Complete Genomics, a U.S.-based innovator in genomic sequencing technology, today confirmed that it has entered into a definitive agreement, subject to customary closing conditions and approval by MGI ...
General Meeting 2026 in Orlando, FL, Volta Labs, a leader in next-generation sequencing (NGS) sample preparation automation, today announced the launch of the Callisto™ Complete Kit for DNA EF Library ...
Every living organism has its own genetic "blueprint": the source code for how it grows, functions and reproduces. This ...
In many countries, newborn screening programmes test babies for certain inherited conditions shortly after birth.
Element Biosciences created a high-throughput benchtop device that can deliver a whole genome for $100 – half the price of ...
SickKids helping to expand access to genomic using the C-GUIDE measurement tool in the iHope program
SickKids is providing the C-GUIDE™ tool evaluation of iHope's genomic testing for the diagnosis, care, and well-being ...
It is hoped screening babies’ DNA could detect hundreds more rare, treatable diseases in their first years of life ...
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Combining gene and biomarker screening for newborn health
For more than six decades, biomarker-based newborn screening has played a pivotal role in reducing infant mortality and ...
Discover how an ancient gene influences the sex of ant, bee, and wasp embryos, impacting conservation and breeding practices.
The Epstein-Barr virus (EBV) can cause certain types of cancer or autoimmune diseases, but how the body controls this common viral infection is largely unknown. Researchers at the University Hospital ...
A 10-year study shows that a multipronged approach using whole exome sequencing can improve diagnostic yield in patients with ...
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