Question: family based linkage study - design and analysis
gravatar for User6891
4.1 years ago by
User6891250 wrote:


We want to perform a linkage analysis study (using an Illumina SNP array) in a family affected with an autosomal dominant disorder

Could someone give some advice on how much family members (affected + unaffected) we would need? I suppose that the more family members you have, the better it is. And is it also necessary to genotype the unaffected parent of affected children? And what about the grandparents, do you need them both? I've read that most tools can handle missing data, but I'm not sure to what extent.

I've read that tools like MERLIN or PLINK are suited to perform the data analysis. Are there other recommended ones?


linkage • 1.4k views
ADD COMMENTlink written 4.1 years ago by User6891250

What's the rationale for doing this on an array rather than via exome sequencing just out of interest?

ADD REPLYlink written 4.1 years ago by Daniel Swan13k

It's to narrow down the regions-of-interest where the causal variant can be located. We have done exome sequencing for two family members, but too expensive to do it for all.

ADD REPLYlink written 4.1 years ago by User6891250
Please log in to add an answer.


Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 1333 users visited in the last hour