Special GATK Use Cases
Information here covers items that are not in Best Practices but may someday be a part of Best Practices
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After apply gatk ApplyBQSR, the total reads become less1 vote 2 comments
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Mutect2 Somatic-vs-Somatic calling1 vote 6 comments
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Picard CrosscheckFingerprints with multi-sample VCF1 vote 5 comments
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ASEReadCounter - What to use as the VCF variant reference1 vote 1 comment
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does GATK offers to match alleles in two vcf files?1 vote 1 comment
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gatk pileup result lost some reads cover?1 vote 2 comments
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Using Mutect2 on Mac M11 vote 1 comment
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How do I know why gatk is removing some of my reads for geotyping?1 vote 0 comments
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Read Group (UNKNOWN) is not a recognized platform1 vote 1 comment
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Maximum performance HaplotypeCaller Answered1 vote 10 comments
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Mutect for Somatic SNVs in Highly Polymorphic Genome Regions Answered1 vote 3 comments
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Common germline variants sites VCF for GetpileupSummaries for mouse data Answered1 vote 7 comments
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has sample entries that don't match the other files. Answered1 vote 1 comment
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Generating COSMIC.db Data Source for Funcotator0 votes 0 comments
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DetermineGermlineContigPloidy generating error0 votes 2 comments
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Mutect2 Calls for non-tumor pooled samples - no variants pass filters0 votes 7 comments
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snp calling using a reference VCF file to define all interesting position0 votes 5 comments
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GATK-VQSR issue0 votes 12 comments
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gatk baserecalibrator no error reported, but no output generated0 votes 6 comments
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Mutect2 calls germline variants not present in germline resource0 votes 4 comments
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1001_Genome project0 votes 1 comment
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CombineGVCFs produces .bcf incompatible with recommended bcftools (v1.19).0 votes 7 comments
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CreateSomaticPanelOfNormals (BETA) workflow0 votes 1 comment
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haplotypecaller: possible to generate phased vcf from phased bam?0 votes 1 comment
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GenomicsDBImport Memory and Disks0 votes 1 comment