SNUBI Research ::   (182 talks satisfying Presenter = 권호식)
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2024-06:
13 권호식   TopicSem
22 권호식   J.Club

2024-05:
18 권호식   J.Club
20 권호식   TopicSem

2024-04:
01 권호식 Human Protein Atlas in our study for Contrast media-induced Immediate Hypersensitivity  TopicSem
17 권호식 dbGaP Data Access  MAInfo
25 권호식 Replication of potential variants influencing HD-MTX delayed excretion in pediatric ALL  TopicSem

2024-03:
06 권호식 SNU OA 게재료 지원 서비스 소개  MAInfo
14 권호식 GVB R package development  TopicSem
30 권호식 CellAnn: a comprehensive, super-fast, and user-friendly single-cell annotation web server     J.Club

2024-02:
17 권호식 The burden of splice-disrupting variants in inherited heart disease and unexplained sudden cardiac death     J.Club
22 권호식 GVB R package development - update functions  TopicSem

2024-01:
04 권호식 GVB R package development  TopicSem
13 권호식 DNA Sequencing to Detect Residual Disease in Adults With Acute Myeloid Leukemia Prior to Hematopoietic Cell Transplant     J.Club
24 권호식 Example data and vignette in R package  MAInfo
29 권호식 GVB R package development - Example data  TopicSem

2023-12:
07 권호식 GVB R package development  TopicSem

2023-11:
13 권호식 Design for GVB R package  TopicSem
22 권호식 R packages to develop R package  MAInfo
25 권호식 Systematic pan-cancer analysis of mutation-treatment interactions using large real-world clinicogenomics data     J.Club

2023-10:
14 권호식 Germline rare deleterious variant load alters cancer risk, age of onset and tumor characteristics     J.Club
23 권호식 Design for GVB R package  TopicSem

2023-09:
18 권호식 Candidate genomic variations in patients with adverse reactions to contrast media  TopicSem
20 권호식 (Review) Tutorial: guidelines for annotating single-cell transcriptomic maps using automated and manual methods  MAInfo

2023-08:
03 권호식 Busulfan and Hepatic veno-occlusive disease  TopicSem
12 권호식 Single-cell transcriptome profiling of the stepwise progression of head and neck cancer     J.Club
16 권호식 AnnotSV: Annotation of Human Structural Variations  MAInfo
28 권호식 Summary of Results for Pharmacogenomic Study of Contrast media-induced adverse reactions   TopicSem

2023-07:
15 권호식 Cell type prioritization in single-cell data     J.Club

2023-06:
03 권호식 STOmicsDB: a database of Spatial Transcriptomic data     J.Club
12 권호식 Copy number variations in Patients receiving contrast media  TopicSem
26 권호식 Copy number variations in patients receiving contrast media  TopicSem
28 권호식 Performance of CNV callers for WES data  MAInfo

2023-05:
10 권호식 Busulfan and Adverse Drug Events  MAInfo
15 권호식 Further analysis for candidate genes derived from CNV analysis in CTM  TopicSem

2023-04:
15 권호식 Confronting false discoveries in single-cell differential expression     J.Club
20 권호식 Potential genomic variations related with adverse effects of contrast media  TopicSem

2023-03:
02 권호식 Variants in two candidate genes related with adverse effects of contrast media  TopicSem
02 권호식   TopicSem
04 권호식 Association of Genetic Ancestry and Molecular Signatures with Cancer Survival Disparities: A Pan-Cancer Analysis     J.Club
20 권호식 Potential genomic variations related with adverse effects of contrast media  TopicSem
29 권호식 Cell types and Functions  MAInfo

2023-02:
09 권호식 Cell markers and Stem cells  MAInfo

2023-01:
14 권호식 Computational comparison of common event based differential splicing tools     J.Club
26 권호식 Candidate genes related with adverse effects of contrast media  TopicSem

2022-12:
03 권호식 Association of altered folylpolyglutamate synthetase pre-mRNA splicing with methotrexate unresponsiveness in early rheumatoid arthritis     J.Club
22 권호식 Candidate variants related with adverse effects of contrast media  TopicSem

