Identify Rare Disease Causing Mutations in Trio (WGS)

The Identify Rare Disease Causing Mutations in a Trio (WGS) 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 (WGS) ready-to-use workflow accepts sequencing reads as input.



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