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.Whole genome re-sequencing and targeted re-sequencing of genomes of any size and type – from bacteria and vira to humans De novo assembly of an unlimited number of reads, for genomes up to human size SNP/DIP detection and identification of genomic rearrangements Visualization and interactive graphical manipulation of results.