Genomics, Proteomics, & Metabolomics

|2 min read

Combining Laboratory Techniques Yields Wealth of Information About Deadly Brain Tumors

Even small tissue samples can yield additional insights into a tumor’s biology, immune interactions, and molecular pathways
Updated |2 min read

Introducing a New Single-Cell Multiomics Workflow for Sequencing-Ready Libraries in Less than 10 Hours

The new workflow enables scalable, high-throughput analysis of hundreds to thousands of single cells, advancing applications in cancer research, drug development, and precision medicine
|2 min read

Element Biosciences Accelerates Rollout of Direct in Sample Sequencing for the AVITI24™ Intelligent Multiomics System to Meet Growing Demand

Direct in sample sequencing, or DISS, is a high-demand and transformative technology that unlocks library-prep free research possibilities across a variety of new use cases
Available on Demand

Optimizing Genetic Health Risk Testing: The Power of Preanalytical Systems

Join Today’s Clinical Lab with experts from Targeted Genomics and DNA Genotek for an in-depth discussion on the role of Genetic Health Risk Tests (GHR) in advancing personalized healthcare, and how integrating sample collection devices validated for their analytical performance can enhance the reliability and accessibility of GHRs
Sponsored by
|3 min read

UK and European Experts Release Landmark Clinical Guidance for Breast Cancer Prevention

This new publication sets the standard, enabling more personalized and targeted breast cancer prevention and detection
|2 min read

Cepheid and Oxford Nanopore Technologies Partner to Advance Automated Sequencing-Based Solutions

Collaboration to leverage Oxford Nanopore's sequencing platform and Cepheid's GeneXpert system to advance the field of sequencing for infectious diseases
|4 min read

Minimally Invasive Approach Could Change Standard of Care for Normal Pressure Hydrocephalus

New treatments are moving away from open surgery and toward minimally invasive techniques
|1 min read

The Missing Factor in Reliable Sequencing: Fragmentation Control

Small changes in fragmentation lead to significant shifts in data quality. See the comparison
Sponsored by
|2 min read

We Must Not Ignore Eugenics in Our Genetics Curriculum, Says Biology Professor

Professor Mark Peifer explains why understanding the history of eugenics is critical for up-and-coming scientists
|2 min read

A Smoother Path From Sample To Sequencing

With whole genome sequencing gaining traction in clinical labs, consistent sample prep is more important than ever
Sponsored by
|2 min read

Belay Diagnostics Partners with GenomOncology to Support High-Performance Liquid Biopsy Test for Central Nervous System Cancer Detection

The customized solution enables the team to make informed variant interpretations and treatment recommendations
|2 min read

Revvity Expands Alliance with Genomics England to Drive Research into Newborn Genomic Sequencing in England

New agreement to support newborn health adds sequencing lab services to the existing extraction services collaboration
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