Journal
NATURE BIOTECHNOLOGY
Volume 40, Issue 2, Pages 245-+Publisher
NATURE PORTFOLIO
DOI: 10.1038/s41587-021-01033-z
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Funding
- European Molecular Biology Laboratory
- Cancer Research UK [C9545/A29580]
- Wellcome Sanger core funding [WT206194]
- Wellcome Trust Senior Research Fellowship in Clinical Science [219542/Z/19/Z]
- Medical Research Council
- Chan Zuckerberg Initiative Seed Network Grant
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Milo is a scalable statistical framework that performs differential abundance testing by assigning cells to partially overlapping neighborhoods on a k-nearest neighbor graph. It can identify perturbations obscured by discretizing cells into clusters and outperforms alternative testing strategies. Milo is based on cell-cell similarity structure and may be applicable to various single-cell data beyond scRNA-seq.
Current computational workflows for comparative analyses of single-cell datasets typically use discrete clusters as input when testing for differential abundance among experimental conditions. However, clusters do not always provide the appropriate resolution and cannot capture continuous trajectories. Here we present Milo, a scalable statistical framework that performs differential abundance testing by assigning cells to partially overlapping neighborhoods on a k-nearest neighbor graph. Using simulations and single-cell RNA sequencing (scRNA-seq) data, we show that Milo can identify perturbations that are obscured by discretizing cells into clusters, that it maintains false discovery rate control across batch effects and that it outperforms alternative differential abundance testing strategies. Milo identifies the decline of a fate-biased epithelial precursor in the aging mouse thymus and identifies perturbations to multiple lineages in human cirrhotic liver. As Milo is based on a cell-cell similarity structure, it might also be applicable to single-cell data other than scRNA-seq. Milo is provided as an open-source R software package at https://github.com/MarioniLab/miloR.
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