R. D. Patton, A. P. McDeed, A. Netzley, A. Pawar, T. W. Persse, A. Nair, P. C. Galipeau, I. M. Coleman, P. Itagi, P. Chandra, E. Sayar, M. Adil, M. Vashisth, J. B. Hiatt, R. Dumpit, L. Kollath, R. A. Demirci, A. Ghodsi, H.-M. Lam, C. Morrissey, D. L. Chen, M. T. Schweizer, A. Iravani, A. C. Hsieh, D. MacPherson, M. C. Haffner, P. S. Nelson, G. Ha
Tumor gene expression profiling provides crucial diagnostic information for guiding therapy, but standard tissue biopsies are invasive, spatially biased, and may inadequately sample metastatic disease. Cell-free DNA (cfDNA) provides a minimally invasive alternative for tumor genotyping, yet reconstructing robust, transcriptome-wide expression from standard-depth cfDNA whole-genome sequencing (WGS) remains a major challenge. We developed a deep learning framework comprising Triton, for comprehensive cfDNA feature extraction, and Proteus, a probabilistic model that infers single-gene expression from standard-depth cfDNA WGS. Proteus outperformed prior cfDNA approaches in reconstructing molecular phenotypes from matched tumor transcriptomes across multiple cancer types, including prostate, lung, and bladder cancer cohorts, with uncertainty-guided withholding improving model reliability. Proteus further enabled assessment of therapeutic target activity, prognostic transcriptional programs, and candidate treatment-emergent resistance states, establishing a generalizable framework for minimally invasive functional genomics in precision oncology.