Next-Generation Sequencing – News and Features

The MALDI Biotyper has obtained the IVD-CE Mark, and is currently for Research Use Only outside of the European Union.

The sequence is reported in BioMed Central's open access journal, Genome Biology and provides insight into the evolutionary history of this distinct lineage.

HapMap 3 points the way forward for human genetics studies; results reported in Nature.

Genetic variant may increase susceptibility to migraine triggers.

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.