alona
alona performs end-to-end analysis of single-cell RNA sequencing (scRNA-seq) data to enable quality control, normalization and batch correction, graph-based clustering, marker-gene-based cell-type annotation, and differential gene expression analysis.
Key Features:
- Flexible Analysis Pipeline: Integrates multiple single-cell analysis algorithms and exposes a Python module framework for constructing custom workflows.
- Quality Filtering: Implements filters to retain high-quality cells and features for downstream analysis.
- Normalization and Batch Correction: Applies normalization and batch-correction methods to reduce technical variability across samples.
- Clustering and Cell Type Annotation: Uses a graph-based clustering strategy and annotates clusters using an extensive collection of marker genes or user-defined markers.
- Differential Gene Expression Analysis: Identifies genes with condition- or cluster-specific expression differences.
- Data Input: Accepts compressed gene expression matrices as input.
Scientific Applications:
- Cell Type Discovery: Identification of novel cell types and cellular heterogeneity from scRNA-seq datasets.
- Cell Atlas Construction: Generation of tissue- and organ-specific cellular atlases based on clustered and annotated single-cell profiles.
- Gene Expression Dynamics: Investigation of single-cell gene expression changes across biological conditions and experimental groups.
Methodology:
Computational steps explicitly include quality filtering, normalization and batch correction, graph-based clustering for cell identification, cluster annotation using predefined or user-specified marker genes, and differential gene expression analysis, implemented via a Python module and accepting compressed gene expression matrices.
Topics
Details
- Tool Type:
- web application, workflow
- Programming Languages:
- JavaScript, Python
- Added:
- 1/18/2021
- Last Updated:
- 1/23/2021
Operations
Publications
Franzén O, Björkegren JLM. alona: a web server for single-cell RNA-seq analysis. Bioinformatics. 2020;36(12):3910-3912. doi:10.1093/bioinformatics/btaa269. PMID:32324845. PMCID:PMC7320629.