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Exco InTouch launches Gather™
Tuesday, January 26, 2016
A revolutionary new product suite which supports patients, sites and sponsors throughout the clinical journey.

Visual Assay to Address Data Reproducibility, Integrity at SLAS 2016
Wednesday, January 20, 2016
Presentation to focus on using mobile devices in lab to capture & share data in real time.

Titian Software Launches Mosaic SampleBank™
Tuesday, January 19, 2016
Company offers a simple route to sample management best practice.

BioDiscovery Releases Nexus Copy Number 8.0
Thursday, January 14, 2016
Software with cutting-edge features like estimation of copy number and allelic events from NGS data.

University of Lyon Researchers Leverage ACD/Percepta in Search of Green Rocket Fuel
Wednesday, January 13, 2016
Software solution provides deeper understanding of new chemicals and their impact on the environment.

Illumina Extends Genomics Portfolio
Tuesday, January 12, 2016
MiniSeqTM sequencing system makes Illumina NGS accessible for every laboratory.

NanoOK: Quality Control for Portable, Rapid, Low-Cost DNA Sequencing
Monday, December 21, 2015
Scientists at TGAC have been putting Oxford Nanopore’s MinION sequencer through its paces with an open-source, sequence alignment-based genome analysis tool called ‘NanoOK’.

MorphoSys Deploys Dotmatics’ Vortex to Accelerate Antibody Research
Friday, December 18, 2015
Dotmatics’ Vortex will enable MorphoSys to rapidly analyse and visualise their screening data, informing the decision-making process.

Exco InTouch Announces the Demonstration of Equivalence for EQ-5D-5L
Friday, December 11, 2015
ScHARR completes independent, scientific, peer reviewed study, funded by Exco InTouch, comparing EQ-5D-5L equivalence across mobile phone and paper administration modes.

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Scientific News
New Database for Sharing MS Clinical Trial Data
A new database containing nearly 2500 patient records from the placebo arms of nine multiple sclerosis (MS) clinical trials is now available for research by qualified investigators.
‘Precision Prevention’ for Colorectal Cancer
New risk prediction model — not yet ready for clinical use — incorporates genetic, lifestyle and environmental risk factors.
Characterizing Cancerous Genomic Variations
Tested on large tumor genomics database, REVEALER method allows researchers to connect genomics to cell function.
Uncovering Hidden Genomic Alterations that Drive Cancers
Tested on large tumor genomics database, REVEALER method allows researchers to connect genomics to cell function.
Spotting DNA Repair Genes Gone Awry
Ludwig researchers develop a two-pronged approach for identifying genes responsible for fixing DNA damage that can trigger cancer when compromised.
Interpreting “Dark Matter” DNA
Scientists at the Gladstone Institutes have invented a new way to read and interpret the human genome.
A Programming Language for Living Cells
New language lets researchers design novel biological circuits.
The Epigenetics of Childhood Cancer
Qlucore software enables researchers to more easily study the genetic influences behind childhood cancer.
Mining Whole Exome Data to Improve Cancer Therapies
New tool interprets the raw data of whole exome tumor sequencing and then matches the cancer’s unique genetics to FDA-approved targeted treatments.
Pittcon 2016: Accelerating Innovation And Enhancing Productivity With Technology
Collaboration and externalization of data highlight evolving lab operations.
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