SNUBI Research ::   (46 talks satisfying Title has 'CNV')
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2020:
11-9 이우승 Result of BRCA2 CNV qPCR Validation  xMutant
11-23 이우승 CNV Benchmark Results with Validation data  TopicSem
08-27 이우승 CNV Validation Candidate Selection  MAInfo
04-13 이우승 GATK - Germline copy number variant discovery (CNVs)  xMutant

2019:
03-14 이우승 Inhouse CNV Algorithm  TopicSem
01-28 이우승 Comparison of Inhouse CNV Algorithms and Ioncopy with Microarray CNV Data  TopicSem
01-25 이우승 Comparison of Inhouse CNV Algorithms and Ioncopy with Microarray CNV Data  MAInfo

2018:
05-24 민병주 Somatic second hit mutation candidates in CNV-PTC patients  TopicSem
04-19 민병주 CNV-PTC in a family with compound heterozygous APC gene mutations  TopicSem
01-18 이우승 CNV algorithm for KPCDx Panel   xMutant
01-18 이우승 CNV algorithm for KPCDx Panel  xMutant
01-18 이우승 CNV algorithm for KPCDx Panel  xMutant
01-18 이우승 CNV algorithm for KPCDx Panel  xMutant

2017:
09-18 이우승 CNV analysis of Cancer Panel 2.0 Data  TopicSem
08-29 이우승 CNV analysis of Cancer Panel 2_0 Data from Pathology Department  xMutant
03-15 이우승 Result : CNV Detection Algorithm for Cancer Samples  xMutant

2016:
05-02 김주연 Predicting drugs related to treatment failure based on CNVs  TopicSem
04-25 김주연 Association between CNV and gene expression using 1000 Genomes data  SysBiol
04-25 김주연 CNV and gene expression profile in 1000 Genomes phase 3 population  SysBiol
04-25 김주연 Association between CNV and gene expression using 1000 Genomes data  SysBiol
04-25 김주연 CNV and gene expression profile in 1000 Genomes phase 3 population  SysBiol
03-23 김주연 Predicting high risk drugs in 1KP based on pharmacogene CNVs  TopicSem

2015:
12-22 이정훈 How to use MuTect, ExomeCNV and EXPANDS.  xMutant

2014:
07-15 백수연 CNV and gene expression profile in 1000 Genomes phase 3 population  SysBiol

2013:
11-06 민병주 CNV Detection by using aCGH method  TopicSem

2011:
09-15 Rocky [Replication- Work Progress] - Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes  xMutant
08-25 김도균 CNV Data Analysis  TopicSem
07-02 Rocky [Replication] - Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes  xMutant

2009:
01-19 김도균 Identify co-effects of SNP and CNV on gene expression  Seminar

2008:
07-14 김도균 Integrative studies for SNPs and CNVs with gene expression data  Seminar
07-10 김도균 Integrative studies for SNPs and CNVs with gene expression data  Seminar
06-23 김도균 Integrated association studies for SNPs and CNVs with gene expression data  Seminar

2007:
09-08 김도균 Challenges and standards in integrating surveys of structural variation [CNVreview]      J.Club
08-29 김도균 Copy number variation from Korean SNP data [KoreanCNVSNP data] Seminar
07-20 김도균 Copy number and loss of heterozygosity estimation [CNVSNPLOH] Seminar
07-06 김도균 Work plan: Integrated SNP database and Analysis system [SNPCNVsystem] Seminar
06-20 김도균 Effects of copy number variations on classical genetic studies [SNPCNV] Seminar
05-30 김도균 Analysis plan for GAW data [CNVGenome-wide associationSNP] Seminar
05-26 김도균 Completing the map of human genetic variation [CNVstructural variation]      J.Club
03-28 김도균 Progress in detecting CNVs from Korean population data [SNPKorean] Seminar
03-24 김도균 Relative impact of nucleotide and copy number variation on gene expression phenotypes [CNV SNP expression]      J.Club
03-09 김도균 Detect CNVs using GEMCA [CNVGEMCA] Seminar
02-26 김도균 Alogorithms for detecting copy number variation using SNP genotyping arrays [CNVAlgorithm] Seminar
02-21 김도균 Tool for organizing and visualizing SNP-level summaries of copy number and genotype calls [SNPCNV] Seminar
02-10 김도균 Copy number variation: New insights in genome diversity [CNVcopy number variants]      J.Club

2006:
12-30 김도균 Global variation in copy number in the human genome [CNV] J.Club

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