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GENOMICS UNLOCKED

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Dive deep with us into the fascinating world of genomic science. Experience the revolution of genomics applications through a series of webinars driven by top scientists.

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Harnessing Ai for Precision Medicine

Speakers

Luciana De Cesare

Luciana De Cesare

LEE Chee Yang

Lee Chee Yang

Reshma Suresh

Reshma Suresh

Harnessing Ai for Precision Medicine

18 sept. 2024

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Join us for an insightful webinar where we delve into the latest advancements in precision oncology, featuring industry-leading experts from Agilent, Genoox, and MGI.

Discover how Agilent's SureSelect CGP Panel, integrated with Genoox's Franklin AI platform and MGI's cutting-edge DNBSEQ™ technology, is transforming the landscape of genetic analysis. Luciana De Cesare, Field Application Scientist at Genoox, will demonstrate how Franklin simplifies variant analysis and interpretation, providing actionable insights for both germline and somatic NGS data. Chee Yang, Senior Field Applications Scientist at Agilent, will explore the innovative SureSelect Cancer CGP portfolio, highlighting its capabilities in detecting critical somatic alterations and emerging biomarkers.

Reshma Suresh, Product Manager at MGI, will introduce the versatile DNBSEQ™ technology, showcasing its applications in sequencing. Attendees will gain practical knowledge on leveraging these technologies for comprehensive tumor profiling, enhancing their genomic research and clinical outcomes.

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Making the implementation of monogenic hereditary diseases diagnosis easy Speaker details but you dont need to include this in the description Dr. Paula Sancho Salmerón, PhD, Product Manager GeneSystems @Sistemas Genómicos
Comprehensive Molecular Tumour Analysis (CMTA) integrates RNA-seq and the Tumour Microenvironment (TME) for targeted therapy Speaker, Dr. Marie-laure Yaspo
Population-based surveillance for inherited disorders Speaker, Dr. Davide Cacchiarelli

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All your greatest webinars and expert speakers at the tip of your fingers.

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  • Comprehensive Molecular Tumour Analysis (CMTA) integrates RNA-seq and the Tumour Microenvironment (TME) for targeted therapy Speaker, Dr. Marie-laure Yaspo
    The Advantage Of Using DNBSEQ Technology​ | ESHG 2024, Speaker, Dr. Samantha Mendonsa
    Transforming Clinical Diagnostics, DNBSEQ-T7: Your gateway to Whole Genome Sequencing
    Closing the Cancer Care Gap with the Power of Precision Oncology
    Building the Largest Database of Human Microbiomes
    OncoPanels with DNBSEQ
    Immune Repertoire Profiling with DNBSEQ
    Comprehensive Molecular Tumor Analysis (CMTA) integrating RNAseq and TME for targeted therapy
    Harnessing The Power of Genomics
    Whole Exome Sequencing with DNBSEQ
    Clinical Exome Sequencing to reporting

Explore MGI's Blog

Complete Human Y to ask more "Why" in biology

Unravel the enigma of the human Y chromosome with MGI's latest insights. Discover how the Telomere-to-Telomere (T2T) consortium's milestone study deciphers the complete genomic sequence of Y, correcting GRCh38 errors and uncovering over 30Mb of new sequence data. Explore how advancements in sequencing technologies—combining short and long reads—illuminate the chromosome's intricate structures and ampliconic gene families. Dive deep into the implications for evolution, sex determination, and the ever-expanding questions in the Omic-verse of Biology.

Author: Weilin Liu Senior Field Application Scientist MGI
Date: 09-01-23
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