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  • huan
    Member
    • Oct 2010
    • 56

    #1

    How should I compute the sampling depth or cells when I use pacbio RNA sequencing?

    I want to do the RNA sequencing using pacbio SMRT, I have got the transcriptome information, but I don't know how many cells should I use ? And what the sampling depth is enough?


    Thank for any adviceO(∩_∩)O~
    happy
  • Brian Bushnell
    Super Moderator
    • Jan 2014
    • 2709

    #2
    It depends on your goal and the organism's clade, of course. Are you doing novel transcript discovery from a well-known organism, for example? And what kingdom is it in?

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    • huan
      Member
      • Oct 2010
      • 56

      #3
      Thanks for reply@Brian BushnelllO(∩_∩)O~ Yes. I want to do the novel transcript discovery and to accomplish one species's annotiation....
      happy

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