Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • sdvie
    Member
    • Jul 2010
    • 68

    #1

    bfast postprocess "AlignedEntryGetAlignment" error

    Dear all,

    unexpectedly, I am getting the following error when trying to run bfast postprocess (alignment of 95 bp Illumina paired-end reads):

    Code:
    bfast+bwa-0.6.4e/bin/bfast postprocess -i t_8.baf -f hg19_indices/hg19.fa -a 3 -z -A 0 -R -O 1 -n 4 -U > t_8_alternative.sam
    ************************************************************
    Checking input parameters supplied by the user ...
    Validating fastaFileName /projects/bg/genomed/data/hg19_indices_ucsc/hg19.fa. 
    Validating alignFileName t_8.baf. 
    Input arguments look good!
    ************************************************************
    ************************************************************
    Printing Program Parameters:
    programMode:			[ExecuteProgram]
    fastaFileName:			/projects/bg/genomed/data/hg19_indices_ucsc/hg19.fa
    alignFileName:			t_8.baf
    algorithm:			[Best Score]
    space:				[NT Space]
    unpaired:			[Using]
    reversePaired:			[Not Using]
    avgMismatchQuality:		10
    scoringMatrixFileName:		[Not Using]
    randomBest:			[Not Using]
    minMappingQuality:		-2147483648
    minNormalizedScore:		-2147483648
    pairingStandardDeviation:	2.000000
    gappedPairingRescue		[Not Using]
    numThreads:			4
    queueLength:			50000
    outputFormat:			[SAM]
    outputID:			[Not Using]
    RGFileName:			[Not Using]
    timing:				[Not Using]
    ************************************************************
    ************************************************************
    Reading in reference genome from /projects/bg/genomed/data/hg19_indices_ucsc/hg19.fa.nt.brg.
    In total read 93 contigs for a total of 3137161264 bases
    ************************************************************
    Postprocessing...
    ************************************************************
    In function "AlignedEntryGetAlignment": Fatal Error[OutOfRange]. Message: Could not get reference sequence.
     ***** Exiting due to errors *****
    ************************************************************
    I do not know what to make of this error - I ran a lot of analysis with the same reference sequence (in the same folder).

    Suggestions are very much appreciated.

    thanks and cheers,
    Sophia
  • nilshomer
    Nils Homer
    • Nov 2008
    • 1283

    #2
    Originally posted by sdvie View Post
    Dear all,

    unexpectedly, I am getting the following error when trying to run bfast postprocess (alignment of 95 bp Illumina paired-end reads):

    Code:
    bfast+bwa-0.6.4e/bin/bfast postprocess -i t_8.baf -f hg19_indices/hg19.fa -a 3 -z -A 0 -R -O 1 -n 4 -U > t_8_alternative.sam
    ************************************************************
    Checking input parameters supplied by the user ...
    Validating fastaFileName /projects/bg/genomed/data/hg19_indices_ucsc/hg19.fa. 
    Validating alignFileName t_8.baf. 
    Input arguments look good!
    ************************************************************
    ************************************************************
    Printing Program Parameters:
    programMode:			[ExecuteProgram]
    fastaFileName:			/projects/bg/genomed/data/hg19_indices_ucsc/hg19.fa
    alignFileName:			t_8.baf
    algorithm:			[Best Score]
    space:				[NT Space]
    unpaired:			[Using]
    reversePaired:			[Not Using]
    avgMismatchQuality:		10
    scoringMatrixFileName:		[Not Using]
    randomBest:			[Not Using]
    minMappingQuality:		-2147483648
    minNormalizedScore:		-2147483648
    pairingStandardDeviation:	2.000000
    gappedPairingRescue		[Not Using]
    numThreads:			4
    queueLength:			50000
    outputFormat:			[SAM]
    outputID:			[Not Using]
    RGFileName:			[Not Using]
    timing:				[Not Using]
    ************************************************************
    ************************************************************
    Reading in reference genome from /projects/bg/genomed/data/hg19_indices_ucsc/hg19.fa.nt.brg.
    In total read 93 contigs for a total of 3137161264 bases
    ************************************************************
    Postprocessing...
    ************************************************************
    In function "AlignedEntryGetAlignment": Fatal Error[OutOfRange]. Message: Could not get reference sequence.
     ***** Exiting due to errors *****
    ************************************************************
    I do not know what to make of this error - I ran a lot of analysis with the same reference sequence (in the same folder).

    Suggestions are very much appreciated.

    thanks and cheers,
    Sophia
    Please submit a test case to the bfast mailing list.

    Comment

    • sdvie
      Member
      • Jul 2010
      • 68

      #3
      Dear all and Nils,

      when preparing the test set, I realized that the reference genome used for bfast postprocess was not the same I had used for alignment after all. (Too many editions of the hg19 around!) That is what caused the error.
      However, as so often, to post the problem helped me to solve it .

      Sorry for the confusion!

      cheers,
      Sophia

      Comment

      • nilshomer
        Nils Homer
        • Nov 2008
        • 1283

        #4
        Excellent, thanks for the great insight.

        Comment

        • xiangwulu
          Member
          • Apr 2014
          • 18

          #5
          what does "avgMismatchQuality" mean?
          does it refer to something with the base quality of mismach base?

          Comment

          Latest Articles

          Collapse

          • SEQadmin2
            Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
            by SEQadmin2



            Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

            Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
            ...
            Yesterday, 09:55 AM
          • SEQadmin2
            New Genomics Technologies Take Aim at Long-Standing Limits
            by SEQadmin2


            Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

            We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
            ...
            09-28-2026, 10:25 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, Yesterday, 05:39 AM
          0 responses
          12 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-13-2026, 09:56 AM
          0 responses
          14 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-09-2026, 11:14 AM
          0 responses
          27 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 09-29-2026, 09:51 AM
          0 responses
          78 views
          0 reactions
          Last Post SEQadmin2  
          Working...