Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • seeker
    Member
    • Jan 2011
    • 26

    #1

    Weird confidence intervals from Cuffdiff

    Hi All,

    Something odd seems to be going on with an analysis I'm doing. I have run the tuxedo suite through to using cummerbund but am seeing some genes which have confidence intervals that do not encompass the FPKM value. The whole confidence interval is lower than the actual FPKM (see attached barplot last pair, and fourth from last pair of bars)

    Any ideas what's going on here?

    command line call and version info:
    Code:
     cuffdiff -o diff_out_NA_AA -b Bter_gDNA.fa -p 16 -L NA,AA -u merged_asm/merged.gtf ./tophat_out_CNA/accepted_hits.bam,./tophat_out_DNA/accepted_hits.bam,./tophat_out_ENA/accepted_hits.bam ./tophat_out_CAA/accepted_hits.bam,./tophat_out_DAA/accepted_hits.bam,./tophat_out_EAA/accepted_hits.bam 
    version	2.1.1
    SVN_revision	4046M
    boost_version	104900
    Attached Files
  • Zapages
    Member
    • Oct 2012
    • 98

    #2
    Apparently if you are using Cufflinks 2.1.1 the confidence intervals will be off due to an internal bug. But the actual FPKM values will still be correct.

    Hence, I am still using Cufflinks 2.0.2, which from my knowledge does not have this problem.

    I hope this helps.

    Comment

    • seeker
      Member
      • Jan 2011
      • 26

      #3
      Wow, really? Ugh.

      Thanks for that. Can you point me to where you found that info or if you found some other work around? I guess it's not the end of the world to rerun it but it is annoying.

      Comment

      • Zapages
        Member
        • Oct 2012
        • 98

        #4
        I read it on seqanswers: http://seqanswers.com/forums/showthread.php?t=39758

        I was experiencing the same issues as you were by looking through the expression results from Cufflinks and was very concerned as to why confidence values were off.

        Also when you continue on to Cuffmerge and Cuffdiff. Please use the same version ie.if you used 2.0.2 for Cufflinks then use 2.0.2 version for Cuffmerge and Cuffdiff. Likewise for Cufflink/Cuffmerge/Cuffdiff 2.1.1.

        All the best with your project.

        Comment

        • seeker
          Member
          • Jan 2011
          • 26

          #5
          I searched and didn't see that. Thanks for pointing me to it. Fingers crossed that the next version arrives fairly quickly.

          Comment

          • seeker
            Member
            • Jan 2011
            • 26

            #6
            At the risk of hijacking my own thread. Does anyone know what's going on when the expression values are associated with more than one locus? eg. LOC100648144,LOC100648258 in the barplot? They are genes that are right next to one another.

            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, 10:13 AM
            0 responses
            14 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-31-2026, 02:55 AM
            0 responses
            27 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-24-2026, 12:17 PM
            0 responses
            20 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-23-2026, 11:41 AM
            0 responses
            19 views
            0 reactions
            Last Post SEQadmin2  
            Working...