Identify Rare Disease Causing Mutations in Trio (WES)
The Identify Rare Disease Causing Mutations in a Trio (WES) 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 (WES) ready-to-use workflow accepts sequencing reads as input.
Subsections
- How to run the Identify Rare Disease Causing Mutations in a Trio (WES) workflow
- Output from the Rare Disease Causing Mutations in a Trio (WES) workflow