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Venugopalan, S.

Publications and source records attributed to Venugopalan, S..

2 recordsLinked to original sources

Deep learning and automated Cell Painting reveal Parkinson's disease-specific signatures in primary patient fibroblasts

Drug discovery for diseases such as Parkinsons disease are impeded by the lack of screenable cellular phenotypes. We present an unbiased phenotypic profiling platform that combines automated cell culture, high-content imaging, Cell Painting, and deep learning. We applied this platform to primary fibroblasts from 91 Parkinsons disease patients and matched healthy controls, creating the largest publicly available Cell Painting image dataset to date at 48 terabytes. We use fixed weights from a convolutional deep neural network trained on ImageNet to generate deep embeddings from each image and train machine learning models to detect morphological disease phenotypes. Our platforms robustness and sensitivity allow the detection of individual-specific variation with high fidelity across batches and plate layouts. Lastly, our models confidently separate LRRK2 and sporadic Parkinsons disease lines from healthy controls (receiver operating characteristic area under curve 0.79 (0.08 standard deviation)), supporting the capacity of this platform for complex disease modeling and drug screening applications.

cell biology↗

Batch Equalization with a Generative Adversarial Network

Advances in automation and imaging have made it possible to capture large image datasets for experiments that span multiple weeks with multiple experimental batches of data. However, accurate biological comparisons across the batches is challenged by the batch-to-batch variation due to uncontrollable experimental noise (e.g., different stain intensity or illumination conditions). To mediate the batch variation (i.e. the batch effect), we developed a batch equalization method that can transfer images from one batch to another while preserving the biological phenotype. The equalization method is trained as a generative adversarial network (GAN), using the StarGAN architecture that has shown considerable ability in doing style transfer for consumer images. After incorporating an additional objective that disentangles batch effect from biological features using an existing GAN framework, we show that the equalized images have less batch information as determined by a batch-prediction task and perform better in a biologically relevant task (e.g., Mechanism of Action prediction).

cell biology↗