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.

PMID: 31359028
Funding: - Office of Biological and Environmental Research: DE-FC02-02ER63421

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