CLC Genomics Workbench for analyzing and visualizing Next Generation Sequencing data, incorporates cutting-edge technology and algorithms, while also supporting and integrating with the rest of your typical NGS workflow.Features include read mapping of Sanger, 454, Illumina Genome Analyzer, Helicos, and SOLiD sequencing data. Advanced SNP detection, including choice of ploidity, advanced DIP detection, including choice of ploidity, identification of structural variations, and DIP reporting.
|License||Free to try|
|File Size||89.25 MB|
|Operating System||Windows 2003 Windows Server 2008 Windows XP Windows 7 Windows Vista Windows|