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  • robelb4
    Member
    • Jul 2011
    • 10

    #1

    Mira assembly -shell script

    hello,

    I'm a beginner in Assembly and shell scripting. My question is I already have pair-end reads generated using solexa. and on the MIRA documentation about mira input file processing (processing to make /1/2 illumina naming scheme), there is a shell script called prepdata.sh .

    but my two reads are not form NCBI website;they're already unziped, so how can i modify the script to just work for an already unzipped file???

    thanks,
    R
  • gaffa
    Member
    • Oct 2010
    • 82

    #2
    I'm not familar with this, but is this the script in question? (from http://mira-assembler.sourceforge.ne...deToMIRA.html):

    Code:
    ######################################################################
    #######
    ####### Prepare paired-end Solexa downloaded from NCBI
    #######
    ######################################################################
    
    # srrname:    is the SRR name as downloaded form NCBI SRA
    # numreads:   maximum number of forward (and reverse) reads to take from
    #              each file. Just to avoid bacterial projects with a coverage
    #              of 200 or so.
    # strainname: name of the strain which was re-sequenced
    
    srrname="SRR030257"
    numreads=5000000
    strainname="REL8593A"
    
    ################################
    
    numlines=$((4*${numreads}))
    
    # put "/1" Solexa reads into file
    echo "Copying ${numreads} reads from _1 (forward reads)"
    zcat ../origdata/${srrname}_1.fastq.gz | head -${numlines} | sed -e 's/SRR[0-9.]*/&\/1/' >${strainname}-${numreads}_in.solexa.fastq
    
    # put "/2" Solexa reads into file
    echo "Copying ${numreads} reads from _2 (reverse reads)"
    zcat ../origdata/${srrname}_2.fastq.gz | head -${numlines} | sed -e 's/SRR[0-9.]*/&\/2/' >>${strainname}-${numreads}_in.solexa.fastq
    
    # make file with strainnames
    echo "Creating file with strain names for copied reads (this may take a while)."
    grep "@SRR" ${strainname}-${numreads}_in.solexa.fastq | cut -f 1 -d ' ' | sed -e 's/@//' -e "s/$/ ${strainname}/" >>${strainname}-${numreads}_straindata_in.txt
    If so, then it should probably just be a matter of changing the "zcat" commands to "cat" (aswell as changing the appropriate file names of course, e.g. it shouldn't say ".gz"). I haven't tried this or anything but it should work. "zcat" is for printing gzipped files to screen, cat is for normal, non-zipped files.

    Comment

    • robelb4
      Member
      • Jul 2011
      • 10

      #3
      gaffa,

      Thanks, that's what I thought and tried, but it's i'm getting a 'No such file ..' error . May be I misplaced the reads directory.

      now I know the command is correct.

      thanks
      Robel

      Comment

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