Demonstrating faster, simpler, more cost-efficient NGS workflows that turn complex agrigenomics data into practical ...

Geneticist Dr. Robert Green is sequencing the DNA of healthy newborns to find hidden disease risks. This knowledge can save ...

NIH funding has allowed scientists to see the DNA blueprints of human life—completely. In 2022, the Telomere-to-Telomere Consortium, a group of NIH-funded scientists from research institutions around ...

A new study indicates that noninvasive prenatal screening (NIPS) performed using a low-cost form of whole genome sequencing ...

Scientists and physicians can better assess precision genome editing technology using a new method made public today by St.

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

Genetic variants that cause rare disorders may remain elusive even after expansive testing, such as exome sequencing. The diagnostic yield of genome sequencing, particularly after a negative ...

Biology has always been an unruly science. Cells divide when they want to. Genes switch on and off like temperamental lights.

A reduced genome in an island species raises evolutionary questions.