The collection of high-quality genomic DNA remains a major barrier in pediatric and neurodevelopmental research, particularly ...

A new study indicates that noninvasive prenatal screening (NIPS) performed using a low-cost form of whole genome sequencing can detect the risk in pregnant mothers of transmitting cytomegalovirus (CMV ...

An updated edition of the Nov. 18, 2025, article. Genomics is a broad and detailed study of genomes (an organism’s complete set of deoxyribonucleic acid or DNA). Recent scientific advances in this ...

Scientists and physicians can better assess precision genome editing technology using a new method made public today by St. Jude Children's Research Hospital. Significant amounts of time and resources ...

Michigan Tech's Genomic Sequencing Lab, part of the University's Health Research Institute, plays a leading role in tracking animal-borne illnesses in the Upper Peninsula region while also advancing ...

The Roundtable on Genomics and Precision Health hosted a public workshop to evaluate how evidence for genomic applications is gathered and assessed for clinical decision-making, reimbursement ...

An analysis of genetic data from over 900,000 people shows that certain stretches of DNA, made up of short sequences repeated ...

A streamlined, automated process helps scientists coordinate site-ready production-level whole genome sequencing results.

Up to 5% of Americans may carry genetic variants associated with cancer risk, according to a cross-sectional analysis.The ...