Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • buthercup_ch
    Member
    • Apr 2014
    • 41

    #1

    Time Course RNA-Seq

    Hello,

    We just finished the QC for the total reads obtain from a Time Course RNA-Seq experiment (Illumina HiSeq2000), and are satisfied with the quality.
    Now we have started the Differential Expression Gene analysis, and the strategy proposed by our bioinformatican was the following:
    Calculating DEG for every condition compared with the initial one, so we will have at the end 5 comparisons. DEG for each gene will show a certain p-value in each case, so we would count as statistically significant those genes with p-value<0.05 in all 5 comparisons.

    Do you think this is a right approach?

    Thanks in advance for your comments and advices.
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    I hope he/she proposed that as only a quick and easy first go while a more useful analysis was being performed...

    If your goal is to find "all genes that change with time" (this is at least biologically interesting), then tell your bioinformatician to "fit the samples with a model of the form '~time', with 'time' as a factor, and then perform an LRT with '~1' as the reduced model".

    Analysing time-course data is a bit of an art in itself if what I wrote above isn't the question you're interested in answering. At that point, you're best of doing a bit of clustering and trying to determine the proper course of action from how the samples cluster together.

    Comment

    • bastianwur
      Member
      • Feb 2014
      • 98

      #3
      I'd make DE all vs all, then sort out the statistically significant ones (no matter where they are significant) and do clustering on these (as suggested), to see which patterns are in there.

      I don't have any experience with time course data myself, but this is probably what I'm going to do with my current time course (running the clustering on the whole dataset though....right now; might sort the DE ones out afterwards...or maybe I'll change that again the other way round, not sure yet).

      Comment

      • Dario1984
        Senior Member
        • Jun 2011
        • 166

        #4
        You should provide more guidance to the bioinformatician collaborating with you. What is your biological hypothesis? Why did you do the experiment? There must have been particular reasons for choosing the timepoints you chose, which you need to inform the bioinformatician about.

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
          by SEQadmin2



          Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

          Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
          ...
          10-14-2026, 09:55 AM
        • SEQadmin2
          New Genomics Technologies Take Aim at Long-Standing Limits
          by SEQadmin2


          Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

          We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
          ...
          09-28-2026, 10:25 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, 10-22-2026, 11:13 AM
        0 responses
        27 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-22-2026, 10:48 AM
        0 responses
        20 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-15-2026, 10:52 AM
        0 responses
        36 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-14-2026, 05:39 AM
        0 responses
        43 views
        0 reactions
        Last Post SEQadmin2  
        Working...