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  • pony2001mx
    Member
    • Aug 2013
    • 32

    #1

    How to identify mismatch and gap positions

    Dear all,

    I need to identify the homologs of many short sequences, and then make statistics of the mismatch and gap positions between each short sequence and its homolog. The first step can be readily done by BLAST, FASTA or patscan, but the second step is a little bit troublesome for me. I am wondering if it's feasible to parse the BLAST or FASTA result, and transform the alingment to mismatch and gap information using a perl script. Would you please suggest me some tools and methods to achieve this analysis? Is there a perl script to extract the information i need from BLAST/FASTA output?

    Thank you very much!
  • maubp
    Peter (Biopython etc)
    • Jul 2009
    • 1544

    #2
    Have you looked at BioPerl for parsing the output inside Perl?

    Comment

    • lindenb
      Senior Member
      • Apr 2010
      • 143

      #3
      cross posted on http://www.biostars.org/p/89151/

      Comment

      • pony2001mx
        Member
        • Aug 2013
        • 32

        #4
        Thank you very much. I have sorted it out.

        Comment

        • GenoMax
          Senior Member
          • Feb 2008
          • 7142

          #5
          Originally posted by pony2001mx View Post
          Thank you very much. I have sorted it out.
          For the sake of completeness: a solution was provided on the biostars thread that was posted above.

          pony2001mx: If you found an alternate (better) solution then please include it here.

          Comment

          • pony2001mx
            Member
            • Aug 2013
            • 32

            #6
            Hi GenoMax,

            Lindenb's solution (https://github.com/lindenb/jvarkit/wiki/BlastnToSnp) should be a nice one. I am performing blast for short sequences and testing his java program.

            I am a perl beginner. I believe parsing blast or fasta output using perl should be another solution. There are handful of websites including SEQAnswers that describe methods parsing blast output, for examples,
            Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc




            Actually, my case may be a little bit more complicated. I used Patscan to identify miRNA targets, the output is like below.

            Code:
            miRNA_ID    miRNA_sequence                            target_sequence
            miR1            AUGCGGUGUACACGUACGUCG        AGGCGGUGUACACGUACGUG
            ......................
            miR1 and its target has one mismatch (the second nt) and one insertion (the 20th nt). I need to make statistics of this information, which has not been given by Patscan.

            I plan to perform blast using miRNA sequence as query and its target as subject, and then use Linenb's java program to identify SNPs.

            Honestly, I am testing and my problem has not been completely sorted out. But I think i am closer. If you and others have better solutions or ideas, please feel free to let me know. I believe it is a general question for many biologists. Really thank you very much!
            Last edited by pony2001mx; 12-18-2013, 05:27 AM.

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