Scientists sequence hundreds of thousands of genomes for crucial large-scale research efforts, such as population genomics initiatives that process more than 10,000 samples per year, to explore ...

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 ...

UT researchers have developed the first viable alternative to a 75-year-old method for sequencing proteins. Image of amino acids, the building blocks of proteins. Scientists at The University of Texas ...

With the ongoing interest in the latest iteration of next-gen sequencing, we thought it would be a good time to take a look back at some early developments in the automated diagnostic DNA seqeuncing ...

Collaboration to leverage Oxford Nanopore's sequencing platform and Cepheid's GeneXpert system to advance the field of sequencing for infectious diseases OXFORD, United Kingdom and SUNNYVALE, Calif., ...

This automated application will enhance researchers' ability to analyze complex genomic variations with minimal hands-on time and additional benefits in cost, productivity, and consistency of results.

INTEGRA Biosciences and Parse Biosciences have partnered to automate single cell RNA sequencing (scRNA-seq) on the ASSIST PLUS pipetting robot. This new protocol combines Parse Biosciences’ Evercode™ ...

One in every 10 people worldwide is impacted by a rare genetic disease but about 50% of them remain undiagnosed despite rapid increases in genetic technology and testing. Even when a person does have ...

The purpose of the whole-genome sequencing module is to provide an overview of whole-genome sequencing and next-generation sequencing, including historical, technical and utilization perspectives. The ...