Hi all
I'm trying to evaluate variants called by GATK UnifiedGenotyper, FreeBayes and mpileup/bcftools. I'm using GATK VariantEval but although the VCF files are showing different concordance, FP and FN fields in the GATK report are zero. I've tried VariantEval providing dbSNP and not providing it. The dataset I'm using is from Broad NA12878.
Any suggestions is appreciated.
Thanks
Mahtab
I'm trying to evaluate variants called by GATK UnifiedGenotyper, FreeBayes and mpileup/bcftools. I'm using GATK VariantEval but although the VCF files are showing different concordance, FP and FN fields in the GATK report are zero. I've tried VariantEval providing dbSNP and not providing it. The dataset I'm using is from Broad NA12878.
Any suggestions is appreciated.
Thanks
Mahtab
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