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Joseph Paul Cohen

Publications and source records attributed to Joseph Paul Cohen.

At least 37 records · Page 2Linked to original sources

ivadomed: A Medical Imaging Deep Learning Toolbox

ivadomed is an open-source Python package for designing, end-to-end training, and evaluating deep learning models applied to medical imaging data. The package includes APIs, command-line tools, documentation, and tutorials. ivadomed also includes pre-trained models such as spinal tumor segmentation and vertebral labeling. Original features of ivadomed include a data loader that can parse image metadata (e.g., acquisition parameters, image contrast, resolution) and subject metadata (e.g., pathology, age, sex) for custom data splitting or extra information during training and evaluation. Any dataset following the Brain Imaging Data Structure (BIDS) convention will be compatible with ivadomed without the need to manually organize the data, which is typically a tedious task. Beyond the traditional deep learning methods, ivadomed features cutting-edge architectures, such as FiLM and HeMis, as well as various uncertainty estimation methods (aleatoric and epistemic), and losses adapted to imbalanced classes and non-binary predictions. Each step is conveniently configurable via a single file. At the same time, the code is highly modular to allow addition/modification of an architecture or pre/post-processing steps. Example applications of ivadomed include MRI object detection, segmentation, and labeling of anatomical and pathological structures. Overall, ivadomed enables easy and quick exploration of the latest advances in deep learning for medical imaging applications. ivadomed's main project page is available at https://ivadomed.org.

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DiVA: Diverse Visual Feature Aggregation for Deep Metric Learning

Visual Similarity plays an important role in many computer vision applications. Deep metric learning (DML) is a powerful framework for learning such similarities which not only generalize from training data to identically distributed test distributions, but in particular also translate to unknown test classes. However, its prevailing learning paradigm is class-discriminative supervised training, which typically results in representations specialized in separating training classes. For effective generalization, however, such an image representation needs to capture a diverse range of data characteristics. To this end, we propose and study multiple complementary learning tasks, targeting conceptually different data relationships by only resorting to the available training samples and labels of a standard DML setting. Through simultaneous optimization of our tasks we learn a single model to aggregate their training signals, resulting in strong generalization and state-of-the-art performance on multiple established DML benchmark datasets.

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A Benchmark of Medical Out of Distribution Detection

Motivation: Deep learning models deployed for use on medical tasks can be equipped with Out-of-Distribution Detection (OoDD) methods in order to avoid erroneous predictions. However it is unclear which OoDD method should be used in practice. Specific Problem: Systems trained for one particular domain of images cannot be expected to perform accurately on images of a different domain. These images should be flagged by an OoDD method prior to diagnosis. Our approach: This paper defines 3 categories of OoD examples and benchmarks popular OoDD methods in three domains of medical imaging: chest X-ray, fundus imaging, and histology slides. Results: Our experiments show that despite methods yielding good results on some categories of out-of-distribution samples, they fail to recognize images close to the training distribution. Conclusion: We find a simple binary classifier on the feature representation has the best accuracy and AUPRC on average. Users of diagnostic tools which employ these OoDD methods should still remain vigilant that images very close to the training distribution yet not in it could yield unexpected results.

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Revisiting Training Strategies and Generalization Performance in Deep Metric Learning

Deep Metric Learning (DML) is arguably one of the most influential lines of research for learning visual similarities with many proposed approaches every year. Although the field benefits from the rapid progress, the divergence in training protocols, architectures, and parameter choices make an unbiased comparison difficult. To provide a consistent reference point, we revisit the most widely used DML objective functions and conduct a study of the crucial parameter choices as well as the commonly neglected mini-batch sampling process. Under consistent comparison, DML objectives show much higher saturation than indicated by literature. Further based on our analysis, we uncover a correlation between the embedding space density and compression to the generalization performance of DML models. Exploiting these insights, we propose a simple, yet effective, training regularization to reliably boost the performance of ranking-based DML models on various standard benchmark datasets. Code and a publicly accessible WandB-repo are available at https://github.com/Confusezius/Revisiting_Deep_Metric_Learning_PyTorch.

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Uniformizing Techniques to Process CT scans with 3D CNNs for Tuberculosis Prediction

A common approach to medical image analysis on volumetric data uses deep 2D convolutional neural networks (CNNs). This is largely attributed to the challenges imposed by the nature of the 3D data: variable volume size, GPU exhaustion during optimization. However, dealing with the individual slices independently in 2D CNNs deliberately discards the depth information which results in poor performance for the intended task. Therefore, it is important to develop methods that not only overcome the heavy memory and computation requirements but also leverage the 3D information. To this end, we evaluate a set of volume uniformizing methods to address the aforementioned issues. The first method involves sampling information evenly from a subset of the volume. Another method exploits the full geometry of the 3D volume by interpolating over the z-axis. We demonstrate performance improvements using controlled ablation studies as well as put this approach to the test on the ImageCLEF Tuberculosis Severity Assessment 2019 benchmark. We report 73% area under curve (AUC) and binary classification accuracy (ACC) of 67.5% on the test set beating all methods which leveraged only image information (without using clinical meta-data) achieving 5-th position overall. All codes and models are made available at https://github.com/hasibzunair/uniformizing-3D.

