C2i Genomics Platform
Whole-genome sequencing platform for minimal residual disease detection and cancer monitoring
Company profile
Company profile
C2i Genomics is a precision oncology company that leverages artificial intelligence and whole genome sequencing to transform cancer detection and monitoring. The company has developed a proprietary platform that analyzes the entire genome rather than targeted panels, enabling unprecedented sensitivity in detecting circulating tumor DNA (ctDNA) for minimal residual disease (MRD) monitoring and early cancer detection. C2i's technology addresses critical unmet needs in oncology by providing clinicians with actionable genomic intelligence to guide treatment decisions, monitor treatment response, and detect cancer recurrence earlier than traditional methods. By combining comprehensive whole genome analysis with advanced AI algorithms, C2i Genomics aims to improve patient outcomes through more precise, personalized cancer care. The company serves oncologists, cancer centers, and health systems seeking to implement cutting-edge genomic testing for their patients.
Company description C2i Genomics official website
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02 · Flagship portfolio
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Whole-genome sequencing platform for minimal residual disease detection and cancer monitoring
03 · Research intelligence
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Research
The Journal of molecular diagnostics : JMD · Jul 30, 2026
Ultrasensitive ctDNA monitoring for organ preservation in patients with locally advanced rectal cancer.NPJ precision oncology · Dec 11, 2025
Detection of circulating tumor DNA by tumor-informed whole-genome sequencing enables prediction of recurrence in stage III colorectal cancer patients.European journal of cancer (Oxford, England : 1990) · Nov 1, 2024
Whole-genome Mutational Analysis for Tumor-informed Detection of Circulating Tumor DNA in Patients with Urothelial Carcinoma.European urology · Oct 1, 2024
Enhanced clinical assessment of hematologic malignancies through routine paired tumor and normal sequencing.Nature communications · Oct 28, 2023
Expert Panel Curation of 113 Primary Mitochondrial Disease Genes for the Leigh Syndrome Spectrum.Annals of neurology · Oct 1, 2023
Clinical validation
NCT05629442 · Sponsor · NOT YET RECRUITING
Clinical Performance Evaluation of the C2i-TestNCT05221827 · Sponsor · TERMINATED
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minimal residual disease monitoring and early cancer detection
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Market context
Companies using AI to analyze genomic, proteomic, metabolomic, or multi-omics data to provide personalized treatment recommendations, identify genetic risks, or develop targeted therapies. Includes genomic sequencing platforms with AI analysis, preventive medicine based on genetic risk assessment, and longevity care based on molecular and genetic data.
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