Output from the Identify Causal Inherited Variants in a Trio (WES) workflow
Six types of output are generated:
- Reads Tracks One for each family member
- Coverage Report One for each family member
- Per-region Statistics Track Three for each family member
- Filtered Variant Track One for each affected family member and one for the putative causal variants in the affected child
- An Amino Acid Track Shows the consequences of the variants at the amino acid level in the context of the original amino acid sequence. A variant introducing a stop mutation is illustrated with a red amino acid.
- An Annotation Track Gene list with putative causal variants
- A Genome Browser View