Reconstructing developmental and disease progression with sample-level embeddings

Abstract

Single-cell genomics is transformative for characterizing cellular heterogeneity, but many translational questions require comparing samples rather than individual cells. Typical analyses compare "case" and "control" groups, ignoring sample-level variation within them. Here we present scSLIDE, a framework that transforms each samples single-cell data into a compact profile describing where its cells fall in high-dimensional space. By comparing these density profiles, scSLIDE calculates embeddings to characterization variation across samples. Applied to COVID-19 infection, Alzheimers disease, and zebrafish embryogenesis, we show that scSLIDE can be used to cluster patients, reconstruct sample-level disease trajectories, and identify coordinated cellular programs across samples. We discover independent axes of infection and severity, a molecular disease progression that aligns with pathology-based estimates of neurodegeneration, and embryonic "pseudostages" varying across and within timepoints. In each case, we demonstrate how case-control analyses collapse rich biological variation into binary labels, and how sample-level embedding represents a powerful analytical alternative.