I've noticed that missing data in my merged vcf file following genotyping are haploid ".:" while all genotypes with data are correctly diploid. Running thesed -e 's/ \.\:/ \.\/\.\:/g'line on the merged vcf file does not resolve the issue. However, using 's/.:.:.:.:.:.:.:./.\/\.:.:.:.:.:.:.:./g' does resolve ploidy of missing genotypes. Just curious as to why the line from the pipeline was not functioning.
Missing data within the raw*.vcf files is coded as a single "." without additional fields
I've noticed that missing data in my merged vcf file following genotyping are haploid ".:" while all genotypes with data are correctly diploid. Running the
sed -e 's/ \.\:/ \.\/\.\:/g'
line on the merged vcf file does not resolve the issue. However, using's/.:.:.:.:.:.:.:./.\/\.:.:.:.:.:.:.:./g'
does resolve ploidy of missing genotypes. Just curious as to why the line from the pipeline was not functioning.Missing data within the raw*.vcf files is coded as a single "." without additional fields
Using vcflib ver 1.0.2 for vcfcombine.
Cheers, -Alex