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  • GeneTalk: a platform to find the second patient of its kind

    Hi folks,

    we started GeneTalk - a platform that is designed to find the second
    patient of its kind. If you are analyzing a human exome and filtered
    all your mutations down to a hand full of candidates you might wonder:
    Is someone out there analyzing another data set with exactly one of
    these mutations? Well, simply log in to GeneTalk and find out.
    If couldn't find a match, don't be sad. Just leave an annotation for
    your mutation and maybe, Doctor X will see your note just on the next
    day and contact you!

    Visit https://www.gene-talk.de and find the needle in the haystack of your NGS data!

Latest Articles

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  • seqadmin
    Advancing Precision Medicine for Rare Diseases in Children
    by seqadmin




    Many organizations study rare diseases, but few have a mission as impactful as Rady Children’s Institute for Genomic Medicine (RCIGM). “We are all about changing outcomes for children,” explained Dr. Stephen Kingsmore, President and CEO of the group. The institute’s initial goal was to provide rapid diagnoses for critically ill children and shorten their diagnostic odyssey, a term used to describe the long and arduous process it takes patients to obtain an accurate...
    12-16-2024, 07:57 AM
  • seqadmin
    Recent Advances in Sequencing Technologies
    by seqadmin



    Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.

    Long-Read Sequencing
    Long-read sequencing has seen remarkable advancements,...
    12-02-2024, 01:49 PM

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