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BioInform s Licensing Roundup: March s Software and IT Deals

BioInform's Licensing Roundup: March's Software and IT Deals
Company Product Licensees
Software Advanced Chemistry Development ACD/Labs Online Carnegie Mellon University
CambridgeSoft Chem & Bio Office Suite WuXi PharmaTech (expansion of existing license)
Eidogen-Sertanty Target Informatics Platform National Center for Biotechnology Information
Genedata Expressionist, Phylosopher Bayer Healthcare
GeneGo MetaCore Berlex
InforSense KDE, In-Oracle Environment, TextSense, BioSense Windber Research Institute (expansion of existing agreement)
Ingenuity Systems Ingenuity Pathway Analysis Pritzker Neuropsychiatric Disorders Research Consortium, Sanofi-Aventis (expansion of existing agreement)
Nonlinear Dynamics Progenesis PF240 UCD Conway Institute of Biomolecular and Biomedical Research
Rosetta Biosoftware Rosetta Resolver Almac Diagnostics, FoxHollow Technologies
Spotfire DecisionSite Organon
Databases Aureus Pharma AurScope ADME Drug-Drug and GPCR databases Servier (renewal)
Integrated Genomics ERGO Danone's Daniel Carasso Center
IT Infrastructure Sun Microsystems Sun Grid Compute Utility Applied Biosystems (beta customer)

Filed under

The Scan

LINE-1 Linked to Premature Aging Conditions

Researchers report in Science Translational Medicine that the accumulation of LINE-1 RNA contributes to premature aging conditions and that symptoms can be improved by targeting them.

Team Presents Cattle Genotype-Tissue Expression Atlas

Using RNA sequences representing thousands of cattle samples, researchers looked at relationships between cattle genotype and tissue expression in Nature Genetics.

Researchers Map Recombination in Khoe-San Population

With whole-genome sequences for dozens of individuals from the Nama population, researchers saw in Genome Biology fine-scale recombination patterns that clustered outside of other populations.

Myotonic Dystrophy Repeat Detected in Family Genome Sequencing Analysis

While sequencing individuals from a multi-generation family, researchers identified a myotonic dystrophy type 2-related short tandem repeat in the European Journal of Human Genetics.