scPNMF
scPNMF selects informative genes from single-cell RNA sequencing (scRNA-seq) data by applying a projective non-negative matrix factorization (PNMF) framework to identify gene bases that capture cell-type–relevant variation.
Key Features:
- Unsupervised Gene Selection: Performs unsupervised identification of informative genes without requiring predefined labels or categories.
- Enhanced Cell Type Distinction: Selects gene bases that improve separation and distinction among different cell types.
- Alignment with Targeted Gene Profiling Data: Enables alignment of targeted gene profiling datasets with reference scRNA-seq data in a low-dimensional space to support cell-type prediction.
- Technical Innovations: Extends Non-negative Matrix Factorization (NMF) by employing projective NMF with altered initialization procedures and an additional basis selection step to choose informative bases.
- Performance Superiority: Empirically outperforms existing state-of-the-art gene selection methods across multiple scRNA-seq datasets.
Scientific Applications:
- Targeted Gene Profiling Experiment Design: Guides selection of genes for targeted gene profiling experiments to focus assays on informative transcripts.
- Cell-Type Annotation: Supports cell-type annotation of targeted profiling data by integrating with reference scRNA-seq datasets in a shared low-dimensional representation.
Methodology:
Modifies the conventional PNMF algorithm by incorporating altered initialization procedures and an additional basis selection step and projects data into a low-dimensional space for alignment between targeted profiling and reference scRNA-seq datasets.
Topics
Details
- License:
- MIT
- Cost:
- Free of charge
- Tool Type:
- library
- Operating Systems:
- Mac, Linux, Windows
- Programming Languages:
- R
- Added:
- 11/20/2021
- Last Updated:
- 11/20/2021
Operations
Publications
Song D, Li K, Hemminger Z, Wollman R, Li JJ. scPNMF: sparse gene encoding of single cells to facilitate gene selection for targeted gene profiling. Bioinformatics. 2021;37(Supplement_1):i358-i366. doi:10.1093/bioinformatics/btab273. PMID:34252925. PMCID:PMC8275345.