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  • Fastq files containing more than one species

    Hi,

    simple query with probably a simple answer, I've got some sequence files (FASTQ) that I know contain several species - definitely several virus species for a start. What is a good way to find out what what is in my files, just BLAST?
    thanks.

  • #2
    Compile all the genomes that are present into a fasta file, build a bowtie index against it and then run bowtie (or do a similar thing for which ever mapper you prefer).

    We've has success doing this looking for HPV in human samples...as an aside for HPV, RNAseq is a more accurate serotyper than serotyping.

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    • #3
      mikep's answer is good ... if you know before-hand the genomes that are present. If not then taking a random 5000 or so reads and using BLAST should work.

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      • #4
        Thanks, useful comments. I found this post - http://www.cureffi.org/2013/01/25/al...viral-genomes/ which also addresses what I am after, the idea of compiling all the genomes together is an excellent one and exactly what I was after, results look good so far, thanks for your help.

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