Ultra-sensitive molecular residual disease detection through whole genome sequencing with single-read error correction.
Xinxing LiTao LiuAntonella BacchiocchiMengxing LiWen ChengTobias WittkopFernando MendezYingyu WangPaul TangQianqian YaoMarcus W BosenbergMario SznolQin YanMalek FahamLi WengRuth HalabanHai JinZhiqian HuPublished in: medRxiv : the preprint server for health sciences (2024)
While whole genome sequencing (WGS) of cell-free DNA (cfDNA) holds enormous promise for molecular residual disease (MRD) detection, its performance is limited by WGS error rate. Here we introduce AccuScan, an efficient cfDNA WGS technology that enables genome-wide error correction at single read level, achieving an error rate of 4.2×10 -7 , which is about two orders of magnitude lower than a read-centric de-noising method. When applied to MRD detection, AccuScan demonstrated analytical sensitivity down to 10 -6 circulating tumor allele fraction at 99% sample level specificity. In colorectal cancer, AccuScan showed 90% landmark sensitivity for predicting relapse. It also showed robust MRD performance with esophageal cancer using samples collected as early as 1 week after surgery, and predictive value for immunotherapy monitoring with melanoma patients. Overall, AccuScan provides a highly accurate WGS solution for MRD, empowering circulating tumor DNA detection at parts per million range without high sample input nor personalized reagents.
Keyphrases
- circulating tumor
- single molecule
- cell free
- loop mediated isothermal amplification
- circulating tumor cells
- label free
- real time pcr
- genome wide
- end stage renal disease
- ejection fraction
- clinical trial
- dna methylation
- chronic kidney disease
- randomized controlled trial
- peritoneal dialysis
- prognostic factors
- artificial intelligence