Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • keebs42
    Member
    • May 2009
    • 17

    Cufflinks (Cuffdiff) v0.9.3 multiple samples

    Hi all,

    I'm running through the cufflinks-cuffcompare-cuffdiff pipeline using three samples, but for some reason cuffdiff is only producing one of each kind of differential expression file (*_exp.diff) rather than one for each pair of samples. In the *.fpkm_tracking files, all 3 samples are showing up (q1,q2,q3) but I'm only getting expression files comparing q1 and q2. Any ideas?? Here's the basics of the cuffdiff command I'm using:

    cuffdiff -q -r ref.fa cuffcompare_6hr.4/stdout.combined.gtf tophat_out_1/sample1.bam tophat_out_2/sample2.bam tophat_out_3/sample3.bam

    Anyone else running cuffdiff on >2 samples using the latest version?

    Thanks!
  • roryk
    Member
    • Aug 2010
    • 15

    #2
    Originally posted by keebs42 View Post
    Hi all,

    I'm running through the cufflinks-cuffcompare-cuffdiff pipeline using three samples, but for some reason cuffdiff is only producing one of each kind of differential expression file (*_exp.diff) rather than one for each pair of samples. In the *.fpkm_tracking files, all 3 samples are showing up (q1,q2,q3) but I'm only getting expression files comparing q1 and q2. Any ideas?? Here's the basics of the cuffdiff command I'm using:

    cuffdiff -q -r ref.fa cuffcompare_6hr.4/stdout.combined.gtf tophat_out_1/sample1.bam tophat_out_2/sample2.bam tophat_out_3/sample3.bam

    Anyone else running cuffdiff on >2 samples using the latest version?

    Thanks!
    I think if you look carefully at the .diff files, you will see that they are doing all pairwise comparisons for each sample (q1 vs q2, q2 vs q3, etc).

    Comment

    • keebs42
      Member
      • May 2009
      • 17

      #3
      Yep.. you're right. Just didn't check down within the file. Thanks for the tip!

      Comment

      • jp.
        Senior Member
        • Jul 2013
        • 142

        #4
        Hi
        I got problem with cuffdiff. I am working of Linuxe server and when give commands:
        cuffdiff -o diff_out -b genome.fa -p 8 –L 1,2 -u merged_asm/merged.gtf \
        ./1_R1_thout/accepted_hits.bam,./1_R2_thout/accepted_hits.bam,./1_R3_thout/accepted_hits.bam \
        ./2_R1_thout/accepted_hits.bam,./2_R_thout/accepted_hits.bam,./2_R3_thout/accepted_hits.bam
        Error: cannot open alignment file

        When I changed (removed \ and ./):
        cuffdiff -o diff_out -b genome.fa -p 8 –L 1,2 -u merged_asm/merged.gtf /1_R1_thout/accepted_hits.bam /2_R1_thout/accepted_hits.bam
        It goes well.
        I can not add replicates. any idea ?
        Thank you

        Originally posted by keebs42 View Post
        Yep.. you're right. Just didn't check down within the file. Thanks for the tip!

        Comment

        • moredd
          Junior Member
          • May 2013
          • 8

          #5
          If you have more than one replicate for a sample, supply the SAM files for the sample as a single comma-separated list. It is not necessary to have the same number of replicates for each sample, says the manual @ http://cufflinks.cbcb.umd.edu/manual.html#cuffdiff

          Comment

          Latest Articles

          Collapse

          • SEQadmin2
            Cancer Drug Resistance: The Lingering Barrier to Rising Survival
            by SEQadmin2



            Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

            There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
            Yesterday, 05:17 AM
          • GATTACAT
            Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
            by GATTACAT
            Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
            07-01-2026, 11:43 AM
          • 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

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, Yesterday, 10:08 AM
          0 responses
          6 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-07-2026, 11:05 AM
          0 responses
          8 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-02-2026, 11:08 AM
          0 responses
          31 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-30-2026, 05:37 AM
          0 responses
          29 views
          0 reactions
          Last Post SEQadmin2  
          Working...