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Variant Discovery in High-Throughput Sequencing Data

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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

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Somatic

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Show no status All Planned Not planned Completed Answered No status Sort by votes Newest post Recent activity Votes Comments
  • strand bias and orientation bias
    • that girl
    • December 02, 2020 06:51
    5 votes 1 comment
  • Custom made Panel of Normals required?
    • Pedro Miguel Raposo
    • July 07, 2020 10:01
    • Edited
    2 votes 2 comments
  • Generating ACS like output from new GATK CNV pipeline (WGS)
    • Jett Crowdis
    • June 26, 2020 18:11
    2 votes 4 comments
  • Funcotator maf has different alt allele than vcf for some variants
    • Balthasar
    • July 11, 2022 11:34
    1 vote 1 comment
  • Funcotator Errors : I/O error in the advisory file locking logic (disk I/O error)
    • Min-Hwan Sohn
    • November 26, 2020 03:56
    • Edited
    1 vote 1 comment
  • How do I merge f1r2.tar.gz files when parallelizing Mutect2 pipeline?
    • Jenifer
    • October 28, 2020 17:25
    • Edited
    1 vote 1 comment
  • MarkDuplicatesSpark error missing Read Group fields
    • Field -Ye Tian
    • October 09, 2020 16:45
    1 vote 1 comment
  • CalculateContamination "there is no such column: contig"
    • Jensen Richardson
    • July 05, 2020 18:02
    1 vote 8 comments
  • gatk CollectAllelicCounts error
    • peterchung
    • May 26, 2020 03:23
    • Edited
    1 vote 6 comments
  • Mutect2 MISSING Low Frequency key (TP53 and KRAS) mutations
    • Saba
    • April 29, 2020 15:54
    • Edited
    1 vote 15 comments
  • Mutect2 - somatic variant calling with/without matched normal sample
    • D B
    • February 26, 2020 19:33
    • Edited
    1 vote 14 comments
  • MergeBamAlignment Error: ArrayIndexOutOfBoundsException
    • Jared Jurss
    • February 19, 2020 22:02
    1 vote 3 comments
  • Problems combining gVCFs that have thousands of scaffolds
    • Dch
    • February 11, 2020 23:24
    • Edited
    1 vote 5 comments
  • Mutect2 variant calling output with tumor and matched normal: 0/1 in all variants called
    • RicPin
    • February 10, 2020 15:41
    • Edited
    1 vote 5 comments
  • Call germline mutations from Mutect2
    • Chadi Saad
    • January 14, 2020 10:30
    1 vote 3 comments
  • Huge number of variants in tumor only mode as compared to T/N paired mode using Mutect2
    • Shivangi Agarwal
    • March 09, 2023 22:26
    0 votes 3 comments
  • Somatic CNV Workflow Tutorials
    • Yuwei Bao
    • March 02, 2023 20:45
    0 votes 1 comment
  • Mutect2 VCF out Tumor Normal
    • Charitra K
    • March 01, 2023 07:53
    0 votes 5 comments
  • Strange differences in detected variants called by mutect2 --dont-use-soft-clipped-bases true vs false
    • Jana Marie Schwarz
    • February 22, 2023 16:26
    0 votes 1 comment
  • How to recover a mutation from secondary alignment
    • Laurent MANCHON
    • February 01, 2023 08:41
    0 votes 2 comments
  • Is it ok to use -L for each chromosome separately when running Mutect2?
    • Xuning Wang
    • January 30, 2023 21:41
    0 votes 1 comment
  • Asking for advice on Mutect2 calling in somatic but amplicon data
    • yangjw
    • January 30, 2023 07:32
    • Edited
    0 votes 2 comments
  • How to call somatic variants without normal matched sample (cfDNA)
    • Abel G
    • January 26, 2023 11:45
    0 votes 0 comments
  • Somatic mutations detection using mutect2
    • Varun Gupta
    • January 23, 2023 16:17
    0 votes 0 comments
  • GatherPileupSummaries does not sort input variants
    • Evan Wu
    • January 20, 2023 23:00
    0 votes 0 comments
  • Problem generating germline resource file for Mutect2
    • Jaime Schwoch
    • January 04, 2023 01:51
    0 votes 0 comments
  • Mutect2 VCF sample order in tumor normal paired call
    • Thomas Sunghoon Huh
    • December 20, 2022 08:49
    0 votes 0 comments
  • How do if remove Germline Variants from my variant calling file ?
    • Seke Keretsu
    • December 08, 2022 21:23
    0 votes 0 comments
  • Error - Mutect2 PG tag
    • A
    • December 08, 2022 02:56
    0 votes 0 comments
  • sample size for somatic CNV
    • Muntadher Jihad
    • December 02, 2022 12:04
    0 votes 1 comment
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