Scientist-friendly, scalable epigenomics analysis

We have reinvented how epigenomics data is efficiently processed, identified, and interpreted in the context of other omics data – and bringing a user-friendly bioinformatics software solution to the fingertips of life scientists. CLC Genomics Workbench was developed to deliver deep insight into biology by incorporating state-of-the art tools to support genomics, transcriptomics, and epigenomics data analysis and achieve more timely, accurate, and transparent result interpretation.

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See a presentation of our new epigenomics features and find out how to fully benefit from the advances of CLC Genomics Workbench for detecting DNA methylation through bisulfite sequencing, transcription factor ChIP-Seq, and histone ChIP-Seq.

Watch the webinar


The ability to analyze our bisulfite sequencing data within the CLC environment is a real advantage for us. We’ve analyzed whole genome, genome wide oligonulcotide capture, and amplicon bisulfite data sets. Being able to get base specific quantitation of CG and non-CG methylation in a strand specific manner all within one program and with an intuitive GUI has been a hit with the lab and is much simpler than our previous work flows.

Willard M. Freeman, Ph.D.

Prof. Freeman leads the Targeted DNA Methylation & Mitochondrial Heteroplasmy Core offering
DNA methylation analysis and other services to researchers at the University of Oklahoma Health Sciences Center.

Other affiliations: Donald W. Reynolds Chair in Aging Research, Associate Professor of Physiology, Adjunct Associate Professor of Geriatric Medicine, Member, Harold Hamm Diabetes Institute, Associate Member, Stephenson Cancer Center, University of Oklahoma Health Sciences Center.

Request a trial

Request a trial and get started using our step-by-step tutorials on ChIP-seq and Bisulfite Sequencing.

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