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  • tineax
    Junior Member
    • Apr 2012
    • 2

    Questions about RNA-seq experiment design

    I try to sequence the RNAs from 2 conditions, 5 replicates per condition, using multiplex Illumina Hiseq 2000. I would like to consult about experiment design. There are 3 plans. Any suggestions are greatly appreciated, especially for the third one.

    First, 5 samples are put in one sequencing lane (2 for condition A, 3 for condition B, and vice versa). This will be asymmetric.

    Second, randomly choose 4 samples in one lane (2 for condition A, 2 for condition B). This reduce the replicates but increase the reads number for each sample.

    Third, keep 5 reps each and pool all 10 and then run half a pool each on two lanes. Each lane would generate 10 separate fastq files and one could then concatenate the 2 fastq files (from the 2 lanes) for the same samples to get more reads for each sample, ending up with a total of 10 fastq files. We are not sure if there are other considerations in this scenario.
  • Bukowski
    Senior Member
    • Jan 2010
    • 388

    #2
    We do all our RNA-Seq through option 3.

    Obviously this is not always possible when you have hundreds of samples, and then the randomised/mixed approach is fine.

    But with 10 samples, just index them all separately, pool and sequence down two lanes and combine the Fastq.

    Comment

    • james hadfield
      Moderator
      Cambridge, UK
      Community Forum
      • Feb 2008
      • 224

      #3
      Option 3 every time.

      You can multiplex up to 96 samples in one pool on HiSeq. I always recommend pooling the whole experiment if possible, and if not consulting with a statistician beforehand to get a controlled randomisation.

      A MiSeq QC can help chekc your pool is balanced. However for your experiment I'd suggest getting the seqeuncing done without MiSeq as a single-end 50bp read (what we'd use for DGE) is cheaper thana MISeq QC run in many labs!

      Comment

      • westerman
        Rick Westerman
        • Jun 2008
        • 1104

        #4
        A problem we have is balancing the number of reads between samples. As James suggested using a MiSeq is a good way to do figure out the balance before running the HiSeq. But even a better method (if you have the time) is to run a pooled sample in a single HiSeq lane and use the information from that lane to balance a second run. You'll get much more data that way.

        Comment

        • tineax
          Junior Member
          • Apr 2012
          • 2

          #5
          Thank you very much. I really appreciate your help.

          Comment

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