[note: cross-posted on GATK forum - still awaiting a response]
I have a GVCF (generated using GATK's HaplotypeCaller w/ -ERC GVCF parameter) of 36 related samples and would like to determine the (potentially de novo) variants that are unique to each sample. Short of creating 36 N-1 GVCFs for discordance testing, or extracting individual sample VCFs for subtraction, is there a straightforward method to obtain the desired information?
As usual, @PierreLindenbaum has the right tool for the job. Thanks!
Now this post needs to be added to the list there, I guess?
Will do. I cross-posted here only b/c the response time there can be... slow.
Sorry, what? I was saying that this post would be linked in Pierre's post page, which he has done now.
@Ram: Sorry for the confusion. I thought your comment was directed at me, since I mentioned cross-posting on GATK. I still intend to share Pierre's solution there, so others will be aware of it.
Ah, OK. No, I was referring to the cross-linking that Pierre does on his tool-page. Sorry, I should have been clearer in my comment.
I added
-F VCF
to run the code while used for gvcf file. Is there any user manual to understand the syntax?