A new study indicates that noninvasive prenatal screening (NIPS) performed using a low-cost form of whole genome sequencing ...
Geneticist Dr. Robert Green is sequencing the DNA of healthy newborns to find hidden disease risks. This knowledge can save lives — but gene sequencing is not a crystal ball.
Demonstrating faster, simpler, more cost-efficient NGS workflows that turn complex agrigenomics data into practical ...
The collection of high-quality genomic DNA remains a major barrier in pediatric and neurodevelopmental research, particularly ...
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 streamlined, automated process helps scientists coordinate site-ready production-level whole genome sequencing results.
Scientists and physicians can better assess precision genome editing technology using a new method made public today by St.
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