The Naive cfDNA approach delivers Q20-25 reads but achieves higher coverage at 10x, allowing for more in-depth exploration of cfDNA. This method is particularly suited for applications requiring detailed methylation analysis and base modification detection, offering both genetic and epigenetic insights.

Key Features:

Q20-25 Reads: Moderate accuracy but high coverage, ensuring a deep dive into cfDNA.

10x Genome Coverage: High-coverage sequencing for comprehensive analysis.

Methylation and Base Modifications: Detects methylation patterns and other epigenetic modifications, making it valuable for cancer epigenomics and disease monitoring.