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  • Giorgio C
    Member
    • Oct 2010
    • 89

    #1

    Scripting help to identify adaptors in reads

    Hi everybody,

    i have some reads (454) where there are adaptors (NNNN...), one,two or three adaptors for each reads depending on the reads. Is there any way to establish for exemple how many reads have 1 adaptors, how many 2 and how many 3 adaptors over the total ???

    >271-88
    GCCTTGCCAGCCGCTCAGATTGATNNNNNNNNNNNNNNNATCAGGTGCCTACG
    >272-88
    GCCTTGCCAGCCGCTCAGATTGATNNNNNNNNNNNNNNNATCANNNNNNNNNNNNNNNCTGATGGCGCGAGGGAGGCGCCTTGCCAGCCCGCTCAGATTGATNNNNNNNNNNNNNNNCTGATGGCGCGAGGGAGGC
    >273-88
    GCCTCCCTCGCGCATCAGATCGTAGGCACCATCAATCTGAGCGGGCTGGCAAGGCGCCTCCCTCGCGCCA
    >274-88
    GCCTTGCCAGCCGCTCAGATTGATNNNNNNNNNNNNNNNCTGATGGCGCGAGGGAGGCGCCTCCCTCGCGCCATCAGATCGTNNNNNNNNNNNNNNNNNNTCGTAGGCACCATCAATCTGAGCGGGCTGGCAAGGCGCCTCCCTCGCGCCATCAGATCGTAGGCACCATCAA

    Can anyone suggests me a script to fix this ???

    Thank you very much
  • maasha
    Senior Member
    • Apr 2009
    • 153

    #2
    You could run a couple of rounds of find_adaptor - which is pretty clever - from Biopieces (www.biopieces.org).

    Comment

    • Giorgio C
      Member
      • Oct 2010
      • 89

      #3
      Thank you it's a very good tool. But the problem is that some adpators occur in the middle of the sequences because they coming out from a concameration experimental design (they are miRNAs between NNNNNN...). So i want to know a script or tool that may say how many reads have 1 adapt, how many 2, (max are 4) in respect to the total number of reads. Do you know any tool/script that may help ? Tnx

      Comment

      • maasha
        Senior Member
        • Apr 2009
        • 153

        #4
        Hm, perhaps patscan_seq then:

        Code:
        read_fasta -i data.fna | patscan_seq -ip "p1=<adaptor sequence> 0...50 p1 0...50 p1 0...50 p1" | write_fasta -xo got4_adaptors.fna
        Code:
        read_fasta -i data.fna | patscan_seq -ip "p1=<adaptor sequence> 0...50 p1 0...50 p1" | write_fasta -xo got3_adaptors.fna
        etc

        of cause you need to separate the sequences in piles. Clever use of grab should do that.

        Martin
        Last edited by maasha; 11-10-2011, 04:17 AM.

        Comment

        • Giorgio C
          Member
          • Oct 2010
          • 89

          #5
          Wonderful Thanks !!!

          Comment

          • maasha
            Senior Member
            • Apr 2009
            • 153

            #6
            of cause you could perhaps also use REGEX of some sort. egrep, agrep or nrgrep springs to mind. you could also use grab --regex in Biopieces.

            Comment

            • Giorgio C
              Member
              • Oct 2010
              • 89

              #7
              Thanks maasha,

              another rapid way:

              nawk -F'[N]+' '/^[^>]/{a[NF-1]++}END{for(i in a) print a[i] " have " i " ADAPTOR"}' myFile.fasta > result.txt

              Comment

              • Giorgio C
                Member
                • Oct 2010
                • 89

                #8
                Also in perl with the same result:

                perl -ne '$count{s/N+//g}++ if /^[^>]/;END{for $i (keys %count){print "$count{$i} have $i ADAPTOR\n";}}' myFile.fasta > result.txt

                Comment

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