A scalable deep-learning framework for cancer detection using cell-free DNA shallow whole-genome sequencing.

Abstract:: Cell-free DNA (cfDNA) in body fluids enables noninvasive cancer detection. Multifeature artificial intelligence (AI) can improve sensitivity by integrating diverse biomarkers when cancer signals are sparse. Tumor-informed assays that rely on mutations have limited practicality for early cancer detection. Emerging fragmentomic and epigenetic features underpin tumor-naive approaches to screening for individuals with low tumor burden. Here, we designed UNITE-a universal cfDNA feature ensemble framework that provides scalable cancer detection methods based on "genomic bin-fragment length" matrices derived from shallow whole-genome sequencing (sWGS) data at 0.1× depth. Using sWGS data from 2063 plasma samples (631 controls and 1432 cases from 26 cancer types), we systematically evaluated both XGBoost (UNITE-XGB) and convolutional neural networks (UNITE-CNN) across multiple feature spaces and cancer stages. In stage I-II cancer, UNITE-XGB and UNITE-CNN achieved 31 and 21% sensitivity, respectively, at 95% specificity. These findings provide roadmaps for developing multifeature AI beyond plasma biopsies.

Authors:: H Wang, PD Mennea, G McAndrew, O Sonmezler, DS Shcherbo, E-J Ditter, SØ Jensen, AIG Buma, CG Smith, Z Cheng, C Harris, RJ Cutts, S Hrebien, PAJ Crosbie, PG Corrie, MM van den Heuvel, A Roshan, F McCaughan, RC Rintoul, F Markowetz, T Kaplan, WN Cooper, H Zhao, N Rosenfeld

Themes