Unconfigured Ad

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

    #1

    Differentially expressed genes

    Hi,
    I am doing RNA-seq analysis using Tuxedo pipeline. I wonder when do you name it DIFFERENTIALY expressed genes? Does it have to be significant genes out of cuffdiff analysis or any sort of fold changes between two conditions.
    I am asking it because my two conditions show very few significant changes in gene expression. And that is between G2 and S phase cells I just get 16 significant differentialy expressed genes.
    Let me know if you need further information.

    thanks.
  • Bukowski
    Senior Member
    • Jan 2010
    • 388

    #2
    Significance in cuffdiff is when the q-value (FDR adjusted p-value) is less than the p-value itself and it is not dependent on the magnitude of the fold change.

    (Source, the cuffdiff manual : http://cufflinks.cbcb.umd.edu/manual.html#gene_exp_diff )

    It's impossible to tell why you have few significant genes without more information about your experimental set up. Too few reads per sample, or too few replicates would be possible explanations.
    Last edited by Bukowski; 02-24-2014, 02:04 PM. Reason: added link

    Comment

    • Parharn
      Member
      • Jul 2013
      • 84

      #3
      Yes, I understood how Cuffdiff defines significant, but my question is if differentially expressed genes are specifically those that are expressed significantly?

      Second, since we were establishing RNA-seq for the first time in our lab, we did only one replicate of each condition. We just wanted to go all the way to the end before doing actual experiment. I recently read that number of replicates have great impact on the accuracy of data analysis. My data has between 10 to 20 million reads per sample. I guess having one replicate is making the problem. What do you think?

      How many replicates do you suggest with how many reads in each?
      Please let me know what other information will make it more clear.

      Thanks.

      Comment

      • TiborNagy
        Senior Member
        • Mar 2010
        • 329

        #4
        Great article about the replicates/read numbers

        Comment

        • Jeremy
          Senior Member
          • Nov 2009
          • 190

          #5
          Most qPCR papers use a minimum fold change of 2 and statistical significance before calling anything differentially expressed. Since RNA-seq is basically high throughput qPCR it would make sense to use the same thresholds.

          Comment

          • reema
            Member
            • Feb 2014
            • 27

            #6
            How about using logFold change?

            Comment

            • Parharn
              Member
              • Jul 2013
              • 84

              #7
              Thanks people.

              Comment

              • Krish_143
                Member
                • Jan 2012
                • 45

                #8
                When we have no replicates.. then i suggest u to try Gfold.
                Gfold > 0 || gfold < 0 means it Upregulated or down regulated.

                For more information check.
                Krishna

                Comment

                • Parharn
                  Member
                  • Jul 2013
                  • 84

                  #9
                  Thanks a lot Krish. Looks very interesting, how can I get the software? Apt-get I guess? I am new to Linux environment.

                  Comment

                  • Krish_143
                    Member
                    • Jan 2012
                    • 45

                    #10
                    You can download at


                    For downlading to linux :

                    wget https://bitbucket.org/feeldead/gfold....V1.1.1.tar.gz

                    Check Readme and installation files in gfold.
                    Last edited by Krish_143; 02-27-2014, 11:35 PM.
                    Krishna

                    Comment

                    • Parharn
                      Member
                      • Jul 2013
                      • 84

                      #11
                      Thanks a million Krish. I will give it a try.

                      Comment

                      • Parharn
                        Member
                        • Jul 2013
                        • 84

                        #12
                        This Gfold was a game changing program. Thanks for suggesting it Krish.

                        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
                          ...
                          Today, 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, Today, 02:55 AM
                        0 responses
                        7 views
                        0 reactions
                        Last Post SEQadmin2  
                        Started by SEQadmin2, 07-24-2026, 12:17 PM
                        0 responses
                        12 views
                        0 reactions
                        Last Post SEQadmin2  
                        Started by SEQadmin2, 07-23-2026, 11:41 AM
                        0 responses
                        12 views
                        0 reactions
                        Last Post SEQadmin2  
                        Started by SEQadmin2, 07-20-2026, 11:10 AM
                        0 responses
                        24 views
                        0 reactions
                        Last Post SEQadmin2  
                        Working...