WES & WTS (22,000 genes) provide assurances to accelerate your development programs with data-driven decisions.
Unmatched breadth and depth of profiling coverage from a single platform enables a seamless transition from clinical trial data to real world applications.
Tissue profiling: Analyze DNA, RNA, and proteins through Whole Exome Sequencing (WES), Whole Transcriptome Sequencing (WTS), and IHC.
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Blood-based profiling: Overcome the challenges of insufficient material, poor sensitivity and false positives by analyzing DNA, RNA, and identifying somatic CHIP mutations.
MI Trials: Accelerate enrollment by identifying biomarker+ patients from our extensive network of clinical sites, supported by dedicated clinical trial navigators.
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RWE projects: Access a dedicated cross-functional team to address questions and enhance programs by leveraging Caris’ matched clinico-genomic database.
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Enable the future of precision medicine with a platform built to last.
Uncover the complete molecular and clinical context to deliver on the promise of precision medicine.
Caris has amassed a longitudinal multiomic data library that spans over 275k+ patients across 55+ indications. Biopsies come to Caris for sequencing across the standard of care. Our partners can interrogate the data to understand the tumor biology within the context of clinical care. Caris RWD is an unmatched resource for discovery and developmental programs. Data available includes, but is not limited to:
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