mNSF: multi-sample non-negative spatial factorization
Analyzing multi-sample spatial transcriptomics data requires accounting for biological variation. We present multi-sample non-negative spatial factorization (mNSF), an alignment-free framework extending single-sample spatial factorization to multi-sample datasets. mNSF incorporates sample-specific spatial correlation modeling and extracts low-dimensional data representations. Through simulations and real data analysis, we demonstrate mNSF's efficacy in identifying true factors, shared anatomical regions, and region-specific biological functions. mNSF's performance is comparable to alignment-based methods when alignment is feasible, while enabling analysis in scenarios where spatial alignment is unfeasible. mNSF shows promise as a robust method for analyzing spatially resolved transcriptomics data across multiple samples.
Authors
- Chaichontat Sriworarat (ORCID: https://orcid.org/0000-0002-1917-3409)
- Yi Wang (ORCID: https://orcid.org/0000-0002-0558-7491)
- Loyal A. Goff (ORCID: https://orcid.org/0000-0003-2875-451X)
- Kasper D. Hansen (ORCID: https://orcid.org/0000-0003-0086-0687)
- Kyla Woyshner (ORCID: https://orcid.org/0000-0002-1005-9896)
- Genevieve Stein-O’Brien (ORCID: https://orcid.org/0000-0001-8681-9110)
Institutions
- Johns Hopkins University (US)
- Johns Hopkins Medicine (US)
Publication Details
- Journal
- Genome biology
- Published
- 2025-06-02
- DOI
- https://doi.org/10.1186/s13059-025-03601-x
- Citations
- 1
- Primary Topic
- Single-cell and spatial transcriptomics
- Type
- article
- Field-Weighted Citation Impact
- 0.81
Funders
- National Institute on Aging
- National Institute of General Medical Sciences
- National Institute of Neurological Disorders and Stroke