by phenotype and genome-wide association study in autism		TopicSem
13	배소정	Phylogenetic analysis		MAInfo
14	이시은	Defining the distance between diseases using SNOMED CT embeddings(Replication)		TopicSem
14	전예진	Mendelian Randomization as a tool to support pgx		TopicSem
16	부은경	Extremely sparse models of linkage disequilibrium in ancestrally diverse association studies		J.Club
16	조민아	Genetic Structure and Forensic Feature of 38 X-Chromosome InDels in the Henan Han Chinese Population		J.Club
18	안세환	Star-allele associated haplogroups of 25 pharmacogenes		TopicSem
18	권호식	Candidate genomic variations in patients with adverse reactions to contrast media		TopicSem
18	임성수	Identifying SAM pairs from TCGA dataset		SysBiol
21	최선	Survival analysis of colon cancer screening test implementation		TopicSem
21	윤미선	Population-Specific Pharmacogenetic Profiling in South Korean Population: Genotype-Based Drug Interventions		TopicSem
23	유준기	Allelic imbalance of chromatin accessibility in cancer identifies candidate causal risk variants and their mechanisms		J.Club
23	전예진	Mendelian randomization analyses support causal relationships between blood metabolites and the gut microbiome		J.Club
25	배소정	Genome wide association study about susceptibility to bacterial and viral infection		TopicSem
25	조민아	Change study design of IBD compared with healthy people		TopicSem
28	...	추석연휴		TopicSem
28	...	추석연휴		TopicSem
30	...	추석연휴		J.Club
30	...	추석연휴		J.Club

02	배소정	One-stage object detectors		MAInfo
02	배소정	One-stage object detectors		MAInfo
03	안세환	Summarize the results of haplogroups		TopicSem
03	권호식	Busulfan and Hepatic veno-occlusive disease		TopicSem
05	부은경	Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases		J.Club
05	차재현	Sex-dependent shared and nonshared Genetic Architecture across mood and psychotic disorders		J.Club
07	최선	Query design for DNET analysis		TopicSem
07	윤미선	Exploring WES data of CKD cohort (EPO resistance)		TopicSem
07	임성수	Identifying SAM pairs - calculate GVB by defining LOF mutations		SysBiol
10	배소정	A genome-wide association study identifies multiple loci associated with susceptibility to bacterial and viral infections		TopicSem
10	조민아	Integrated interpretation of single variant analysis and pair-gvb analysis in extension of ulcerative colitis		TopicSem
12	안세환	Chracterizing the combined effects of cytochrome P450 missense variation within star allele definitions		J.Club
12	권호식	Single-cell transcriptome profiling of the stepwise progression of head and neck cancer		J.Club
14	유준기	Biased genetic predisposition in cancer and neurodegeneration		TopicSem
14	부은경	Variant- and gene-wise analyses of PD		TopicSem
16	권호식	AnnotSV: Annotation of Human Structural Variations		MAInfo
17	임성수	Identifying synthetic anti-metastasis gene pairs from TCGA		TopicSem
17	박유미	Research outline of the Human Disease Genome Map construction project		TopicSem
19	조민아	A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer		J.Club
19	배소정	Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits		J.Club
21	차재현	Study of ASD		TopicSem
21	전예진	Mendelian randomization as a tool to support PGx		TopicSem
21	조민아	Code for network analysis of pair-wide gvb		SysBiol
23	차재현	genomic studies of ASD		MAInfo
24	이시은	(replication) Defining the distance between diseases using SNOMED-CT embeddings		TopicSem
24	안세환	Association between haplogroups and star-alleles in 1KGP		TopicSem
26	임성수	Identification of core genes and pathways in melanoma metastasis via bioinformatics analysis		J.Club
26	유준기	An allelic-series rare-variant association test for candidate-gene discovery		J.Club
28	권호식	Summary of Results for Pharmacogenomic Study of Contrast media-induced adverse reactions		TopicSem
28	최선	Dnet data analysis		TopicSem
30	윤미선	Visualizing genomic information across chromosomes with PhenoGram		MAInfo
31	윤미선	Population-Specific Pharmacogenetic Profiling in South Korean Population: Genotype-Based Drug Interventions		TopicSem
31	배소정	A genome-wide association study identifies multiple loci associated with susceptibility to bacterial and viral infections		TopicSem

01	조민아	From gene to dose: Long-read sequencing and *-allele tools to refine phenotype predictions of CYP2C19		J.Club
01	배소정	A cross-population atlas of genetic associations for 220 human phenotypes		J.Club
03	전예진	review_pgx of BRONJ		TopicSem
03	안세환	Constructing Haplogroups for Pharmacogenes		TopicSem
03	임성수	Identifying SAM pair from TCGA-SKCM		SysBiol
