Would haplotype analysis is enough for a rare disease?
0
0
Entering edit mode
2.3 years ago
nuketbilgen ▴ 40

Hi, I want to analyze the WGS data from the following work,
- the aim of the project finding a pathogenic variant. - samples are core family (father, mother and two affected offspring) and one nonfamily member. - penetrance is observed in the sample group, (female offspring affected severely and male affected offspring moderately)

Would haplotype analysis is enough for a rare disease? What else do I need?

kind regards.

genome next-gen haplotype rare disease • 360 views
ADD COMMENT

Login before adding your answer.

Traffic: 2784 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6