Scientists

Better understand the biology of targets and compounds with a genomic reference

Integrate, extract, map, query, compare sequence and annotation data in genomic contexts

Simplify research projects by accessing powerful, easy-to-use analysis tools that facilitate complex workflows involving vast amounts of disparate data

Benefit from a shared repository of knowledge and work performed by colleagues and collaborators on expression and pathways analysis, splice variant and ortholog detection, and more Simplify integration of licensed data sources (Incyte, Celera, Derwent Patent DB, etc.) to maximize value

Informaticists

Design, adapt and expand workflows to manage the scheduled acquisition and integration of public sequence data behind your firewall

Create high-throughput pipelines for Sequence Mapping, Data Extraction and Complex Genomic Data Analysis.

Create proprietary gene models based on complete in-house knowledge

Collect, manage and integrate large data sets (public, proprietary and licensed) to be presented in a customized manner to scientists.

Support for Sun Grid Engine Distributed Compute Clusters for high speed genomic sequence mapping.

Perl API facilitates the creation of custom workflows and analysis pipelines

Comprehensive set of generic Perl scripts turbo-charge data integration, extraction and genome analysis.

Simplify integration of licensed data sources (Incyte, Celera, Derwent Patent DB, etc.) to maximize value

Research Executives

Increase return on investment by monitoring research projects and controlling information critical to decision making about target and compound selection to make the most of research budgets

Eliminate redundancy and increase productivity by sharing and managing data and research projects across functional research groups, collaborators and geographical sites

Generate and evaluate novel IP by merging and leveraging in-house, licensed and public data sources in a common environment