05	차재현	Network characteristics and clustering		MAInfo
06	이시은	Defining the distance between diseases using SNOMED CT embeddings(Replication)		TopicSem
06	차재현	.		TopicSem
08	임성수	Harnessing synthetic lethality to predict the response to cancer treatment		J.Club
08	유준기	Prioritizing autoimmunity risk variants for functional analyses by fine-mapping mutations under natural selection		J.Club
10	최선	Question answering task using aact db		TopicSem
10	윤미선	Population-Specific Pharmacogenetic Profiling in South Korean Population: Genotype-Based Drug Interventions		TopicSem
10	조민아	Code of trend of GVB in m-core analysis		SysBiol
12	윤미선	EPO resistance index design & Mixed Effects Model		MAInfo
13	배소정	A genome‐wide association studyabout susceptibility to bacterial and viral infections		TopicSem
13	조민아	M-core analysis of GVB in pair with cutoff of improvement p value ratio		TopicSem
15	안세환	PharmaGScore scores of compound genetic variant burden for psychiatric treatment optimization		J.Club
15	권호식	Cell type prioritization in single-cell data		J.Club
17	유준기	Inverse relationship and positive selection in Cancer and Neurodegeneration		TopicSem
17	부은경	K-core decomposition analysis using PPMI dataset		TopicSem
20	임성수	Identifying synthetic anti-metastasis gene pairs from TCGA		TopicSem
20	박유미	Deciphering sequence-structure-function relationships to predict individual drug-intolerance with minimal uncertainty		TopicSem
22	최선	Medical Question Understanding and Answering with Knowledge Grounding and Semantic Self-Supervision		J.Club
22	윤미선	The pharmacogenomic landscape of an Indigenous Australian population		J.Club
24	인턴	이수민-TTN mutation in Colorectal Cancer Patients and Future Studies		TopicSem
24	인턴	Journal review and replication trial		TopicSem
24	인턴	노서준 - Web Development: Federated Learning System for Breast mass segmentation in ultrasound		TopicSem
26	유준기	Positive selection scoring method		MAInfo
27	이시은	Defining the distance between diseases using SNOMED CT embeddings(Replication)		TopicSem
27	Lilia	INFLUENCE OF THE FAMILY HISTORY OF DEPRESSION IN THE CLINICAL CONSEQUENCES OF DEPRESSION		TopicSem
29	이시은	Improving graph embeddings via entity linking: A case study on Italian clinical notes		J.Club
29	전예진	Genetic validation of neurokinin 3 receptor antagonist for IHD prevention in men		J.Club
31	차재현	Genomic study of Major Depressive Disorder		TopicSem
31	전예진	Genetic validation of Antiepileptic drugs for Parkinson disease		TopicSem

01	박유미	Study design to identify candidate genetic variants associated with cervical insufficiency		TopicSem
01	Lilia	DEPRESSION DATASET ANALYSIS PT2		TopicSem
03	최선	biomedgpt		J.Club
03	권호식	STOmicsDB: a database of Spatial Transcriptomic data		J.Club
05	차재현			TopicSem
05	이시은	CKD Variants Analysis		TopicSem
05	조민아	igraph: r package for network graph (code)		SysBiol
05	조민아	igraph: r package for network graph (code)		SysBiol
05	조민아	igraph: r package for network graph (code)		SysBiol
07	유준기	Computational genomic approaches to interpret non-coding disease risk variants		MAInfo
08	전예진	Natural selection of pharmacogene in UK biobank		TopicSem
08	안세환	Identifications of associations between star alleles and haplogroups		TopicSem
10	임성수	Synthetic lethality-mediated precision oncology via the tumor transcriptome		J.Club
10	윤미선	Multiomic analysis of malignant pleural mesothelioma identifies molecular axes and specialized tumor profiles driving intertumor heterogeneity		J.Club
12	권호식	Copy number variations in Patients receiving contrast media		TopicSem
12	최선	Query design for Dnet analysis		TopicSem
14	최선	R packages for ML		MAInfo
15	윤미선	Exploring WES data of CKD cohort		TopicSem
15	조민아	Network analysis of pair-wise gvb in UC extension comparison		TopicSem
17	부은경	Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine		J.Club
17	전예진	Assessing Digital Phenotyping to Enhance Genetic Studies of Human Diseases		J.Club
19	임성수	Identifying synthetic anti-metastasis gene pairs from TCGA-SKCM		TopicSem
19	유준기	Molecular genetic features of Cancer Predisposition Genes (CPG) and Alzheimer's Disease Genes		TopicSem
21	배소정	Heterogeneous response to Glucocorticoids in breast cancer cells		MAInfo
22	부은경	Pair gvb-based network analysis in parkinson’s disease		TopicSem
22	배소정	genome wide association study about infection disease		TopicSem
24	이시은	Defining the distance between diseases using SNOMED CT embeddings		J.Club
24	차재현	.		J.Club
