Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • bioBob
    Member
    • Mar 2011
    • 72

    #1

    DESeq2 paired plus condition

    Hi,

    I am having some trouble getting my head around it today, its Monday.

    Essentially, I have a design matrix like so:

    Patient Condition
    58 2
    58 3
    64 2
    64 3
    ...

    So, according the the vignette, I need to do ~Patient + Condition. I really want condition differences, NOT patient differences.

    I can view the results via results(slim_dds_1, contrast=c("Condition","3","2")). How do I know what was a patient difference? I suppose I could do the reduced formula and compare?
    Last edited by bioBob; 02-23-2015, 01:29 PM.
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    You're going to need to provide rather more detail.

    Comment

    • fanli
      Senior Member
      • Jul 2014
      • 197

      #3
      You can extract patient differences like so:
      Code:
      results(slim_dds_1, contrast=c("Patient", "58", "64")
      Specifying the design as you did will explicitly account for differences in Patient when looking at Condition.

      Comment

      • dpryan
        Devon Ryan
        • Jul 2011
        • 3478

        #4
        @bioBob: for future reference, we don't get easily notified when a post gets edited. For a speedier reply, post a comment after editing (or just post the edit as a new comment). Anyway, I suspect that fanli answered your question. If instead you really want to see what genes vary with patient in general (i.e., not between any individual pair of patients but generally across them), then you can use the LRT test with a reduced model of ~Condition.

        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
        • SEQadmin2
          Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
          by SEQadmin2



          Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
          ...
          07-09-2026, 11:10 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, 08-06-2026, 07:41 AM
        0 responses
        13 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-03-2026, 10:13 AM
        0 responses
        30 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-31-2026, 02:55 AM
        0 responses
        40 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-24-2026, 12:17 PM
        0 responses
        26 views
        0 reactions
        Last Post SEQadmin2  
        Working...