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Ignite hope in the quest for cancer care

Your passion in fighting cancer transforms precious sample into hope. When you trust your results throughout the cancer research process, that gives you the power to confidently drive the future of precision cancer care.

Our deep expertise in Cancer Genomics enables us to help you in your cancer research, whether you are looking for a partner in development of companion diagnostics, or you are searching for innovative technologies to help you answer the questions you seek.

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Drive the future of cancer care

Our deep expertise in Cancer Genomics enables us to help you in your cancer research, whether you are looking for a partner in development of companion diagnostics, or you are searching for innovative genomics technologies to help you answer the questions you seek.  See how our broad portfolio helps you answer your questions for tumor analysis, liquid biopsy, inherited and somatic cancer research.


Optimizing liquid biopsy for liver cancer analysis

Liquid biopsies give researchers a powerful, non-invasive tool to investigate cancer where tissue biopsies can fall short. One of these advances comes from Dr. Villanueva (Assistant Professor, Icahn School of Medicine at Mount Sinai, New York) and his work on advanced hepatocellular carcinoma (aHCC). Learn now his work with Custom SureSelect assays in the detection of cfDNA in his NGS workflow helped him uncover new findings about aHCC.


Advancing the promise of precision oncology with our tumor analysis workflow

Dr. Antonio Marchetti, a professor at the Anatomical Pathology Laboratory at SS Annunziata Hospital (Chieti, Italy), is passionate about precision oncology for non-small cell lung cancer (NSCLC). That passion ignited research that led to his pathology lab developing and optimizing an end-to-end NGS workflow for NSCLC FFPE samples.  Find out more about his approach which enabled greater yield, increased library complexity and improved detection of difficult variants compared to traditional methods.



Key applications

Somatic cancer research

These have been developed to address technical challenges, including assaying small or heterogeneous samples, degraded FFPE samples, and detecting variants at only very low allele frequencies.

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Liquid biopsy research

Our solutions include sample QC and NGS library prep to detect variants with low allele frequencies, & miRNA microarrays to detect mature miRNAs. These assays provide ultrahigh sensitivity and specificity.

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Inherited cancer research

Working in inherited cancer research, you need access to a portfolio of solutions make progress fighting cancer. Our NGS solutions include easy-to-use catalog and custom options with complete workflows.

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Hematological cancer research

Our NGS solutions not only offer high sensitivity detection with molecular barcodes, and but also simplify your workflow from sample to report.

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Cancer cytogenetics research

Our cytogenetics solutions offer the most complete CGH workflow from sample QC to data interpretation and enables genome-wide analysis of CNCs and cnLOH.

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Partner with precision

Accelerate your companion diagnostic development by taking advantage of our global infrastructure and decades of experience enabling targeted therapeutics.

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For Research Use Only. Not for use in diagnostic procedures.

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