Identify Rare Disease Causing Mutations in Trio (TAS)
The Identify Rare Disease Causing Mutations in a Trio (TAS) identifies de novo and compound heterozygous variants from a Trio. The workflow includes a back-check for all family members.
The Identify Rare Disease Causing Mutations in a Trio (TAS) ready-to-use workflow accepts sequencing reads as input.
Subsections
- How to run the Identify Rare Disease Causing Mutations in a Trio (TAS) workflow
- Output from the Rare Disease Causing Mutations in a Trio (TAS) workflow