Single nucleotide polymorphism (SNP) & Variation Suite (SVS) is an analytic tool created to empower researchers to perform complex analyses and visualizations on genomic and phenotypic data. Genome-Wide Association Studies (GWAS) continues to be an effective method for identifying disease susceptible genes in humans and other organisms. Attendees will learn how SVS can be used to perform GWAS and genomic prediction, how to analyze high-quality SNPs by performing the association test, how to use quality control metrics, and how to use genomic prediction with K-Fold to estimate which genotypes best predict a desired phenotype.
SNP and Variation Suite (SVS) for Genome-Wide Association Studies (GWAS)
Upcoming Sessions
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