Aug 21 to Aug 25
UC Davis Campus
Participants will explore experimental design, cost estimation, data generation, and processing of genomic data generated on the Illumina sequencing platform to discover and analyze variants. Topics will include mapping data to a genome, variant discovery pipelines, SNP annotation, effect prediction, structural variants, copy number variants, Genome-Wide Association Studies (GWAS), and Cancer datasets. This workshop will include a rich collection of lectures and hands-on sessions, covering both theory and tools associated with command-line variant analysis.