Video Tip of the Week: The New Database of Genomic Variants – DGV2

submitted by: OpenHelix

For more information about this resource, please see our blog post at URL http://blog.openhelix.eu/?p=10185. In today’s tip I will briefly introduce you to the beta version of the updated Database of Genomic Variants, or DGV.

Demo: Structural variation for a region

submitted by: gspudich

Large structural variations like CNVs (copy number variation) are explored for a region of the human genome. We use the Ensembl genome browser at www.ensembl.org

Demo: Variation for the ZAP70 gene with Ensembl

submitted by: gspudich

We use the Ensembl genome browser at www.ensembl.org to view small scale sequence variants such as SNPs (single nucleotide polymorphims) along with larger structural variations like CNVs (copy number variation) for the human ZAP70 gene.

Array CGH Computational Lab - Chris Miller

submitted by: ralanharris

An introduction to computational methods for analyzing Array Comparative Genomic Hybridization data by Chris Miller. This was presented as a lab within the Computer Aided Discovery Methods course offered within the Graduate Program at Baylor College of Medicine.