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  • how is the minimum read counts to do a transcriptome assembly?

    Hi everyone, i have Illumina short read data of 2X150 bp tight now, araound of 12,35 G of data.
    I want to know if you have knowledge about the exactly number of reads to do a good transcriptome assembly of a plant.
    Best regards to everyone!

  • #2
    Depends on the ploidy of your organism and if you are aligning to a reference or not.
    For de-novo bi-allelic SNP detection I have previously used a min of 20x and a min allele frequency of 20%.

    I think with RADseq de-novo in a diploid organism around 30x is recommended per SNP.

    If you have a reference to validate SNPs against you could probably go a little lower

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    • #3
      Hi JackieBadger, the problem on my analysis is that i don't know about the ploidy of the organism and i'm not alignin to any reference because is a denovo transcriptome...

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      • #4
        The only information that i know is that de genome of the plant is from the large of 325 Mb.

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