scVAE
scVAE models single-cell RNA sequencing (scRNA-seq) count data using variational auto-encoders (VAEs) to learn latent representations and enable likelihood-based model comparison.
Key Features:
- Direct Use of Raw Count Data: Models raw scRNA-seq count data directly without requiring intermediate normalization or transformation steps.
- Latent Representation Learning: Learns a latent representation for each cell to capture underlying biological variability and cellular heterogeneity.
- Deep Generative Models: Employs variational auto-encoders as deep generative models to represent complex gene expression distributions across cells.
- Likelihood-Based Model Comparison: Uses likelihood-based criteria to compare and evaluate alternative models on scRNA-seq data.
- Incorporation of Count Likelihood Functions: Tests and employs various count likelihood functions to model gene expression counts accurately.
- A Priori Clustering in Latent Space: Integrates a priori clustering within the latent space to inform and improve cell clustering outcomes.
Scientific Applications:
- Cell Type Identification and Clustering: Produces latent-space clustering of single cells that reflects distinct cell types for cellular taxonomy and population analyses.
- Gene Expression Estimation: Estimates expected gene expression levels from modeled count distributions to support downstream analysis of gene regulation and differential expression.
Methodology:
Applies variational auto-encoders to model raw count scRNA-seq data, evaluates multiple count likelihood functions, performs likelihood-based model comparison, incorporates a priori clustering in latent space, and is implemented in Python using TensorFlow.
Topics
Details
- License:
- Apache-2.0
- Programming Languages:
- Python
- Added:
- 1/18/2021
- Last Updated:
- 2/13/2021
Operations
Publications
Grønbech CH, Vording MF, Timshel PN, Sønderby CK, Pers TH, Winther O. scVAE: variational auto-encoders for single-cell gene expression data. Bioinformatics. 2020;36(16):4415-4422. doi:10.1093/bioinformatics/btaa293. PMID:32415966.
PMID: 32415966
Funding: - Lundbeck Foundation: R190 2014-3904
- Novo Nordisk Foundation: NNF18CC0034900
- Novo Nordisk Foundation Center for Basic Metabolic Research: NNF16OC0021496