scholarly journals Combining weakly and strongly supervised learning improves strong supervision in Gleason pattern classification

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Sebastian Otálora ◽  
Niccolò Marini ◽  
Henning Müller ◽  
Manfredo Atzori

Abstract Background One challenge to train deep convolutional neural network (CNNs) models with whole slide images (WSIs) is providing the required large number of costly, manually annotated image regions. Strategies to alleviate the scarcity of annotated data include: using transfer learning, data augmentation and training the models with less expensive image-level annotations (weakly-supervised learning). However, it is not clear how to combine the use of transfer learning in a CNN model when different data sources are available for training or how to leverage from the combination of large amounts of weakly annotated images with a set of local region annotations. This paper aims to evaluate CNN training strategies based on transfer learning to leverage the combination of weak and strong annotations in heterogeneous data sources. The trade-off between classification performance and annotation effort is explored by evaluating a CNN that learns from strong labels (region annotations) and is later fine-tuned on a dataset with less expensive weak (image-level) labels. Results As expected, the model performance on strongly annotated data steadily increases as the percentage of strong annotations that are used increases, reaching a performance comparable to pathologists ($$\kappa = 0.691 \pm 0.02$$ κ = 0.691 ± 0.02 ). Nevertheless, the performance sharply decreases when applied for the WSI classification scenario with $$\kappa = 0.307 \pm 0.133$$ κ = 0.307 ± 0.133 . Moreover, it only provides a lower performance regardless of the number of annotations used. The model performance increases when fine-tuning the model for the task of Gleason scoring with the weak WSI labels $$\kappa = 0.528 \pm 0.05$$ κ = 0.528 ± 0.05 . Conclusion Combining weak and strong supervision improves strong supervision in classification of Gleason patterns using tissue microarrays (TMA) and WSI regions. Our results contribute very good strategies for training CNN models combining few annotated data and heterogeneous data sources. The performance increases in the controlled TMA scenario with the number of annotations used to train the model. Nevertheless, the performance is hindered when the trained TMA model is applied directly to the more challenging WSI classification problem. This demonstrates that a good pre-trained model for prostate cancer TMA image classification may lead to the best downstream model if fine-tuned on the WSI target dataset. We have made available the source code repository for reproducing the experiments in the paper: https://github.com/ilmaro8/Digital_Pathology_Transfer_Learning

2015 ◽  
Author(s):  
Lisa M. Breckels ◽  
Sean Holden ◽  
David Wojnar ◽  
Claire M. Mulvey ◽  
Andy Christoforou ◽  
...  

AbstractSub-cellular localisation of proteins is an essential post-translational regulatory mechanism that can be assayed using high-throughput mass spectrometry (MS). These MS-based spatial proteomics experiments enable us to pinpoint the sub-cellular distribution of thousands of proteins in a specific system under controlled conditions. Recent advances in high-throughput MS methods have yielded a plethora of experimental spatial proteomics data for the cell biology community. Yet, there are many third-party data sources, such as immunofluorescence microscopy or protein annotations and sequences, which represent a rich and vast source of complementary information. We present a unique transfer learning classification framework that utilises a nearest-neighbour or support vector machine system, to integrate heterogeneous data sources to considerably improve on the quantity and quality of sub-cellular protein assignment. We demonstrate the utility of our algorithms through evaluation of five experimental datasets, from four different species in conjunction with four different auxiliary data sources to classify proteins to tens of sub-cellular compartments with high generalisation accuracy. We further apply the method to an experiment on pluripotent mouse embryonic stem cells to classify a set of previously unknown proteins, and validate our findings against a recent high resolution map of the mouse stem cell proteome. The methodology is distributed as part of the open-source Bioconductor pRoloc suite for spatial proteomics data analysis.AbbreviationsLOPITLocalisation of Organelle Proteins by Isotope TaggingPCPProtein Correlation ProfilingMLMachine learningTLTransfer learningSVMSupport vector machinePCAPrincipal component analysisGOGene OntologyCCCellular compartmentiTRAQIsobaric tags for relative and absolute quantitationTMTTandem mass tagsMSMass spectrometry


2016 ◽  
Vol 53 ◽  
pp. 172-191 ◽  
Author(s):  
Eduardo M. Eisman ◽  
María Navarro ◽  
Juan Luis Castro

iScience ◽  
2021 ◽  
pp. 103298
Author(s):  
Anca Flavia Savulescu ◽  
Emmanuel Bouilhol ◽  
Nicolas Beaume ◽  
Macha Nikolski

2018 ◽  
Vol 42 (1) ◽  
pp. 39-61 ◽  
Author(s):  
Marko Gulić ◽  
Marin Vuković

Ontology matching plays an important role in the integration of heterogeneous data sources that are described by ontologies. In order to determine correspondences between ontologies, a set of matchers can be used. After the execution of these matchers and the aggregation of the results obtained by these matchers, a final alignment method is executed in order to select appropriate correspondences between entities of compared ontologies. The final alignment method is an important part of the ontology matching process because it directly determines the output result of this process. In this paper we improve our iterative final alignment method by introducing an automatic adjustment of final alignment threshold as well as a new rule for determining false correspondences with similarity values greater than adjusted threshold. An evaluation of the method is performed on the test ontologies of the OAEI evaluation contest and a comparison with other final alignment methods is given.


Sign in / Sign up

Export Citation Format

Share Document