2022-11:
17 권호식 Candidate variant related with adverse effects of contrast media  TopicSem

2022-10:
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
17 권호식 HLA alleles in patients administrated with Contrast media   TopicSem
27 권호식 NGS-based HLA genotyping tools  MAInfo

2022-09:
19 권호식 Candidate variations related with adverse effects of contrast media  TopicSem

2022-08:
04 권호식 Candidate copy number variations related with adverse effects of contrast media  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

2022-07:
07 권호식 Candidate variants related with adverse effects of contrast media including Sex chromosomes  TopicSem

2022-06:
09 권호식 Candidate variants related with adverse effects of contrast media  TopicSem
11 권호식 The frequency of the known mitochondrial variants associated with drug‑induced toxicity in a Korean population     J.Club
30 권호식 Association test for variants on X chromosome  MAInfo

2022-05:
12 권호식 Comparison of the clinical information by genotypes of potential candidate variants  TopicSem

2022-04:
14 권호식 Candidate variants related with MTX delayed excretion and Subgroup analysis  TopicSem
23 권호식 Mitochondrial DNA variation across 56,434 individuals in gnomAD     J.Club
28 권호식 Mitochondrial DNA variants in gnomAD Browser  MAInfo

2022-03:
12 권호식 Changes in Plasma Amyloid and Tau in a Longitudinal Study of Normal Aging, Mild Cognitive Impairment, and Alzheimer’s Disease     J.Club
17 권호식 [Review] Repeated Measures Designs and Analysis of Longitudinal Data  MAInfo
21 권호식 Candidate variants related with MTX-induced delayed excretion  TopicSem

2022-02:
21 권호식 Candidate variants related with MTX-induced nephrotoxicity or delayed excretion  TopicSem

2022-01:
15 권호식 Genetic Background of Mesalamine-induced Fever and Diarrhea in Japanese Patients with Inflammatory Bowel Disease     J.Club
20 권호식 Candidate variants related with MTX-induced elevations in creatinine or MTX plasma concentrations  TopicSem
27 권호식 Human CNV and complex genetic disease  MAInfo

2021-12:
16 권호식 Useful functions for preprocessing clinical data in R  MAInfo

2021-10:
21 권호식 Sequencing and Imputation  MAInfo
28 권호식 Adverse effects of Contrast Media  TopicSem

2021-09:
18 권호식 Copy number variation profiling in pharmacogenes using panel-based exome resequencing and correlation to human liver expression     J.Club
23 권호식 Association between Traits in UK Biobank and Potential variant related with Methotrexate-induced nephrotoxicity  TopicSem

2021-08:
23 권호식 Identification of potential variants related with Methotrexate-induced nephrotoxicity  TopicSem
30 권호식 Genebass  MAInfo

2021-07:
17 권호식 Systematic single-variant and gene-based association testing of 3,700 phenotypes in 281,850 UK Biobank exomes     J.Club
19 권호식 Interpretation and literature review for the results of HD-MTX induced nephrotoxicity analysis  TopicSem

2021-06:
10 권호식 Adverse Effects of Contrast Media  TopicSem
28 권호식 Filtering out false positive variants  MAInfo

2021-05:
15 권호식 A comparison of tools for copy-number variation detection in germline whole exome and whole genome sequencing data     J.Club

2021-04:
08 권호식 review : Contrast media  MAInfo
26 권호식 Candidate variants related with Methotrexate-induced nephrotoxicity  TopicSem
29 권호식 Adverse Effects of Contrast Media  MAInfo

2021-03:
04 권호식 Clinical characteristics according to the presence or absence of candidate variants in UK Biobank  TopicSem
11 권호식 Charlson comorbidity index  MAInfo
15 권호식 Propensity score analysis and R packages  xMutant
20 권호식 Analysis of Drug Metabolizing Gene Panel in Osteosarcoma Patients Identifies Association Between Variants in SULT1E1, CYP2B6 and CYP4F8 and Methotrexate Levels and Toxicities     J.Club
23 권호식 MTX-induced Nephrotoxicity in ALL  Seminar
25 권호식 Methotrexate induced renal toxicity  TopicSem

