FDA Approves Companion Test to Identify Patients Eligible for New NSCLC Treatment
The test is approved to identify patients eligible for Hernexeos, an orally administered targeted treatment for HER2 (ERBB2)-mutant non-small cell lung cancer.
Category: Sequencing Systems
Sequencing Systems
Latest
Sequencing Systems
Latest
Thermo Fisher Scientific introduces One Lambda HybriType Assay
Thermo Fisher Scientific has launched the One Lambda HybriType HLA Plus Typing Flex kit, an NGS hybrid capture assay.
Sequencing Systems
Latest
OGT Launches Myeloid MRD Panel for Sensitive AML Biomarker Detection
OGT's SureSeq Myeloid MRD Panel offers a NGS solution for ultra-sensitive detection of MRD biomarkers in acute myeloid leukemia.
Illumina Launches New Series of Benchtop Sequencing Systems
Illumina’s new MiSeq i100 Series sequencing systems provide faster, simpler, and more cost-efficient next-generation sequencing solutions.
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Healthcare-Associated Infections Can Be Reduced with DNA Sequencing
Reducing the incidence of healthcare-associated infections, and the antimicrobial resistance they can trigger, is critical for patient care.
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NeoGenomics Launches New Sequencing Assay for Rapid Genetic Profiling of AML
The next-generation sequencing assay delivers rapid and comprehensive genetic profiling for AML patients, guiding precise treatment decisions.
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Breakthroughs in Diagnosing Colorectal Cancer with Rare Genetic Variants
A new study emphasizes the potential of advanced sequencing techniques in improving outcomes for CRC patients with rare genetic variants.
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Ambry Genetics Announces New Multiomic Exome Test for Improved Rare Disease Detection
Ambry Genetics unveiled a new multiomic exome sequencing test that incorporates RNA analysis to enhance the detection of rare diseases.
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GeneDx Announces Whole Genome Sequencing Product Enhancements to Accelerate Diagnoses
GeneDx announced enhancements to its whole genome sequencing services, all aimed at accelerating diagnoses and improving health outcomes.
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Baylor Genetics and Baylor College of Medicine Launch New Lab
Baylor Genetics and Baylor College of Medicine have launched the Medical Genetics Multi-Omics Laboratory to innovate genetic testing.
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Unlock Behind the Seizure Program Provides Testing for Pediatric Epilepsy
The Unlock Behind the Seizure program aims to provide accessible and affordable genetic testing for pediatric epilepsy patients.
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Whole Genome Sequencing Improves Pediatric Cancer Care
Whole genome sequencing has improved care for some children with cancer in England and can potentially replace multiple standard tests.
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Rapid Cerebrospinal Fluid Test Decreases Time for Brain Tumors Diagnosis
A new genotyping test using cerebrospinal fluid can rapidly diagnose brain cancers, reducing the need for invasive biopsies.
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Foundation Medicine Launches RNA Sequencing Test
Foundation Medicine launched a tissue-based RNA sequencing test in the U.S. for the detection of cancer-related fusions across 318 genes.Â
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AI-powered Microbiome Test Gets New Distribution Partner
Jona announced a new distribution partnership where practitioners can order Jona kits, the company’s AI-powered gut microbiome profile test.
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Researchers Discover Urine-Based Test to Detect Head and Neck Cancer
Researchers developed a urine-based test utilizing whole genome sequencing to detect DNA fragments released by head and neck tumors.
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Quest’s New Collaboration to Evaluate WGS for Developmental Delays
The collaboration seeks to demonstrate the value of WGS as a first-line genetic test for postnatal diagnosis of developmental delay disorders.
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Data-Processing Tool Could Support Early-Stage Cancer Detection
Researchers developed a platform for integrating DNA and RNA data from single-cell sequencing with improved speed and precision.
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