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Predicting COVID-19 Pneumonia Severity on Chest X-ray with Deep Learning

Purpose: The need to streamline patient management for COVID-19 has become more pressing than ever. Chest X-rays provide a non-invasive (potentially bedside) tool to monitor the progression of the disease. In this study, we present a severity score prediction model for COVID-19 pneumonia for frontal chest X-ray images. Such a tool can gauge severity of COVID-19 lung infections (and pneumonia in general) that can be used for escalation or de-escalation of care as well as monitoring treatment efficacy, especially in the ICU. Methods: Images from a public COVID-19 database were scored retrospectively by three blinded experts in terms of the extent of lung involvement as well as the degree of opacity. A neural network model that was pre-trained on large (non-COVID-19) chest X-ray datasets is used to construct features for COVID-19 images which are predictive for our task. Results: This study finds that training a regression model on a subset of the outputs from an this pre-trained chest X-ray model predicts our geographic extent score (range 0-8) with 1.14 mean absolute error (MAE) and our lung opacity score (range 0-6) with 0.78 MAE. Conclusions: These results indicate that our model's ability to gauge severity of COVID-19 lung infections could be used for escalation or de-escalation of care as well as monitoring treatment efficacy, especially in the intensive care unit (ICU). A proper clinical trial is needed to evaluate efficacy. To enable this we make our code, labels, and data available online at https://github.com/mlmed/torchxrayvision/tree/master/scripts/covid-severity and https://github.com/ieee8023/covid-chestxray-dataset

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Automatic segmentation of spinal multiple sclerosis lesions: How to generalize across MRI contrasts?

Despite recent improvements in medical image segmentation, the ability to generalize across imaging contrasts remains an open issue. To tackle this challenge, we implement Feature-wise Linear Modulation (FiLM) to leverage physics knowledge within the segmentation model and learn the characteristics of each contrast. Interestingly, a well-optimised U-Net reached the same performance as our FiLMed-Unet on a multi-contrast dataset (0.72 of Dice score), which suggests that there is a bottleneck in spinal MS lesion segmentation different from the generalization across varying contrasts. This bottleneck likely stems from inter-rater variability, which is estimated at 0.61 of Dice score in our dataset.

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On the limits of cross-domain generalization in automated X-ray prediction

This large scale study focuses on quantifying what X-rays diagnostic prediction tasks generalize well across multiple different datasets. We present evidence that the issue of generalization is not due to a shift in the images but instead a shift in the labels. We study the cross-domain performance, agreement between models, and model representations. We find interesting discrepancies between performance and agreement where models which both achieve good performance disagree in their predictions as well as models which agree yet achieve poor performance. We also test for concept similarity by regularizing a network to group tasks across multiple datasets together and observe variation across the tasks. All code is made available online and data is publicly available: https://github.com/mlmed/torchxrayvision

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COVID-19 Image Data Collection

This paper describes the initial COVID-19 open image data collection. It was created by assembling medical images from websites and publications and currently contains 123 frontal view X-rays.

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Spine intervertebral disc labeling using a fully convolutional redundant counting model

Labeling intervertebral discs is relevant as it notably enables clinicians to understand the relationship between a patient's symptoms (pain, paralysis) and the exact level of spinal cord injury. However manually labeling those discs is a tedious and user-biased task which would benefit from automated methods. While some automated methods already exist for MRI and CT-scan, they are either not publicly available, or fail to generalize across various imaging contrasts. In this paper we combine a Fully Convolutional Network (FCN) with inception modules to localize and label intervertebral discs. We demonstrate a proof-of-concept application in a publicly-available multi-center and multi-contrast MRI database (n=235 subjects). The code is publicly available at https://github.com/neuropoly/vertebral-labeling-deep-learning.

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Quantifying the Value of Lateral Views in Deep Learning for Chest X-rays

Most deep learning models in chest X-ray prediction utilize the posteroanterior (PA) view due to the lack of other views available. PadChest is a large-scale chest X-ray dataset that has almost 200 labels and multiple views available. In this work, we use PadChest to explore multiple approaches to merging the PA and lateral views for predicting the radiological labels associated with the X-ray image. We find that different methods of merging the model utilize the lateral view differently. We also find that including the lateral view increases performance for 32 labels in the dataset, while being neutral for the others. The increase in overall performance is comparable to the one obtained by using only the PA view with twice the amount of patients in the training set.

