CLC Genomics Workbench 4.5

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.

Main Features:

- De novo assembly of Sanger, 454, Illumina Genome Analyzer, and SOLiD data
- De novo assembly of mixed datasets (e.g. 454 and Illumina Genome Analyser)
- Contig report that records various statistics and graphs for contigs, including e.g. N75, N50 and N25 statistics, coverage distribution, contig size distributions.
- Read mapping in native Color Space
- Read mapping of Sanger, 454, Illumina Genome Analyzer, Helicos, and SOLiD sequencing data
- Read mapping of mixed datasets (e.g. 454 and Illumina Genome Analyser)
- Read mapping of genomes of any size
- Assembly of standard read data and support for assembly of paired end reads / mate pair reads of any sequencing technology
- Advanced graphical tools for detection of large scale mutations and rearrangements