26	박유미	Investigating gene-pairs contributing to cervical insufficiency		TopicSem
26	권호식	Copy number variations in patients receiving contrast media		TopicSem
28	권호식	Performance of CNV callers for WES data		MAInfo
29	Lilia	Overview of depression dataset analysis process and future considerations		TopicSem
29	이시은	Defining the distance between diseases using SNOMED CT embeddings		TopicSem

01	차재현	Genome-wide association of polygenic risk extremes for Alzheimer		TopicSem
01	배소정	A genome‐wide association study in a large community‐based cohort identifies multiple loci associated with susceptibility to bacterial and viral infections		TopicSem
03	배소정	Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies		MAInfo
04	박유미	Identification of candidate gene variants associated with cervical insufficiency		TopicSem
04	부은경	Progress of pair-gvb analysis in PD patients		TopicSem
06	배소정	Infectious disease outbreak prediction using machine learning articles with machine learning models		J.Club
06	조민아	Participation bias in the UK Biobank distorts genetic associations and downstream analyses		J.Club
08	Lilia	DEPRESSION DATASET ANALYSIS		TopicSem
08	이시은	CKD Patients’ Variants Analysis		TopicSem
10	권호식	Busulfan and Adverse Drug Events		MAInfo
11	전예진	GWAS in complex disease and pharmacogenomics		TopicSem
11	안세환	Association between haplogroups and star-alleles		TopicSem
13	부은경	Inference of chronic obstructive pulmonary disease with deep learning on raw spirograms identifies new genetic loci and improves risk models		J.Club
13	안세환	A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variants		J.Club
15	권호식	Further analysis for candidate genes derived from CNV analysis in CTM		TopicSem
15	최선	sun_colon_cancer		TopicSem
15	임성수	(Replication) Identifying SAM pairs from TCGA-COAD patients		SysBiol
18	윤미선	CKD cohort grouping by EPO responsiveness		TopicSem
18	조민아	Differences in GVB at variant levels when comparing UC with 1000 genome project data		TopicSem
20	이시은	The Effect of Genotyping on the Number of Pharmacotherapeutic Gene–Drug Interventions in Chronic Kidney Disease Patients		J.Club
20	유준기	The genetic deteriminants of recurrent somatic mutations in 43,693 blood genomes		J.Club
22	배소정	Genome wide association study about bacterial and viral infections		TopicSem
22	유준기	Rare variants and deleterious variants in Cancer predisposition Genes (CPG) and Alzheimer associated Genes		TopicSem
24	차재현	GWA Studies with UKBB data		MAInfo
25	부은경	Single- and pair-gvb analysis in Parkinson’s disease		TopicSem
25	임성수	(Replication) Identifying SAM pairs from TCGA-SKCM patients		TopicSem
27	...	부처님 오신날		J.Club
27	...	부처님 오신날		J.Club
29	...	대체공휴일		TopicSem
29	...	대체공휴일		TopicSem

01	이시은	Novel Genetic Variants Associated with Chronic Kidney Disease Progression		J.Club
01	조민아	A comparison of the genes and genesets identified by GWAS and EWAS of fifteen complex traits		J.Club
02	임성수	(Replication) Overall process of identifying SAM gene pairs from TCGA		SysBiol
03	배소정	A genome‐wide association study in a large community‐based cohort identifies multiple loci associated with susceptibility to bacterial and viral infections		TopicSem
03	유준기	Comparing Cancer predisposition gene (CPG) and Alzheimer associated genes		TopicSem
05	최선	GWAS		MAInfo
06	부은경	Identifying gene pairs associated with Parkinson’s disease		TopicSem
06	임성수	(Replication) Identifying synthetic anti-metastatis gene pairs		TopicSem
08	안세환	A unifying model to predict variable drug response for personalised medicine.		J.Club
08	유준기	Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes		J.Club
10	박유미	Importance of rare pharmacogenomic variants in interpreting drug response		TopicSem
10	차재현	Analyzing Genomic Data from the 1000 Genomes Project		TopicSem
13	Lilia	CADD scoring for depression data		TopicSem
13	이시은	CKD,NSAID,PPI and Comparison with the Control		TopicSem
15	임성수	Clinical and bionarker analyses of sintilimab plus gemcitabine and cisplatin as first-line treatment for patients with advanced biliary tract cancer		J.Club
15	권호식	Confronting false discoveries in single-cell differential expression		J.Club
17	전예진	Association between AEDs and incident PD in the UK Biobank		TopicSem
17	안세환	Distribution of haplogroups and star-alleles		TopicSem
17	조민아	Downloading data using pyega3		SysBiol
20	권호식	Potential genomic variations related with adverse effects of contrast media		TopicSem
20	윤미선			TopicSem
22	전예진	Global Biobank Meta-analysis Initiative_Powering genetic discovery across human disease		J.Club
