Next-generation sequencing (NGS) has transformed genomic research and healthcare by enabling the rapid and cost-effective sequencing of DNA and RNA, surpassing traditional techniques such as Sanger ...

The most comprehensive, family-based variant dataset ever published will improve variant classification using AI-based toolsMENLO PARK, Calif., Aug. 04, 2025 (GLOBE NEWSWIRE) -- PacBio (NASDAQ ...

Sanger sequencing continues to be an efficient and effective method for identifying known genetic variants, making it a good initial method for genetic tests. With resolution down to a single base ...

Discover the latest Sequencing Buyer's Guide. Compare platforms, technologies, and key features to find the best solution for your research or clinical needs.

Another exciting use for this method is in DNA barcoding, a way to tag proteins with tiny strands of DNA to track or analyze them. Until now, scientists couldn’t combine DNA barcoding with traditional ...

The study introduces a method for analyzing complex regions of the human genome using Paraphase and HiFi long-read sequencing. How does Paraphase improve genetic analysis?

Delve Bio presents data from the largest study of its kind showing the diagnostic yield of mNGS was greater than conventional test methods.

12. Zhu L, Huang Y, Fang X, et al: A novel and reliable method to detect microsatellite instability in colorectal cancer by next-generation sequencing. J Mol Diagn 20:225-231, 2018 13. Middha S, Zhang ...

Next-generation metagenomic sequencing test developed at UCSF proves its effectiveness in quickly diagnosing almost any kind of pathogen.

A decade-long effort has resulted in a new, rapid genomic test to diagnose rare infectious diseases in the brain and lungs.

Large-Scale Pharmacogenomics Analysis of Patients With Cancer Within the 100,000 Genomes Project Combining Whole-Genome Sequencing and Medical Records to Inform Clinical Practice The following ...