Agilent Magnis NGS Automated Library Preparation System

Magnis Automated NGS Library Preparation System Diagnostech is excited to announce the Agilent Magnis Automated NGS library preparation platform! The adoption and implementation of Next Generation Sequencing (NGS) in both clinical and research laboratories has seen significant progress in the past several years. The use of massively parallel sequencing allows us to study and better…

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Agilent on Reproductive Genetics

Agilent Technologies Extends Collaboration on Reproductive Genetics New Two-Year Agreement with Belgian University to Focus on Detecting Genetic Abnormalities in Cell-free DNA and Embryo Biopsies   Agilent Technologies Inc.today announced that it is extending its collaboration with the Centre for Human Genetics of the University of Leuven and the University Hospital of Leuven in Belgium.…

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Diagnostech Cloning Promotion

Agilent Cloning 3 for 2 promotion We’ll get you stocked up and ready to go with our 3 for 2 promotion. Buy three of the same listed items, and we’ll give you the third one FREE! Promotion runs for October 19th to November 22nd 2017.    The items below are covered by the promotion.  …

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New High-Sensitivity NGS Target Enrichment Solution

Agilent Technologies Introduces New High-Sensitivity NGS Target Enrichment Solution New Solution Streamlines Workflow and Eliminates Sequencing Errors SANTA CLARA, Calif., July 17, 2017 Agilent Technologies Inc. today introduced its newest next-generation sequencing (NGS) library prep solution — Agilent SureSelectXT HS — a complete target enrichment research solution that provides total workflow management for laboratories, from QC…

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Agilent expands Data Processing offering for Molecular Pathology

We are proud to be associated with the new products and developments from Agilent Technologies. In their most recent article on their blog, they feature the release of the Cartagenia Bench Lab, designed to help laboratories involved in clinical genetics and molecular pathology efficiently interpret and report on genomic variants. Read the full article below…

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