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 (www.clcbio.com).
Company
Qiagen
Access Information
You must submit a request through “NCI at Your Service” to obtain access to CLC Software.