Output from the Identify Causal Inherited Variants in a Family of Four (WGS) workflow
Five types of output are generated:
- 4 Reads Track, one for each family member
- 4 Reports Read Mapping, one for each family member
- A 4 Filtered Variant Track, one for each family member
- An Annotation Track
- 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.
- A Genome Browser View, where the putative causal variants are presented together with the reference genome and the mapped reads from the proband and the parents.