Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • SS00
    PhD Student
    • Jun 2012
    • 33

    #1

    RNA-seq: Population diversity for a gene based on normalized counts?

    Hi all,

    A little Bioinformatics/Population Genetics question. I have a list of significant differentially expressed genes from two experimental conditions (each with 5 biological replicates). I have compared this to DE genes reported in previous literature (about 6 studies) to see how consistent these are, which I have done nicely using upSetR.

    What I want to do now is to see if consistency in literature correlates with consistency in the experimental group, e.g. if a gene is upregulated in all biological replicates in condition 2, is it more likely to be reported in the majority of the other studies as opposed to a gene which is upregulated in only 3 out of the 5 replicates. To do this, I thought of converting my normalized counts for each DE gene (about 150 genes) into some sort of diversity index and visualizing this against literature consistency.

    Does anyone know how to do this? In my undergrad studies I briefly dabbled in population genetics in regards to repeat polymorphisms using Fixation Index and diversity index but I am not sure how to apply this to normalized counts (e.g. 600cpm, 200cpm) instead of genotype (e.g. AA, AT).

    Any thoughts appreciated. Thanks!

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
26 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...