22	차재현	Single-nucleus gene and gene set expression-based similarity network fusion identifies autism molecular subtypes		J.Club
24	최선	Research idea using clinical trials DB		TopicSem
24	유준기	Rare variants in Cancer predisposition Gene (CPG) and Alzheimer associated genes		TopicSem
26	유준기	Single-cell whole genome sequencing (scWGS) in degenrative diseases		MAInfo
27	조민아	Cases between GVB and pair wise GVB in UC patients		TopicSem
27	임성수	(Replication) Identifying synthetic anti-metastatis gene pairs for COAD		TopicSem
29	최선	GPT4		J.Club
29	윤미선			J.Club

02	권호식	Variants in two candidate genes related with adverse effects of contrast media		TopicSem
02	조원일	pgwatch_database		TopicSem
02	권호식			TopicSem
02	최선	RD1		MAInfo
04	권호식	Association of Genetic Ancestry and Molecular Signatures with Cancer Survival Disparities: A Pan-Cancer Analysis		J.Club
04	유준기	Germline mutations in mitochondrial complex I reveal genetic and targetable vulnerability in IDH1-mutant acute myeloid leukaemia		J.Club
06	최선	Cohort analysis for the retinal detachment research using UKB		TopicSem
06	배소정	Replication: A genome‐wide association study in a large community‐based cohort identifies multiple loci associated with susceptibility to bacterial and viral infections		TopicSem
09	윤미선	Study design using WES of CKD (EPO resistance)		TopicSem
09	조민아	exploring pair-wise GVB score in UC patients		TopicSem
09	윤미선	Study design using WES of CKD (EPO resistance)		TopicSem
09	조민아	exploring pair-wise GVB score in UC patients		TopicSem
09	윤미선	Diffusion model		MAInfo
09	윤미선	Diffusion model		MAInfo
11	최선	Language Is Not All You Need: Aligning Perception with Language Models		J.Club
11	윤미선	Diffusion Models for Implicit Image Segmentation Ensembles		J.Club
13	유준기	Distribution of allele frequency and Insilico scores in Cancer Predisposition Gene (CPG)		TopicSem
13	부은경	Study design using PWGVB in patients with PD		TopicSem
15	유준기	LRT-q: Rare variant association test for gene expression in multiple tissues		MAInfo
16	박유미	Investigating gene-pairs contributing to sex differences in depression		TopicSem
16	Lilia	OVERVIEW OF THE DEPRESSION DATASET ANALYSIS AND FUTURE CONSIDERATIONS		TopicSem
16				TopicSem
16				TopicSem
18	전예진	A 12-gene pharmacogenetic panel to prevent adverse drug reactions_an open-label, multicentre, controlled, cluster-randiomised crossover implementation study		J.Club
18	조원일	Utility of long-read sequencing for All of Us		J.Club
20	이시은	Comparison of genotypes between CKD patients and the Control		TopicSem
20	권호식	Potential genomic variations related with adverse effects of contrast media		TopicSem
23	안세환	Identifying associations between haplogroups and star-alleles		TopicSem
23	조원일	concordance of star calling and GeT-RM		TopicSem
23				TopicSem
23				TopicSem
25	배소정	Single-cell RNA sequencing reveals a heterogeneous response to Glucocorticoids in breast cancer cells		J.Club
25	부은경	Network expansion of genetic associations defines a pleiotropy map of human cell biology		J.Club
27	전예진	pgx-passport		SysBiol
27	전예진	Association between AEDs and incident PD in the UK Biobank		TopicSem
27	최선	Cohort analysis for the retinal detachment research using UKB		TopicSem
29	권호식	Cell types and Functions		MAInfo
30	윤미선	Exploring WES data of CKD cohort		TopicSem
30	조민아	Classifying Bladder cancer patients using gene set identified by SCISSOR		TopicSem

02	조민아	Replication of UC candidates in 100 UC patients		TopicSem
02	유준기	Classification and characterization of Cancer Predisposition Gene (CPG) variants		TopicSem
04	전예진	Association Between Antiepileptic Drugs and Incident Parkinson Disease in the UK Biobank		J.Club
04	김나영	A State-of-the Art Review of SNOMED CT Terminology Binding and Recommendations for Practice and Research		J.Club
06	임영균			TopicSem
06	부은경	PPMI Data Overview		TopicSem
09	박유미	Real-world data analysis of warfarin dose-associated variants of CYP2C9 and VKORC1 in subjects with unclear molecular phenotypes		TopicSem
09	이시은	Distribution Graph of CKD Patients Genotypes		TopicSem
09	권호식	Cell markers and Stem cells		MAInfo
11	부은경	Pairwise effects between lipid GWAS genes modulate lipid plasma levels and cellular uptake		J.Club
11	임영균	Mono- and biallelic variant effects on disease at biobank scale		J.Club
13	인턴	Variant filtering workflow in 1000 depression dataset		TopicSem
13	전예진	Association between AEDs and incident PD in the UK Biobank		TopicSem
