Most features of a cell are determined by gene programs — sets of co-expressed genes that execute a specific function. By incorporating existing knowledge about gene programs and cell types, the Spectra factor analysis method improves how we decode single-cell transcriptomic data and offers insights into challenging tumor immune contexts.
This is a preview of subscription content, access via your institution
Access options
Access Nature and 54 other Nature Portfolio journals
Get Nature+, our best-value online-access subscription
$29.99 / 30 days
cancel any time
Subscribe to this journal
Receive 12 print issues and online access
$209.00 per year
only $17.42 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
References
Levitin et al. De novo gene signature identification from single-cell RNA-seq with hierarchical Poisson factorization. Mol. Syst. Biol. 15, e8557 (2019). Unsupervised Bayesian factorization approach for identifying highly coherent gene programs.
Buettner, F. et al. f-scLVM: scalable and versatile factor analysis for single-cell RNA-seq. Genome Biol. 18, 212 (2017). The first method to successfully identify gene programs from scRNA-seq data using pathway annotations.
Kartha, V. K. et al. Functional inference of gene regulation using single-cell multi-omics. Cell Genom. 2, 100166 (2022). This dataset was used to benchmark Spectra’s performance.
Bassez, A. et al. A single-cell map of intratumoral changes during anti-PD1 treatment of patients with breast cancer. Nat. Med. 27, 820–755 (2021). ScRNA-seq datasets from patients with breast cancer before and after immunotherapy that we used to associate gene expression programs in tumor-infiltrating immune cells with surrogates of therapy response.
Salcher, S. et al. High-resolution single-cell atlas reveals diversity and plasticity of tissue-resident neutrophils in non-small cell lung cancer. Cancer Cell 40, 1503–1520 (2022). An scRNA-seq atlas of lung tumors from 318 patients with data from over 1.2 million cells that we used to interrogate Spectra’s generalizability.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
This is a summary of: Kunes, R. Z. et al. Supervised discovery of interpretable gene programs from single-cell data. Nat. Biotechnol. https://doi.org/10.1038/s41587-023-01940-3 (2023).
Rights and permissions
About this article
Cite this article
Decoding the building blocks of cellular processes from single-cell transcriptomics data. Nat Biotechnol 42, 1034–1035 (2024). https://doi.org/10.1038/s41587-023-01967-6
Published:
Issue Date:
DOI: https://doi.org/10.1038/s41587-023-01967-6