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First expressions last

Analyzing RNA-seq data is no longer complicated. With our solutions you’ll get a lasting impression of how easy gene expression analysis can be.

The complete path to biological insight

At QIAGEN we’re dedicated to guiding scientists from Sample to Insight with solutions that start with the processing of biological samples and end with the interpretation of RNA-Seq data.

No background in bioinformatics required

Would you prefer to own both the experimental design and the data analysis? We’re bringing sophisticated bioinformatics to the fingertips of the life scientists, making sure that critical information isn’t lost.

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.

When data turns to insights

Are you getting the most out of your RNA-Seq data? How are you getting from FastQ files to differential gene expression data today? We provide you a smooth workflow from raw NGS data to gene expression, which you can use to generate biological insights.

Bioinformatics tools for Somatic Cancer Research

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CLC

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QCI Interpret for Somatic Can

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Integrated Workflows

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Clinical Knowledge Base

CLC

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QCI Interpret for Somatic Can

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Integrated Workflows

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Clinical Knowledge Base

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