Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Parharn
    Member
    • Jul 2013
    • 84

    #1

    cuffdiff - cummerbund - fold change

    Hi,
    Is there a way that I can have a list of genes with expression fold change of X, instead of significant genes, using cummeRbund and cuffdiff?

    Thanks,
    Parham
  • TiborNagy
    Senior Member
    • Mar 2010
    • 329

    #2
    Yes, in the cuffdiff output folder there is a gene_exp.diff file, the 10th column is the log2 fold change.
    awk -F"\t" '{if($10==X)print $1}' gene_exp.diff # where X is the specified fold change.

    Comment

    • Parharn
      Member
      • Jul 2013
      • 84

      #3
      Yes, I could see the log2 in the data file but I didn't know how to list them using command lines. I am not a linux expert. However I tried your command line but it gives this error:

      > awk -F"\t" '{if($10==1.5)print $1}' gene_exp.diff #
      Error: unexpected string constant in "awk -F"\t""

      and could you write what if I want it to show all the genes with a fold change of equal and bigger than X? thanks.

      Comment

      • Parharn
        Member
        • Jul 2013
        • 84

        #4
        oops I guess I made a mistake. I ran the command in R then!
        Now I tried it in normal terminal, I don't know what you call it. But it gave me a long list! So it seems it works. I still appreciate to know how to change it to show values equal and bigger/smaller! thanks.

        Update: all the files it sorted has a characteristic like:

        SPATRNATHR.02 SPATRNATHR.02 SPATRNATHR.02 I:2433047-2433119 tag5 tag7 NOTEST 0 0 0 0 1 1 no
        Last edited by Parharn; 01-14-2014, 04:59 AM.

        Comment

        • jeales
          Member
          • Oct 2012
          • 13

          #5
          If you're not familiar with R or cmd line then just import it into excel, sort by log2 fold change then remove the range of values you don't want

          Comment

          • Parharn
            Member
            • Jul 2013
            • 84

            #6
            Thanks jeales.

            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, Today, 10:35 AM
            0 responses
            7 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-06-2026, 07:41 AM
            0 responses
            24 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-03-2026, 10:13 AM
            0 responses
            42 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-31-2026, 02:55 AM
            0 responses
            47 views
            0 reactions
            Last Post SEQadmin2  
            Working...