Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • Chinney14
    Junior Member
    • Feb 2013
    • 2

    Cuffdiff timecourse replicates

    I am trying to figure out if CuffDiff handles replicates in its timecourse option.

    so it would be something like this...

    cuffdiff -T sampleA_20min_a.bam,sampleA_20min_b.bam,sampleA_20min_c.bam sampleA_40min_a.bam,sampleA_40min_b.bam,sampleA_40min_c.bam sampleA_1hr_a.bam,sampleA_1hr_b.bam,sampleA_1hr_c.bam

    and, of course, I would include the other options. But basically, can I use a space to separate time points and commas to separate replicates?

    Thanks in advance.
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    Sort of, but that's not really a time-series analysis, cuffdiff will simply treat those as different groups. Cuffdiff isn't the most flexible package, you'd be better served with limma, DESeq2, or edgeR.

    Comment

    • Chinney14
      Junior Member
      • Feb 2013
      • 2

      #3
      dpryan - I truncated the input for simplicity sake... I have the same treated/untreated cell line harvested in triplicate at 5 different time points. Do you have a preference for one of those for something like this?
      you'd be better served with limma, DESeq2, or edgeR.
      I appreciate the response.

      Comment

      • dpryan
        Devon Ryan
        • Jul 2011
        • 3478

        #4
        Since these aren't the exact same sample extracted at multiple time-points, I would normally use DESeq2. Others will have their own preferred tool.

        Comment

        • danwiththeplan
          Member
          • Sep 2011
          • 72

          #5
          Originally posted by dpryan View Post
          Sort of, but that's not really a time-series analysis, cuffdiff will simply treat those as different groups. Cuffdiff isn't the most flexible package, you'd be better served with limma, DESeq2, or edgeR.
          My interpretation of the cuffdiff manual says this is not true.

          "If you have more than one replicate for a sample, supply the SAM files for the sample as a single comma-separated list."

          -T/--time-series Instructs Cuffdiff to analyze the provided samples as a time series, rather than testing for differences between all pairs of samples. Samples should be provided in increasing time order at the command line (e.g first time point SAM, second timepoint SAM, etc.)


          So my interpretation is that you could analyse a time-course with repeats for each time point, by supplying the individual BAM/CXB files for a time point as a comma-separated list, separating the time points by a space, and using the -T flag. Like so:

          Code:
          cuffdiff -T time1rep1.bam,time1rep2.bam,time1rep3.bam time2rep1.bam,time2rep2.bam,time2rep3.bam time3rep1.bam,time3rep2.bam,time3rep3.bam
          Going to send this to [email protected] to get a confirmation of this as I haven't personally tested this and I'm not sure if my interpretation is correct.
          Last edited by danwiththeplan; 08-19-2014, 03:16 PM.

          Comment

          • pocket_helix
            Junior Member
            • Nov 2014
            • 1

            #6
            Any update from this query? I am having the same trouble coding a time series with multiple conditions and replicates.

            Comment

            Latest Articles

            Collapse

            • SEQadmin2
              Nine Things a Sample Prep Scientist Thinks About Before Sequencing
              by SEQadmin2


              I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.


              Here are nine questions we think about, in roughly the order they matter, before...
              06-18-2026, 07:11 AM
            • SEQadmin2
              From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
              by SEQadmin2


              Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


              The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
              ...
              06-02-2026, 10:05 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, 06-17-2026, 06:09 AM
            0 responses
            24 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-09-2026, 11:58 AM
            0 responses
            42 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-05-2026, 10:09 AM
            0 responses
            48 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-04-2026, 08:59 AM
            0 responses
            49 views
            0 reactions
            Last Post SEQadmin2  
            Working...