BeginNGS Archives

Media Coverage
September 12, 2023

How Rapid Whole Genome Sequencing Can Change the Rare Disease Game for Every Newborn

FIERCE Healthcare

FIERCE Healthcare: The rare disease journey can be long and difficult. rWGS could offer newborns a greater chance of successful diagnosis and intervention at birth.

Media Coverage
September 8, 2023

Dr Stephen Kingsmore Describes the Participants of the BeginNGS Consortium

AJMCtv

Dr. Stephen Kingsmore explains how the BeginNGS consortium members help the project to continually evolve.

Media Coverage
August 29, 2023

Dr. Stephen Kingsmore Highlights Disparities Seen in Genetic Testing

AJMCtv

AJMCtv: Stephen Kingsmore discusses the types of disparities seen in genetic testing as the BeginNGS phase 2 clinical trial is underway.

Media Coverage
August 14, 2023

Interview with Patricio A. Frias, President and CEO of Rady Children’s Hospital – San Diego

Becker's Healthcare Podcast

Becker's Healthcare Podcast: RCHSD President and CEO Patricio A. Frias shares the exciting innovative research being conducted at Rady Children's Institute for Genomic Medicine.

Media Coverage
August 14, 2023

Dr Stephen Kingsmore Discusses Rapid Diagnostic Genome Sequencing Program for Newborns

AJMCtv

Stephen Kingsmore, MD, DSc, president and CEO, at Rady Children's Institute for Genomic Medicine, shares details of the BeginNGS newborn screening program and its future goals.

Media Coverage
August 3, 2023

Rady’s newborn screening program prepares to expand

San Diego Union-Tribune

SAN DIEGO UNION-TRIBUNE: Rady Children’s hospital has set its sights on expanding the use of a screening test that it says can detect 411 genetic disorders in newborns.

Press Releases
July 10, 2023

Rady Children’s Institute for Genomic Medicine Launches Phase 2 of BeginNGS Program for Identifying Treatable Genetic Diseases for Newborns

During its first year, the BeginNGS newborn whole genome sequencing program welcomed 22 founding members, completed its first phase, and launched next-phase screening for 31 additional genetic disorders.

Media Coverage
March 28, 2023

The doctor will see your phone now: Sequencing and speedy diagnosis give chance of timely care

New Zealand Doctor

NEW ZEALAND DOCTOR: In this cover story, journalist Alan Perrott grills a leader in genome sequencing and artificial intelligence on the future of healthcare.

Media Coverage
March 13, 2023

England’s National Health Service to Offer Widespread Rapid Whole Genome Sequencing for Children and Babies

Dark Daily

DARK DAILY: Research in the UK and US into how rapid WGS can prevent deaths and improve outcomes for kids with rare genetic diseases may lead to more genetic testing based in local clinical laboratories.

Press Releases
February 9, 2023

Study Finds Association of Genetic Disease and Infant Mortality Higher Than Previously Recognized: 41% of Infant Deaths Associated with Genetic Diseases

Rapid, Diagnostic Whole Genome Sequencing May Have Prevented Deaths in Some Cases

News Center Archives

About us

Tag: BeginNGS

How Rapid Whole Genome Sequencing Can Change the Rare Disease Game for Every Newborn

Dr Stephen Kingsmore Describes the Participants of the BeginNGS Consortium

Dr. Stephen Kingsmore Highlights Disparities Seen in Genetic Testing

Interview with Patricio A. Frias, President and CEO of Rady Children’s Hospital – San Diego

Dr Stephen Kingsmore Discusses Rapid Diagnostic Genome Sequencing Program for Newborns

Rady’s newborn screening program prepares to expand

Rady Children’s Institute for Genomic Medicine Launches Phase 2 of BeginNGS Program for Identifying Treatable Genetic Diseases for Newborns

The doctor will see your phone now: Sequencing and speedy diagnosis give chance of timely care

England’s National Health Service to Offer Widespread Rapid Whole Genome Sequencing for Children and Babies

Study Finds Association of Genetic Disease and Infant Mortality Higher Than Previously Recognized: 41% of Infant Deaths Associated with Genetic Diseases

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