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  • jfo
    Junior Member
    • Oct 2016
    • 5

    "bioinformatically pooling" replicates for SNP discovery from Pooled RNA-seq

    Dear all,

    What I have:
    3 populations duplicate, 25M 100-PE reads each. That will be 6 libraries (using sample > 40 per lib) all in all.

    Objective: discover SNP and use it for SNP genotyping and pop gen studies

    Question:

    Should I just combine Pop1_replicate1 and Pop1_replicate2 libraries (e.g., concatenate the two read1's and two read2's to get finalread1 and 2) before doing alignment, sorting, and SNP discovery? Any thoughts?

    Thanks!

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