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  • ritzriya
    Member
    • Jun 2010
    • 49

    #16
    @thorondor - From all this, one thing for sure I've learnt is I need to know much more about the wetlab experiment also. Yes I will be assembling the reads into contigs.

    @colindaven - Yes I will have to learn R for that. I was plain curious to know how one would calculate RNA-seq coverage? that's all ..

    Bottom-line is (hope I've understood), is that the number of singletons you get in your assembly of reads as well as its coverage value - assesses your quality of data at the basic level of analysis.

    Thanks everyone for helping!!

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