Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Caitriona McEvoy
    Junior Member
    • Aug 2014
    • 3

    #121
    Hi all,
    I am very new to r & DEseq2 but have been following the excellent vignette. I have encountered a problem though. I can create the object rld as per the command in the vignette, but when I try to run PCA as suggested I repeatedly encounter the following error:

    plotPCA(rld, intgroup=c("Fibrosis", "Sample.ID"))

    Error in (function (classes, fdef, mtable) :
    unable to find an inherited method for function ‘plotPCA’ for signature ‘"SummarizedExperiment"’
    I have also tried:
    plotPCA( DESeqTransform(rld ) )
    and get the following:
    Error in plotPCA(DESeqTransform(rld)) :
    error in evaluating the argument 'x' in selecting a method for function 'plotPCA': Error: could not find function "DESeqTransform"
    Can anyone advise?
    Caitriona

    Comment

    • dpryan
      Devon Ryan
      • Jul 2011
      • 3478

      #122
      How did you make "rld" and what version of DESeq2 are you using?

      Comment

      • Caitriona McEvoy
        Junior Member
        • Aug 2014
        • 3

        #123
        Thanks for replying. I am using DESeq2 1.6.3.
        First I made dds:
        dds <- DESeqDataSetFromMatrix(countData = countData,
        colData = colData,
        design = ~ Organ + Fibrosis)
        then:
        rld = rlog (dds)
        I went on to examine rld using: head(assay(rld)), and it is listed in my environment as a large SummarisedExperiment.
        Caitriona

        Comment

        • Michael Love
          Senior Member
          • Jul 2013
          • 333

          #124
          hi Caitriona

          It looks like you have a mix of out-of-date and new packages. These often generate conflicts. This can occur if you install Bioconductor packages using install.packages() rather than with biocLite().

          Try this:

          source("http://bioconductor.org/biocLite.R")
          biocValid()

          Comment

          • Caitriona McEvoy
            Junior Member
            • Aug 2014
            • 3

            #125
            Hi Michael, Thank you for your reply. I installed packages as suggested, and it's working. Thanks! Caitriona

            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, Yesterday, 07:41 AM
            0 responses
            12 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-03-2026, 10:13 AM
            0 responses
            26 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-31-2026, 02:55 AM
            0 responses
            39 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-24-2026, 12:17 PM
            0 responses
            25 views
            0 reactions
            Last Post SEQadmin2  
            Working...