Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • nmfly
    Junior Member
    • Jul 2012
    • 4

    #1

    Issues with gene id after using Cufflinks

    Hi,

    I am very new and very much a beginner when it come to NGS technologies. I have aligned my RNAseq reads to the dm3 genome in galaxy (UCSC dm3 Drosophila annotation). For some reason the gene_ids are all annotated as CUFF.6 or CUFF.1 etc. but I would hope and expect gene-id to be CG numbers from the annotation...

    Would anyone know what I have done wrong?

    Thanks in advance for any insight
  • Krish_143
    Member
    • Jan 2012
    • 45

    #2
    I do not know about galaxy, but if you use tophat with -G option (Annotation file)and cufflinks ( annotation file) you will get output with scaffold names.. else it would be like this CUFF.XXXXX.
    It's not a problem your doing correct, those are Cufflinks transcripts.
    Krishna

    Comment

    • nmfly
      Junior Member
      • Jul 2012
      • 4

      #3
      Sorry I still don't understand

      I am using UCSC drosophila genome annotation when performing cufflinks so shouldn't the annotation come from the UCSC file and therefore display gene_id from USCS annotation?

      If I can't change the output from CUFF.XXXX, does anyone know how I can identify the gene easily with the CUFF.XXXX gene_ID?

      Comment

      • Krish_143
        Member
        • Jan 2012
        • 45

        #4
        if you want to identify gene names for Cuff.XXX
        i.e 2 ways :

        1) you have to run tophat for mapping instead of galaxy and use -G option in tophat and provide ur UCSC annotation file and run cufflinks for tophat data.

        2) perform Blast2go for Cuff.xxxx transcripts here you will identify gene names.

        i hope you will understand !
        Krishna

        Comment

        • nmfly
          Junior Member
          • Jul 2012
          • 4

          #5
          Hi Krishna,

          Thank you, now I understand

          I recieved BAM and BED files from another institute which were from tophat. I am not sure what reference genome they used, so maybe that is my issue!

          I will contact them and in the meantime give Blast2go a go.

          Comment

          • Krish_143
            Member
            • Jan 2012
            • 45

            #6
            Thats fine.. you can ask exactly what genome and annotation file they used.. that has to be fixed through out the project so be clear with that.
            tc good luck with blast2go.
            Krishna

            Comment

            • cufflinksman
              Junior Member
              • Jun 2012
              • 2

              #7
              Cufflinks

              Thats excellent.. you can ask exactly what genome and annotation computer file they used.. that has to be set through out the venture so be obvious with that.
              tc best of fortune with blast2go.
              Last edited by cufflinksman; 07-20-2012, 11:41 PM.
              cufflinks | New York cufflinks

              Comment

              Latest Articles

              Collapse

              • SEQadmin2
                Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
                by SEQadmin2



                Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

                Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
                ...
                10-14-2026, 09:55 AM
              • SEQadmin2
                New Genomics Technologies Take Aim at Long-Standing Limits
                by SEQadmin2


                Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

                We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
                ...
                09-28-2026, 10:25 AM

              ad_right_rmr

              Collapse

              News

              Collapse

              Topics Statistics Last Post
              Started by SEQadmin2, 10-22-2026, 11:13 AM
              0 responses
              26 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-22-2026, 10:48 AM
              0 responses
              20 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-15-2026, 10:52 AM
              0 responses
              36 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-14-2026, 05:39 AM
              0 responses
              43 views
              0 reactions
              Last Post SEQadmin2  
              Working...