Is FPM the only normalisation method recommended for CircRNAs?
Hi all,
I have a question. For circRNAs detected by RNA-seq, I've read various articles suggesting to use FPM (Fragments per million mapped reads) for normalisation of the raw counts. Is it wrong to use FPKM for circRNA normalisation - the difference being FPKM also corrects for the gene length.
Thanks and best!
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Hey,
Can you cite the sources? FPKM may correct for gene length, but it fails to correct for cross-sample differences.
Kevin
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