mkVCFfreq | R Documentation |
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 |
prefix for .freq file (frequency) |
markers |
data.frame of markers being processed |
recode |
use 1/2 instead of two given alleles (eg. A/C) |
envir |
"environment" containing SQLite database and other globals |
None
## Not run:
mkVCFfreq(prefix, NULL, FALSE, envir)
## End(Not run)
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