Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • blairw
    Junior Member
    • Feb 2015
    • 1

    #1

    How do you determine which a gene annotation is correct?

    Using the program Artemis, I have to get the annotation of one specific gene. I then have to do a blast search on other databases (Ecocyc, KEGG, etc.) and compare those results to Artemis (to see if the Artemis annotation is correct). If the databases do not give the same annotations for that gene, how do I decide which is correct (Artemis vs. the others)?

    Sorry if I used any of the incorrect terms, I'm an undergrad and a lot of this is new to me.
  • mastal
    Senior Member
    • Mar 2009
    • 666

    #2
    I'm not sure that you can determine which annotation is 'correct' without doing loads of additional work.

    You would have to consider the source of the annotations, and which you would consider to be more reliable - whether it is from a manually curated database, or from a computational gene-prediction pipeline, or a mixture of both, for example.

    Comment

    • GenoMax
      Senior Member
      • Feb 2008
      • 7142

      #3
      It is always better to start with protein sequence when you are working with an unknown gene sequence. Start with Swissprot/Uniprot/RefSeq (http://www.uniprot.org/blast/) to see if you are able to find a conserved domain (or something that looks like one) even if the rest of the sequence match is not great.

      Comment

      Latest Articles

      Collapse

      • SEQadmin2
        Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
        by SEQadmin2



        CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

        Despite this, “CRISPR helped turn genome editing from a specialized technique into
        ...
        07-31-2026, 11:01 AM
      • SEQadmin2
        Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
        by SEQadmin2


        Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

        The systematic characterization of the human proteome has
        ...
        07-20-2026, 11:48 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 08-13-2026, 12:22 PM
      0 responses
      18 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-11-2026, 10:35 AM
      0 responses
      16 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-06-2026, 07:41 AM
      0 responses
      32 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-03-2026, 10:13 AM
      0 responses
      50 views
      0 reactions
      Last Post SEQadmin2  
      Working...