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Make multisample exomedepth VCF files then annotate with contextual info:
GC content
MQ
MQRankSum
MQRMSE
Number of heterozygous calls
?B-allele frequency
?Overlap with polymorphic CNVs
The text was updated successfully, but these errors were encountered:
Make multisample exomedepth VCF files then annotate with contextual info:
GC content
MQ
MQRankSum
MQRMSE
Number of heterozygous calls
?B-allele frequency
?Overlap with polymorphic CNVs
The text was updated successfully, but these errors were encountered: