SNUBI Research ::   (173 talks satisfying Presenter = 안세환)
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2024-05:
04 안세환 Polygenic scores for cardiovascular risk factors improve estimation of clinical outcomes in CCB treatment compared to pharmacogenetic variants alone     J.Club
16 안세환   TopicSem

2024-04:
01 안세환 OEIS to OMOP CDM  TopicSem
22 안세환 Converting OEIS to OMOP CDM  TopicSem

2024-03:
11 안세환 Comparing VAMP-seq and star alleles  TopicSem
30 안세환 Empowering personalized pharmacogenomics with generative AI solutions     J.Club

2024-02:
03 안세환 Integrating rare genetic variants into DPYD pharmacogenetic testing may help preventing fluoropyrimidine-induced toxicity     J.Club
19 안세환 Embedded System  TopicSem

2024-01:
25 안세환   TopicSem

2023-12:
04 안세환 The association between haplogroups and star alleles  TopicSem
23 안세환 Frequencies of pharmacogenomic alleles across biogeographic groups in a large-scale biobank     J.Club
28 안세환 Improving star allele nomenclature based on haplogroups  TopicSem

2023-11:
13 안세환 Classification of star alleles based on haplogroups  TopicSem
25 안세환 Deep mutational scanning of CYP2C19 reveals a substrate specificity-abundance tradeoff     J.Club

2023-10:
07 안세환 Structural variation of the coding and non-coding human pharmacogenome     J.Club
19 안세환 Classification of star alleles by haplogroups  TopicSem

2023-09:
18 안세환 Star-allele associated haplogroups of 25 pharmacogenes  TopicSem

2023-08:
03 안세환 Summarize the results of haplogroups  TopicSem
12 안세환 Chracterizing the combined effects of cytochrome P450 missense variation within star allele definitions     J.Club
24 안세환 Association between haplogroups and star-alleles in 1KGP  TopicSem

2023-07:
03 안세환 Constructing Haplogroups for Pharmacogenes  TopicSem
15 안세환 PharmaGScore scores of compound genetic variant burden for psychiatric treatment optimization     J.Club

2023-06:
08 안세환 Identifications of associations between star alleles and haplogroups  TopicSem

2023-05:
11 안세환 Association between haplogroups and star-alleles  TopicSem
13 안세환 A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variants     J.Club

2023-04:
08 안세환 A unifying model to predict variable drug response for personalised medicine.     J.Club
17 안세환 Distribution of haplogroups and star-alleles  TopicSem

2023-03:
23 안세환 Identifying associations between haplogroups and star-alleles  TopicSem

2023-02:
18 안세환 Identification and functional validation of novel pharmacogenomic variants using a next-generation sequencing-based approach for clinical pharmacogenomics     J.Club
27 안세환 Identifying novel functional PGx variants based on haplogroup  TopicSem

2023-01:
05 안세환 test     SysBiol
16 안세환   TopicSem

2022-12:
19 안세환 Identify novel variants in haplogroup  TopicSem
31 안세환 Evaluating the frequency and the impact of pharmacogenetic alleles in an ancestrally diverse Biobank population     J.Club

2022-11:
14 안세환 Enrichment analysis of haplogroups  TopicSem
19 안세환 PharmaKU: A web-based tool aimed at improving outreach and clinical utility of pharmacogenomics     J.Club

2022-10:
01 안세환 Aldy 4:An efficient genotypes and star-allele caller for pharmacygenomics     J.Club
20 안세환 Haplogrouping performance evaluation  TopicSem

2022-09:
22 안세환 Evaluate haplogrouping by star-allele  TopicSem

2022-08:
01 안세환 Evaluate haplogroups by populations  TopicSem

2022-07:
04 안세환 Evaluate haplogrouping and K-means clustering  TopicSem
18 안세환 Adjusted Rand Index between haplogroups and populations   SysBiol
23 안세환 Dating genomic variants and shared ancestry in population scale sequencing data     J.Club

2022-06:
02 안세환 Evaluate constructing haplogroup method  TopicSem
18 안세환 Evaluation of population-level pharmacogenetic actionability in Alabama     J.Club
20 안세환 Evaluate the haplogrouping method by DNA evolution pairwise distances  SysBiol

2022-05:
09 안세환 Evaluation of haplogroups in 25 pharmacogenes  TopicSem
16 안세환 Summary of variants in 25 pharmacogenes  SysBiol

2022-04:
07 안세환 Evaluation of haplogrouping results  TopicSem
09 안세환 Pharmacogenomic landscape of Indian population using whole genomes     J.Club

2022-03:
05 안세환 Massively parallel characterization of CYP2C9 variant enzyme activity and abundance     J.Club
14 안세환 Association between haplogroups and star-alleles in 25 pharmacogenes  TopicSem

2022-02:
17 안세환 Haplogroups of 25 pharmacogenes  TopicSem

2022-01:
08 안세환 Phenotype prediction and characterization of 25 pharmacogenes in Thais from whole genome sequencing for clinical implementation     J.Club
13 안세환 Enrichment analysis of TPMT haplogroups  TopicSem

2021-12:
20 안세환 TPMT haplogroups enrichment analysis  TopicSem
28 안세환 TPMT star-alleles in high-coverage T1GP  SysBiol

2021-11:
06 안세환 Population-scale predictions of DPD and TPMT phenotypes using a quantitative pharmaacogene-specific ensemble classifier     J.Club
23 안세환 Comparison of phasing strategies for whole human genomes  SysBiol
25 안세환 Phylogenetic TPMT haplogroups  TopicSem

2021-10:
12 안세환 Segmented haplotype estimation and imputation tools (SHAPEIT4)  SysBiol
12 안세환 Segmented haplotype estimation and imputation tools (SHAPEIT4)  SysBiol
25 안세환 Phylogenetic clustering results of T1GP  TopicSem

2021-09:
16 안세환 Results of matching Health Showcase data with T1GP haplogroups  TopicSem
25 안세환 High coverage whole genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios     J.Club

2021-08:
19 안세환 Hierarchical clustering of TPMT haplgroups  TopicSem
24 안세환 TPMT star-alleles and haplogroups of Health Showcase data  SysBiol

2021-07:
06 안세환 Querying against cell viability data(PRISM) in CMap LINCS website  SysBiol
08 안세환 Compare star-alleles and haplogroups in TPMT  TopicSem
24 안세환 Haplotype-resolved diverse human genomes and integrated analysis of structural variation     J.Club

2021-06:
07 안세환 Haplogroupswith hierarchical clustering  TopicSem

2021-05:
08 안세환 Genetic ancestry plays a central role in population pharmacogenomics     J.Club

2021-04:
22 안세환 Deleterious TPMT haplogroups in T1GP  TopicSem
27 안세환 Calling star-alleles from NGS data  SysBiol

2021-03:
04 안세환 Star-allele based phenotypes and haplogroups  TopicSem
13 안세환 Systems Pharmacogenomic Landscape of Drug Similarities from LINCS data: Drug Association Networks     J.Club
23 안세환 Factor-specific Pattern Mining of Gene Expression  Seminar
25 안세환 Diplogroups and star-allele based phenotypes  TopicSem

2021-02:
04 안세환 Introduction of Hail  TopicSem

2021-01:
16 안세환 A systematic comparison of pharmacogene star allele calling bioinformatics algorithm: a focus on CYP2D6 genotyping     J.Club
21 안세환 Functional or Deleterious variants in each haplogroup  TopicSem

2020-12:
05 안세환 A Proteotranscriptomic-Based Computational Drug-Repositioning Method for Alzheimer’s Disease     J.Club
07 안세환 Compare TPMT haplogroup clusterings  BioEMR
10 안세환 Discovering three-dimensional FSGPs  TopicSem
28 안세환 TPMT haplogroup construction  TopicSem

2020-11:
16 안세환 FSGPs with LINCS L1000 data  TopicSem

2020-10:
17 안세환 Drug-induced adverse events prediction with the LINCS L1000 data     J.Club
26 안세환 Discovering cell- and drug-specific patterns with the LINCS L1000 data  TopicSem
26 안세환 Introduction of Phylip  BioEMR

2020-09:
03 안세환 Enrichment Test of drug-specific genes  TopicSem
03 안세환 Enrichment Test of drug-specific genes  TopicSem
14 안세환 The PRISM drug repurposing dataset  BioEMR
21 안세환 Discovering significant and interpretable patterns with LINCS L1000 data  TopicSem

2020-08:
06 안세환 Interpretation significant cell- and drug-specific FSGPs  TopicSem
22 안세환 Improving cell-specific drug connectivity mapping with collaborative filtering     J.Club

2020-07:
02 안세환 Interpretation FSGPs in activator group  TopicSem
02 안세환 Interpretation FSGPs in activator group  TopicSem
06 안세환 Significant FSGPs estimating FDR  BioEMR

2020-06:
01 안세환 Integrative web platform for analysis of LINCS data (iLINCS)  BioEMR
04 안세환 Discovering FSGPs using small molecules classified by Moa  TopicSem
08 안세환 Mechanism of action lists in L1000 data  SysBiol
13 안세환 Evaluation of Connectivity Map shows limited reproducibility in drug repositioning     J.Club

2020-05:
11 안세환 Discovering FSGP using gene expression signature and fold change  TopicSem

2020-04:
06 안세환 The Comparative Toxicogenomics Database  SysBiol
09 안세환 Top 50 FSGPs in LINCS L1000 data  TopicSem
18 안세환 Predict New Therapeutic Drugs for Hepatocellular Carcinoma Based on Gene Mutation and Expression     J.Club
27 안세환 Fold changes of LINCS L1000 data  BioEMR

2020-03:
16 안세환 Determining significant FSGP using permutation  TopicSem
23 안세환 Discovering FSGP for UKBiobank  BioEMR

