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  • HTSeq.BAM_Reader error: .bam-file has no index ...

    I'm running into a problem with HTSeq that I can't seem to solve on my own:

    As running through the entire bam file to find alignments corresponding to a genomic position (from a gtf file) works, but takes a long time, I'm trying to use the indexed random access approach. Code is identical (except filenames and window postitions) to the docs tutorial for HTSeq, and my input file is a coordinate-sorted bam file with index file of the same name (but with .bai extension of course) in same folder as sorted bam file. Bam file was sorted with Picard Tools if that matters. After attempting to run the code below, I get the following error:

    sortedbam = \
    HTSeq.BAM_Reader("729_GCCAAT_L007_R1_001_trimmed.sorted.bam")
    for alnmt in sortedbam[ window ]:
    print alnmt

    ERROR: ValueError: The .bam-file has no index, random-access is disabled!

    The index filename is 729_GCCAAT_L007_R1_001_trimmed.sorted.bai

    I'm stumped.

    For what it's worth, htseq_count and dexseq_count both work fine (obviously fewer chances to screw something up passing arguments to a script but I wanted to mention it).

  • #2
    Try renaming the index to 729_GCCAAT_L007_R1_001_trimmed.sorted.bam.bai

    Comment


    • #3
      Worked beautifully, thank you.

      Any idea why that filename format is assumed? Is there a standard for naming bam index files?

      Comment


      • #4
        Well, if you just
        Code:
        samtools index blah.bam
        then the index file will be automatically named "blah.bam.bai". Generally, whatever samtools does is the standard

        Comment


        • #5
          Fair enough. Thanks again for your help.

          Comment

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