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Generate the initial boiler plate VCF, then generate ##INFO entries for each entry tag. Finally, generate the ##contig entries for each chromosome.
mkVCFfreq(prefix, markers, recode = FALSE, envir)
prefix for .freq file (frequency)
data.frame of markers being processed
use 1/2 instead of two given alleles (eg. A/C)
"environment" containing SQLite database and other globals
None
# NOT RUN { mkVCFfreq(prefix, NULL, FALSE, envir) # }
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