Clinical Exome Sequencing to reporting
On Demand
1 hr 6 min
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Sequencing larger regions of the genome offers more information to clinicians looking for potential disease causing variants to help diagnose their patients. This webinar demonstrates the full workflow from sample to report generation covering, exome sequencing with MGI’s DNBSeq-T7, NGS data analysis and interpretation with VarSome Clinical, and Gencell's approach and experience using both.
Professor. Charles E. Chappel - Chief Scientific Officer @ Saphetor
Dr. Marcela Galvez - Medical & Scientific Director @ Gencell
Dr. Manuel Delpero - Bioinformatician @ MGI
