Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Can't run GATK HaplotypeCaller set ploidy = 1

    Greetings!

    I have been attempting to call variants on a haploid genome using GATK HaplotypeCaller, however when I set ploidy = 1, I get an error:

    Code:
    INFO 21:05:57,644 HelpFormatter - -------------------------------------------------------------------------------- 
    INFO 21:05:57,648 HelpFormatter - The Genome Analysis Toolkit (GATK) v3.2-2-gec30cee, Compiled 2014/07/17 15:22:03 
    INFO 21:05:57,648 HelpFormatter - Copyright (c) 2010 The Broad Institute 
    INFO 21:05:57,651 HelpFormatter - For support and documentation go to http://www.broadinstitute.org/gatk 
    INFO 21:05:57,658 HelpFormatter - Program Args: -T HaplotypeCaller -R Ref.fa -I aln-pe_RG_sorted_dedup_realigned.bam -o aln-pe_RG_sorted_dedup_realigned_HC_ploidy1.vcf -ploidy 1 -maxAltAlleles 2 
    INFO 21:05:57,666 HelpFormatter -on Linux 2.6.32-504.8.1.el6.x86_64 amd64; OpenJDK 64-Bit Server VM 1.7.0_75-mockbuild_2015_01_20_23_39-b00. 
    INFO 21:05:57,667 HelpFormatter - Date/Time: 2015/08/25 21:05:57 
    INFO 21:05:57,667 HelpFormatter - -------------------------------------------------------------------------------- 
    INFO 21:05:57,668 HelpFormatter - -------------------------------------------------------------------------------- 
    INFO 21:05:57,913 GenomeAnalysisEngine - Strictness is SILENT 
    INFO 21:05:58,027 GenomeAnalysisEngine - Downsampling Settings: Method: BY_SAMPLE, Target Coverage: 250 
    INFO 21:05:58,040 SAMDataSource$SAMReaders - Initializing SAMRecords in serial 
    INFO 21:05:58,067 SAMDataSource$SAMReaders - Done initializing BAM readers: total time 0.03 
    INFO 21:05:58,079 HCMappingQualityFilter - Filtering out reads with MAPQ < 20 
    INFO 21:05:58,213 GenomeAnalysisEngine - Preparing for traversal over 1 BAM files 
    INFO 21:05:58,302 GenomeAnalysisEngine - Done preparing for traversal 
    INFO 21:05:58,303 ProgressMeter - [INITIALIZATION COMPLETE; STARTING PROCESSING] 
    INFO 21:05:58,305 ProgressMeter - | processed | time | per 1M | | total | remaining 
    INFO 21:05:58,306 ProgressMeter - Location | active regions | elapsed | active regions | completed | runtime | runtime 
    INFO 21:05:58,520 HaplotypeCaller - Using global mismapping rate of 45 => -4.5 in log10 likelihood units 
    INFO 21:05:58,828 AFCalcFactory - Requested ploidy 1 maxAltAlleles 2 not supported by requested model EXACT_INDEPENDENT looking for an option 
    INFO 21:05:58,829 AFCalcFactory - Selecting model EXACT_GENERAL_PLOIDY 
    INFO 21:06:28,312 ProgressMeter - Starting 0.0 30.0 s 49.6 w 100.0% 30.0 s 0.0 s
    
    ERROR stack trace
    java.lang.NullPointerException
    at org.broadinstitute.gatk.tools.walkers.genotyper.afcalc.GeneralPloidyExactAFCalc.assignGenotype(GeneralPloidyExactAFCalc.java:559)
    at org.broadinstitute.gatk.tools.walkers.genotyper.afcalc.GeneralPloidyExactAFCalc.subsetAlleles(GeneralPloidyExactAFCalc.java:527)
    at org.broadinstitute.gatk.tools.walkers.genotyper.GenotypingEngine.calculateGenotypes(GenotypingEngine.java:286)
    at org.broadinstitute.gatk.tools.walkers.genotyper.UnifiedGenotypingEngine.calculateGenotypes(UnifiedGenotypingEngine.java:335)
    at org.broadinstitute.gatk.tools.walkers.genotyper.UnifiedGenotypingEngine.calculateGenotypes(UnifiedGenotypingEngine.java:320)
    at org.broadinstitute.gatk.tools.walkers.genotyper.UnifiedGenotypingEngine.calculateGenotypes(UnifiedGenotypingEngine.java:310)
    at org.broadinstitute.gatk.tools.walkers.haplotypecaller.HaplotypeCaller.isActive(HaplotypeCaller.java:844)
    at org.broadinstitute.gatk.engine.traversals.TraverseActiveRegions.addIsActiveResult(TraverseActiveRegions.java:618)
    at org.broadinstitute.gatk.engine.traversals.TraverseActiveRegions.access$800(TraverseActiveRegions.java:78)
    at org.broadinstitute.gatk.engine.traversals.TraverseActiveRegions$ActiveRegionIterator.hasNext(TraverseActiveRegions.java:378)
    at org.broadinstitute.gatk.utils.nanoScheduler.NanoScheduler.executeSingleThreaded(NanoScheduler.java:268)
    at org.broadinstitute.gatk.utils.nanoScheduler.NanoScheduler.execute(NanoScheduler.java:245)
    at org.broadinstitute.gatk.engine.traversals.TraverseActiveRegions.traverse(TraverseActiveRegions.java:273)
    at org.broadinstitute.gatk.engine.traversals.TraverseActiveRegions.traverse(TraverseActiveRegions.java:78)
    at org.broadinstitute.gatk.engine.executive.LinearMicroScheduler.execute(LinearMicroScheduler.java:99)
    at org.broadinstitute.gatk.engine.GenomeAnalysisEngine.execute(GenomeAnalysisEngine.java:314)
    at org.broadinstitute.gatk.engine.CommandLineExecutable.execute(CommandLineExecutable.java:121)
    at org.broadinstitute.gatk.utils.commandline.CommandLineProgram.start(CommandLineProgram.java:248)
    at org.broadinstitute.gatk.utils.commandline.CommandLineProgram.start(CommandLineProgram.java:155)
    at org.broadinstitute.gatk.engine.CommandLineGATK.main(CommandLineGATK.java:107)
    
    ERROR ------------------------------------------------------------------------------------------
    ERROR A GATK RUNTIME ERROR has occurred (version 3.2-2-gec30cee):
    My arguments are set as follows:

    Code:
    -T HaplotypeCaller -R Ref.fa -I aln-pe_RG_sorted_dedup_realigned.bam -o aln-pe_RG_sorted_dedup_realigned_HC_ploidy1.vcf -ploidy 1 -maxAltAlleles 2
    However it runs perfectly with ploidy = 2.

    Any help is appreciated.

  • #2
    Did you try to run it with GATK 3.4 ?

    Comment

    Latest Articles

    Collapse

    • seqadmin
      Essential Discoveries and Tools in Epitranscriptomics
      by seqadmin


      The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist on Modified Bases...
      Yesterday, 07:01 AM
    • seqadmin
      Current Approaches to Protein Sequencing
      by seqadmin


      Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
      04-04-2024, 04:25 PM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, 04-11-2024, 12:08 PM
    0 responses
    55 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    51 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    45 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-04-2024, 09:00 AM
    0 responses
    55 views
    0 likes
    Last Post seqadmin  
    Working...
    X