Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • archananraja
    Junior Member
    • Dec 2010
    • 3

    Gene Finding

    Hi All,

    I am trying to identify genes in a specific pathway from an unannotated draft genome assembly?
    Below are the details of what I have:
    1.I have identified orthologs for the genes of interest
    2.I have also identified the putative gene regions in my assembly


    Now,
    How do I identify gene duplicates and missing regions in my predicted gene?
    I am a little confused because I have a list of nearly 70 genes to identify.


    Any help would be greatly appreciated.
  • krobison
    Senior Member
    • Nov 2007
    • 734

    #2
    At the most basic, you'll want to use TBLASTN to search the protein sequences of your collection of pathway members vs. the contigs from the reference genome.

    Identifying which hits are really the same thing (but from incompletely assembled regions) and which are paralogs/pseudogenes will take a bunch of work. In some cases, mate pair/paired end information may be available to assist in inferring which contigs are near each other in the genome. Similarly, frameshifts and other sequencing/assembly errors are likely to be present & may require close inspection to distinguish biology from artifact.

    Ideally, you would have access to DNA from that genome & the resources to do some PCR & sequencing experiments to test hypotheses as to which fragments belong together.

    Comment

    • archananraja
      Junior Member
      • Dec 2010
      • 3

      #3
      Thanks

      Thankyou....Let me see how it goes.

      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, Yesterday, 05:37 AM
      0 responses
      6 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-26-2026, 11:10 AM
      0 responses
      16 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-17-2026, 06:09 AM
      0 responses
      51 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-09-2026, 11:58 AM
      0 responses
      110 views
      0 reactions
      Last Post SEQadmin2  
      Working...