Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • pm2012
    Member
    • Apr 2012
    • 18

    #1

    Extracting statistically significant differentially expressed exons from DEXseq resu

    Hi

    I am trying to extract some data from my DEXseq results. I was able to get the final HTML report for my analysis. However, I was wondering if there's a way I could extract specific exons that are significantly differentially expressed between two conditions. I am interested in getting the gene id (ensembl gene id ok), exon or exon bin id (if applicable), their exon boundaries, fold change & adjusted p value. I am a R/bioconductor newbie. Any help is appreciated.

    Thanks
  • amandinette
    Junior Member
    • Mar 2014
    • 4

    #2
    see the DEUresultTable function

    Hi,

    You can have a look at the DEUresultTable function, to create a table with gene id and number of exon bin, log2(fold change), adjusted p value...

    You can see the DEXSeq vignette on page 18 for usage of the DEUresultTable function :

    Code:
    > res1 <- DEUresultTable(ecs)
    > head( res1 )
    geneID exonID dispersion pvalue padjust meanBase
    FBgn0000256:E001 FBgn0000256 E001 0.046 0.94 1 58.34
    FBgn0000256:E002 FBgn0000256 E002 0.040 0.47 1 103.33
    FBgn0000256:E003 FBgn0000256 E003 0.035 0.92 1 326.48
    FBgn0000256:E004 FBgn0000256 E004 0.035 0.81 1 253.65
    FBgn0000256:E005 FBgn0000256 E005 0.046 0.87 1 60.64
    FBgn0000256:E006 FBgn0000256 E006 1.067 NA NA 0.79
    log2fold(untreated/treated)
    FBgn0000256:E001 0.025
    FBgn0000256:E002 -0.045
    FBgn0000256:E003 0.025
    FBgn0000256:E004 0.038
    FBgn0000256:E005 -0.013
    FBgn0000256:E006 0.126
    I think you can extract exon boundaries from the file you made earlier when preparing the annotation (the xxx_flattened.gff file).

    Hope that helps
    Best regards

    Comment

    • amandinette
      Junior Member
      • Mar 2014
      • 4

      #3
      Another piece of information : to extract a table with only significant results (FDR < 10 % for example), you can try something like this

      Code:
       na.omit(res1[res1$padjust < 0.1, ])

      Comment

      Latest Articles

      Collapse

      • SEQadmin2
        Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
        by SEQadmin2



        CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

        Despite this, “CRISPR helped turn genome editing from a specialized technique into
        ...
        07-31-2026, 11:01 AM
      • SEQadmin2
        Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
        by SEQadmin2


        Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

        The systematic characterization of the human proteome has
        ...
        07-20-2026, 11:48 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, Yesterday, 12:22 PM
      0 responses
      12 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-11-2026, 10:35 AM
      0 responses
      13 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-06-2026, 07:41 AM
      0 responses
      30 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-03-2026, 10:13 AM
      0 responses
      48 views
      0 reactions
      Last Post SEQadmin2  
      Working...