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Combining variants from different WES capture types

Hi there!
I've googled on GATK forum with no success for the following topic. I have a set of wes (around 110 samples in total) all of them from an specific population. The aim of the project is to study population genetic variation. All samples have been processed with GATK 4.1.2. The issue is that I have two subsets of samples, each generated with a different capture technology.

Not sure how to proceed to study variants for the whole set since it is desired to reduce the batch effect as much as possible. I've run the following: gVCF files were generated for each sample and then a joint analysis has been applied using all gVCF files (GenomicsDBImport and genotypeGVCFs). Not sure if this approach is the best one (it is the same as assuming a single capture technology). For GenomicsDBImport, the intervals used were all chromosomes although another try would be to build de database using a specific set of regions given just by the intersection of the two capture BEDs.

Another approach would be to perform joint variant calling separately for each subset and then combine results somehow (not sure how) using again the intersection of capture BEDs, but may be this might introduce a worse batch effect.

Any suggestions?
Thanks,
Javier

Answers

  • Tiffany_at_BroadTiffany_at_Broad Cambridge, MAMember, Administrator, Broadie, Moderator admin

    Hi @jpflorido ,

    The GATK support team is focusing on resolving questions about GATK tool-specific errors and abnormal results from GATK tools. For all other questions, such as this one, we are building a backlog to work through when we have the capacity.

    Please continue to post your questions because we will be mining them for improvements to documentation, resources, and the tools.

    We cannot guarantee a reply, however we ask other community members to help out if you know the answer.

    For context, see this announcement and check out our support policy.

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