In a clinical laboratory setting, a robust framework for quickly and accurately detecting and reviewing new publications is essential for the successful interpretation of CNVs and sequence variants - and can significantly impact patient care.

In our upcoming live webinar, Kai Lee Yap, PhD, FACMG from Lurie Children’s Hospital and Genomenon’s Brittnee Jones, PhD will discuss a variety of real-life clinical cases that illustrate how the Mastermind Genomic Search Engine is increasing patient diagnoses for rare pediatric germline conditions that may otherwise go uncovered. Register now to join the conversation!

Overcoming Challenges of CNV and Sequence Variant Interpretation in the Clinical Lab

 

 

THURSDAY, JULY 21, 2022 | 11am EDT

EVENT SPEAKERS Kai Lee Yap, PhD, FACMG Director of Molecular Diagnostics, Ann & Robert H. Lurie Children’s Hospital of Chicago Kai Lee is the Director of the Lurie Children's Molecular Diagnostics Laboratory. Her clinical expertise lies in the genetic diagnosis of pediatric constitutional disorders and childhood malignancies.

Brittnee Jones, PhD Director of Customer Success, Genomenon With over a decade of experience in clinical NGS applications, from assay development to enterprise software implementation, Brittnee’s genomics expertise ensures Mastermind users get the most out of the software.

 

 

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About Genomenon
Genomenon is an AI-driven genomics company that organizes the world’s genomic knowledge to connect patient DNA to scientific research in the diagnosis and development of treatments for patients with rare genetic diseases and cancer.

For more information, visit Genomenon.com