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Applying Deep Neural Network Analysis to High-Content Image-Based Assays
Samuel J Yang1, Scott L Lipnick2,3,4, Nina R Makhortova2,5
11 Google, LLC, Mountain View, CA, USA.
SLAS Discovery : Advancing Life Sciences R & D
|July 10, 2019
Summary
High-content imaging of skin cells can identify disease patterns. This approach, using Cell Painting and machine learning, successfully differentiated healthy individuals from those with spinal muscular atrophy (SMA).
Area of Science:
- Cellular imaging
- Machine learning
- Genetics
Background:
- Central nervous system (CNS) disorders often have unclear causes due to multiple pathological subtypes and complex genetic factors.
- Integrating diverse patient data, including imaging and genetic information, with machine learning offers a path to understanding disease heterogeneity.
Purpose of the Study:
- To investigate if high-content imaging of primary skin fibroblasts using the Cell Painting method can reveal disease-specific information.
- To develop and validate a machine learning model capable of distinguishing between healthy controls and patients with spinal muscular atrophy (SMA).
Main Methods:
- Utilized Cell Painting, a high-content imaging technique, on primary skin fibroblasts.
- Employed a pre-trained deep neural network and deep image embeddings to identify and account for technical nuisance signals in imaging data.
- Developed a convolutional neural network (CNN) using a subset of cells and tested its ability to differentiate unseen control and SMA patient cells, while controlling for batch effects.
Main Results:
- Technical variations (batch/plate type, location) introduced detectable signals but were manageable with appropriate experimental design.
- The developed CNN model successfully differentiated between healthy controls and SMA patients.
- Model performance was robust and not significantly affected by batch or plate type variations.
Conclusions:
- High-content imaging of fibroblasts, combined with machine learning, can effectively stratify patients based on disease state.
- This methodology provides a foundation for studying complex genetic neurological disorders with unknown subtypes.
- Further research is warranted to explore broader applications in CNS disorder subtyping.
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