Live webinar 'Implication of Next Generation Sequencing in Molecular Diagnosis of Cancer' on 28 September 2016.
In this webinar we will discuss the implications of next generation sequencing based tests in multi-gene testing. We will also show how NGS based tests help to identify copy number variations, split read analysis and breakpoint identification. Finally, we will show a brief glimpse of Indian cohort data, where NGS based tests have shown improved mutation detection. In this webinar, we will present clinical case studies in on Hereditary Breast and Ovarian Cancer (HBOC) and Retinoblastoma patients to demonstrate how CNV analysis in Strand NGS enables researchers to detect and visualize copy number changes ranging from single exon to full gene.
Session 1: 2:30 PM IST
Session 2: 10:00 PM IST
Registration : http://www.strand-ngs.com/webinar_registration
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