13	조민아	RNA-seq deconvolution		SysBiol
16	...	GDA		TopicSem
16	...	GDA		TopicSem
18	안세환	Identification and functional validation of novel pharmacogenomic variants using a next-generation sequencing-based approach for clinical pharmacogenomics		J.Club
18	조민아	An Improved Phenotype-Driven Tool for Rare Mendelian Variant Prioritization: Benchmarking Exomiser on Real Patient Whole-Exome Data		J.Club
20	...	GDA		TopicSem
20	...	GDA		TopicSem
23	...	GDA		TopicSem
23	...	GDA		TopicSem
25	이시은	Impact of SGLT2 inhibitors on old age patients with heart failure and chronic kidney disease		J.Club
25	배소정	Genetic common variants associated with cerebellar volume and their overlap with mental disorders: a study on 33,265 individuals from the UK-Biobank		J.Club
27	김나영	Semantic enrichment of Data Elements using ChatGPT		TopicSem
27	안세환	Identifying novel functional PGx variants based on haplogroup		TopicSem

02	유준기	Characteristics of Cancer predisposition gene (CPG) variants in the general population		TopicSem
02	임영균	Analysis of metastatic potential by somatic mutations in cancer cell		TopicSem
05	부은경	Research Idea for Neurodegenerative Diseases		TopicSem
05	박유미	Replication study of the association of rs4653328 (EPHA10) with cervical insufficiency		TopicSem
05	안세환	test		SysBiol
07	배소정	The landscape of host genetic factors involved in immune response to common viral infections		J.Club
07	조원일	Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants		J.Club
09	이시은	Chronic Kidney Disease and DialysisNet		TopicSem
09	전예진	variant-wise analysis to discover phenytoin adverse reaction related genes		TopicSem
12	안선주	Pharmacogenomics Watch(PGWatch) - Intro, Terms, DB		TopicSem
12	김나영	Master's thesis revisions		TopicSem
14	유준기	The impact of rare germline variants on human somatic mutation processes		J.Club
14	권호식	Computational comparison of common event based differential splicing tools		J.Club
16	안세환			TopicSem
16	최선	SUN_CKD		TopicSem
19	인턴	ANALYSIS OF A DATASET OF 1000 SOUTH KOREAN DEPRESSIVE PATIENTS		TopicSem
19	인턴			TopicSem
19	유준기	Histological category of cancer and classification of Cancer predisposition genes		MAInfo
21	...	설날		J.Club
21	...	설날		J.Club
23	...	설날		TopicSem
23	...	설날		TopicSem
26	조원일	Starallele_calling 4_healthshowcase data		TopicSem
26	권호식	Candidate genes related with adverse effects of contrast media		TopicSem
28	최선	Temporal phenotyping using Deep predictive clustering of disease progression		J.Club
28	윤미선	Identification of pathogenic genes associated with CKD: An integrated bioinformatics approach		J.Club
30	윤미선	Pharmacogenomic Profile of Korean population using whole genome sequencing (HLA)		TopicSem
30	배소정	Replication: A genome‐wide association study in a large community‐based cohort identifies multiple loci associated with susceptibility to bacterial and viral infections		TopicSem

01	...	GDA		TopicSem
01	...	GDA		TopicSem
03	부은경	An integral genomic signature approach for tailored cancer therapy using genome-wide sequencing data		J.Club
03	권호식	Association of altered folylpolyglutamate synthetase pre-mRNA splicing with methotrexate unresponsiveness in early rheumatoid arthritis		J.Club
05	조민아	Single cell analysis in Bladder cancer		TopicSem
05	유준기	Rare variant analysis with gene tolerance		TopicSem
08	임영균			TopicSem
08	부은경	Evaluation of pharmacogenetic influences on thiopurine-induced leukopenia in patients with inflammatory bowel disease (Results)		TopicSem
08	배소정	Rare-Variant Association Analysis: Study Designs and Statistical Tests		MAInfo
10	최선	Association of Genome-Wide Polygenic Scores for Multiple Psychiatric and Common Traits in Preadolescent Youths at Risk of Suicide		J.Club
10	김나영	Harvesting metadata in clinical care: a crosswalk between FHIR, OMOP, CDISC and openEHR metadata		J.Club
12	박유미	Comparison of average daily drug dose between subjects with unclear molecular phenotypes and non-ambiguous normals		TopicSem
12	전예진	Active surveillance of AEDs using RWD		TopicSem
15	이시은	Natural Language Processing in Clinical Data		TopicSem
15	김나영	Master's thesis revisions		TopicSem
17	윤미선	EagleImp: fast and accurate genome-wide phasing and imputation in a single tool		J.Club
17	임영균	Genetic risk factors have a substantial impact on healthy life years		J.Club
19	정문경	CDEs for modeling meaningful clinical documents to achieve semantic interoperability		TopicSem
19	안세환	Identify novel variants in haplogroup		TopicSem
