CNV (copy number variations) Identification
Commercial tools
Downstream Analysis of Variants
Germline Callers
Germline + Somatic Callers
Metagenomics Tools
Other Tools
Public Resources Related to Clinical Impacts of SNPs
Somatic Callers
Structural Variant Indenification
Structural Variant Tools
ToolKits
Tool Repositories, Analytical Pipelines, & Workflow Systems
Variant Annotation
Authors and Contributors
Updated July 2016
Created by: Ben Busby, Kaitlyn Williams, and Farrah Hermes
An additional thanks to OMICtools
