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New Database of Ethnically and Phenotypically Diverse Whole Genome Information
Tuesday, June 09, 2015
QIAGEN and Inova Translational Medicine Institute have announced the launch of Inova Genomes, a unique compendium of ethnically, phenotypically, and ancestrally diverse whole-genome sequencing data for researchers seeking to accelerate cohort analysis programs or improve success rates in diagnostic odyssey cases.

Manchester First to Adopt Congenica's Sapientia Technology for Clinical Service
Monday, June 08, 2015
Manchester Centre for Genomic Medicine becomes the first NHS genetics service in the country to use genome DNA sequence analysis supported by Sapientia, a technology developed by Cambridge, UK based Congenica.

Agilent Releases New Target-Enrichment Solutions for Disease Research
Friday, June 05, 2015
Products address current limitations of exome sequencing.

New Single-Cell T-cell Receptor Assay
Wednesday, June 03, 2015
New assay for immunology and immuno-oncology research available from Cellular Research.

Fluxion Biosciences and Swift Biosciences Announce New Workflow
Friday, May 29, 2015
Jointly developed next-generation sequencing workflow for somatic mutation detection from liquid biopsy samples.

EKF Diagnostics Highlighting Cancer Molecular Diagnostics Products at ASCO 2015
Thursday, May 28, 2015
New PrecisionPath™ NGS panel molecular test for colon cancer to be key focus on Booth #19141.

PrimePCR™ Assays Used to Create qPCR Reference Data for FDA-Led Sequencing Project
Tuesday, May 19, 2015
Biogazelle recently used Bio-Rad Laboratories’ PrimePCR Real-Time PCR Assays in a global analysis of NGS reproducibility that was published in Nature Biotechnology.

Kapa Biosystems Launches New RNA Prep Kit to Maximize Sequencing Efficiency
Tuesday, May 19, 2015
Ribodepletion kit boosts NGS throughput and data quality for more comprehensive view of transcriptome.

New Affordable Advanced NGS Cancer Test Launched by EKF Subsidiary
Saturday, May 16, 2015
Selah and GHS partner to pave the way for accessible, low-cost personalized medicine.

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Scientific News
DNA Damage Seen in Patients Undergoing CT Scanning
Along with the burgeoning use of advanced medical imaging tests over the past decade have come rising public health concerns about possible links between low-dose radiation and cancer.
Web App Helps Researchers Explore Cancer Genetics
Brown University computer scientists have developed a new interactive tool to help researchers and clinicians explore the genetic underpinnings of cancer.
New Research Advances Genetic Studies in Wildlife Conservation
‘Next-gen’ DNA sequencing of non-invasively collected hair expands field of conservation genetics.
Gene Testing Now Allows Precision Medicine for Thoracic Aneurysms
Researchers at the Aortic Institute at Yale have tested the genomes of more than 100 patients with thoracic aortic aneurysms, a potentially lethal condition, and provided genetically personalized care.
OGT’s Popular ESHG Workshop Free to View Online
Learn about the next generation of microarrays in one of the best attended workshops of the conference.
Discordant NIPT Test Results May Reflect Presence of Maternal Cancer
Results published in Journal of the American Medical Association.
Sperm RNA Test May Improve Evaluation of Male Infertility
To help resolve uncertainty—and guide prospective parents to the right fertility treatments—scientists propose the use of a new kind of fertility test. It involves examining sperm RNA by means of next-generation sequencing.
How the Mammoth Got its Wool
Evolutionary change in a gene reconstructed in the lab from the woolly mammoth was part of a suite of adaptations that allowed the mammoth to survive in harsh arctic environments, according to new research.
NuGEN Scientists Screen 400+ Genes for Fusion Events in Single Assay
Breakthrough proves efficacy of new sample preparation method that could accelerate cancer research and development of treatments and diagnostic tests.
More Accurate and Comprehensive Whole Genome Assembly
Scientists from the Icahn School of Medicine at Mount Sinai have developed a new approach to build nearly complete genomes by combining high-throughput DNA sequencing with genome mapping.
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