iScienceBioinformaticsPeer-reviewed journal article
scMILD: Single-cell Multiple Instance Learning for Sample Classification and Associated Subpopulation Discovery
Abstract
Linking cellular states to clinical phenotypes is a major challenge in single-cell analysis. Here, we present scMILD, a weakly supervised Multiple Instance Learning framework that robustly identifies condition-associated cells using only sample-level labels. After systematically validating scMILDs accuracy through controlled simulations, we applied it to diverse disease datasets, confirming its ability to retrieve known biological signatures. Building on this, our sample-informed analysis of scMILD-identified monocytes in COVID-19 revealed a temporal transition from an early antiviral to a late stress-response state. Furthermore, in a novel cross-disease application, a model trained on COVID-19 successfully stratified Lupus patients and distinguished shared inflammatory states from disease-specific ones. scMILD thus provides a validated and versatile strategy to dissect cellular heterogeneity, bridging single-cell observations with high-level phenotypes.
- organism: human
- assay: scRNA-seq
- research focus: cell type annotation
- research focus: clustering
- research focus: differential expression
- research focus: cell-cell communication
- approach: machine learning (classical)
- Citations
- 3
- FWCI
- 4.16
- Field percentile
- top 7%
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