2021-02:
08 권호식 Clinical characteristics according to the presence or absence of candidate variant in UK Biobank  TopicSem

2021-01:
18 권호식 Candidate variant as a biomarker for MTX-Induced nephrotoxicity in UK Biobank  TopicSem
30 권호식 Real world scenarios in rare variant association analysis: the impact of imbalance and sample size on the power in silico     J.Club

2020-12:
07 권호식 Candidate variants related with HD-MTX Induced Toxicity in Pediatric ALL  TopicSem
19 권호식 Combining clinical and candidate gene data into a risk score for azathioprine-associated leukopenia in routine clinical practice     J.Club
31 권호식 Candidate variant in UK Biobank  TopicSem

2020-11:
16 권호식 Analysis of renal toxicity induced by MTX in Korean pediatric ALL and UKB  TopicSem

2020-10:
22 권호식 Analysis of renal toxicity induced by MTX based on fold Cr in Korean pediatric ALL and UKB  TopicSem
31 권호식 A novel statistical method for interpreting the pathogenicity of rare variants     J.Club

2020-09:
24 권호식 Candidates related with Methotrexate induced acute kidney injury  TopicSem
28 권호식 review : Oligonucleotide microarray  xMutant

2020-08:
03 권호식 MTX and AKI in UK Biobank   TopicSem
06 권호식 Sex chromosomes and genetic association studies   MAInfo
29 권호식 A functional polymorphism in the ATP-Binding Cassette B1 transporter predicts pharmacologic response to combination of nortriptyline and morphine in neuropathic pain patients     J.Club
31 권호식 Candidate variants related with HD-MTX Induced Toxicity in Pediatric ALL  TopicSem

2020-07:
04 권호식 Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes     J.Club
09 권호식 Adverse Effects of Contrast Media   TopicSem
20 권호식 Error and Trouble shooting In TVC and GATK  xMutant

2020-06:
01 권호식 Candidate variants related with HD-MTX Induced Toxicity in Pediatric ALL  TopicSem
08 권호식 Difference in clinical information according to candidate variants in HD-MTX Study  xMutant
18 권호식 Variants related to MTX efficacy or toxicity reported in PharmGKB and Clinical significance in ClinVar   MAInfo

2020-05:
07 권호식 HD-MTX : BUN & Candidates from Fold-Cr  MAInfo
11 권호식 TM7SF3 induced Renal Toxicity in ALL administered with MTX  TopicSem

2020-04:
13 권호식 TM7SF3 in UK Biobank  TopicSem
25 권호식 Genetic and clinical prediction models for the efficacy and hepatotoxicity of methotrexate in patients with rheumatoid arthritis: a multicenter cohort study     J.Club
27 권호식 Study of contrast agent to side effects from additional samples  xMutant

2020-03:
16 권호식 TM7SF3 candidate variant : Renal Toxicity in Pediatric ALL patients administered with HD-MTX  TopicSem
19 권호식 Discussion for defining phenotypes from UKB  xMutant
26 권호식 TM7SF3 variant in UKB  MAInfo

2020-02:
20 권호식 BiobankRead  MAInfo
24 권호식 Clinical Data in UK Biobank   TopicSem
29 권호식 Identification of pathogenic variant enriched regions across genes and gene families     J.Club

2020-01:
02 권호식 HD-MTX induced Renal Toxicity in Pediatric ALL  TopicSem
02 권호식 HD-MTX induced Renal Toxicity in Pediatric ALL  TopicSem
04 권호식 Evaluating potential drug targets through human loss-of function genetic variation     J.Club
30 권호식 GeneHancer: genome-wide integration of enhancers and target genes in GeneCards  xMutant

2019-12:
12 권호식 MAC: identifying and correcting annotation for multi-nucleotide variations  xMutant
26 권호식 The genome Aggregation Database  MAInfo

2019-11:
07 권호식 Analysis of HD-MTX induced renal toxicity In Pediatric Patients with ALL   MAInfo
28 권호식 HD-MTX induced renal toxicity in pediatric ALL  TopicSem

