Logo
User Guide Tool Index Blog Forum DRAGEN-GATK Events Download GATK4
Sign in

Genome Analysis Toolkit

Variant Discovery in High-Throughput Sequencing Data

GATK process banner

Need Help?

Search our documentation

Community Forum

Hi, How can we help?

Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size. Learn more

  1. GATK
  2. Community
  3. Documentation Questions

Documentation Questions

Follow New posts New posts and comments

Show all All Planned Not planned Completed Answered No status Sort by newest post Newest post Recent activity Votes Comments
  • producing strandedness metrics from rnaseq data Answered
    • AMN
    • July 02, 2021 16:45
    0 votes 1 comment
  • --dbsnp option in HaplotypeCaller and other programs Answered
    • gwotto
    • July 01, 2021 12:21
    0 votes 3 comments
  • Using -"-allow-old-rms-mapping-quality-annotation-data" to force genotyping gvcf created with old version Answered
    • Muriel Gros-Balthazard
    • June 25, 2021 08:54
    0 votes 1 comment
  • Theorical model for Active region detection Answered
    • Naomie Abecassis
    • June 22, 2021 14:26
    0 votes 6 comments
  • What does PCT_MIX from CreateVerifyIDIntensityContaminationMetricsFile mean?
    • Lucas Taniguti
    • June 21, 2021 13:40
    0 votes 2 comments
  • MTLowHeteroplasmyFilterTool documentation Answered
    • jorgez
    • June 11, 2021 12:58
    0 votes 7 comments
  • Confirmation that Mutect2 /haplotype caller only use reads mapped within the active region
    • JW
    • June 03, 2021 16:19
    1 vote 3 comments
  • Is it okay to run multiple instances of BQSR with the -L argument in order to increase the speed of the workflow? Answered
    • Jenifer
    • May 24, 2021 11:44
    0 votes 1 comment
  • I have question about stats file after using mutect2 Answered
    • 황신원
    • May 21, 2021 00:56
    0 votes 1 comment
  • Ploidy as an argument in Mutect2 Answered
    • Michael Weinstein
    • May 21, 2021 00:46
    0 votes 5 comments
  • Calculation method of the global_read_depth.tsv file of the DetermineGermlineContigPloidy tool Answered
    • Tintest
    • May 20, 2021 14:35
    0 votes 7 comments
  • How do I calculate QD for multiple samples, if all samples are homozygous? Answered
    • Martin Grasshoff
    • May 19, 2021 16:02
    0 votes 1 comment
  • STRANDQ missing from mutect2 vcf records Answered
    • Rebecca Halperin
    • May 12, 2021 19:26
    0 votes 6 comments
  • What is the difference between "CNVSomaticPairWorkflow.common_sites" and "CNVSomaticPairWorkflow.intervals"? Answered
    • Hiro Ama
    • May 12, 2021 07:18
    0 votes 2 comments
  • VariantRecalibrator latest recommandations Answered
    • nhaus
    • May 04, 2021 15:48
    0 votes 3 comments
  • gatk FilterByOrientationBias Answered
    • Nishtha Tanwar
    • May 04, 2021 09:15
    0 votes 2 comments
  • GenomicsDBImport java error
    • TONG ZHOU TAO
    • May 04, 2021 06:33
    0 votes 1 comment
  • GATK VariantEval no concordance between dbSNP and our data Answered
    • Pierre_Bioinfo
    • May 03, 2021 07:50
    0 votes 6 comments
  • What does mutect2 do if two bams are input and --normal-sample is not specified? Answered
    • Tyler Borrman
    • April 27, 2021 05:07
    • Edited
    0 votes 1 comment
  • ApplyBQSRSpark ApplyBQSR has different results
    • AMN
    • April 22, 2021 15:40
    • Edited
    0 votes 3 comments
  • GC DROPOUT AND AT DROPOUT Answered
    • asqt96
    • April 22, 2021 13:16
    0 votes 1 comment
  • Determining Optimal Number of Samples to include in Panel of Normal Answered
    • Gannon Cottone
    • April 16, 2021 16:56
    0 votes 2 comments
  • every exon junctions in Bam files got softclipped after run SplitNCigarReads Answered
    • 이한새
    • July 21, 2021 00:49
    • Edited
    0 votes 4 comments
  • How does Picard basecalling make decisions on NovaSeq data? Answered
    • James Webber
    • April 14, 2021 17:12
    0 votes 4 comments
  • If base quality scores set at 2 for clipped regions are restored to the original score with MergeBamAlignment, how will clipped regions not contribute to downstream analyses? Planned
    • ISmolicz
    • April 07, 2021 15:07
    • Edited
    0 votes 0 comments
  • How do adapter sequences not contribute to alignment if the base quality is set to 2 with SamToFastq but BWA-MEM does not consider base quality scores? Answered
    • ISmolicz
    • April 07, 2021 14:37
    • Edited
    0 votes 5 comments
  • GATK 4.2.0.0 Haplotype caller --genotyping_mode DISCOVERY Option Answered
    • M.R-E.H
    • April 07, 2021 11:30
    0 votes 2 comments
  • Error remove 0x1 from alternate contigs tutorial Answered
    • Linda Do
    • April 05, 2021 16:18
    0 votes 5 comments
  • CreateSomaticPanelOfNormals BETA tag Answered
    • G E
    • April 01, 2021 19:38
    0 votes 2 comments
  • Sensitivity analysis for GATK CNV PoN Answered
    • Kimal Rajapakshe
    • March 29, 2021 21:51
    0 votes 1 comment
  • «
  • ‹
  • 1
  • 2
  • 3
  • 4
  • 5
  • 6
  • ›
  • »

Welcome

Forum Guidelines

GATK Announcements

Become a GATK Guru

Read Before You Post

Get Email Notifications

Didn't find what you were looking for?

New post

Quick Links

GATK Latest Releases

Known Issues & Troubleshooting

Submitting a Bug Report

How to Track a Github issue

GATK on the Cloud with Terra

Recent GATK News

GATK Blog Posts

GATK Twitter Page

About the GATK community

  • 133,119 Total Users
  • 0 Comments
  • 0 Posts
  • 0 Votes

footer-logo © Broad Institute

  • twitter icon
  • facebook icon
  • linkedin icon
Powered by Zendesk