DNASTAR Solutions
SeqMan NGen is a High Accuracy NGS Assembler:  Assessment with NA12878 Reference Materials

 

Cancer Genomics

DNASTAR's Lasergene Genomics Suite includes comprehensive functionality for all aspects of cancer genomics. Features of the Lasergene Genomics Suite software include:

  • Industry leading accuracy of greater than 99.8%
  • The ability to identify mutations and genes that contribute to the development of a cancer cell
  • Streamlined workflows for cancer gene panels
  • Quick assembly of large data sets from all major next-gen technologies on a desktop computer - check out our benchmarks below
  • Powerful analysis and filtering capabilities for both prospective and retrospective studies
  • 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
  • Streamlined Workflow for Cancer Gene Panels

    Quickly narrow your focus to identify tumor-specific variants with a streamlined approach to cancer gene panel data assembly and analysis.

     

    Analyze and Compare Mutations Across Groups

    For more information on using Lasergene Genomics Suite in your cancer genomics research, please see the following video, which briefly demonstrates an assembly of the exomes of four individuals, and the subsequent analysis and comparison of SNPs across the group.

     

    PDF Icon SeqMan NGen is a High Accuracy NGS Assembler: Assessment with NA12878 Reference Materials

     

    Request a fully-functional, free trial of Lasergene Genomics Suite.