Emerging Diagnostic Modalities & Innovation

|5 min read

Breast Cancer Remains the Most Common Cancer in Women, with Cases Projected to Exceed 3.5 Million by 2050

Six modifiable risks drive over a quarter of healthy years lost to breast cancer
|4 min read

Digital Pathology Market Continues to Battle Low Adoption, High Costs

Analyst Imogen Fitt highlights vendors that are pushing boundaries with new digital pathology business models
|3 min read

Direct-to-Consumer Gut Microbiome Testing Kit Results Vary Between Kits and Manufacturers

The accuracy of gut health tests remains uncertain and no study has systematically evaluated their performance until now
|3 min read

Researchers Develop New Laser Technique to Test mRNA-Based Therapeutics

Deep-UV Raman technology enables precise mRNA measurement with minimal lipid interference
|2 min read

Noninvasive ‘Fragmentome’ Test Expands Liquid Biopsy to Liver Cirrhosis and Other Conditions

The assay builds on the clinical potential of liquid biopsy platforms and could expand this technology’s utility to detect conditions besides cancer
|3 min read

AI Adoption and Evolving Leadership in Clinical Laboratories

Explore the transformative impact of artificial intelligence on executive hiring and its role in the future of lab operations
|3 min read

Blood Test Predicts Which Bladder Cancer Patients May Safely Skip Surgery

Positive results from the RETAIN-2 trial demonstrate that a response-adapted bladder-preservation approach involving neoadjuvant chemoimmunotherapy can be considered in select patients
|1 min read

Standardizing Oncology Assays: A Guide to Cell Line-Derived Reference Materials

Identify the limitations of patient tissue controls in genetic testing and examine the verification data supporting cell line-derived standards
Sponsored by
|1 min read

Move Past the Limitations of Synthetic Reference Standards in Cancer Research

A review of cell line-derived reference standards for the investigation and molecular profiling of myeloid malignancies
Sponsored by
|3 min read

FDA Fast-Tracks Ultra-Rare Therapies with Plausible Mechanism Guidance

Framework enables approval of individualized genome editing and RNA-based treatments when traditional trials aren’t feasible
|1 min read

Labcorp Expands Digital Pathology Rollout with FDA-Cleared PathAI Platform

Nationwide deployment of AISight® Dx aims to support fully digital workflows and AI-assisted diagnostics across anatomic pathology labs
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