CLC Genomics Workbench includes all features of CLC Main Workbench and the following additional functionalities:
- 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.
- Read mapping in native Color Space
- Read mapping of Sanger, 454, Illumina Genome Analyzer, Helicos, and SOLiD sequencing data
- Advanced graphical tools for detection of large scale mutations and rearrangements