Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • lsantome
    Junior Member
    • Feb 2013
    • 8

    #1

    NGS data: append annotations from HGMD

    Hi all,

    Trying to give sense to the big amount of variants detected after exome sequencing, I was figuring out wether is it possible to append HGMD annotations to my VCF data in order to select only those with reported clinical impact.

    I've purchased a copy of HGMD pro.

    Thank you in advance,

    Best

    Luis
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    Have you tried to contact BioBase tech support? Since you are referring to a commercial product not many on this forum are likely to have access to HGMD pro.

    Comment

    • lsantome
      Junior Member
      • Feb 2013
      • 8

      #3
      Maybe I should do that, but I was confident to get a quickier answer in this forum.

      I'll try it!

      Thanks,

      Luis

      Comment

      • Aquarius
        Junior Member
        • Feb 2013
        • 2

        #4
        Hgmd

        If you purchased HGMD Professional download version you get the data and can work with e.g. VCF files. But not with the online version.

        Comment

        Latest Articles

        Collapse

        • 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
        • SEQadmin2
          New Genomics Technologies Take Aim at Long-Standing Limits
          by SEQadmin2


          Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

          We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
          ...
          09-28-2026, 10:25 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, Yesterday, 11:13 AM
        0 responses
        17 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, Yesterday, 10:48 AM
        0 responses
        18 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-15-2026, 10:52 AM
        0 responses
        36 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-14-2026, 05:39 AM
        0 responses
        42 views
        0 reactions
        Last Post SEQadmin2  
        Working...