Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • Debu_013
    Junior Member
    • Jul 2013
    • 3

    Fusion or Chimeric gene discovery tools

    I browsed through a few fusion gene discovery tools like deFuse and SOAPfuse and found that they all have established a pipeline wherein they accept input as fastq and do the alignment with a tools like Bowtie2 or BWA and then do the down stream analysis.

    I have already generated alignments- SAM/BAM files using both STAR and Bowtie2.

    I wanted to know if there are any tools that I could now use to do downstream analysis of the data to find fusion genes.
  • kopi-o
    Senior Member
    • Feb 2008
    • 319

    #2
    FusionMap (http://www.omicsoft.com/fusionmap/#[[%283%29%20Options]]) is one program that does allow BAM/SAM input (although I have only used it starting from .fastq myself).

    I guess you need to be careful about how you map your FASTQ files initially to make sure that possible fusions are not filtered out. Perhaps that's why most packages do the mapping internally.

    Comment

    • Debu_013
      Junior Member
      • Jul 2013
      • 3

      #3
      I guess that is reasonable.
      By the way, in your experience which Fusion detection tool would you suggest?

      I was thinking of using deFuse or SOAPfuse and Tophat2.

      Comment

      • ndaniel
        Member
        • Feb 2009
        • 33

        #4
        Also FusionCatcher is very good and very easy to use! It found plenty of novel fusion genes!

        Finder of Somatic Fusion Genes in RNA-seq data. Contribute to ndaniel/fusioncatcher development by creating an account on GitHub.
        Last edited by ndaniel; 07-10-2013, 12:08 PM.

        Comment

        Latest Articles

        Collapse

        • 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
        • SEQadmin2
          From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
          by SEQadmin2


          Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


          The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
          ...
          06-02-2026, 10:05 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, 06-26-2026, 11:10 AM
        0 responses
        15 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-17-2026, 06:09 AM
        0 responses
        49 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-09-2026, 11:58 AM
        0 responses
        107 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-05-2026, 10:09 AM
        0 responses
        125 views
        0 reactions
        Last Post SEQadmin2  
        Working...