Hi,
Running TASSEL 5.0 for -mxTagL 64 I produce, after ProductionSNPCallerPluginV2 step, a .h5 file. I open this file in GUI and all things OK. But, I try to export a vcf file with goal to see the depth of SNP calling and using vcftools (vcftools --vcf <vcf_file.vcf> --out <output_file> --depth) to estimate this depth, the result was "-nan". Look:
INDV N_SITES MEAN_DEPTH
Male 0 -nan
Female 0 -nan
Female 0 -nan
Female 0 -nan
Male 0 -nan
Female 0 -nan
unknown 0 -nan
Male 0 -nan
Looking (head -20 <vcf_file>) in vcf file, it doesn't have information about depth:
##fileformat=VCFv4.0
##Tassel=<ID=GenotypeTable,Version=5,Description="Reference allele is not known. The major allele was used as reference allele">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=AD,Number=.,Type=Integer,Description="Allelic depths for the reference and alternate alleles in the order listed">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read Depth (only filtered reads used for calling)">
##FORMAT=<ID=GQ,Number=1,Type=Float,Description="Genotype Quality">
##FORMAT=<ID=PL,Number=3,Type=Float,Description="Normalized, Phred-scaled likelihoods for AA,AB,BB genotypes where A=ref and B=alt; not applicable if site is not biallelic">
##INFO=<ID=NS,Number=1,Type=Integer,Description="Number of Samples With Data">
##INFO=<ID=DP,Number=1,Type=Integer,Description="Total Depth">
##INFO=<ID=AF,Number=.,Type=Float,Description="Allele Frequency">
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT Male Female Female Female Male Female unknown Female
1 70989 S1_70989 C T . PASS . GT 1/1 0/0 0/1 0/1 1/1 0/1 0/0 1/1
1 289370 S1_289370 C A . PASS . GT 0/0 0/0 0/1 1/1 ./. 0/0 ./. 1/0
1 344682 S1_344682 G A . PASS . GT 1/0 0/1 0/0 0/0 1/0 0/0 0/0 1/0
I would be happy for some help with this issue...
Thank you