Unraveling the complexity of Cancer. Expedite your understanding of cancer with CLC Cancer Research Workbench


Seeking the meaning of the sequence? Gain valuable insights into cancer with Cancer Research Workbench!

  • Quickly analyze complex data
  • Modify or personalize workflows
  • Conveniently filter and visualize your data
  • Compare your results with relevant databases

The truth lurking behind the sequences…

Accelerate next-generation sequencing (NGS) data interpretation and uncover meaningful insights in cancer research with CLC Cancer Research Workbench — the world’s first comprehensive, user-friendly, and customizable cancer-focused informatics solution!

CLC Cancer Research Workbench provides you with all the tools you need to:

  • Discover prognostic markers
  • Identify subclonal somatic mutations
  • Detect inherited traits
  • Find biomarkers for drug response
  • Determine new oncogenes

Comprehensive analysis so you don’t miss a single detail!

To perform comprehensive cancer data analysis, CLC Cancer Research Workbench offers specialized tools that allow you to:

  • Remove germline variants
  • Identify rare subclonal mutations and mutated genes for further analysis
  • Annotate identified variants with information from COSMIC and ClinVar
  • Test the presence of specific variants
  • Compare samples and identify new biomarkers

Compare and share your data

Inspect identified variants in the context of mapped sequencing reads, human genes, and relevant variants in clinical databases, including:

  • Human genome
  • dbSNP
  • dbSNP common from UCSC
  • ClinVar
  • HapMap
  • 1000 genomes data
  • Ensembl genes

The intuitive software interface allows you to customise workflows or create new ones. You can also easily share workflows with your collaborators and colleagues.

End-to-end workflows for analysis of cancer data

Whether it is targeted amplicon, exome, or whole genome sequencing data, CLC Cancer Research Workbench is compatible with data generated using all sequencing platforms. From identifying known and novel variants with information from databases, amino acid changes, and conservation scores – versatile CLC Cancer Research Workbench provides comprehensive analysis to help you uncover all the details!


The looks


Application Manual


Need something bigger?

The underlying strategy of our enterprise platform is the smooth integration between desktop clients and our server back-end. As a user, you’re never confronted with scripts or advanced IT questions – you simply use your client as usual, and our platform takes care of all the analysis and data management in the background.

We provide an enterprise platform for building and managing a flexible and powerful sequence analysis setup in organizations of any size; from small biotech start-ups to large pharmaceutical or agricultural companies.

Check out CLC Genomics Workbench for more information and quote requests


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