Next-Generation Sequencing – News and Features

Researchers found gene mutations through whole exome sequencing - a new gene scanning technology that cuts the cost and time of searching for rare mutations.

Focus on new testing systems for the rapid diagnosis of cancer and infectious diseases.

The acquisition of Illumina systems allows Ambry to expand its sequencing and genotyping capabilities.

The Latest SureSelect product to emerge from close collaboration with The Broad Institute.

IMGM Laboratories and the Center for Human Genetics and Laboratory Medicine will use the GS FLX System and GS Junior System for the joint development program.

Bioo Scientific chose Eureka Genomics based on their extensive sequencing experience, quick turnaround times and strong bioinformatics support.

NHGRI-supported researchers streamlined DNA sequencing strategies to find rare disease genes quickly.

New poster describes how Access Array™ chip technology has been used at NCI’s core facility to capture and sequence the entire EBV genome.

The Company will develop human isogenic disease models to predict the activity of potential therapeutic agents for the program.

Researcher can now have direct access to whole-genome processing previously found only inside genome centers.