팀:AllSeminarBioEMRxMutantSysBiolMAInfoJ.ClubTopicSemBookReading   발표자: All강성훈국수경권호식김나영김민정김재환김지헌문성희민유정배소정부은경안선주안세환유경훈유승원유승원유준기윤미선이시은인턴임성수전예진정문경조동영조민아조원일차재현채정환최선최선한봄허지허지연홍진희...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 JacksonNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLNULLPPPrabinRockySo Jeongabe torkeltonbenhjkyutest강기원강병희강병희강병희강석훈강소영고인석김경화김경화김기태김도균김동호김민구김보성김승빈김승호김영성김영훈김주연김주한김준호김지미김지훈김지희김진환김현대김형준김혜현김효정김효진나영지류영재민병주박원준박유랑박유미박은영박이영박정수박지연박지혜박찬희박호경백수연서명의서희원손경아송영수심재현심재현심혜진안빈안선주양웅철엄세인오가희우정훈윤선민윤영조이계화이수연이수연S이수현이우승이정우이정훈이현임영균임재현임준호전은주정상원정승원정용정태수정해원정희준조성범조용래주경민초빙강연최광윤최윤영최준영한미령한지예한현욱홍승권홍주영황동현源����������臾닿�����理���ㅼ��김기원김미현김세영김예진김옥구김윤희김지훈(H)박지연박지연변상재서화정신용준신현정온정헌윤혜성이석호이영주이정애이혜원임수아안성준권혜진유방암센터유수영유의혁(세종대)이권무황기태unknown세종대외부특강전체정혜림팀원권창혁송유림윤준희정제균   제목/키워드:    날짜:   

21	유준기	(Revision) Genome-wide investigation of synthetic rescue interactions in Alzheimer disease		TopicSem
24	유준기	The virtual lab of AI agents designs new SARS-CoV-2 nanobodies		J.Club

05	유준기	Review of current therapies and protective cell-cell interaction in Alzheimer disease		TopicSem
10	유준기	muscat: tool for subpopulation-specific snRNA-seq analysis		MAInfo
15	유준기	Multicellular communities are perturbed in the aging human brain and Alzheimer disease		J.Club
26	유준기	Identifying protective cellular interactions in Alzheimer disease		TopicSem

10	유준기	Issues in OPLL risk gene analysis		TopicSem
20	유준기	Unraveling the intercellular communication disruption and key pathways in Alzheimer disease: an integrative study of single-nucleus transcriptomes and genetic association		J.Club

04	유준기	Single cell analysis for SR pairs in ROSMAP dataset		TopicSem
04	유준기	CS-CORE: Cell type specific co-expression inference in scRNA-seq data		MAInfo
21	유준기	Single cell transcriptomes and multiscale networks from persons with and without Alzheimer disease		J.Club

12	유준기	A single nuclear transcriptomic characterisation of mechanisms responsible for impaired angiogenesis and blood-brain barrier function in Alzheimer disease		J.Club
16	유준기	.		TopicSem
30	유준기	scCODA a Bayesian model for compositional single cell data analysis		MAInfo

06	유준기	Replication of SR pairs using Polygenic Rescued Hazard Score		TopicSem
18	유준기	Cell state dependent allelic effects and contextual mendelian randomization analysis for human brain phenotypes		J.Club
23	유준기	OPLL WES analysis: Clinical variables and analysis plan		TopicSem

11	유준기	OPLL analysis		MAInfo
16	유준기	Synthetic rescue pairs identified in ADSP and ROSMAP dataset		TopicSem
28	유준기	Multi trait association analysis reveals shared genetic loci between Alzhimer disease and cardiovascular traits		J.Club

07	유준기	Replication of SR pairs for Alzheimer disease in ROSMAP dataset		TopicSem
16	유준기	Genes with diffrential expression across ancestries are enriched in ancestry specific disease effects likely due to gene by environment interactions		J.Club
28	유준기	Replication of SR pairs for Alzheimer disease in external datasets		TopicSem

12	유준기	Identifying genetic variants that influence the abndance of cell states in single cell data		J.Club
21	유준기	Identifying SR pairs for Alzheimer disease using different GVB thresholds		TopicSem
30	유준기	The complex genetic architecture of Alzheimer disease novel insights and future directions		MAInfo

05	유준기	Identification of synthetic rescue pairs for Alzheimer disease		TopicSem
24	유준기	Cell subtype specific effects of genetic variation in the Alzheimer disease brain		J.Club

11	유준기	Genome wide identification of synthetic rescue pairs for Alzheimer disease: Figures and Tables		TopicSem
27	유준기	Cell type specific Alzhimer disease polygenic risk scores are associated with distinct disease process in Alzhimer disease		J.Club
31	유준기	VarCards2: an integrated genetic and clinical database for ACMG-AMP variant-interpretation guidelines in the human whole genome		MAInfo

01	유준기	APOE4 homozygosity represents a distinct genetic form of Alzheimer disease		J.Club
20	유준기	Genome-wide identification of synthetic rescue pairs for Alzheimer disease		TopicSem
26	유준기	Polygenic resilience scores capture protective effects for Alzheimer disease		MAInfo