22	조원일	The result of pharmacogene in healthshowdata and PGwatch		TopicSem
22	권호식	Candidate variants related with adverse effects of contrast media		TopicSem
22	최선	Time series in healthcare_1		MAInfo
24	전예진	Loss of function, gain of function and dominant negative mutations have profoundly different effects on protein structure		J.Club
24	조민아	Gene Size Matters: An Analysis of Gene Length in the Human Genome		J.Club
26	최선	K-cdm Research design		TopicSem
26	윤미선	Pharmacogenomic Profile of Korean population using WGS		TopicSem
26	전예진	FoldX_variant stability and effect prediction		SysBiol
29	배소정	Infection disease genetic analysis with UK Biobank		TopicSem
29	조민아	Single cell analysis in bladder cancer and troubleshooting		TopicSem
31	안세환	Evaluating the frequency and the impact of pharmacogenetic alleles in an ancestrally diverse Biobank population		J.Club
31	이시은	A pre-trained BERT for Korean medical natural language processing		J.Club

03	부은경	Evaluation of pharmacogenetic influences on thiopurine-induced leukopenia in patients with inflammatory bowel disease (Results with figures)		TopicSem
03	박유미	Distribution of unclear molecular phenotypes for genes with published CPIC guidelines in UK Biobank		TopicSem
03	최선	Data valuation		MAInfo
05	조원일	The genetic landscape of major drug metabolizing cytochrome P450 genes an updated analysis of population scale sequencing data		J.Club
05	임영균	Pan-Cancer Analysis of Potential Synthetic Lethal Drug Targets Specific to Alterations in DNA Damage Response		J.Club
07	이시은	Intro to Natural Language Processing in Clinical Data		TopicSem
07	전예진	active surveillance of phenytoin using UK biobank		TopicSem
09	김나영	Covid-19 vaccination and menstrual cycle length in the Apple Women’s Health Study		BioEMR
10	정문경	빈즈 8주 교육 프로그램 임상연구 현황		TopicSem
10	김나영	Plotting results of unique CDE from 10 hospitals		TopicSem
10	윤미선	A gene set-integrated approach for predicting disease-associated genes		MAInfo
12	정문경	Association of step counts over time with the risk of chronic disease in the All of Us Research Program		J.Club
12	유준기	The mutational signatures of formalin fixation on the human genome		J.Club
14	안세환	Enrichment analysis of haplogroups		TopicSem
14	조원일	star allele caller		TopicSem
17	권호식	Candidate variant related with adverse effects of contrast media		TopicSem
17	최선	sun_kcdm		TopicSem
17	유준기	Disease-gene Database: DisGeNET		MAInfo
19	이시은	Extracting seizure frequency from epilepsy clinic notes: a machine reading approach to natural language processing		J.Club
19	안세환	PharmaKU: A web-based tool aimed at improving outreach and clinical utility of pharmacogenomics		J.Club
21	윤미선	Study design using WES of CKD (EPO resistance)		TopicSem
21	배소정	Infection disease genetic analysis with UK Biobank		TopicSem
21	조민아	SCISSOR: tutorial		SysBiol
24	...	GDA		TopicSem
24	...	GDA		TopicSem
26	조민아	Identifying phenotype-associated subpopulations by integrating bulk and single-cell sequencing data		J.Club
26	배소정	Frequency and Phenotype Associations of Rare Variants in 5 Monogenic Cerebral Small Vessel Disease Genes in 200,000 UK Biobank Participants		J.Club
28	...	GDA		TopicSem
28	...	GDA		TopicSem

01	배소정	Ultrafast search of all deposited bacterial and viral genomic data		J.Club
01	안세환	Aldy 4:An efficient genotypes and star-allele caller for pharmacygenomics		J.Club
03	...	개천절		TopicSem
03	...	개천절		TopicSem
03	...	개천절		SysBiol
06	부은경	Evaluation of pharmacogenetic influences on thiopurine-induced leukopenia in patients with inflammatory bowel disease(Methods)		TopicSem
06	이시은	Natural Language Processing in clinical data		TopicSem
08	유준기	Identifying disease-critical cell types and cellular processes by integrating single-cell RNA-sequencing and human genetics		J.Club
08	권호식	Identification of differentially expressed genes in lung adenocarcinoma cells using single-cell RNA sequencing not detected using traditional RNA sequencing and microarray		J.Club
10	...	대체공휴일		TopicSem
10	...	대체공휴일		TopicSem
10	...	대체휴일		SysBiol
13	김나영	Common data elements for modeling meaningful clinical documents to achieve semantic interoperability		TopicSem
13	정문경			TopicSem
15	이우승	Impact of integrating genomic data into the electronic health record on genetics care delivery		J.Club
15	윤미선	Returning individual genomic results to population‑based cohort study participants with BRCA1/2 pathogenic variants		J.Club
17	전예진	Rare genetic variants can be important determinants of interindividual differences		TopicSem
