Cyclomics offers two distinct approaches for cfDNA sequencing and analysis, each tailored to provide high-resolution insights into circulating cell-free DNA (cfDNA). Both approaches enable multi-omics data extraction, delivering layers of information from genetic mutations to epigenetic modifications, ensuring comprehensive genomic and epigenomic analysis.

​

NanoRCS
NanoRCS provides highly accurate consensus reads (Q40) with 1x-3x coverage across the human genome. This approach is ideal for detecting rare genetic mutations and structural variations. By producing high-quality reads, NanoRCS ensures reliable and trustworthy data for both research and clinical applications.

​

Key Features:

Q40 Consensus Reads: Ultra-accurate, high-quality sequencing data for detailed genetic analysis.

1x-3x Genome Coverage: Low-coverage sequencing that balances accuracy with sufficient breadth for whole-genome analysis.​​