Opinion

Baylor Genetics Supports Bipartisan House Bill to Broaden Medicaid Access to Genomic Sequencing for Children who Meet Medical Criteria

In 2025, Baylor Genetics was named an official genetic testing partner of the Child Neurology Society.
Business Wire

Whole Exome Sequencing Market Research Report 2024-2034: Adoption in Clinical Diagnostics, Integration with AI and Bioinformatics, & Increasing Focus on Precision Medicine ...

DUBLIN--(BUSINESS WIRE)--The "Whole Exome Sequencing Market - A Global and Regional Analysis: Focus on Product, Workflow, Application, End User, and Country - Analysis and Forecast, 2024-2034" report ...
ascopubs.org

Concordance of somatic whole exome sequencing and germline genotyping of DPYD to screen for DPD deficiency.

NuGenA (Nurse Led Genetic Counselling and Awareness): A proof-of-concept to implementation of genetic counseling for HBOC in LMICs. Clinical features and occurrence of other cancers in patients with ...
EurekAlert!

Pediatric investigation review highlights the future of newborn screening with next-generation sequencing

Routine newborn screening (NBS) has transformed early disease detection. However, traditional biochemical tests limit the ...
Business Wire

GeneDx to Expand Access to Exome Testing for Pediatric Epilepsy Patients with New Partners

STAMFORD, Conn.--(BUSINESS WIRE)--GeneDx (Nasdaq: WGS), a leader in delivering improved health outcomes through genomic insights, today announced Biogen (Nasdaq: BIIB), Praxis Precision Medicines ...
GEN - Genetic Engineering and Biotechnology News

Simple Workflows for Complex Genomics: Expanding Clinically Relevant Findings with Enhanced Exomes

In this GEN webinar, Guilherme Yamamoto, MD, PhD, and Sevana Yaghoubian will present a novel whole-exome assay for detecting high-confidence variants across multiple applications.
Seeking Alpha

GeneDx Announces Data Demonstrating that Whole Exome and Genome Sequencing Report Fewer Variants of Uncertain Significance (VUS) than Multi-Gene Panel Testing Published in ...

STAMFORD, Conn., Aug. 21, 2023 (GLOBE NEWSWIRE) -- GeneDx, a leader in delivering improved health outcomes through genomic and clinical insights, today announced that Genetics in Medicine, the ...
Morningstar

Illumina whole-genome sequencing provides greater insight into genetic signals behind common diseases—according to Nature study

Study shows that rare variants captured by Illumina WGS with DRAGEN™ variant calling explain most of the "missing heritability" in complex human diseases and traits, including those related to blood ...
Baylor College of Medicine

Integrative exome sequencing and machine learning identify new genes contributing to systemic sclerosis risk

Systemic sclerosis (SSc) is a severe autoimmune disease with complex genetic causes. Some genetic contributors have been identified, but others remain unknown, which has impeded development of ...