CLC GENOMIC WORKBENCH 

When working with Next Generation Sequencing, data analysis represents a serious bottleneck in the pipelines of most R&D departments. CLC Genomics Workbench solves this problem by facilitating rapid and visual analysis of the enormous amounts of data that are generated by Next Generation Sequencing.

The CLC Genomics workbench is the first comprehensive analysis package that allows for the analysis and visualization of data from all major NGS platforms. In doing so this software enables you to compare the results of BaseClear's Genome Analysis services with your own older data or with data obtained from other laboratories.

CLC Genomics Workbench includes the following features:

• Reference assembly of all types of sequencing data 
• Assembly of genomes of any size (only limited by TRAM available), de novo assembly of genomes of up to 50 mega bases. 
• Colour space assembly 
• SNP detection using advanced statistical models 
• Advanced visualization, scrolling and zooming tools 
• Support for multiplexing with DNA bar-coding 
• Transcriptomics, like RNA-seq and tagged expression profiling 
• ChIP-seq analysis 
• Classical sequence analysis tools, such as primer design, molecular cloning, alignments, BLAST, phylogenetic trees and much more. 

For further information see www.clcbio.com.