Heys,
I am doing the SNP calling with Haplotypecaller BP_Resolution, CombineGVCFs with convert-to-base-pair-resolution and GenotypeGVCFs with include-non-variant-sites with GATK and when I get my vcf file, the non-variant sites does not have any quality at all:
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT Leopards_1 Leopards_2
NC_001700.1 1 . G . . . DP=40 GT:AD:DP:RGQ 0/0:26:26:78 0/0:14:14:42
NC_001700.1 2 . G . . . DP=43 GT:AD:DP:RGQ 0/0:29:29:87 0/0:14:14:42
NC_001700.1 3 . A . . . DP=43 GT:AD:DP:RGQ ./.:0:29:0 ./.:0:14:0
NC_001700.1 4 . C . . . DP=43 GT:AD:DP:RGQ ./.:0:29:0 ./.:0:14:0
NC_001700.1 5 . T . . . DP=71 GT:AD:DP:RGQ 0/0:50:50:99 0/0:21:21:63
NC_001700.1 6 . A . . . DP=74 GT:AD:DP:RGQ 0/0:53:53:99 0/0:21:21:63
NC_001700.1 7 . A . . . DP=85 GT:AD:DP:RGQ 0/0:59:59:99 0/0:26:26:78
Except for the variant ones:
NC_001700.1 63 . T A 6198.13 . AC=4;AF=1.00;AN=4;DP=252;ExcessHet=3.0103;FS=0.000;MLEAC=4;MLEAF=1.00;MQ=48.90;QD=24.60;SOR=0.709 GT:AD:DP:GQ:PL 1/1:0,166:166:99:4057,496,0 1/1:0,86:86:99:2157,258,0
Do you know what is this happening?
It seems there is a version problem, I just did the same runs with gatk v.4.1.3 and I got the quality parameter I was looking for, just in case it helps to anybody