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Single-Tube, Multiplex Amplicon Sequencing for Illumina® Platforms
Wednesday, November 12, 2014
Swift Biosciences, Inc. announced the launch of an early access program for Accel-NGS™ Amplicon Panels for use with Illumina Next Generation Sequencing (NGS) systems.

Quest Diagnostics Introduces BRCAvantage Plus™
Friday, November 07, 2014
First major service extension to the company's BRCAvantage™ BRCA1 and BRCA2 mutation test menu offers screening for five new non-BRCA genes shown to increase risk of inherited breast cancer.

Thermo Fisher Scientific Launches Industry’s Only End-to-End, NGS Genotyping Solution for Expanded Microbial Analysis
Tuesday, October 28, 2014
Ion 16S Metagenomics Kit leverages the Ion Torrent sequencing platform and Ion Reporter for seamless assessment of mixed bacterial populations.

Next Generation Sequencing Library Sample Preparation Kits
Monday, October 27, 2014
AMSBIO announces RapidSeq – new convenient and cost-effective library sample preparation kits for Next Generation Sequencing (NGS) research and diagnostic work.

Agilent Introduces Focused Exome Kit with Unparalleled Coverage, Speed, Flexibility for Disease Research
Monday, October 27, 2014
Solution Ideal for Both High-Throughput and Benchtop Next-Generation Sequencing Applications.

Agilent Introduces SureSelect Focused Exome Kit
Saturday, October 25, 2014
Solution ideal for both high-throughput and benchtop next-generation sequencing applications.

NIBMG Accelerates Oral Cancer Research Using DDN Storage
Friday, October 24, 2014
India’s first biomedical genomics institute relies on DDN’s exceptional performance and complete end-to-end file and object solution for big data ingest, processing, collaboration and archive.

DNA Sequencing Analysis Kits Added to HIPAA Compliant Maverix Analytic Platform
Monday, October 20, 2014
Highly scalable analysis solutions for large volumes of whole genome, exome, and targeted resequencing data.

Illumina Launches New Reagent Kits for HiSeq X Ten and HiSeq 2500 Systems
Saturday, October 18, 2014
Enhancements offer improved performance for high throughput sequencing.

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Showing Results 21 - 30 of 238
Scientific News
TAU Researchers Solve Disease Mystery Through Crowdfunding
Tel Aviv University researcher identifies novel genetic mutations through DNA sequencing of afflicted child and family.
A Gene That Shaped The Evolution Of Darwin's Finches
Researchers from Princeton University and Uppsala University in Sweden have identified a gene in the Galápagos finches studied by English naturalist Charles Darwin that influences beak shape and that played a role in the birds' evolution from a common ancestor more than 1 million years ago.
DNA ‘Cage’ Could Improve Nanopore Technology
Scientists at Brown University have designed a nanoscale cage that can trap a single DNA strand and allow before-and-after sequencing of the same DNA strand in research trials.
Epigenetic Signatures that Differentiate Triple-Negative Breast Cancers
Australian researchers have identified epigenetic ‘signatures’ that could help clinicians tell the difference between highly aggressive and more benign forms of triple-negative breast cancer.
New Techniques Reveal “Extreme” Gene Copy Range
New findings give scientists the first precise way to study places in the genome where the number of copies of a sequence varies widely from person to person.
New Software Analyzes Human Genomes Faster than Other Available Technologies
The new software will empower population scale genomic analysis.
Major Study Links Gene to Drug Resistance in Testicular Cancer
Researchers used a genetic technique called whole-exome sequencing to examine tumour samples.
Titin' Gene Mutations Will Help Identify Patients At Risk Of Heart Failure
A new study has identified genetic mutations that cause the heart condition dilated cardiomyopathy (DCM), paving the way for more accurate diagnosis.
Blood Test For Prostate Cancer
Vanderbilt team demonstrates that prostate cancer can accurately be detected by liquid biopsy.
Whole-Genome Sequencing Successfully Identifies Cancer-Related Mutations
UT Southwestern Medical Center cancer researchers have demonstrated that whole-genome sequencing can be used to identify patients’ risk for hereditary cancer.
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