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  • chayan
    Member
    • Nov 2012
    • 52

    #1

    Assembly using Illumina Paired-end reads from SRA with MIRA

    Hii

    I have downloaded a Pair-end data set from SRA and used fastq-dump from SRA tool-kit to generate the fastq file for that..well everything works fine till here..now i wanted to reassemble it with MIRA..but from SRA i got only one file for pair end reads, as they mentioned that it will be a joined (may be by cat ???) file...now i am not sure how to a single file for a PE assembly with MIRA..somewhere i found that they mention it to use as a unpaired one but then should i use readgroup = unpaired/PE... in both cases MIRA is complaining...little confuse..any one has any experiences with this???

    thanks for any help

    best ...
  • JackieBadger
    Senior Member
    • Mar 2009
    • 385

    #2
    use the MIRA mailing list for quick and accurate response

    Comment

    • maubp
      Peter (Biopython etc)
      • Jul 2009
      • 1544

      #3
      But first, search the mira_talk mailing list as people have discussed using SRA data there before. http://www.freelists.org/list/mira_talk
      Last edited by maubp; 02-24-2014, 03:40 AM. Reason: Fixed autocorrected typo

      Comment

      • chayan
        Member
        • Nov 2012
        • 52

        #4
        thanks to both of you..yes, i got the answer from the mira-mailing list indeed

        Comment

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