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Biology subjects

Martel, A. L.

Publications and source records attributed to Martel, A. L..

2 recordsLinked to original sources

General stain deconvolution of histopathology images with physics-guided deep learning

Advances have been made in the use of deep learning to extract quantitative and predictive information from digital pathology slides, yet many barriers remain before clinical translation and deployment. In particular, models need to be generalizable despite the wide variations in image characteristics due to inter-scanner variability and differences in slide preparation protocols. This has led to an interest in stain deconvolution methods that could correct for the variability in image appearances. However, most existing stain deconvolution methods were developed and validated on specific datasets and perform poorly on unseen data. We developed Physics-Guided Deep Image Prior network for Stain deconvolution (PGDIPS), a method that combines a novel optical physics model and a self-supervised deep neural network to perform deconvolution for various classes and any number of stains, without the need of training data. PGDIPS outperformed state-of-the-art approaches for the deconvolution of conventional stain combinations, enabled analysis of previously unsupported special stains, and provided superior interpretability by explicitly encoding representations for stain properties and the light transmittance/absorbance process. PGDIPS is publicly available as an end-to-end off-the-shelf tool that does not require data curation, domain knowledge or high computation power.

bioinformatics↗

Automated and Manual Quantification of Tumour Cellularity in Digital Slides for Tumour Burden Assessment

AimsThe residual cancer burden index is an important quantitative measure used for assessing treatment response following neoadjuvant therapy for breast cancer. It has shown to be predictive of overall survival and is composed of two key metrics: qualitative assessment of lymph nodes and the percentage of invasive or in-situ tumour cellularity (TC) in the tumour bed (TB). Currently, TC is assessed through eye-balling of routine histopathology slides estimating the proportion of tumour cells within the TB. With the advances in production of digitized slides and increasing availability of slide scanners in pathology laboratories, there is potential to measure TC using automated algorithms with greater precision and accuracy.\n\nMethodsWe describe two methods for automated TC scoring: 1) a traditional approach to image analysis development whereby we mimic the pathologists workflow, and 2) a recent development in artificial intelligence in which features are learned automatically in deep neural networks using image data alone.\n\nResultsWe show strong agreements between automated and manual analysis of digital slides. Agreements between our trained deep neural networks and experts in this study (0.82) approach the inter-rater agreements between pathologists (0.89). We also reveal properties that are captured when we apply deep neural network to whole slide images, and discuss the potential of using such visualisations to improve upon TC assessment in the future.\n\nConclusionsTC scoring can be successfully automated by leveraging recent advancements in artificial intelligence, thereby alleviating the burden of manual analysis.

pathology↗