796 research outputs found
SubCMap: subject and condition specific effect maps
Current methods for statistical analysis of neuroimaging data identify condition related structural alterations in the human brain by detecting group differences. They construct detailed maps showing population-wide changes due to a condition of interest. Although extremely useful, methods do not provide information on the subject-specific structural alterations and they have limited diagnostic value because group assignments for each subject are required for the analysis. In this article, we propose SubCMap, a novel method to detect subject and condition specific structural alterations. SubCMap is designed to work without the group assignment information in order to provide diagnostic value. Unlike outlier detection methods, SubCMap detections are condition-specific and can be used to study the effects of various conditions or for diagnosing diseases. The method combines techniques from classification, generalization error estimation and image restoration to the identify the condition-related alterations. Experimental evaluation is performed on synthetically generated data as well as data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. Results on synthetic data demonstrate the advantages of SubCMap compared to population-wide techniques and higher detection accuracy compared to outlier detection. Analysis with the ADNI dataset show that SubCMap detections on cortical thickness data well correlate with non-imaging markers of Alzheimer's Disease (AD), the Mini Mental State Examination Score and Cerebrospinal Fluid amyloid-β levels, suggesting the proposed method well captures the inter-subject variation of AD effects
Learning to Detect and Track Cells for Quantitative Analysis of Time-Lapse Microscopic Image Sequences
© 2015 IEEE.Studying the behaviour of cells using time-lapse microscopic imaging requires automated processing pipelines that enable quantitative analysis of a large number of cells. We propose a pipeline based on state-of-the-art methods for background motion compensation, cell detection, and tracking which are integrated into a novel semi-automated, learning based analysis tool. Motion compensation is performed by employing an efficient nonlinear registration method based on powerful discrete graph optimisation. Robust detection and tracking of cells is based on classifier learning which only requires a small number of manual annotations. Cell motion trajectories are generated using a recent global data association method and linear programming. Our approach is robust to the presence of significant motion and imaging artifacts. Promising results are presented on different sets of in-vivo fluorescent microscopic image sequences
Encoding atlases by randomized classification forests for efficient multi-atlas label propagation
Uncertainty-driven Forest Predictors for Vertebra Localization and Segmentation
Accurate localization, identification and segmentation of vertebrae is an important task in medical and biological image analysis. The prevailing approach to solve such a task is to first generate pixelindependent features for each vertebra, e.g. via a random forest predictor, which are then fed into an MRF-based objective to infer the optimal MAP solution of a constellation model. We abandon this static, twostage approach and mix feature generation with model-based inference in a new, more flexible, way. We evaluate our method on two data sets with different objectives. The first is semantic segmentation of a 21-part body plan of zebrafish embryos in microscopy images, and the second is localization and identification of vertebrae in benchmark human CT
Deformable Registration through Learning of Context-Specific Metric Aggregation
We propose a novel weakly supervised discriminative algorithm for learning
context specific registration metrics as a linear combination of conventional
similarity measures. Conventional metrics have been extensively used over the
past two decades and therefore both their strengths and limitations are known.
The challenge is to find the optimal relative weighting (or parameters) of
different metrics forming the similarity measure of the registration algorithm.
