Note that a "Commercial Services" license is required for organizations that use our software as part of an analysis pipeline that is provided as a service for others. Please request a quote for pricing and additional information.
DNASTAR's Lasergene Genomics Suite includes a full-spectrum of functionality for clinical research. Features include:
- Streamlined workflows for Mendelian and Cancer Gene Panels
- Access to DNASTAR's new human variant annotation database, which bundles together data from dbNSFP as well as 1000 Genomes and ESP's Exome Variant Server
- Powerful analysis and filtering capabilities for both prospective and retrospective studies
- #1 in accuracy for NGS alignment and variant calling
- Quick assembly of large data sets from all major next-gen technologies on a desktop computer
- Ability to identify variants using live, interactive views and comprehensive filtering tools
- The ability to perform large-scale comparisons of variants across individuals and groups of indivduals, and determine the level of disruption to each gene caused by the variants present
Request QuoteFree Trial
*Linux operating systems are supported for SeqMan NGen only.