Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • bjoernoest
    Member
    • Feb 2013
    • 11

    #1

    Pipeline for DESeq and annotation

    Hi, i am new to this and I would like to be able to feed my RNA data into the VST algorithm from DESeq, to normalize my data. But since there is so many different informations in here, I am not sure if I do it the right way, what I do is for each experiment/replicate:

    python tophat -p 8 -G genome.gtf -o output_dir genome.bt2 X1.fastq X2.fastq

    This generates a directory containing accepted_hits.bam

    I then sort this using

    Samtools sort –n input.bam out.sam

    I then run cufflinks and use the transcripts.gtf file

    cufflinks -p 8 -o newoutputDir outputdir/accepted_hits.bam

    To generate the list of counts I then do:

    htseq-count --stranded=no out.sam transcripts.gtf > output-htseq.txt

    which then gives me a list like this:

    CUFF.1 745
    CUFF.10 14
    CUFF.100 0
    CUFF.1000 1
    CUFF.10000 0
    CUFF.10001 1
    CUFF.10002 57


    Would this be a correct way of doing it? The output I get is just assigned to arbitrary values in the GTF file, and I have not been able to find that much about assigning the count values to gene identifiers, does anyone have any experience with that?
    Bjørn Øst
  • super0925
    Senior Member
    • Feb 2014
    • 206

    #2
    What is your input.bam? is that accepted_hits.bam?

    Comment

    • Simon Anders
      Senior Member
      • Feb 2010
      • 995

      #3
      Are you looking for new genes, or do you you want to look for differential expression of known and annotated genes?

      If the former: Well, a new gene will not have a name; after all, it is new.

      If the latter: What did you run 'cufflinks' for?

      Comment

      Latest Articles

      Collapse

      • SEQadmin2
        16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
        by SEQadmin2




        NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...
        Today, 06:46 AM
      • 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

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 10-28-2026, 09:57 AM
      0 responses
      23 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-28-2026, 09:51 AM
      0 responses
      15 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-22-2026, 11:13 AM
      0 responses
      68 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-22-2026, 10:48 AM
      0 responses
      48 views
      0 reactions
      Last Post SEQadmin2  
      Working...