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Image-Pro Plus Version 6.0, Ingenuity Pathways Analysis 3.1, Benchware LibraryMaker 6.0, Benchware LibraryDesigner 2.4, Cellenger MVA, BioModels Database, Cate Sabatini, Don Listwin


Downloads & Upgrades

Media Cybernetics has released Image-Pro Plus Version 6.0. The latest version of the company's scientific image processing and analysis software includes support for Windows XP x64 operating systems as well as new analysis features, such as color management tools, the ability to classify more than 100,000 objects per image frame, and tools to export data via DDE to programs like Origin and Microsoft Excel.

Ingenuity Systems has launched Ingenuity Pathways Analysis 3.1, a web-based software application for analyzing biological mechanisms, pathways, and functions. The new release integrates with third-party and customer applications through dedicated APIs and supports Affymetrix's GeneChip Human Mapping 10K, 100K, and 500K arrays. The content in IPA 3.1 has also been updated, and currently contains 1.4 million biological findings. Trials are available at

Tripos has released Benchware LibraryMaker 6.0 and Benchware LibraryDesigner 2.4. Product enhancements include increased flexibility for handling compound-protecting groups and improved integration of third-party chemical sketchers, Tripos said. Benchware LibraryMaker's library-enumeration functionality is also being integrated into the company's Benchware Notebook electronic laboratory notebook.

Definiens has released Cellenger MVA, a multivariate image analysis software package for cell-based assays. Cellenger is a set of workflow tools and modular image analysis components. Cellenger MVA is expected to reduced attritions rate and liability risk, and identify more lead compounds with higher quality, the company said.

Release 4 of the BioModels Database is available from the European Bioinformatics Institute at The release includes six new models that represent 220 reactions, the biggest increase since the creation of the resource, according to EBI. The release also includes the qualification of annotations, following the recommendation of the MIRIAM standard.

People in the News

Iconix Pharmaceuticals has named Cate Sabatini as executive vice president of business development. Sabatini has held previous positions at Incyte, where she was the director of product development and vice president of customer relations Prior to Incyte, Sabatini was the manager of information systems at LSI Logic and a project manager for clinical systems at Syntex (Roche Group). Sabatini also founded Athena Consulting, where she worked with a number of life science companies, including Genentech, Applera, Iconix, and Align Technology.

GenoLogics Life Sciences Software has appointed Don Listwin its board of directors. Listwin most recently served as the president and CEO of Openwave Systems, a software provider for the communications industry. He also founded Canary Foundation, a non-profit organization dedicated to the early detection of cancer, in 2004. Listwin served as executive vice president of Cisco Systems for a decade before leaving the company in 2000.

Robert Tuttle has joined molecular diagnostic developer HistoRx as director of bioinformatics. Tuttle was previously group leader and bioinformatics systems manager at CuraGen. Prior to that, he held senior positions at TurboGenomics (now TurboWorx), and Gerber Scientific. Other recent new hires at HistoRx include Donna Marino, vice president of diagnostics, who most recently served as a principal at Genomic Healthcare Strategies; and Lorah Perlee, vice president of technical operations, who joins the firm from Protedyne, where she served as director of scientific applications.

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The Scan

Genetic Tests Lead to Potential Prognostic Variants in Dutch Children With Dilated Cardiomyopathy

Researchers in Circulation: Genomic and Precision Medicine found that the presence of pathogenic or likely pathogenic variants was linked to increased risk of death and poorer outcomes in children with pediatric dilated cardiomyopathy.

Fragile X Syndrome Mutations Found With Comprehensive Testing Method

Researchers in Clinical Chemistry found fragile X syndrome expansions and other FMR1 mutations with ties to the intellectual disability condition using a long-range PCR and long-read sequencing approach.

Team Presents Strategy for Speedy Species Detection in Metagenomic Sequence Data

A computational approach presented in PLOS Computational Biology produced fewer false-positive species identifications in simulated and authentic metagenomic sequences.

Genetic Risk Factors for Hypertension Can Help Identify Those at Risk for Cardiovascular Disease

Genetically predicted high blood pressure risk is also associated with increased cardiovascular disease risk, a new JAMA Cardiology study says.