2019-10:
05 권호식 Exome-wide assessment of the functional impact and pathogenicity of multinucleotide mutations     J.Club
21 권호식 Identification of potential genomic markers related with adverse effects of Contrast Media  Seminar
24 권호식 Impact of outdated gene annotation on Enrichment analysis  xMutant
28 권호식 Identification of potential genomic variants related with adverse effects of Contrast Media  TopicSem

2019-09:
16 권호식 Adverse Effects of Contrast Media  TopicSem

2019-08:
01 권호식 Adverse Effects of Contrast Media  TopicSem
01 권호식 Rare-Variant Association  MAInfo
08 권호식 Markers related with Iopromide from Literatures  xMutant

2019-07:
20 권호식 Pathogenic Germline Variants in 10,389 Adult Cancers     J.Club

2019-06:
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
24 권호식 Adverse effects of Contrast media  TopicSem

2019-05:
02 권호식 MTX Genomic markers from literatures  xMutant
18 권호식 The germline genetic component of drug sensitivity in cancer cell lines     J.Club
27 권호식 The List of Public Databases and Discussion  TopicSem

2019-04:
11 권호식 Clinical data of HD-MTX ALL samples and the progress  TopicSem
25 권호식 Considerations in Assigning Star Alleles to 1KGP  MAInfo

2019-03:
09 권호식 Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions     J.Club
14 권호식 Variants of Star Allele Wild Type samples from 1KGP  TopicSem
14 권호식 Clinical data of HD-MTX samples   xMutant

2019-02:
07 권호식 HD-MTX induced renal toxicity In Pediatric Patients with ALL  TopicSem
07 권호식 star allele assignment and annotation  MAInfo

2019-01:
02 권호식 discussion about HD-MTX analysis  xMutant
05 권호식 ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants     J.Club

2018-12:
17 권호식 HD-MTX induced renal toxicity in pediatric ALL  TopicSem
27 권호식 High dose MTX induced renal toxicity in pediatric acute lymphoblastic leukemia   Seminar
29 권호식 ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants     J.Club

2018-11:
10 권호식 Intersect-then-combine approach: improving the performance of somatic variant calling in whole exome sequencing data using multiple aligners and callers     J.Club
15 권호식 preliminary investigation : Variants and Genes related with adverse effects of MTX  TopicSem
22 권호식 Variants related with MTX-induced renal toxicity or HDMTX from research papers  MAInfo

2018-10:
04 권호식 GDM visualization on the web  TopicSem
30 권호식 HGVS nomenclature  xMutant

2018-09:
01 권호식 The landscape of genomic alterations across childhood cancers     J.Club
04 권호식 KOVA : Korean Variant Archive  xMutant
13 권호식 GDM conversion and visualization  TopicSem
20 권호식 Study : Leukemia and Anticancer drugs  MAInfo

2018-07:
16 권호식 Mutational Signatures of COSMIC  MAInfo
17 권호식 GDM Visualization using maftools  xMutant

2018-06:
04 권호식 Leukemia WXS Conversion  MAInfo
30 권호식 Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes     J.Club

2018-04:
02 권호식 Leukemia QC and Annotation  MAInfo
07 권호식 Analysis of a gene panel for targeted sequencing of colorectal cancer samples     J.Club

2018-03:
27 권호식 xCell : cell types enrichment analysis  xMutant

2018-01:
11 권호식 Exercise for Visualizing TCGA data   TopicSem
20 권호식 Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma     J.Club

2017-12:
11 권호식 Plan for my Study Using TCGA data   TopicSem

2017-11:
06 권호식 Alamut Visual: Visualization engine for NGS analysis  TopicSem
18 권호식 Multiregion Whole-Exome Sequencing Uncovers the Genetic Evolution and Mutational Heterogeneity of Early-Stage Metastatic Melanoma     J.Club

2017-10:
11 권호식 Alamut-Focus : interactive variant filtration application for NGS analysis.  TopicSem

2017-09:
04 권호식 Alamut-Batch : annotation engine for NGS analysis  TopicSem

2017-08:
26 권호식 Burden of Nonsynonymous Mutations among TCGA Cancers and Candidate Immune Checkpoint Inhibitor Responses     J.Club

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