Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • hyates
    Member
    • Jan 2014
    • 18

    #1

    Inquiry: p-values & q-values for cummeRbund volcano?

    Hi,

    Suppose I have the following command:
    Code:
    sigGene <- csVolcano(genes(cuffData), "A, "B")
    It shows no differential expressed genes in the plot. It now can show some differential gene expression. Why? What changed? Is what being reported not taking into account the q-values which are adjusted?
    Code:
    sigGene <- csVolcano(genes(cuffData), "A, "B", alpha = 0.01, showSignificant =T)
    Thanks,
    GeekyOmega

    PS - I looked at the bioconductor manual for cummeRbund. What is the default alpha for csVolcano()? Is it alpha = 0.05 for p-value/q-value? I can't figure out how it works exactly in the default/manual situation. Thanks.
  • sazz
    Member
    • Oct 2012
    • 28

    #2
    Hello Hyates,

    Depending on the output, I can say alpha is for q-value. But in the volcano plot it is the corresponding p-value. If your cutoff for q-value is 0.01 you should see that red dots for p-value starts around -log(2.42) in volcano plot (it would be exactly at -2.00 if alpha was accounted for p-value).

    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, Yesterday, 11:13 AM
    0 responses
    21 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, Yesterday, 10:48 AM
    0 responses
    18 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
    42 views
    0 reactions
    Last Post SEQadmin2  
    Working...