About CLC Genomics Workbench
Using super-fast, integrated, high-performance computing algorithms, CLC Genomics Workbench sets a new standard for desktop based reference assembly and de novo assembly of SOLiD, Solexa, 454, and Helicos sequencing data# De novo assembly of Sanger, 454, Solexa, Helicos, and SOLiD data
- Reference assembly of Sanger, 454, Solexa, Helicos, and SOLiD sequencing data
- Assembly of genomes of any size (only limited by RAM available)
- Assembly of standard read data and support for assembly of paired end reads / mate pair reads of any sequencing technology
- Advanced graphical tools for the detection of large scale mutations/rearrangements like inversions, translocations, duplications, and deletions
- Support for multiplex sequencing using 454, Solexa, or SOLiD technology
- Integration with CLC bio’s High Performance Computing solutions, making assemblies very fast
- Many more features.

What’s New in this Version
- New ChIP seq tool
- Contig report that records various statistics and graphs for contigs, including e.g. N75, N50 and N25 statistics, coverage distribution, contig size distributions.
- Extension of RNA-seq functionality to also handle color space data
- Many more enhancements.