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
  • 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


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Free Trial


Applications included in the Lasergene Genomics Suite for Clinical Research

SeqMan NGen NGS Assembly Software

SeqMan NGen


Next-Gen Sequence Assembly
ArrayStar Multi-Sample Variation Comparisons

ArrayStar


Large-Scale, Multi-Sample Variation Comparisons
GenVision Pro

GenVision Pro


Genomic Visualization Software
Lasergene Molecular Biology Suite

Molecular Biology Suite


Essential Sequence Analysis Software

Technical Requirements


Windows 7 64-bit or higher

Mac OSX 10.9, 10.10, or 10.11

Linux Ubuntu 12.04*

Linux CentOS 7*
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*Linux operating systems are supported for SeqMan NGen only.

Next-Gen Software For All Major Sequencing Technologies