This image illustrates the typical steps in next-generation sequencing (excluding single-molecule sequencing methods). The process begins with isolating genomic DNA (a) and breaking it into short ...

In the United States, healthcare professionals classify a disease as rare if it affects fewer than 200,000 individuals. As of August 7, 2024, the U.S. population consists of just under 336.9 million ...

The ongoing Italian clinical and research FPG500 program is designed to tailor matched targeted therapies (MTTs) based on "biomarkers predictive of response identified by comprehensive genome profiling ...

Next-generation sequencing (NGS), especially long-read DNA sequencing, is transforming infectious organism detection by ...

As demand for high-throughput genomic profiling continues to grow, laboratories and research organizations face increasing pressure to maximize sample throughput The post Optimizing Sample Throughput ...

Variant detection of multiple genes from a single tumor sample requires high-throughput molecular testing. To meet this demand, targeted next-generation sequencing (NGS) panels are useful in clinical ...

The AutoNorm(TM) adaptive amplification technology transforming library preparation at leading genomics cores is now available in a 16-well format, purpose-built for labs running smaller sequencing ...

SAN FRANCISCO, Nov. 13, 2025 /PRNewswire/ -- The global next-generation sequencing market size is anticipated to reach USD 42.25 billion by 2033, growing at a CAGR of 18.0% from 2025 to 2033. The next ...

A major pitfall is that most next-generation sequencing assays fail to detect the underlying genetic mechanisms of SMARCB1 ...

Automated library preparation is critical for reducing errors, increasing repeatability, and reducing hands-on time, allowing researchers to generate sequence data from DNA more quickly. The CyBio ...