Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • adrian
    Member
    • Oct 2009
    • 90

    #1

    How do I identify splicing differences from RNA-Seq

    Dear group,

    I think I am back to square 1 on this issue.

    I have RNA-Seq data from 3 samples.

    I used tophat / cufflinks pipeline.

    From PCR experiment I know that a Gene xyz (that has only 1 known transcript) is spliced at exons 4, 5 and 6. In sample 1, exons 4-6 are joined and also have transcripts 4-5-6.

    In sample 2, I know exon joining 4-6 is not happening. Only one form 4-5-6 happening.

    In sample 3, there should be both 4-6 and 4-5-6 exon join.

    My question:

    1. From various cufflink outputs, how do I find this splicing differences in samples 1, 2 and 3.

    2. How do Identify other genes that behave the same way.

    3. How can I visually observe the identified genes where splicing is happening.

    Could any one please help me this. I am desperate and need help.

    I just cant wrap my around this. If cufflinks is not designed to answer these questions, what other softwares could help me.

    thanks
  • adrian
    Member
    • Oct 2009
    • 90

    #2
    sorry again to bump another question by me.

    I see over 100 hits, and no answers.

    I am wondering if my question is really stupid or a basic question that is obvious or my question don't make sense. I appreciate also any reply stating that or pointing me to a resource where I can find the answer.

    Thanks
    Adrian.

    Comment

    • kopi-o
      Senior Member
      • Feb 2008
      • 319

      #3
      No, it's not a stupid question, these issues are not straightforward.

      From Cufflinks output, you could use something like ASProfile and go from there. From Cuffdiff, you could take a look at CummeRbund and see if that fits.

      Check out this list of related software:

      Comment

      • adrian
        Member
        • Oct 2009
        • 90

        #4
        Thank you very much for your reply.

        it is frustrating to sift through 400 genes from isoforms.diff file and identify what exon arrangement is different between isoforms of each gene.

        Currently I am lining up junctions.bed and bam file in IGV which is a pain in eyes and confusing.

        Comment

        Latest Articles

        Collapse

        • kinpict.com
          Reply to 16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
          by kinpict.com
          The part about this topic feels surprisingly grounded, and the details on the page is the bit that made me slow down. I’d keep <a href="https://kinpict.com/">ai family photo generator</a> bookmarked for later.
          Today, 06:37 PM
        • 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,...
          10-30-2026, 06:46 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, 11-12-2026, 07:59 AM
        0 responses
        27 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 11-05-2026, 09:25 AM
        0 responses
        35 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 11-03-2026, 11:54 AM
        2 responses
        56 views
        0 reactions
        Last Post kinpict.com  
        Started by SEQadmin2, 10-28-2026, 09:57 AM
        0 responses
        175 views
        0 reactions
        Last Post SEQadmin2  
        Working...