Next-Generation Sequencing – News and Features

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.

Sandia self-assembly and atomic-layer deposition improve process fivefold.

Creation of the Illumina Genome Network will link researchers interested in conducting large-scale whole human genome sequencing projects using Illumina sequencing.

Study to evaluate gene identification ability to predict patient response and improve safety when dosing this anti-blood clotting drug.

INRA core facility is now providing a wide range of services on a Fluidigm BioMark™ System for Genetic Analysis to all European researchers.

Joint services offered for human exome targeted re-sequencing based on Roche NimbleGen format.

Study sheds new light onto the mysterious disease which has cause widespread damage to farmed salmon populations.