2020-02:
03 안세환 Permutation testing for the distance measures  BioEMR
06 안세환 Interpretable patterns from LINCS-L1000 data  TopicSem
15 안세환 eVIP2: Expression-based variant impact phenotypic to predict the function of gene variants     J.Club

2020-01:
13 안세환 Visualize interpretable pattern from LINCS-L1000  SysBiol

2019-12:
07 안세환 .     J.Club
23 안세환 Streamlined analysis of LINCS L1000 data with the slinky package for R  BioEMR
30 안세환 Discovering interpretable pattern from LINCS-L1000 data  TopicSem

2019-11:
11 안세환 Introduction to Genetic Algorithm  SysBiol
18 안세환 Breast cancer(adenocarcinoma) data in L1000  BioEMR
25 안세환 Discovering significant and interpretable pattern from L1000 data  TopicSem

2019-10:
05 안세환 Drug Gene Budger (DGB): an application for ranking drugs to modulate a specific gene based on transcriptomic signatures.     J.Club
07 안세환 Use of Sharesource in Remote Patient Management in Peritoneal Dialysis: A UK Nurse  BioEMR
24 안세환 FSGP for L1000 breast carcinoma cancer cell lines   TopicSem

2019-09:
02 안세환 L1000 data overview  BioEMR
09 안세환 Overview of L1000 data  TopicSem
16 안세환 Subtype of Cell Lines in L1000 data  SysBiol

2019-07:
20 안세환 L1000 Viewer: A Search Engine and Web Interface for the LINCS Data Repository     J.Club
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

2019-06:
03 안세환 Errors in importing Leukemia Data  SysBiol
17 안세환 Datasets in cBioPortal  BioEMR
24 안세환 Importing Leukemia Dataset into cBioPortal  TopicSem

2019-05:
11 안세환 New drug candidates for treatment of atypical meningiomas: An integrated approach using gene expression signatures for drug repurposing     J.Club
13 안세환 Clinical data for each project in GDM  BioEMR
16 안세환 The issues of importing gdm into cbioportal  TopicSem

2019-04:
08 안세환 File Formats of cBioPortal  TopicSem
15 안세환 Select available columns in cBioPortal mutation file  SysBiol

2019-03:
07 안세환 Importing sample data into cBioPortal  TopicSem
07 안세환 File Formats for cBioPortal  SysBiol
25 안세환 About cBioPortal on GDPortal  BioEMR

2019-02:
23 안세환 GenIO: a phenotype-genotype analysis web server for clinical genomics of rare diseases     J.Club

2019-01:
21 안세환 The Mutation Significance Cutoff(MSC)  TopicSem
21 안세환 How to use cBioPortal in GDPortal  BioEMR

2018-12:
03 안세환 VVA Plots include Protein domains  TopicSem
10 안세환 VVA background data of protein domians  BioEMR
20 안세환 Protein domain layer in VVA Plot  SysBiol
22 안세환 PopViz: a webserver for visualizing minor allele frequencies and damage prediction scores of human genetic variations     J.Club
27 안세환 Gene-centered Visualization and Annotation for Exome Variant Analysis(VVA) using GDM  Seminar

2018-11:
05 안세환 How to visualize protein domain in VVA  TopicSem

2018-10:
01 안세환 Changed result table of VVA using GDM  BioEMR
08 안세환 Upgraded VVA Table using GDM  TopicSem
25 안세환 The Cochran-Armitage Trend Test(CATT) in result table of VVA  SysBiol
27 안세환 VarCards: an integrated genetic and clinical database for coding variants in the human genome     J.Club
29 안세환 Re-Calculate Allele Frequency of VVA result Table  BioEMR

2018-09:
06 안세환 Add VEP data to VVA  TopicSem

2018-08:
23 안세환 Add knowledge bases to VVA plot  SysBiol
25 안세환 Gene Graphics: a genomic neighborhood data visualization web application     J.Club

2018-07:
02 안세환 VVA plot using GDM  TopicSem
14 안세환 Genome U-Plot:a whole genome visualization     J.Club
19 안세환 Modify VVA part interface of GDM portal  BioEMR
30 안세환 Modified VVA Interface  TopicSem

2018-06:
07 안세환 GDM and VVA  BioEMR
28 안세환 Apply VVA to GDM  SysBiol

2018-05:
03 안세환 clinical data for VVA  BioEMR
10 안세환 Knowledge Bases for VVA  SysBiol
31 안세환 Add knowledge bases to VVA  TopicSem

2018-04:
23 안세환 Add advanced features to VVA  TopicSem

2018-03:
08 안세환 VVA review and future work  SysBiol
08 안세환 VVA review and future work  SysBiol
08 안세환 VVA review and future work  SysBiol
15 안세환 How to trasfer blood dialyzer data to patients using OCR  BioEMR
19 안세환 Future works of VVA  TopicSem
31 안세환 Visualization portal for genetic variation(VizGVar): a tool for interactive visualization of SNPs and somatic mutations in exons, genes and protein domains     J.Club

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