Hand-tuning these parameters would result in sub optimal solutions and quickly
become infeasible as the number of metrics increases. Furthermore, such
hand-crafted combination can only happen at global scale (entire volume) and
therefore will not be able to account for the different tissue properties. We
propose a learning algorithm for estimating these parameters locally,
conditioned to the data semantic classes. The objective function of our
formulation is a special case of non-convex function, difference of convex
function, which we optimize using the concave convex procedure. As a proof of
concept, we show the impact of our approach on three challenging datasets for
different anatomical structures and modalities.Comment: Accepted for publication in the 8th International Workshop on Machine
Learning in Medical Imaging (MLMI 2017), in conjunction with MICCAI 201
Automatic Segmentation, Localization, and Identification of Vertebrae in 3D CT Images Using Cascaded Convolutional Neural Networks
This paper presents a method for automatic segmentation, localization, and
identification of vertebrae in arbitrary 3D CT images. Many previous works do
not perform the three tasks simultaneously even though requiring a priori
knowledge of which part of the anatomy is visible in the 3D CT images. Our
method tackles all these tasks in a single multi-stage framework without any
assumptions. In the first stage, we train a 3D Fully Convolutional Networks to
find the bounding boxes of the cervical, thoracic, and lumbar vertebrae. In the
second stage, we train an iterative 3D Fully Convolutional Networks to segment
individual vertebrae in the bounding box. The input to the second networks have
an auxiliary channel in addition to the 3D CT images. Given the segmented
vertebra regions in the auxiliary channel, the networks output the next
vertebra. The proposed method is evaluated in terms of segmentation,
localization, and identification accuracy with two public datasets of 15 3D CT
images from the MICCAI CSI 2014 workshop challenge and 302 3D CT images with
various pathologies introduced in [1]. Our method achieved a mean Dice score of
96%, a mean localization error of 8.3 mm, and a mean identification rate of
84%. In summary, our method achieved better performance than all existing works
in all the three metrics
Towards continual learning in medical imaging
This work investigates continual learning of two segmentation tasks in brain MRI with neural networks. To explore in this context the capabilities of current methods for countering catastrophic forgetting of the first task when a new one is learned, we investigate elastic weight consolidation, a recently proposed method based on Fisher information, originally evaluated on reinforcement learning of Atari games. We use it to sequentially learn segmentation of normal brain structures and then segmentation of white matter lesions. Our findings show this recent method reduces catastrophic forgetting, while large room for improvement exists in these challenging settings for continual learning
Algorithmic encoding of protected characteristics in chest X-ray disease detection models
Background It has been rightfully emphasized that the use of AI for clinical decision making could amplify health disparities. An algorithm may encode protected characteristics, and then use this information for making predictions due to undesirable correlations in the (historical) training data. It remains unclear how we can establish whether such information is actually used. Besides the scarcity of data from underserved populations, very little is known about how dataset biases manifest in predictive models and how this may result in disparate performance. This article aims to shed some light on these issues by exploring methodology for subgroup analysis in image-based disease detection models. Methods We utilize two publicly available chest X-ray datasets, CheXpert and MIMIC-CXR, to study performance disparities across race and biological sex in deep learning models. We explore test set resampling, transfer learning, multitask learning, and model inspection to assess the relationship between the encoding of protected characteristics and disease detection performance across subgroups. Findings We confirm subgroup disparities in terms of shifted true and false positive rates which are partially removed after correcting for population and prevalence shifts in the test sets. We find that transfer learning alone is insufficient for establishing whether specific patient information is used for making predictions. The proposed combination of test-set resampling, multitask learning, and model inspection reveals valuable insights about the way protected characteristics are encoded in the feature representations of deep neural networks. Interpretation Subgroup analysis is key for identifying performance disparities of AI models, but statistical differences across subgroups need to be taken into account when analyzing potential biases in disease detection. The proposed methodology provides a comprehensive framework for subgroup analysis enabling further research into the underlying causes of disparities. Funding European Research Council Horizon 2020, UK Research and Innovation
Morpho-MNIST: Quantitative Assessment and Diagnostics for Representation Learning
Revealing latent structure in data is an active field of research, having brought exciting new models such as variational autoencoders and generative adversarial networks, and is essential to push machine learning towards unsupervised knowledge discovery. However, a major challenge is the lack of suitable benchmarks for an objective and quantitative evaluation of learned representations. To address this issue we introduce Morpho-MNIST. We extend the popular MNIST dataset by adding a morphometric analysis enabling quantitative comparison of different models, identification of the roles of latent variables, and characterisation of sample diversity. We further propose a set of quantifiable perturbations to assess the performance of unsupervised and supervised methods on challenging tasks such as outlier detection and domain adaptation
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