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  • apratap
    Member
    • Jan 2009
    • 58

    #1

    Calculating RPKMs from Tophat results : Your advice requested

    I am trying to calculate RPKM on the tophat data but have come across this issue that I believe could skew my results.

    My #input reads to tophat are ~49 million. The number of reads reported by tophat to be mapped are ~55 million. I assume I am getting more reads mapped than the total input due to the "--max-multihits 15" option I had set.

    Now for RPKM calculation I am not sure what number should I use for total mapped reads.

    1. Total reads mapped by Tophat including multireads
    2. Total uniquely mapped reads

    If I go with #2 then I think I should also remove all multi reads when I am doing the counting for reads mapping to my genes.

    Thanks!
    -Abhi
  • carmeyeii
    Senior Member
    • Mar 2011
    • 137

    #2
    Apratap,

    I also have a similar question.

    When TopHat maps a read to more than one place in the genome, thus producing 2+ alignments for read X, at the end of the mapping process we will have more alignments than reads originally input.

    When a program such as Cufflinks does the normalization for a gene/transcript by its length and million mapped reads - which value is it actually using: the total million UNIQUE mapped reads, or the total alignments TopHat found?

    My guess is it takes the former, but I cannot find a logical explanation in my head to support this gut feeling....

    Any thoughts?

    Carmen

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