16	유준기	Genome-wide analyses reveal the contribution of somatic variants to the immune landscape of multiple cancer types		J.Club
21	유준기	Revised onset age analysis for SR pair in Alzheimer Disease		TopicSem

05	유준기	Identifying Synthetic Rescue pairs in Alzheimer Disease using z-test		TopicSem
24	유준기	cLD Rare variant linkage disequilibrium between genomic regions identifies novel genomic interactions		J.Club
28	유준기	CoxPH model for cross-sectional genomic data		MAInfo
29	유준기	The impact of SR pairs on the Onset Age of Alzheimer Disease		TopicSem

14	유준기	Identifying synthetic rescuer in Alzheimer's Disease using enrichment/depletion test		TopicSem
27	유준기	External DBs for filtering Synthetic Rescue Pairs		MAInfo
30	유준기	Identification of Ferroptosis-Related Genes in Alzheimer's Disease Based on Bioinformatic analysis		J.Club

08	유준기	Idea for identifying synthetic rescue pair		MAInfo
18	유준기	Global analysis of suppressor mutations that rescue human genetic defects		J.Club
23	유준기	Variant-wise and gene-wise analysis, and idea for identifying their rescuers in ADSP dataset		TopicSem

04	유준기	Synthetic rescue analysis using TCGA and ADSP data		TopicSem
06	유준기	TCGA PanCanAtlas data		MAInfo
23	유준기	Allelic imbalance of chromatin accessibility in cancer identifies candidate causal risk variants and their mechanisms		J.Club

14	유준기	Biased genetic predisposition in cancer and neurodegeneration		TopicSem
26	유준기	An allelic-series rare-variant association test for candidate-gene discovery		J.Club

08	유준기	Prioritizing autoimmunity risk variants for functional analyses by fine-mapping mutations under natural selection		J.Club
17	유준기	Inverse relationship and positive selection in Cancer and Neurodegeneration		TopicSem
26	유준기	Positive selection scoring method		MAInfo

20	유준기	The genetic deteriminants of recurrent somatic mutations in 43,693 blood genomes		J.Club
22	유준기	Rare variants and deleterious variants in Cancer predisposition Genes (CPG) and Alzheimer associated Genes		TopicSem

03	유준기	Comparing Cancer predisposition gene (CPG) and Alzheimer associated genes		TopicSem
08	유준기	Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes		J.Club
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

04	유준기	Germline mutations in mitochondrial complex I reveal genetic and targetable vulnerability in IDH1-mutant acute myeloid leukaemia		J.Club
13	유준기	Distribution of allele frequency and Insilico scores in Cancer Predisposition Gene (CPG)		TopicSem
15	유준기	LRT-q: Rare variant association test for gene expression in multiple tissues		MAInfo

02	유준기	Characteristics of Cancer predisposition gene (CPG) variants in the general population		TopicSem
14	유준기	The impact of rare germline variants on human somatic mutation processes		J.Club
19	유준기	Histological category of cancer and classification of Cancer predisposition genes		MAInfo

12	유준기	The mutational signatures of formalin fixation on the human genome		J.Club
17	유준기	Disease-gene Database: DisGeNET		MAInfo

08	유준기	Identifying disease-critical cell types and cellular processes by integrating single-cell RNA-sequencing and human genetics		J.Club
31	유준기	Candidate variants of Infliximab induced neutropenia in IBD patients		TopicSem

06	유준기	Rare genetic variability in human drug target genes modulates drug response and can guide precision medicine		J.Club
18	유준기	Variant filtering and Gene-wise analysis of Infliximab induced neutropenia in IBD patients		TopicSem

18	유준기	Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity		J.Club
20	유준기	Infliximab induced neutropenia in IBD patients - subgroups and graphs		TopicSem

07	유준기	All of Us: Genomic data browser		MAInfo
21	유준기	Infliximab induced neutropenia in IBD patients		TopicSem
30	유준기	The individual and global impact of copy-number variants on complex human traits		J.Club

03	유준기	Genetic variants associated with Infliximab response in IBD patients		TopicSem
12	유준기	Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank		J.Club
28	유준기	Variant-wise analysis of Infliximab response in IBD patients		TopicSem

03	유준기	Anti TNF therapy induced ADR		TopicSem
06	유준기	Accessing JGA (Japanese Genotype-Phenotype Archive) data		MAInfo
22	유준기	Exome variant discrepancies due to reference-genome differences		J.Club

15	유준기	Rare variant analysis in Multiple Sclerosis patients		TopicSem
25	유준기	Variant calling from transcriptome data		MAInfo
27	유준기	Calibrated rare variant genetic risk scores for complex disease prediction using large exome sequence repositories		J.Club

06	유준기	Autoimmune disease single tissue eQTL analysis in UK Biobank		TopicSem
25	유준기	Set based rare variant expression quantitative trait loci in blood and brain from Alzheimer Disease study participants		J.Club
30	유준기	Comparing Rare Variant Association Tests		MAInfo

17	유준기	Association between major depressive disorder and multiple disease outcomes: a phenome-wide Mendelian randomisation study in the UK Biobank		J.Club
26	유준기	Combining UKB dataset with eQTL data		MAInfo

05	유준기	Transcript expression-aware annotation improves rare variant interpretation		J.Club
24	유준기	GWAS study design using UK Biobank		TopicSem