Towards high quality reference genomes

QIAGEN CLC Genome Finishing Module automates steps like scaffolding, contig joining, and the ordering of contigs and scaffolds relative to each other or a closely related reference genome. Remaining unresolved regions can visually inspect and edited to further optimize the results.

  • Our capabilities and investments in developing clinical bioinformatics solutions will become increasingly relevant as the research and clinical community scales from panels to exomes and ultimately to whole genomes for personalized medicine. This trend will continue to demand the use of our highly sophisticated computational solutions with the perpetually curated QIAGEN Knowledge Base to predict phenotypic impacts of genomic variation.

    Dr. Michael Hadjisavas,
    VP of Clinical Genomics Program, QIAGEN Bioinformatics.

Scientist friendly genome assembly

QIAGEN CLC Genome Finishing module comes fully integrated into the industry standard for scientist-friendly and scalable NGS data analysis, QIAGEN CLC Genomics Workbench. The workbench includes our trusted de novo assembly tools, plus a comprehensive set of tools to explore:

  • genome
  • transcriptome
  • or epigenome data

Accelerate genome finishing now

QIAGEN CLC Genomics Workbench
QIAGEN CLC Genome Finishing Module
QIAGEN CLC Genomics Workbench
QIAGEN CLC Genomics Workbench is a powerful solution that works for everyone, no matter the workflow. Utilizing cutting-edge technology, unique features and algorithms widely used by scientific leaders in industry and academia to overcome challenges associated with data analysis.
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QIAGEN CLC Genome Finishing Module
Short read lengths and repetitive genomic regions often result in fragmented de novo assemblies. To improve results and convert contigs into high quality assemblies a complex process referred to as genome finishing is needed. QIAGEN CLC Genome Finishing Module is an add-on to QIAGEN CLC Genomics Workbench, designed to accelerate and simplify genome finishing, and make this process accessible to life scientist without deep understanding of bioinformatics.
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One-click PacBio
assembly included

Assemble raw PacBio reads into high quality genomes on your laptop, powered by a preconfigured workflow of fast and compute resource efficient algorithms.

Benchmarking results
Sample to Insight
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