WEBINAR DETAILS
  • About
    At SOPHiA GENETICS, we collaborate with genetic experts to develop specialized next-generation sequencing (NGS) applications that seamlessly integrate into any laboratory workflow. Today, our partners share how the analytical technology and dedicated features in the SOPHiA DDM™️ Platform have enabled the accurate detection and streamlined assessment of variants associated with Rare Diseases.

    Discover how the SOPHiA DDM™️ Platform successfully enabled the discovery of complex variants associated with genetic diseases using exome sequencing.

    This talk took place at on June 11th in Glasgow, UK at the European Society of Human Genetics (ESHG) Conference 2023.
  • Price
    Free
  • Language
    English
  • OPEN TO
    Everyone
  • Dial-in available
    (listen only)
    Not available.
FEATURED PRESENTERS
  • Webinar hosting presenter

    Dr. Berta Almoguera Castillo

    Researcher at the Genetics Department at Fundación Jimenez Díaz University Hospital, Madrid, Spain.
    My research interest focuses on the identification of the genetics basis of human diseases, with an emphasis on pediatric conditions, and the influence of genetics on drug responses.
    I have a bachelor degree in Pharmacy (by the Complutense...
    Full Profile
HOSTED BY
Powered by BigMarker