Identify Rare Disease Causing Mutations in Family of Four (WGS)
You can use the Identify Rare Disease Causing Mutations in a Family of Four (WGS) ready-to-use workflow to identifie de novo and compound heterozygous variants from an extended family of four, where the fourth individual is not affected.
The Identify Rare Disease Causing Mutations in a Family of Four (WGS) ready-to-use workflow accepts sequencing reads as input.
Subsections
- How to run the Identify Rare Disease Causing Mutations in a Family of Four (WGS) workflow
- Output from the Rare Disease Causing Mutations in a Family of Four (WGS) workflow