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  • Danielbenitezr
    Junior Member
    • Dec 2012
    • 9

    #1

    problems with bam file and mpileup

    Hello everyone:

    I have a problem with samtools' mpileup.
    Im trying to map a set of reads (only 1 library for now) against a reference genome, to find SNPs. The command line I used is:

    $ samtools mpileup -uD -f ref_genome.fasta library.sorted.bam | bcftools view -bvcg library.raw.bcf

    the output I get is this:

    open: No such file or directory
    [mpileup] 1 samples in 1 input files
    Segmentation fault

    i dont know what's wrong. I used this same command line with other data and it worked just fine, so I could use some help.

    thank you!
  • zhidkov.ilia
    Member
    • Dec 2010
    • 25

    #2
    Does "ref_genome.fasta" indexed?
    -f FILE faidx indexed reference sequence file [null]

    Comment

    • Danielbenitezr
      Junior Member
      • Dec 2012
      • 9

      #3
      yes, it is.

      I run this command line earlier:

      $ samtools faidx ref_genome.fasta

      generating a ref_genome.fasta.fai file

      I don´t think that's the problem =(

      Comment

      • Dethecor
        Member
        • May 2010
        • 24

        #4
        Fasta file chromosome names

        Hi, can you post the result of:

        Code:
        grep ">" ref_genome.fasta
        You can get these segfaults without message when your fasta header lines have spaces in them.

        Cheers,
        Paul

        "You are only young once, but you can stay immature indefinitely."

        Comment

        • Richard Finney
          Senior Member
          • Feb 2009
          • 701

          #5
          Quick guess ...
          Shouldn't it be
          $ samtools mpileup -uD -f ref_genome.fasta library.sorted.bam | bcftools view -bvcg - > library.raw.bcf

          Comment

          • Danielbenitezr
            Junior Member
            • Dec 2012
            • 9

            #6
            Thank you all!
            actually it was the missing "- >" before the "library.raw.bcf"
            thanks a lot!

            Comment

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