3D-ADA

3D-ADA performs macromolecular structural classification in cellular electron cryo-tomograms (CECT) using adversarial domain adaptation to enable cross-dataset prediction under domain shift conditions.


Key Features:

  • Adversarial Domain Adaptation Framework: Uses deep learning–based adversarial training to minimize feature distribution differences between source and target datasets.
  • Dual Feature Extractor Architecture: Implements separate feature extractors for source and target domains to align feature representations across datasets.
  • Cross-Dataset Classification: Enables classifiers trained on annotated source datasets to predict macromolecular structures in target datasets without additional labeling.
  • Subtomogram Structural Classification: Supports classification of macromolecular structures in cellular electron cryo-tomography subtomograms.

Scientific Applications:

  • Macromolecular Structure Identification: Enables detection and classification of macromolecules within cellular electron cryo-tomograms.
  • Cross-Dataset Structural Analysis: Supports structural prediction across cryo-tomography datasets with differing imaging conditions.
  • Structural Cell Biology Research: Facilitates analysis of in situ macromolecular organization in cellular environments.

Methodology:

The method extracts discriminative features from labeled source-domain subtomograms using a deep learning feature extractor, trains a classifier on these features, and adversarially trains a target-domain feature extractor to align its feature distribution with the source domain for cross-dataset classification.

Topics

Details

License:
GPL-3.0
Tool Type:
command-line tool
Programming Languages:
Python
Added:
11/14/2019
Last Updated:
1/9/2021

Operations

Publications

Lin R, Zeng X, Kitani K, Xu M. Adversarial domain adaptation for cross data source macromolecule <i>in situ</i> structural classification in cellular electron cryo-tomograms. Bioinformatics. 2019;35(14):i260-i268. doi:10.1093/bioinformatics/btz364. PMID:31510673. PMCID:PMC6612867.

PMID: 31510673
PMCID: PMC6612867
Funding: - U.S. National Institutes of Health: P41 GM103712

Links