Genomenon and BeginNGS:
The Promising Future of Newborn Screening

Improving infant patient outcomes by providing clinicians with powerful insight

The new BeginNGS™ program, based at the Rady Children’s Institute for Genomic Medicine (RCIGM), is a novel health care delivery system designed to screen newborns for genetic diseases and connect their doctors with effective treatment options. It will improve infant patient outcomes by providing clinicians with powerful insight on how these diseases form, and how to treat them, creating life-saving opportunities for patients and their families at very early stages.

PRESS RELEASE | Genomenon Partners with Rady Children’s Institute for Genomic Medicine on Newborn Screening by Next Generation Sequencing

Mastermind: The premier resource of BeginNGS


As part of our mission to curate the entire human genome, Genomenon will combine AI-powered organization and expert manual review to fully curate all the genes in the BeginNGS screening panel – genes tied to over 400 diseases – and provide RCIGM with a comprehensive, actionable dataset on the variants that are found to cause disease.


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Mastermind: The premier resource of BeginNGS

Genomenon’s essential role in curating actionable genomic information and making it easily accessible to these professionals is helping transform that goal into a reality.


Dr. Stephen Kingsmore, President & CEO, Rady Children's Institute for Genomic Medicine.
Dr. Stephen Kingsmore, President & CEO, Rady Children’s Institute for Genomic Medicine.

By screening for over 400 treatable conditions and providing treatment guidelines to doctors and other clinicians before symptoms start, BeginNGS is creating life-saving opportunities for patients and their families at very early stages. Genomenon is honored to play a part in this important mission.


Mike Klein, CEO, Genomenon
Mike Klein, CEO, Genomenon

PAPER | An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases

Latest Blog Posts

Read about Genomenon’s mission to curate the entire human genome, how we’re making that happen, and more about our partnership with BeginNGS

READ MORE ABOUT THIS PARTNERSHIP

PAPER | A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases

The World’s Most Comprehensive Source of Genomic Evidence


The World’s Most Comprehensive Source of Genomic Evidence

Meet the engine powering BeginNGS. Accelerate variant interpretation with immediate insight into the full text of millions of scientific articles. Prioritize your search results by clinical relevance and find what you are looking for 5-10 times faster


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