17	권호식	HLA alleles in patients administrated with Contrast media		TopicSem
17	조민아	All variants of CEMIP2 genes in ulcerative colitis patients		SysBiol
20	안세환	Haplogrouping performance evaluation		TopicSem
20	조원일	CPIC PGx Gene:Star allele calling		TopicSem
22	최선	MolTrans_Molecular Interaction Transformer for DTI prediction		J.Club
22	전예진	Integrating rare genetic variants into pharmacogenetic drug response predictions		J.Club
24	최선	toy project for drug discovery		TopicSem
24	윤미선	Pharmacogenomic Profile of Korean population using whole genome sequencing (Methods & Results of HLA)		TopicSem
24	부은경	.		SysBiol
27	배소정	Rare and low-frequency genetic variants in bacterial and viral disease		TopicSem
27	조민아	Prioritizing CD- or UC-specific variants among candidates		TopicSem
27	권호식	NGS-based HLA genotyping tools		MAInfo
29	부은경	Integrative analysis of drug response and clinical outcome in acute myeloid leukemia		J.Club
29	김나영	Harmonization and standardization of data for a pan-European cohort on SARS- CoV-2 pandemic		J.Club
31	유준기	Candidate variants of Infliximab induced neutropenia in IBD patients		TopicSem
31	임영균	Identifying Gene combination affecting Cancer patients��� Survival		TopicSem

01	부은경	Evaluation of association between genetic variants and thiopurine-induced leukopenia in inflammatory bowel disease		TopicSem
01	임영균	Association between IRF2BP1-rs60158447 and incidence of post ERCP pancreatitis.		TopicSem
03	김나영	CASIDE: A data model for interoperable cancer survivorship information based on FHIR		J.Club
03	정문경	Recognizing Emotions among Couples Managing Diabetes in Daily Life using Multimodal Real-World Smartwatch Data		J.Club
05	이시은	Information Retrieval and medical ontology NLP		TopicSem
05	전예진	CYP2C19 phenotype calling in Korean population(HBDS)		TopicSem
08	정문경			TopicSem
08	김나영	Composite CDE modeling in the domain of 5 representative clinical documents: Data-driven approach		TopicSem
08	윤미선	CLIP for Medical Image		MAInfo
08	윤미선	CLIP for Medical Image		MAInfo
10	...	추석		J.Club
10	...	추석		J.Club
12	...	대체휴일		TopicSem
12	...	대체휴일		TopicSem
15	조원일	inhouse _starallele_calling		TopicSem
15	안선주	PGwatch_Review and starallele		TopicSem
15	유준기	Review of recurrent event models		MAInfo
17	조원일	Genomewide pharmacogenetics of antidrug antibody response to bococizumab highlights key residues in HLA DRB1 and DQB1		J.Club
17	이시은	Deep learning-based NLP data pipeline for EHR-scanned document information extraction		J.Club
19	최선	Fall prediction		TopicSem
19	권호식	Candidate variations related with adverse effects of contrast media		TopicSem
22	안세환	Evaluate haplogrouping by star-allele		TopicSem
22	윤미선	Pharmacogenomic Profile of Korean population using whole genome sequencing_2		TopicSem
22	배소정	MIMIC-IV database		MAInfo
24	조민아	A Survey of Compound Heterozygous Variants in Pediatric Cancers and Structural Birth Defects		J.Club
24	부은경	Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility		J.Club
26	배소정	Biological agent genome sequence analysis		TopicSem
26	조민아	Results of selecting pathogenic variants and comparing with clinical data in RP		TopicSem
26	전예진	type of pharmacogenomic evidence and limitation		SysBiol
29	유준기	Survival analysis of infliximab induced neutropenia in IBD patients		TopicSem
29	임영균	Identifying candidate variants of PEP in merged dataset with new PSM control		TopicSem

01	김나영	Semantic data integration of 5 representative Clinical Document items		TopicSem
01	안세환	Evaluate haplogroups by populations		TopicSem
01	조민아	Application of long-read sequencing to elucidate complex pharmacogenomic regions: a proof of principle		SysBiol
03	최선	낙상예측		MAInfo
04	조원일	analysis of chip and report data of showcase		TopicSem
04	권호식	Candidate copy number variations related with adverse effects of contrast media		TopicSem
04	이우승	Data of Signatures of copy number alterations from TCGA		MAInfo
06	배소정	A genome-wide association study in a large community-based cohort identifies multiple loci associated with susceptibility to bacterial and viral infections		J.Club
06	유준기	Rare genetic variability in human drug target genes modulates drug response and can guide precision medicine		J.Club
08	최선	Fall risk prediction		TopicSem
08	윤미선	Pharmacogenomic Profile of Korean population using whole genome sequencing_2		TopicSem
11	배소정	Biological agentsstudy idea and data processing		TopicSem
