SNUBI Research ::   (86 talks satisfying Presenter = 유준기)
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2024-06:
15 유준기   J.Club
24 유준기   TopicSem

2024-05:
11 유준기   J.Club
13 유준기   TopicSem
27 유준기   TopicSem

2024-04:
03 유준기 ssGSEA: single sample Gene Set Enrichment Analysis  MAInfo
11 유준기 Replication of onset age analysis in UK Biobank Alzheimer disease patients  TopicSem

2024-03:
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

2024-02:
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

2024-01:
15 유준기 Filtering synthetic rescue pairs in Alzheimer disease  TopicSem

2023-12:
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

2023-11:
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

2023-10:
05 유준기 Synthetic rescue analysis in cancer and Alzheimer's Disease patients  TopicSem
30 유준기 Variant-wise analysis in ADSP dataset  TopicSem

2023-09:
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

2023-08:
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

2023-07:
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

2023-06:
07 유준기 Computational genomic approaches to interpret non-coding disease risk variants  MAInfo
19 유준기 Molecular genetic features of Cancer Predisposition Genes (CPG) and Alzheimer's Disease Genes  TopicSem

2023-05:
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

2023-04:
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

2023-03:
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

2023-02:
02 유준기 Classification and characterization of Cancer Predisposition Gene (CPG) variants  TopicSem

2023-01:
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

2022-12:
05 유준기 Rare variant analysis with gene tolerance  TopicSem

2022-11:
12 유준기 The mutational signatures of formalin fixation on the human genome     J.Club
17 유준기 Disease-gene Database: DisGeNET  MAInfo

2022-10:
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

2022-09:
15 유준기 Review of recurrent event models  MAInfo
29 유준기 Survival analysis of infliximab induced neutropenia in IBD patients  TopicSem

2022-08:
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

2022-07:
14 유준기 CIBERSORTx: Determining cell type abundance and expression from bulk RNA-seq data  MAInfo
21 유준기 Variant wise analysis of infliximab induced neutropenia in IBD patients  TopicSem

2022-06:
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

2022-05:
23 유준기 Infliximab induced neutropenia in IBD patients - case reconstruction  TopicSem
26 유준기 Neutropenia criteria in Infliximab-treated IBD patients  MAInfo

2022-04:
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

2022-03:
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

2022-02:
07 유준기 Infliximab induced ADR in IBD patients  TopicSem
24 유준기 Study design - Infliximab response in IBD patients  MAInfo

2022-01:
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

2021-12:
13 유준기 Rare variant analysis in MS patients  TopicSem

2021-11:
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

2021-10:
14 유준기 Rare variant analysis incorporating functional annotations  TopicSem

2021-09:
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

2021-08:
02 유준기 Comparative analysis integrating UK Biobank and eQTL data  TopicSem

2021-07:
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

2021-06:
05 유준기 Transcript expression-aware annotation improves rare variant interpretation     J.Club
24 유준기 GWAS study design using UK Biobank  TopicSem

2021-05:
10 유준기 Rarepedia analysis of an individual  TopicSem

2021-04:
08 유준기 Rarepedia analysis of an individual  TopicSem

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