Astir

Astir assigns cell types in single-cell multiplexed imaging and proteomics datasets using a probabilistic framework that integrates marker protein priors and machine learning for automated, reference-free cell-type annotation.


Key Features:

  • Probabilistic Modelling: Astir employs a probabilistic model that integrates prior knowledge of marker proteins to assign cells to known or unknown cell types.
  • Deep Recognition Neural Networks: Utilizing deep recognition neural networks, Astir performs fast Bayesian inference to enable scalable annotation.
  • Scalability and Implementation: Implemented in PyTorch, Astir scales to datasets comprising millions of single cells and supports multiple single-cell technologies and antibody panels, including Imaging Mass Cytometry (IMC).
  • Reference-free Annotation: Astir provides cell type annotations without requiring previously annotated reference datasets, enabling discovery of uncharacterized cell types.

Scientific Applications:

  • Tumor Microenvironment Analysis: Analyze the spatial architecture of tumor microenvironments, quantify immune cell influx, and assess spatial heterogeneity in patient samples.
  • Cancer Research: Support studies of disease processes such as cancer initiation and progression by providing accurate cell type annotations across imaging and proteomics modalities.
  • Multiplexed Imaging and Proteomics Studies: Apply to Imaging Mass Cytometry, suspension mass cytometry, and microscopy datasets to annotate cellular heterogeneity across antibody panels.

Methodology:

Astir integrates prior biological knowledge of marker proteins into a probabilistic model and uses deep recognition neural networks to perform fast Bayesian inference via stochastic variational inference; the implementation uses PyTorch.

Topics

Details

License:
GPL-2.0
Tool Type:
library
Programming Languages:
Python
Added:
3/19/2021
Last Updated:
4/11/2021

Operations

Publications

Geuenich MJ, Hou J, Lee S, Jackson HW, Campbell KR. Automated assignment of cell identity from single-cell multiplexed imaging and proteomic data. Unknown Journal. 2021. doi:10.1101/2021.02.17.431633.

Documentation