CLC Genomics Workbench allows users to analyze and visualize nexg generation sequencing (NGS) data. CLC Genomics Workbench supports the complete resequencing pipeline for detecting and comparing genetic variants.
Free to Use
Open Access
Costs and Fees
This software is not currently licensed by ITS. If you would like to share the licensing costs of this product with other interested users, please register your name using the link below.
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Keywords
resequencing, read mapping,sequence alingment,ChIP-Seq,bisulfite sequencing,de novo assembly,RNA-Seq,variant analysis,metagenomics