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.



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