CyclomicsSeq solves the challenge of finding the proverbial needle in a haystack in the genomic world. Designed for ultra-sensitive detection, CyclomicsSeq is the ideal technology for researchers and clinicians searching for rare genetic variants, especially those associated with cancer. Whether you are tracking minute traces of circulating tumor DNA or identifying low-frequency mutations in a complex sample, CyclomicsSeq delivers unparalleled accuracy and depth, making it the perfect solution for applications where precision is critical.

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Key Features:

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Unmatched Sensitivity and Accuracy: CyclomicsSeq delivers Q40 consensus accuracy, providing confidence in every result and reducing false positives and false negatives in biomarker detection.

Broad Compatibility: Capable of handling a wide range of DNA lengths (50bp to 3kb), CyclomicsSeq accommodates various amplicons and genetic targets, making it versatile for both clinical diagnostics and exploratory research.

High Throughput: With the ability to generate up to 50 million high-quality reads per run, CyclomicsSeq supports large-scale studies, offering both speed and precision for researchers and healthcare providers.