Building a Better Picture of Cancer
Clinical labs are adopting broader cancer diagnostics—including whole-genome sequencing and multi-omic testing—to deliver more comprehensive molecular insights and improve disease monitoring.
Clinical labs are adopting broader cancer diagnostics—including whole-genome sequencing and multi-omic testing—to deliver more comprehensive molecular insights and improve disease monitoring.
The company is showcasing newly cleared tests and platforms for multiple myeloma, lung cancer, connective tissue disease, and other laboratory applications.
Seegene has launched the Global Million Clinical Study to collect real-world data on the clinical utility of syndromic PCR testing for infectious diseases, aiming to inform future global diagnostic standards.
The test utilizes genomic sequencing and AI to identify biological signals associated with early-stage disease.
Read MoreThe transaction includes subsidiaries in the United States, Sweden, and Australia to expand transplantation diagnostic offerings.
Read MoreResearch suggests new sequencing technologies can help labs move from tissue-level averages to cell-specific testing for precision exercise medicine.
Read MoreHerAnova Lifesciences presented validation data for HerResolve, a blood-based endometriosis test, showing 94.4% accuracy and detection of cases missed by imaging.
Read MoreRoche has launched AXELIOS 1, a single-molecule sequencing platform that uses sequencing by expansion technology to deliver same-day whole-genome results.
Read MoreThe agreement combines extraction and PCR technologies to create an end-to-end workflow for DNA and RNA analysis.
Read MoreThe new technologies address library normalization and amplification accuracy for high-throughput and oncology sequencing.
Read MoreThe whole-genome sequencing assay is now available for breast, colorectal, and renal cancers following new clinical study results.
Read MoreThe NCCN has updated its bladder cancer guidelines to include FDA-approved ctDNA-based MRD testing for post-surgical risk assessment and adjuvant immunotherapy decisions in muscle-invasive bladder cancer.
Read MoreThe point-of-care assay provides results in 15 minutes and received a waiver for use in decentralized settings.
Read MoreA study reports that an OpenAI reasoning model improved rare disease diagnostic yield by 4.8% in previously unsolved cases, offering new leads after specialist analysis.
Read MoreThe Fleming Initiative and Cepheid have launched a 30-month study in England to compare rapid molecular and traditional culture screening for drug-resistant carbapenemase-producing Enterobacterales in hospital settings.
Read MoreA study reports that long-read genome sequencing can replace up to 15 separate tests and improve diagnostic yield for rare genetic disorders, according to researchers in the Netherlands.
Read MoreThe NCCN has updated its guidelines to recommend cerebrospinal fluid-based molecular profiling for inoperable high-grade gliomas and glioblastomas, expanding indications for liquid biopsy in CNS cancer care.
Read MoreThe system uses routine blood draws to provide results in 17 minutes, offering an alternative to invasive diagnostic methods.
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