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Chester: A Web Delivered Locally Computed Chest X-Ray Disease Prediction System

In order to bridge the gap between Deep Learning researchers and medical professionals we develop a very accessible free prototype system which can be used by medical professionals to understand the reality of Deep Learning tools for chest X-ray diagnostics. The system is designed to be a second opinion where a user can process an image to confirm or aid in their diagnosis. Code and network weights are delivered via a URL to a web browser (including cell phones) but the patient data remains on the users machine and all processing occurs locally. This paper discusses the three main components in detail: out-of-distribution detection, disease prediction, and prediction explanation. The system open source and freely available here: https://mlmed.org/tools/xray

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Analysis of Gene Interaction Graphs as Prior Knowledge for Machine Learning Models

Gene interaction graphs aim to capture various relationships between genes and can represent decades of biology research. When trying to make predictions from genomic data, those graphs could be used to overcome the curse of dimensionality by making machine learning models sparser and more consistent with biological common knowledge. In this work, we focus on assessing how well those graphs capture dependencies seen in gene expression data to evaluate the adequacy of the prior knowledge provided by those graphs. We propose a condition graphs should satisfy to provide good prior knowledge and test it using `Single Gene Inference' tasks. We also compare with randomly generated graphs, aiming to measure the true benefit of using biologically relevant graphs in this context, and validate our findings with five clinical tasks. We find some graphs capture relevant dependencies for most genes while being very sparse. Our analysis with random graphs finds that dependencies can be captured almost as well at random which suggests that, in terms of gene expression levels, the relevant information about the state of the cell is spread across many genes.

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Is graph-based feature selection of genes better than random?

Gene interaction graphs aim to capture various relationships between genes and represent decades of biology research. When trying to make predictions from genomic data, those graphs could be used to overcome the curse of dimensionality by making machine learning models sparser and more consistent with biological common knowledge. In this work, we focus on assessing whether those graphs capture dependencies seen in gene expression data better than random. We formulate a condition that graphs should satisfy to provide a good prior knowledge and propose to test it using a `Single Gene Inference' (SGI) task. We compare random graphs with seven major gene interaction graphs published by different research groups, aiming to measure the true benefit of using biologically relevant graphs in this context. Our analysis finds that dependencies can be captured almost as well at random which suggests that, in terms of gene expression levels, the relevant information about the state of the cell is spread across many genes.

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Icentia11K: An Unsupervised Representation Learning Dataset for Arrhythmia Subtype Discovery

We release the largest public ECG dataset of continuous raw signals for representation learning containing 11 thousand patients and 2 billion labelled beats. Our goal is to enable semi-supervised ECG models to be made as well as to discover unknown subtypes of arrhythmia and anomalous ECG signal events. To this end, we propose an unsupervised representation learning task, evaluated in a semi-supervised fashion. We provide a set of baselines for different feature extractors that can be built upon. Additionally, we perform qualitative evaluations on results from PCA embeddings, where we identify some clustering of known subtypes indicating the potential for representation learning in arrhythmia sub-type discovery.

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The TCGA Meta-Dataset Clinical Benchmark

Machine learning is bringing a paradigm shift to healthcare by changing the process of disease diagnosis and prognosis in clinics and hospitals. This development equips doctors and medical staff with tools to evaluate their hypotheses and hence make more precise decisions. Although most current research in the literature seeks to develop techniques and methods for predicting one particular clinical outcome, this approach is far from the reality of clinical decision making in which you have to consider several factors simultaneously. In addition, it is difficult to follow the recent progress concretely as there is a lack of consistency in benchmark datasets and task definitions in the field of Genomics. To address the aforementioned issues, we provide a clinical Meta-Dataset derived from the publicly available data hub called The Cancer Genome Atlas Program (TCGA) that contains 174 tasks. We believe those tasks could be good proxy tasks to develop methods which can work on a few samples of gene expression data. Also, learning to predict multiple clinical variables using gene-expression data is an important task due to the variety of phenotypes in clinical problems and lack of samples for some of the rare variables. The defined tasks cover a wide range of clinical problems including predicting tumor tissue site, white cell count, histological type, family history of cancer, gender, and many others which we explain later in the paper. Each task represents an independent dataset. We use regression and neural network baselines for all the tasks using only 150 samples and compare their performance.

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Torchmeta: A Meta-Learning library for PyTorch

The constant introduction of standardized benchmarks in the literature has helped accelerating the recent advances in meta-learning research. They offer a way to get a fair comparison between different algorithms, and the wide range of datasets available allows full control over the complexity of this evaluation. However, for a large majority of code available online, the data pipeline is often specific to one dataset, and testing on another dataset requires significant rework. We introduce Torchmeta, a library built on top of PyTorch that enables seamless and consistent evaluation of meta-learning algorithms on multiple datasets, by providing data-loaders for most of the standard benchmarks in few-shot classification and regression, with a new meta-dataset abstraction. It also features some extensions for PyTorch to simplify the development of models compatible with meta-learning algorithms. The code is available here: https://github.com/tristandeleu/pytorch-meta

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Do Lateral Views Help Automated Chest X-ray Predictions?

Most convolutional neural networks in chest radiology use only the frontal posteroanterior (PA) view to make a prediction. However the lateral view is known to help the diagnosis of certain diseases and conditions. The recently released PadChest dataset contains paired PA and lateral views, allowing us to study for which diseases and conditions the performance of a neural network improves when provided a lateral x-ray view as opposed to a frontal posteroanterior (PA) view. Using a simple DenseNet model, we find that using the lateral view increases the AUC of 8 of the 56 labels in our data and achieves the same performance as the PA view for 21 of the labels. We find that using the PA and lateral views jointly doesn't trivially lead to an increase in performance but suggest further investigation.

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