News & Articles

New whitepaper demonstrates how customizable, medically focused array designs complement NGS for clinical genetics research

From rapid TB diagnostics to genomic breakthroughs, this Lab Week spotlight reveals how a dedicated team in Djibouti is transforming public health — one test at a time

In this guest editorial from INTEGRA Biosciences discover how NGS has transformed genomic research since its initial development, broadening our understanding of genetic variation and gene expression

Population genetics sequencing panel incorporates global genetic variations for superior study of disease and target discovery

Learn how digital PCR is advancing cancer genetics research at Louisiana State University Health Sciences Center

Learn how a generics pharmaceutical company in the U.S. is simplifying chromatography data management for greater productivity

The head of molecular genetics at Munich Leukemia Lab highlights the benefits of sequencing automation to improve the success of leukemia therapy

A new method for screening the genomes of malaria parasites could help malaria programs select the best diagnostic tests

New product offers complete genome coverage and high accuracy for DeNovo assembling reference level genomes at a much lower cost to accelerate agricultural research

Discover the latest technology for the identification of structural variants (SVs) within the human genome

Study shows PacBio's HiFi long-read sequencing can identify genetic causes of rare diseases, potentially simplifying diagnostics

Highly accurate long-read sequencing data from Revio will support Germany’s National Genome Initiative and provide data to the International Male Infertility Consortium