next generation sequencing

Cutting-edge microfluidics enables full automation of NGS protocols.

Learn how nanopore sequencing improves the monitoring of infectious disease outbreaks.

A new protein sequencing technology paves the way for a better understanding of protein function.

Sequencing advances deliver comprehensive insights into how genomic variation drives cancer initiation and progression.

Using a library preparation kit optimized for cell free DNA (cfDNA) provides high quality data for early cancer detection.

Samples are commonly stored in a way that degrades RNA. Scientists are devising new ways to overcome this obstacle for RNA sequencing. 

Nanopore sequencing platforms provide researchers the freedom to rapidly sequence long microbial nucleic acid fragments in the field. 

As a trailblazer in rare disease research and treatment, Wendy Chung captures the big picture of rare disease genetics with the help of next generation sequencing.

Explore a cfDNA library preparation workflow that provides high yield and conversion to improve sensitivity and detection of low variant allele frequencies (VAF).

Proteins interact with DNA to regulate many vital processes in cells. Nearly 40 years ago, researchers developed a way to map these molecular connections.

Scientists employ an RNA exome panel for a targeted RNA-sequencing approach.

Gang Fang’s new metagenomics method helps sequence rare bacteria.

DNA barcoding is a fast sequencing-based technique that scientists use to catalog all life on Earth or perform high throughput bioanalyses.

Ten years ago, scientists put DNA barcodes in AAV vectors, creating an approach that simplified, expedited, and streamlined AAV screening. 

With nanoliter-scale reaction volumes, microfluidics-based real-time PCR (RT-PCR) devices speed up genomic analyses and library prep.

Scientists optimize PCR to ensure successful amplification and analysis.

A novel instrument simplifies and optimizes every sequencing step.

By monitoring disease biomarkers within wastewater, researchers gain insight into disease prevalence within communities.

Learn how researchers across health-related fields identify and characterize disease-causing genomic variants.