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  • Script to remove gap-only sites from fasta alignment?

    Hi all,

    I am trying to find a script or a program that I can call in a pipeline that can remove gap-only sites in a multiple sequence alignment. Can you think of anything I can use? I'd also like to
    delete the columns at either end of each alignment where there are only 2 or fewer sequences with non-gap characters if you can think of anything that can do that.

    Thanks!
    Kevin

  • #2
    I can picture how I would solve this using Biopython, provided the whole alignment can be loaded into RAM.

    How big are the alignments (number of columns, number of rows)?

    Comment


    • #3
      Originally posted by kmkocot View Post
      Hi all,

      I am trying to find a script or a program that I can call in a pipeline that can remove gap-only sites in a multiple sequence alignment. Can you think of anything I can use? I'd also like to
      delete the columns at either end of each alignment where there are only 2 or fewer sequences with non-gap characters if you can think of anything that can do that.

      Thanks!
      Kevin
      Given your alignments in the SAM format, you can remove all alignments with indels with the C-program "dbamfilter -i". You could also easily parse the CIGAR field in the SAM format for any "I" or "D" operators.

      What format are you working with?

      Comment


      • #4
        Hi maubp,

        The alignments vary but all have fewer than 30 taxa and fewer than 1000 amino acids.

        Thanks,
        Kevin

        Comment


        • #5
          Hi maubp,

          The alignments vary but all have fewer than 30 taxa and fewer than 1000 amino acids.

          Thanks,
          Kevin

          Comment

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