Declare class VCFQAParam which will store thresholds to apply to VCFEvaluate object. This is intended for use in batch mode when a large number of vcf files needs to be screened and individual vcf files that fail flagged. All limits follow the format lower limit than upper limit
homref.limits |
lower limit, upper limit, number of homozygous reference |
het.limits |
lower limit, upper limit, number of heterozygous calls |
homvar.limits |
lower limit, upper limit, number of homozygous alternative |
count.limits |
lower limit, upper limit, total number of counts |
percenthets.limits |
lower limit, upper limit, Number of Heterozgyous / (Total Number of Counts) or percent het |
titv.noncoding.limits |
lower limit, upper limit, Transition transversion ratio in noncoding regions |
titv.coding.limits |
lower limit, upper limit, Transition transversion ratio in coding regions |
readdepth.target |
The sequencing depth target (eg 30x) |
readdepth.limits |
lower limit, upper limit, Mean read depth |
readdepth.percent.limits |
lower limit, upper limit, Percent read depth in target (50 percent to 200 percent of target read depth) |
gq.limit |
lower limit, Mean genotype quality (does not make sense to have an upper limit) |
masked.limits |
lower limit, upper limit, (Number of heterozygous in masked regions)/(Total number of heterozygotes) |
non.masked.limits |
lower limit, upper limit, (Number of heterozygous in non-self chained regions)/(Total number of heterozygotes) |
het.gap.limits |
lower limit, upper limit, Largest gap within chromosome between two heterozygous calls |
gq.filter |
filter for the VCF file on genotype quality (eg only GQ > 90) |
dp.filter |
filter for the VCF file on read depth (eg only DP > 0) |
VCFQAParam object
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