About this webinar
Recorded On: Wednesday, January 21, 2015
Many of today's researchers are generating DNA sequence data for large numbers of samples in population-based experiments. This may include whole genomes, exomes, or targeted regions. The Golden Helix SNP and Variation Suite (SVS) provides a powerful computing environment for analyzing these data and performing association tests at the gene and/or variant level.
In this presentation, Dr. Christensen will review fundamentals of population-based variant analysis and demonstrate some of the tools available in SVS for analysis of both common and rare variants. The presentation will feature the recently implemented SKAT-O method, as well as other functions for annotation, visualization, quality control and statistical analysis of DNA sequence variants.
Watch on demand
Please enjoy this webcast recording. Should you have any questions about the content covered, please reach out to our team here.