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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
    Essential Discoveries and Tools in Epitranscriptomics
    by seqadmin




    The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
    Yesterday, 07:01 AM
  • seqadmin
    Current Approaches to Protein Sequencing
    by seqadmin


    Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
    04-04-2024, 04:25 PM

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