SHARP
SHARP applies ensemble random projection and multi-layer meta-clustering to perform fast, scalable dimensionality reduction and clustering of single-cell RNA sequencing (scRNA-seq) data while preserving cell-to-cell distances.
Key Features:
- Ensemble Random Projection (RP): Reduces dimensionality of large-scale scRNA-seq data while preserving critical cell-to-cell distances in the reduced-dimensional space.
- Multi-layer Meta-clustering: Integrates multiple clustering layers to achieve high clustering accuracy on large datasets.
- Scalability: Capable of processing datasets containing up to 10 million cells.
- R-based Implementation: Provided as an R-based solution for clustering very large single-cell RNA-seq datasets.
- Benchmarking: Demonstrated superior speed and accuracy in comprehensive benchmarking on 17 public scRNA-seq datasets, notably for datasets larger than 40,000 cells.
Scientific Applications:
- Large-scale scRNA-seq clustering: Clustering of millions of single cells to identify cell populations and heterogeneity.
- Dimensionality reduction for single-cell transcriptomics: Generating reduced-dimensional representations that preserve intercellular distances for downstream analysis.
- Method benchmarking: Comparative evaluation of speed and accuracy across public scRNA-seq datasets.
Methodology:
Ensemble random projection (RP) for dimensionality reduction, preservation of cell-to-cell distances in the reduced space, and multi-layer meta-clustering; performance assessed on 17 public scRNA-seq datasets.
Topics
Details
- Programming Languages:
- R
- Added:
- 1/18/2021
- Last Updated:
- 2/16/2021
Operations
Publications
Wan S, Kim J, Won KJ. SHARP: hyperfast and accurate processing of single-cell RNA-seq data via ensemble random projection. Genome Research. 2020;30(2):205-213. doi:10.1101/gr.254557.119. PMID:31992615. PMCID:PMC7050522.
PMID: 31992615
PMCID: PMC7050522
Funding: - National Institute of Diabetes and Digestive and Kidney Diseases: R01 DK106027
- Novo Nordisk Foundation: NNF17CC0027852