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  • Biotexcel
    Member
    • Jan 2015
    • 18

    #1

    Genomic Medicine 2017 Cambridge

    The Genomic Medicine 2017 Cambridge meeting on 26th & 27th September will cover areas where Next Generation Sequencing is used in the analysis of human disease. These topics will include different disease areas where particularly promising genomic studies have been performed, whole genome & whole exome studies, large population studies, epigenomics and many other topics.

    Speakers include:

    Prof Carlos Caldas, Cambridge Breast Cancer Research Unit
    Prof Eamonn Maher, University of Cambridge
    Prof David Van Heel, Blizard Institute
    Prof Stephan Beck, UCL
    Dr James Hadfield, CR UK
    Dr Serena Nik-Zainal, Sanger Institute
    Prof Lyn Chitty, UCL
    and more...

    We are still accepting poster submission so please do get in touch if you have some interested work to present.

    Hope you'll join us in Cambridge!!!

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    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
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