11	이우승	SCV Splitting overlapped region between amplicons method to detect somatic copy number variation (CNV) with PCR-based targeted sequencing		TopicSem
11	권호식	Mutect2(Mitochondria mode)		MAInfo
13	권호식	Copy number variation is highly correlated with differential gene expression: a pan-cancer study		J.Club
13	최선	Integrative multiomics-histopathology analysis for breast cancer classification		J.Club
15	...	광복절		TopicSem
15	...	광복절		TopicSem
16	최선	RNA seq research		MAInfo
18	조민아	Results of Classification with patients using known retinitis pigmentosa genes		TopicSem
18	유준기	Variant filtering and Gene-wise analysis of Infliximab induced neutropenia in IBD patients		TopicSem
20	이우승	A pan cancer compendium of chromosomal instability		J.Club
20	윤미선	Development of an extensive workflow for comprehensive clinical pharmacogenomic profiling: lessons from a pilot study on 100 whole exome sequencing data		J.Club
22	...	GDA		TopicSem
22	...	GDA		TopicSem
25	...	GDA		TopicSem
25	...	GDA		TopicSem
25	최선	RNA seq research		MAInfo
27	전예진	Biobank Scale Pharmacogenomics Informs the Genetic Underpinnings of Simvastatin Use		J.Club
27	임영균	Improved pathogenicity prediction for rare human missense variants		J.Club
29	...	GDA		TopicSem
29	...	GDA		TopicSem

02	이시은	Automatically disambiguating medical acronyms with ontology-aware deep learning		J.Club
02	전예진	Combination of Genome-Wide Polymorphisms and CNVs of Pharmacogenes in Koreans		J.Club
04	안세환	Evaluate haplogrouping and K-means clustering		TopicSem
04	조원일	Starallele_calling 3_healthshowcase data		TopicSem
06	김나영	A Digital Health Program Targeting Physical Activity Among Adolescents With Overweight or Obesity: Open Trial		BioEMR
07	권호식	Candidate variants related with adverse effects of contrast mediaincluding Sex chromosomes		TopicSem
07	최선	대장암 선별검사연구		TopicSem
07	윤미선	Identifying interactions in omics data for clinical biomarker discovery using symbolic regression		MAInfo
07	윤미선	Star allele calling in CYP2D6		MAInfo
07	윤미선	Star allele calling in CYP2D6		MAInfo
09	임영균	Identification of discriminative gene-level and protein-level features associated with pathogenic gain-of-function and loss-of-function variants		J.Club
09	김나영	Developing an ETL tool for converting the PCORnet CDM into the OMOP CDM to facilitate the COVID-19 data integration		J.Club
11	윤미선	Star allele calling in CYP2D6 and HLA		TopicSem
11	조민아	Results of Classification with patients using known retinitis pigmentosa genes		TopicSem
14	이우승	Splitting overlapped region between amplicons method to detect somatic copy number variation (CNV) with PCR-based targeted sequencing		TopicSem
14	배소정	Biological agents : Study idea and data preprocessing		TopicSem
14	유준기	CIBERSORTx: Determining cell type abundance and expression from bulk RNA-seq data		MAInfo
16	정문경	Enabling Research and Clinical Use of Patient-Generated HealthData (the mindLAMP Platform): Digital Phenotyping Study		J.Club
16	조민아	Unbiased mosaic variant assessment in sperm: a cohort study to test predictability of transmission		J.Club
18	인턴	Statistical analysis of AKR1C family mutation that lowers cancer risk		TopicSem
18	인턴	Statistical analysis of AKR1C family mutation that lowers cancer risk		TopicSem
18	안세환	Adjusted Rand Index between haplogroups and populations		SysBiol
21	유준기	Variant wise analysis of infliximab induced neutropenia in IBD patients		TopicSem
21	임영균	Analysis of validation samples of Post-ERCP pancreatitis		TopicSem
21	배소정	Bioinformatics in vaccine design and virus detection		MAInfo
23	안세환	Dating genomic variants and shared ancestry in population scale sequencing data		J.Club
23	조원일	Pharmacogenetic genotype and phenotype frequencies in a large Danish population-based case-cohort sample		J.Club
25	부은경	Association of genetic variants in IL6 with thiopurine-induced leukopenia in patients with inflammatory bowel disease		TopicSem
25	전예진	220725_Active surveillance of drug-gene using RWD		TopicSem
27	정문경	Journal Review: Maintaining Outcomes of Internet-Delivered Cognitive-Behavioral Therapy for Depression: A Network Analysis of Follow-Up Effects		BioEMR
28	이시은	lstm		TopicSem
28	정문경	Design ideas for PGHD visualization and incentives		TopicSem
28	임영균	Immune checkpoint inhibitor therapy response data		MAInfo
30	이시은	Leveraging clinical data across healthcare institutions for continual learning of predictive risk models		J.Club
30	부은경	A global overview of genetically interpretable multimorbidities among common diseases in the UK Biobank		J.Club