Oncomine Dx Express Test Receives FDA Approval as a Companion Diagnostic
The FDA has approved Thermo Fisher’s Oncomine Dx Express Test on the Genexus Dx Integrated Sequencer as a companion diagnostic for ZEGFROVY.
The FDA has approved Thermo Fisher’s Oncomine Dx Express Test on the Genexus Dx Integrated Sequencer as a companion diagnostic for ZEGFROVY.
Researchers have developed a revolutionary method using DNA sequencing to rapidly and precisely measure metabolites critical for health.
Delve Bio's Delve Detect is a metagenomic sequencing test capable of quickly identifying over 68,000 pathogens from CSF.
A new study emphasizes the potential of advanced sequencing techniques in improving outcomes for CRC patients with rare genetic variants.
Read MoreAmbry Genetics unveiled a new multiomic exome sequencing test that incorporates RNA analysis to enhance the detection of rare diseases.
Read MoreGeneDx announced enhancements to its whole genome sequencing services, all aimed at accelerating diagnoses and improving health outcomes.
Read MoreBaylor Genetics and Baylor College of Medicine have launched the Medical Genetics Multi-Omics Laboratory to innovate genetic testing.
Read MoreThe Unlock Behind the Seizure program aims to provide accessible and affordable genetic testing for pediatric epilepsy patients.
Read MoreWhole genome sequencing has improved care for some children with cancer in England and can potentially replace multiple standard tests.
Read MoreA new genotyping test using cerebrospinal fluid can rapidly diagnose brain cancers, reducing the need for invasive biopsies.
Read MoreFoundation Medicine launched a tissue-based RNA sequencing test in the U.S. for the detection of cancer-related fusions across 318 genes.Â
Read MoreJona announced a new distribution partnership where practitioners can order Jona kits, the company’s AI-powered gut microbiome profile test.
Read MoreResearchers developed a urine-based test utilizing whole genome sequencing to detect DNA fragments released by head and neck tumors.
Read MoreThe collaboration seeks to demonstrate the value of WGS as a first-line genetic test for postnatal diagnosis of developmental delay disorders.
Read MoreResearchers developed a platform for integrating DNA and RNA data from single-cell sequencing with improved speed and precision.
Read MoreResearchers analyzed data from children who suffered from syndromic conditions and found a high incidence of overlapping genetic alterations.
Read MoreThe new suite of high-quality adapters, universal blockers, and library amplification primer mixes are designed for the AVITI System.
Read MoreThe system features full 24/7 run automation, flexibility for smaller and faster runs, high accuracy for germline applications, and more.
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