CNV analysis with Daniel Howrigan
25:36
Polygenic risk scores: PRSice & lassosum with Shing Wan Choi
1:25:16
Somatic Copy Number Alterations in Cancer
58:38
Detecting CNVs from Whole Exome Sequencing Data Using Nexus Copy Number
42:09
Presentation - Copy Number Variant Interpretation/Dosage Sensitivity Curation (Erica Andersen)
48:50
Infinium Assay: CNV Analysis using GenomeStudio or BlueFuse Multi Software
47:53
Webinar: Unraveling the roles of copy number variants in tumorigenesis
27:18
Family-based GWAS analysis: SAIGE with Wei Zhou
15:38