CLC Genomics Workbench


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.

  • Read mapping of Sanger, Illumina, PacBio, and IonTorrent sequencing data
  • De novo assembly of genomes of any size (only limited by RAM available)
  • Color space mapping
  • Advanced visualization, scrolling, and zooming tools
  • SNP detection using advanced quality filtering
  • Support for multiplexing with DNA barcoding
  • RNA-seq including support for paired data and transcript-level expression
  • Small RNA analysis
  • Expression profiling by tags
  • EST library construction
  • Advanced visualization, scrolling, and zooming tools
  • Gene expression analysis
  • Chromatin immunoprecipitation sequencing (ChIP-seq) analysis
  • Peak finding and peak refinement
  • Graph and table of background distribution and the false discovery rate
  • Peak table and annotations

Click the Here to learn more about CLCBio (



Access Information

You must submit a request through “NCI at Your Service” to obtain access to CLC Software.