3,967 research outputs found
Supervised machine learning based multi-task artificial intelligence classification of retinopathies
Artificial intelligence (AI) classification holds promise as a novel and
affordable screening tool for clinical management of ocular diseases. Rural and
underserved areas, which suffer from lack of access to experienced
ophthalmologists may particularly benefit from this technology. Quantitative
optical coherence tomography angiography (OCTA) imaging provides excellent
capability to identify subtle vascular distortions, which are useful for
classifying retinovascular diseases. However, application of AI for
differentiation and classification of multiple eye diseases is not yet
established. In this study, we demonstrate supervised machine learning based
multi-task OCTA classification. We sought 1) to differentiate normal from
diseased ocular conditions, 2) to differentiate different ocular disease
conditions from each other, and 3) to stage the severity of each ocular
condition. Quantitative OCTA features, including blood vessel tortuosity (BVT),
blood vascular caliber (BVC), vessel perimeter index (VPI), blood vessel
density (BVD), foveal avascular zone (FAZ) area (FAZ-A), and FAZ contour
irregularity (FAZ-CI) were fully automatically extracted from the OCTA images.
A stepwise backward elimination approach was employed to identify sensitive
OCTA features and optimal-feature-combinations for the multi-task
classification. For proof-of-concept demonstration, diabetic retinopathy (DR)
and sickle cell retinopathy (SCR) were used to validate the supervised machine
leaning classifier. The presented AI classification methodology is applicable
and can be readily extended to other ocular diseases, holding promise to enable
a mass-screening platform for clinical deployment and telemedicine.Comment: Supplemental material attached at the en
Methods for Analysing Endothelial Cell Shape and Behaviour in Relation to the Focal Nature of Atherosclerosis
The aim of this thesis is to develop automated methods for the analysis of the
spatial patterns, and the functional behaviour of endothelial cells, viewed under
microscopy, with applications to the understanding of atherosclerosis.
Initially, a radial search approach to segmentation was attempted in order to
trace the cell and nuclei boundaries using a maximum likelihood algorithm; it
was found inadequate to detect the weak cell boundaries present in the available
data. A parametric cell shape model was then introduced to fit an equivalent
ellipse to the cell boundary by matching phase-invariant orientation fields of the
image and a candidate cell shape. This approach succeeded on good quality
images, but failed on images with weak cell boundaries. Finally, a support
vector machines based method, relying on a rich set of visual features, and a
small but high quality training dataset, was found to work well on large numbers
of cells even in the presence of strong intensity variations and imaging noise.
Using the segmentation results, several standard shear-stress dependent parameters
of cell morphology were studied, and evidence for similar behaviour
in some cell shape parameters was obtained in in-vivo cells and their nuclei.
Nuclear and cell orientations around immature and mature aortas were broadly
similar, suggesting that the pattern of flow direction near the wall stayed approximately
constant with age. The relation was less strong for the cell and
nuclear length-to-width ratios.
Two novel shape analysis approaches were attempted to find other properties
of cell shape which could be used to annotate or characterise patterns, since a
wide variability in cell and nuclear shapes was observed which did not appear
to fit the standard parameterisations. Although no firm conclusions can yet be
drawn, the work lays the foundation for future studies of cell morphology.
To draw inferences about patterns in the functional response of cells to flow,
which may play a role in the progression of disease, single-cell analysis was performed
using calcium sensitive florescence probes. Calcium transient rates were
found to change with flow, but more importantly, local patterns of synchronisation
in multi-cellular groups were discernable and appear to change with flow.
