654 research outputs found
Active Mean Fields for Probabilistic Image Segmentation: Connections with Chan-Vese and Rudin-Osher-Fatemi Models
Segmentation is a fundamental task for extracting semantically meaningful
regions from an image. The goal of segmentation algorithms is to accurately
assign object labels to each image location. However, image-noise, shortcomings
of algorithms, and image ambiguities cause uncertainty in label assignment.
Estimating the uncertainty in label assignment is important in multiple
application domains, such as segmenting tumors from medical images for
radiation treatment planning. One way to estimate these uncertainties is
through the computation of posteriors of Bayesian models, which is
computationally prohibitive for many practical applications. On the other hand,
most computationally efficient methods fail to estimate label uncertainty. We
therefore propose in this paper the Active Mean Fields (AMF) approach, a
technique based on Bayesian modeling that uses a mean-field approximation to
efficiently compute a segmentation and its corresponding uncertainty. Based on
a variational formulation, the resulting convex model combines any
label-likelihood measure with a prior on the length of the segmentation
boundary. A specific implementation of that model is the Chan-Vese segmentation
model (CV), in which the binary segmentation task is defined by a Gaussian
likelihood and a prior regularizing the length of the segmentation boundary.
Furthermore, the Euler-Lagrange equations derived from the AMF model are
equivalent to those of the popular Rudin-Osher-Fatemi (ROF) model for image
denoising. Solutions to the AMF model can thus be implemented by directly
utilizing highly-efficient ROF solvers on log-likelihood ratio fields. We
qualitatively assess the approach on synthetic data as well as on real natural
and medical images. For a quantitative evaluation, we apply our approach to the
icgbench dataset
Multi-Atlas Segmentation using Partially Annotated Data: Methods and Annotation Strategies
Multi-atlas segmentation is a widely used tool in medical image analysis,
providing robust and accurate results by learning from annotated atlas
datasets. However, the availability of fully annotated atlas images for
training is limited due to the time required for the labelling task.
Segmentation methods requiring only a proportion of each atlas image to be
labelled could therefore reduce the workload on expert raters tasked with
annotating atlas images. To address this issue, we first re-examine the
labelling problem common in many existing approaches and formulate its solution
in terms of a Markov Random Field energy minimisation problem on a graph
connecting atlases and the target image. This provides a unifying framework for
multi-atlas segmentation. We then show how modifications in the graph
configuration of the proposed framework enable the use of partially annotated
atlas images and investigate different partial annotation strategies. The
proposed method was evaluated on two Magnetic Resonance Imaging (MRI) datasets
for hippocampal and cardiac segmentation. Experiments were performed aimed at
(1) recreating existing segmentation techniques with the proposed framework and
(2) demonstrating the potential of employing sparsely annotated atlas data for
multi-atlas segmentation
Roto-Translation Equivariant Convolutional Networks: Application to Histopathology Image Analysis
Rotation-invariance is a desired property of machine-learning models for
medical image analysis and in particular for computational pathology
applications. We propose a framework to encode the geometric structure of the
special Euclidean motion group SE(2) in convolutional networks to yield
translation and rotation equivariance via the introduction of SE(2)-group
convolution layers. This structure enables models to learn feature
representations with a discretized orientation dimension that guarantees that
their outputs are invariant under a discrete set of rotations. Conventional
approaches for rotation invariance rely mostly on data augmentation, but this
does not guarantee the robustness of the output when the input is rotated. At
that, trained conventional CNNs may require test-time rotation augmentation to
reach their full capability. This study is focused on histopathology image
analysis applications for which it is desirable that the arbitrary global
orientation information of the imaged tissues is not captured by the machine
learning models. The proposed framework is evaluated on three different
histopathology image analysis tasks (mitosis detection, nuclei segmentation and
tumor classification). We present a comparative analysis for each problem and
show that consistent increase of performances can be achieved when using the
proposed framework
Computational exploration of molecular receptive fields in the olfactory bulb reveals a glomerulus-centric chemical map
© The Author(s) 2020. This article is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.Progress in olfactory research is currently hampered by incomplete knowledge about chemical receptive ranges of primary receptors. Moreover, the chemical logic underlying the arrangement of computational units in the olfactory bulb has still not been resolved. We undertook a large-scale approach at characterising molecular receptive ranges (MRRs) of glomeruli in the dorsal olfactory bulb (dOB) innervated by the MOR18-2 olfactory receptor, also known as Olfr78, with human ortholog OR51E2. Guided by an iterative approach that combined biological screening and machine learning, we selected 214 odorants to characterise the response of MOR18-2 and its neighbouring glomeruli. We found that a combination of conventional physico-chemical and vibrational molecular descriptors performed best in predicting glomerular responses using nonlinear Support-Vector Regression. We also discovered several previously unknown odorants activating MOR18-2 glomeruli, and obtained detailed MRRs of MOR18-2 glomeruli and their neighbours. Our results confirm earlier findings that demonstrated tunotopy, that is, glomeruli with similar tuning curves tend to be located in spatial proximity in the dOB. In addition, our results indicate chemotopy, that is, a preference for glomeruli with similar physico-chemical MRR descriptions being located in spatial proximity. Together, these findings suggest the existence of a partial chemical map underlying glomerular arrangement in the dOB. Our methodology that combines machine learning and physiological measurements lights the way towards future high-throughput studies to deorphanise and characterise structure-activity relationships in olfaction.Peer reviewe
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