Hi Everyone
If we test the cummulative effect of a group of variants in a gene (or a region) using burden test and association analysis stuff. If a gene is found very significant, should we validate all variants in the gene using sanger sequence? Doesn't seem reasonable, so what we can do to prove this finding? And also is there any further analyis we should do before any wet lab step? Like something more than pathways, genes functions,GO, etc.
Thanks
I have altered your title to make it more concise, and removed the bold text from your post. There is no need for that. I have also added more appropriate tags to your question. These are important because as such experts can easily find your question.