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  • Samtools view -c Readcount Issue

    I'm using samtools to determine the total number of reads in a uniquely large bam file as shown below. I'm having a hard time interpreting the result. Anyone else receive a negative read count from samtools view -c before?

    $ samtools view -c /run/media/data/Enclosure3/mergedcohort.bam
    -1203401967

  • #2
    Must be an overflow of whatever type they are using in the code. In other words the actual count is larger than what they designed the code to handle.
    /* Shawn Driscoll, Gene Expression Laboratory, Pfaff
    Salk Institute for Biological Studies, La Jolla, CA, USA */

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    • #3
      Is there a reference that would indicate what the maximum count limit is? Would help with converting the overflow into a count. I've tried the samtools manual at sourceforge with no luck.

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      • #4
        If you can read code that seems to be the best reference for samtools. I can take a look unless somebody chimes in with a real answer. Exactly how big is this bam file anyway? Even with a 32 bit unsigned int you should be able to count way higher than any total number of reads I've ever heard of in an experiment.
        /* Shawn Driscoll, Gene Expression Laboratory, Pfaff
        Salk Institute for Biological Studies, La Jolla, CA, USA */

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        • #5
          Its huge. The folks who did the sequencing said to expect well over 2E9 reads. (yep -- billions...)

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          • #6
            You could try this one...

            Code:
            samtools view file.bam | wc -l
            See if that fails.
            /* Shawn Driscoll, Gene Expression Laboratory, Pfaff
            Salk Institute for Biological Studies, La Jolla, CA, USA */

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