The patterns suggest a new functional mechanism in flow-mediation of cell-cell
calcium signalling
Understanding Health and Disease with Multidimensional Single-Cell Methods
Current efforts in the biomedical sciences and related interdisciplinary
fields are focused on gaining a molecular understanding of health and disease,
which is a problem of daunting complexity that spans many orders of magnitude
in characteristic length scales, from small molecules that regulate cell
function to cell ensembles that form tissues and organs working together as an
organism. In order to uncover the molecular nature of the emergent properties
of a cell, it is essential to measure multiple cell components simultaneously
in the same cell. In turn, cell heterogeneity requires multiple cells to be
measured in order to understand health and disease in the organism. This review
summarizes current efforts towards a data-driven framework that leverages
single-cell technologies to build robust signatures of healthy and diseased
phenotypes. While some approaches focus on multicolor flow cytometry data and
other methods are designed to analyze high-content image-based screens, we
emphasize the so-called Supercell/SVM paradigm (recently developed by the
authors of this review and collaborators) as a unified framework that captures
mesoscopic-scale emergence to build reliable phenotypes. Beyond their specific
contributions to basic and translational biomedical research, these efforts
illustrate, from a larger perspective, the powerful synergy that might be
achieved from bringing together methods and ideas from statistical physics,
data mining, and mathematics to solve the most pressing problems currently
facing the life sciences.Comment: 25 pages, 7 figures; revised version with minor changes. To appear in
J. Phys.: Cond. Mat
Patch-based Convolutional Neural Network for Whole Slide Tissue Image Classification
Convolutional Neural Networks (CNN) are state-of-the-art models for many
image classification tasks. However, to recognize cancer subtypes
automatically, training a CNN on gigapixel resolution Whole Slide Tissue Images
(WSI) is currently computationally impossible. The differentiation of cancer
subtypes is based on cellular-level visual features observed on image patch
scale. Therefore, we argue that in this situation, training a patch-level
classifier on image patches will perform better than or similar to an
image-level classifier. The challenge becomes how to intelligently combine
patch-level classification results and model the fact that not all patches will
be discriminative. We propose to train a decision fusion model to aggregate
patch-level predictions given by patch-level CNNs, which to the best of our
knowledge has not been shown before. Furthermore, we formulate a novel
Expectation-Maximization (EM) based method that automatically locates
discriminative patches robustly by utilizing the spatial relationships of
patches. We apply our method to the classification of glioma and non-small-cell
lung carcinoma cases into subtypes. The classification accuracy of our method
is similar to the inter-observer agreement between pathologists. Although it is
impossible to train CNNs on WSIs, we experimentally demonstrate using a
comparable non-cancer dataset of smaller images that a patch-based CNN can
outperform an image-based CNN
A Survey on Deep Learning in Medical Image Analysis
Deep learning algorithms, in particular convolutional networks, have rapidly
become a methodology of choice for analyzing medical images. This paper reviews
the major deep learning concepts pertinent to medical image analysis and
summarizes over 300 contributions to the field, most of which appeared in the
last year. We survey the use of deep learning for image classification, object
detection, segmentation, registration, and other tasks and provide concise
overviews of studies per application area. Open challenges and directions for
future research are discussed.Comment: Revised survey includes expanded discussion section and reworked
introductory section on common deep architectures. Added missed papers from
before Feb 1st 201
Detecting cells and analyzing their behaviors in microscopy images using deep neural networks
The computer-aided analysis in the medical imaging field has attracted a lot of attention for the past decade. The goal of computer-vision based medical image analysis is to provide automated tools to relieve the burden of human experts such as radiologists and physicians. More specifically, these computer-aided methods are to help identify, classify and quantify patterns in medical images. Recent advances in machine learning, more specifically, in the way of deep learning, have made a big leap to boost the performance of various medical applications. The fundamental core of these advances is exploiting hierarchical feature representations by various deep learning models, instead of handcrafted features based on domain-specific knowledge.
In the work presented in this dissertation, we are particularly interested in exploring the power of deep neural network in the Circulating Tumor Cells detection and mitosis event detection. We will introduce the Convolutional Neural Networks and the designed training methodology for Circulating Tumor Cells detection, a Hierarchical Convolutional Neural Networks model and a Two-Stream Bidirectional Long Short-Term Memory model for mitosis event detection and its stage localization in phase-contrast microscopy images”--Abstract, page iii
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