filt1_dip | R Documentation |
filt1_dip: transforming the phred score to relative genotype likelihood
filt1_dip(n, skip, dur, input, output)
n |
an integer, the number of individuals contain in the vcf |
skip |
an integer, lines to skip |
dur |
an ingerger, lines for current chromosome |
input |
a string, the dir to cleaned vcf file |
output |
a string, the dir to the output file |
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