Newborn Screening System Uses Rapid Whole Genome Sequencing to Diagnose Genetic Diseases
Researchers developed a prototype for newborn screening that includes the diagnosis of genetic diseases by rapid Whole Genome Sequencing.
Read MorePosted by Andy Lundin | Aug 25, 2022 | Molecular Diagnostics |
Researchers developed a prototype for newborn screening that includes the diagnosis of genetic diseases by rapid Whole Genome Sequencing.
Read MorePosted by Andy Lundin | Aug 25, 2022 | Cardiovascular |
Researchers found that a novel blood test can be used to easily evaluate disease severity in patients with pulmonary arterial hypertension.
Read MorePosted by Chris Wolski | Aug 22, 2022 | Covid 19 |
The S-Gene dropout is a critical means for helping identify variants in SARS-CoV-2, and how they will be identified in the future.
Read MorePosted by Andy Lundin | Aug 19, 2022 | Prostate |
Men at the highest risk for prostate cancer could be fast-tracked for investigation if their genetic risk was considered in general practice.
Read MorePosted by Andy Lundin | Aug 18, 2022 | Dementias & Alzheimer’s |
A new study identified multiple new risk genes for Alzheimer’s disease and a rare, related brain disorder through new testing methods.
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