ACTINN
ACTINN applies neural network classification to automate cell type identification in single-cell RNA sequencing (scRNA-seq) data using a model with three hidden layers to learn gene expression patterns for cross-dataset prediction.
Key Features:
- Neural Network Architecture: A neural network with three hidden layers is trained on datasets with predefined cell type annotations to learn complex patterns in gene expression data.
- Training Datasets: The model was trained on the Tabula Muris Atlas (mouse) and a human immune cell dataset.
- Application Scope: ACTINN has been applied to predict cell types in mouse leukocytes, human peripheral blood mononuclear cells (PBMCs), and human T cell subtypes.
- Speed and Accuracy: The model is designed for rapid processing and to mitigate unwanted variation and the absence of canonical markers that can affect clustering-based methods.
- Complementary Tool: ACTINN functions alongside existing scRNA-seq methodologies to reduce manual annotation and biases from literature-based lookup.
- Software Implementation: The codebase is implemented in Python.
Scientific Applications:
- Cell Type Identification: Automated classification of cell types in scRNA-seq datasets for large-scale studies.
- Cross-Species Analysis: Application to both mouse and human datasets supports comparative and translational research.
- Research Efficiency: Reduction of manual annotation and literature lookup accelerates annotation of large or complex datasets.
Methodology:
Train a neural network with three hidden layers on datasets with known cell type annotations (e.g., Tabula Muris Atlas and a human immune cell dataset), then apply the trained model to predict cell types for new scRNA-seq datasets based on learned parameters to reduce noise and variability effects.
Topics
Details
- Programming Languages:
- R, Python
- Added:
- 11/14/2019
- Last Updated:
- 12/1/2020
Operations
Publications
Ma F, Pellegrini M. ACTINN: automated identification of cell types in single cell RNA sequencing. Bioinformatics. 2019;36(2):533-538. doi:10.1093/bioinformatics/btz592. PMID:31359028.