Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • angerusso
    Member
    • Oct 2011
    • 47

    #1

    how to look for known fusion in fastq file

    Hello:

    I have an internal data for NCI-h660 file with 8m mapped pairs (HiSeq, 50bp paired end data) and I have an external dataset (4m mapped pairs, 50 bp paired end generated on GAII).

    Questions:
    1. I observe TMPRSS2-ERG fusion with external dataset, not with internal data from HiSeq. What could be the reasons? I use tophat2 fusion with same parameters for both the datasets.

    2. How can I investigate the FASTQ file to see if this fusion is present. The sequence of ERG-TMPRSS2 fusion is as mentioned here:


    3. Does this mean we need more data generated internally to find the same fusion?
    I use the following possible thresholds that are the minimum possible:

    tophat-fusion-post -p $np --skip-read-dist --num-fusion-reads 1 --num-fusion-pairs 1 --num-fusion-both 2 $index

    Any help will be greatly appreciated!! Thanks.
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    You have 2x the reads in internal dataset yet can't find the fusion (how many reads are supporting that observation in the external dataset?). Have you considered the possibility that one of these two data sets may be not what they are supposed to be?

    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...
      Yesterday, 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
    26 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-28-2026, 09:51 AM
    0 responses
    17 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-22-2026, 11:13 AM
    0 responses
    71 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...