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What is the best approach for QC of multi-allelic variant in a GLnexus pVCF? If there is one high quality alternate allele and a poor quality allele at a multi-allelic site, how are they filtered properly? In GATK VQSR, there is now a Allele Specific INFO field (AS_FilterStatus) to filter on. Is there something comparable with GLnexus?
The text was updated successfully, but these errors were encountered:
What is the best approach for QC of multi-allelic variant in a GLnexus pVCF? If there is one high quality alternate allele and a poor quality allele at a multi-allelic site, how are they filtered properly? In GATK VQSR, there is now a Allele Specific INFO field (AS_FilterStatus) to filter on. Is there something comparable with GLnexus?
The text was updated successfully, but these errors were encountered: