The Genomes2People Research Program (G2P), led by Robert Green at Brigham and Women’s Hospital, the Broad Institute, Ariadne Labs, and Harvard Medical School, conducts research to accelerate the implementation of genomic medicine and the promise of precision health. In his talk, "The Path to Universal Newborn Sequencing," Dr. Green discusses the latest advancements in genomics research and the promise it holds for personalized and preventive medicine, drawing on his work leading the MedSeq and BabySeq projects.
Throughout his talk, Dr. Green highlights the progress made by the MedSeq and BabySeq projects in advancing our understanding of genomics and its application to clinical care. MedSeq explored the use of whole genome sequencing in primary health care and cardiology specialty care, while BabySeq focuses on the use of genomic sequencing as screening in newborns. In its current phase, BabySeq is enrolling 1,000 families from diverse populations and using whole genome sequencing as screening to assess clinical utility and cost effectiveness.
Dr. Green discusses how the insights gained through these projects are paving the way for a more personalized and preventive approach to medicine. He emphasizes the importance of integrating genomic data into clinical care and the need for policies and guidelines to ensure that this is done in an ethical and responsible manner.
Through rigorous scientific research, G2P is establishing a foundation of evidence for genomic medicine that will accelerate the adoption of novel genomics-based technologies and hasten the day when illness is not just treated, but prevented.
Level of Instruction: Intermediate
Only the live session qualifies for CEUs but when possible, we host the recordings on our website and NSGC recommends participants to use their personal email instead of work email addresses to ensure they receive their CEU certificates.
Ambry Genetics is approved as a provider for continuing education program by NSGC and ASCLS P.A.C.E ® Program.