Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • attilav
    Junior Member
    • Mar 2011
    • 7

    #1

    BWA 0.6.1 fail to insert infer isize: weird pairing + Segmentation Fault

    Hi all!

    Using the command: bwa sampe refseq.fasta seq_1.aln.sai seq_2.aln.sai seq_1.fastq.gz seq_2.fastq.gz > output.sam , sometimes I get the error that you can see in the title. It looks like this:

    [bwa_sai2sam_pe_core] 5505024 sequences have been processed.
    [bwa_sai2sam_pe_core] convert to sequence coordinate...
    [infer_isize] (25, 50, 75) percentile: (410, 437, 469)
    [infer_isize] fail to infer insert size: weird pairing
    [bwa_sai2sam_pe_core] time elapses: 0.82 sec
    [bwa_sai2sam_pe_core] changing coordinates of 643 alignments.
    [bwa_sai2sam_pe_core] align unmapped mate...
    Segmentation fault

    I did several very similar alignment tasks with BWA, most of them goes through fine, but with a few fastq files this happens. My data is from the 1000genomes, so that shouldn't be the problem I guess.
    Please let me know, if you guys have an idea what's causing this!

    Yours,
    Attila Vikor
  • swbarnes2
    Senior Member
    • May 2008
    • 910

    #2
    The simplest thing is to redo the alignment. If you mistyped a file name somewhere, you might get that result.

    Also, try making the single end .sams separately, and spot check a few pairs of reads, see if thei rcoordiantes and relative orientation make sense. Weird pairing might mean that the reads don't run into each other like they should.

    Comment

    • Richard Finney
      Senior Member
      • Feb 2009
      • 701

      #3
      Is your genome index made with bwa 0.6.1?
      How much memory do you have ?
      Is the error consistent (reproduceable)?

      Comment

      • attilav
        Junior Member
        • Mar 2011
        • 7

        #4
        I made the genome index with bwa 0.6.1.
        I have 2GB RAM on this computer, which is not optimal, but the segfaults only happen, if there is a weird pairing before.
        Its consistent.

        I will align the files separately, and see if something comes up.

        Comment

        • Richard Finney
          Senior Member
          • Feb 2009
          • 701

          #5
          I think you're going to need more that 2GB.
          Try one with 8GB on the problem samples.

          Comment

          • attilav
            Junior Member
            • Mar 2011
            • 7

            #6
            Apparently the problem was some of the files getting corrupted during downloading. Sorry to have wasted your time with this... Guess I have learned a lesson to always check the MD5 sums when downloading huge files from the internet.

            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
              ...
              10-14-2026, 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, 10:52 AM
            0 responses
            8 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-14-2026, 05:39 AM
            0 responses
            19 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-13-2026, 09:56 AM
            0 responses
            16 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-09-2026, 11:14 AM
            0 responses
            27 views
            0 reactions
            Last Post SEQadmin2  
            Working...