Should Everyone Have Their Genome Sequenced at Birth?
Genomics England recently announced a pilot program of whole genome sequencing to screen for genetic diseases in 200,000 healthy seeming newborns.
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Search Results for: genetic testing
Gene Mapping: Multiplex Network Improves Diagnosis, Analysis of Rare Diseases
Researchers have developed a mulitiplex network that reveals underlying mechanisms of rare diseases for more accurate identification of genetic defects.
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Testing Kit Detects Gene Variants Linked to Cystic Fibrosis
Asuragen Inc. has launched a testing kit for research use that is designed to detect pathogenic variants in the CFTR gene that cause cystic fibrosis.
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Genomenon, Inozyme Pharma Partner to Advance Genetic Diagnosis for Rare Disease
A partnership between Genomenon and Inozyme Pharma will make variant data on ENPP1 deficiency available to genetic testing labs across the world.
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IVD System Helps Accelerate Molecular Diagnostics Growth
Thermo Fisher Scientific has expanded its diagnostics portfolio to support full qPCR assay development and testing workflow.
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