Clinical Research

Lasergene Genomics Suite for Clinical Research



Alert 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
  • Powerful analysis and filtering capabilities for both prospective and retrospective studies
  • The new best practice in NGS variant calling
  • Quick assembly of large data sets from all major next-gen technologies on a desktop computer
  • Ability to identify mutations using live, interactive views and comprehensive filtering tools
  • Direct connection to the dbNSFP, dbSNP, COSMIC and GERP databases
  • The ability to perform large-scale comparisons of SNPs across individuals and groups of individuals, and determine the level of disruption to each gene caused by the SNPs present

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Free Trial

Applications included in the Lasergene Genomics Suite for Clinical Research

SeqMan NGen

Next-Gen Sequence Assembly

SeqMan Pro

Next-Gen Assembly Analysis


Large-Scale, Multi-Sample Variation Comparisons


RNA-Seq, ChIP-Seq, and miRNA Analysis

Cloning Suite

Sequence Editing, Virtual Cloning, and Primer Design


Automated Sequence Editing


Publication-Quality Graphics

Technical Requirements

Windows 7, 8, or 8.1 (64-bit)

Mac OSX 10.7 or higher

Linux Ubuntu 12.04*

Linux CentOS 6.5*
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*Linux operating systems are supported for SeqMan NGen only.

Next-Gen Software
For All Major Sequencing Technologies