Now Reading: Limitations of cell embedding metrics assessed using drifting islands
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Limitations of cell embedding metrics assessed using drifting islands
Data availability
All data in this study are publicly available. Statistics, resources and corresponding studies are listed in Extended Data Table 1.
Code availability
The implementation code for Islander, as well as tutorial notebooks to reproduce the results in this paper, can be accessed from GitHub (https://github.com/Genentech/Islander). The standalone scgraph evaluation toolkit can be installed using pip (https://pypi.org/project/scgraph-eval/). For scIB evaluation pipelines, the implementations by Gayso et al. were obtained from GitHub (https://github.com/yoseflab/scib-metrics).
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Acknowledgements
We thank R. Lopez, R. Sosic, P. He, M. Bereket, L. Dony, S.-J. Dunn, G. Eraslan, A. Gayoso, G. Heimberg, K. Huang, J. Marioni, D. Pe’er, L. Peng, Y. Roohani, Y. Rosen, A. Whitehead and J. Zhang for invaluable insights, along with all the members from the J.L. and A.R. labs and colleagues at the Human Cell Atlas, Chan Zuckerberg Initiative and Google DeepMind, for constructive and insightful discussions. J.L. was supported by the National Science Foundation through grants OAC-1835598 (CINES), CCF-1918940 (Expeditions) and DMS-2327709 (IHBEM), the Stanford Data Applications Initiative, the Wu Tsai Neurosciences Institute, the Stanford Institute for Human-Centered Artificial Intelligence, the Chan Zuckerberg Initiative, Amazon, Genentech, GSK, Hitachi, SAP and UCB.
Ethics declarations
Competing interests
H.W. and A.R. are employees of Genentech, a member of the Roche Group. A.R. has equity in Roche. A.R. is a cofounder and equity holder of Celsius Therapeutics and is an equity holder in Immunitas. Until 31 July 2020, A.R. was a scientific advisory board member of Thermo Fisher Scientific, Syros Pharmaceuticals, Neogene Therapeutics and Asimov. A.R. is a named inventor on multiple filed patents related to single-cell and spatial genomics, including for scRNA-seq, spatial transcriptomics, Perturb-Seq, compressed experiments and PerturbView.
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Extended data
Extended Data Fig. 1
Drifting Cell Islands, different runs of Islander on fetal lung atlas (donor).
Extended Data Fig. 2 Design optimization for scGraph using human fetal lung atlas22.
a, b, Distribution of raw (a) and log1p-transformed (b) scRNA-seq counts. c, scGraph scores using log- 1p counts do not effectively flag distortions caused by drifting cell islands. scGraph scores (y axis) for embeddings generated with each method (x axis) using log-1p counts. d,e Effect of trim rate on PCA centroid locations and scGraph scores. d, Normalized mean square error between centroids (MSE, y-axis) at different trimming rates (x-axis), with centroids at 49% trimming as reference. e, Percentage difference (y-axis) between scGraph scores at various trimming rates (x-axis) compared to the score at 49% trimming. While small trim rates lead to larger changes in centroid coordinates, the corresponding changes in scGraph scores are relatively minor. Based on these observations, we selected a trim rate of 5% per side (10% total).
Extended Data Fig. 3 Scoring human fetal lung fibroblast22 embeddings by scIB and scGraph metrics.
a-c, Embeddings of 31,020 human fetal lung fibroblast profiles from 9 fibroblast subtypes across 29 batches, generated by the top scoring methods based on scIB (scANVI and Is- lander) or scGraph (Harmony and Authors’) and colored by developmental stage (a), cell types (b), or batch (c). Each method was trained on this subset and evaluated using both scIB and scGraph (Extended Data Table 5). d-e, Rankings of integration methods. scGraph (d, y axis) and scIB (e, y axis) scores for each of the 9 integration methods (x axis).
Supplementary information
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Wang, H., Leskovec, J. & Regev, A. Limitations of cell embedding metrics assessed using drifting islands.
Nat Biotechnol (2025). https://doi.org/10.1038/s41587-025-02702-z
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DOI: https://doi.org/10.1038/s41587-025-02702-z
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