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  • aarthi.talla
    Member
    • May 2011
    • 16

    454 Mate pair naming convention, for input to BAMBUS

    Hi everyone,

    I am working on 454 assembly of Norton Genome. I havent got the original data yet.

    But I have been trying to test the MIRA2 software followed by BAMBUS to build scaffolds with test data.
    I have a question regarding the .mates file.

    Do we have to create it ?

    If yes, what exactly is the naming convention followed by 454 mate pairs ? Is it fixed?
    What is the perl regular expression for it ?

    I know it goes some thing like this :
    Library threeKB 700 3000 (..............).*
    pair (.*)\.f (.*)\.r

    But is it fixed for 454 ? I know the max and min size numbers vary. But I wanna know about the reg ex.

    Thanks.
    Wud appreciate if anyone helped me out.
  • aarthi.talla
    Member
    • May 2011
    • 16

    #2
    Guys, would be glad if anyone helped me out ! Thanks !

    Comment

    • sklages
      Senior Member
      • May 2008
      • 628

      #3
      Originally posted by aarthi.talla View Post
      Hi everyone,

      I am working on 454 assembly of Norton Genome. I havent got the original data yet.

      But I have been trying to test the MIRA2 software followed by BAMBUS to build scaffolds with test data.
      I have a question regarding the .mates file.

      Do we have to create it ?

      If yes, what exactly is the naming convention followed by 454 mate pairs ? Is it fixed?
      What is the perl regular expression for it ?

      I know it goes some thing like this :
      Library threeKB 700 3000 (..............).*
      pair (.*)\.f (.*)\.r

      But is it fixed for 454 ? I know the max and min size numbers vary. But I wanna know about the reg ex.

      Thanks.
      Wud appreciate if anyone helped me out.
      You're way too impatient .. :-)

      - hopefully you mean MIRA3
      - yes, you have to create the mates file on your own, tab separated
      - your regular expression looks good if you use 'sff_extract' to generate input for MIRA
      - there is no fixed naming convention, the 454 reads just have a linker between f and r read. The format of the downstream conversion is dependent on the software which has to deal with the data (here MIRA)

      Just give it a try and you'll see if the regex works ..

      hth,
      Sven

      Comment

      • aarthi.talla
        Member
        • May 2011
        • 16

        #4
        Thanks sklages

        wud this be the correct output after using sff-extract of the mate paired sff files
        The FASTQ files are clipped, devoid of linkers and each mate pair is separated as follows:


        @GSDFVHG01BWBMB.r
        AACCCGAGCCAAACTACTCAAAGAAA
        +
        IIHHHIIIIIHHHIIIIIIHHHIF?;
        @GSDFVHG01BWBMB.f
        ATAGGTTATGAGTACACGGGCTCGTAATTGGCGTATACACCATCTGCAAGAAAACAAAAGAAGGCA
        +
        IIIIIIIIIIIIIIIIIHHHIIIIIIIIIGGGIIIIIGHHIIIIEEEEEE9999C:===I@@IIII


        so wud that be the correct corresponding .mates file to create ?

        Comment

        • sklages
          Senior Member
          • May 2008
          • 628

          #5
          Originally posted by aarthi.talla View Post
          Thanks sklages

          wud this be the correct output after using sff-extract of the mate paired sff files
          The FASTQ files are clipped, devoid of linkers and each mate pair is separated as follows:


          @GSDFVHG01BWBMB.r
          AACCCGAGCCAAACTACTCAAAGAAA
          +
          IIHHHIIIIIHHHIIIIIIHHHIF?;
          @GSDFVHG01BWBMB.f
          ATAGGTTATGAGTACACGGGCTCGTAATTGGCGTATACACCATCTGCAAGAAAACAAAAGAAGGCA
          +
          IIIIIIIIIIIIIIIIIHHHIIIIIIIIIGGGIIIIIGHHIIIIEEEEEE9999C:===I@@IIII


          so wud that be the correct corresponding .mates file to create ?

          Looks good. Give it a try and see what happens.
          If you want MIRA to use read pair information you should provide a XML file (and fasta/qual AFAIR) with the template info.

          Sven

          Comment

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