We present an Unsupervised Domain Adaptation strategy to compensate for domain shifts on Electron Microscopy volumes. Our method aggregates visual correspondences-motifs that are visually similar across different acquisitions-to infer changes on the parameters of pretrained models, and enable them to operate on new data. In particular, we examine the annotations of an existing acquisition to determine pivot locations that characterize the reference segmentation, and use a patch matching algorithm to find their candidate visual correspondences in a new volume. We aggregate all the candidate correspondences by a voting scheme and we use them to construct a consensus heatmap: a map of how frequently locations on the new volume are matched to relevant locations from the original acquisition. This information allows us to perform model adaptations in two different ways: either by a) optimizing model parameters under a Multiple Instance Learning formulation, so that predictions between reference locations and their sets of correspondences agree, or by b) using high-scoring regions of the heatmap as soft labels to be incorporated in other domain adaptation pipelines, including deep learning ones. We show that these unsupervised techniques allow us to obtain high-quality segmentations on unannotated volumes, qualitatively consistent with results obtained under full supervision, for both mitochondria and synapses, with no need for new annotation effort.

We propose a novel approach to automatically tracking elliptical cell populations in time-lapse image sequences. Given an initial segmentation, we account for partial occlusions and overlaps by generating an over-complete set of competing detection hypotheses. To this end, we fit ellipses to portions of the initial regions and build a hierarchy of ellipses, which are then treated as cell candidates. We then select temporally consistent ones by solving to optimality an integer program with only one type of flow variables. This eliminates the need for heuristics to handle missed detections due to partial occlusions and complex morphology. We demonstrate the effectiveness of our approach on a range of challenging sequences consisting of clumped cells and show that it outperforms state-of-the-art techniques.

Electron and light microscopy imaging can now deliver high-quality image stacks of neural structures. However, the amount of human annotation effort required to analyze them remains a major bottleneck. While machine learning algorithms can be used to help automate this process, they require training data, which is time-consuming to obtain manually, especially in image stacks. Furthermore, due to changing experimental conditions, successive stacks often exhibit differences that are severe enough to make it difficult to use a classifier trained for a specific one on another. This means that this tedious annotation process has to be repeated for each new stack. In this paper, we present a domain adaptation algorithm that addresses this issue by effectively leveraging labeled examples across different acquisitions and significantly reducing the annotation requirements. Our approach can handle complex, nonlinear image feature transformations and scales to large microscopy datasets that often involve high-dimensional feature spaces and large 3D data volumes. We evaluate our approach on four challenging electron and light microscopy applications that exhibit very different image modalities and where annotation is very costly. Across all applications we achieve a significant improvement over the state-of-the-art machine learning methods and demonstrate our ability to greatly reduce human annotation effort.

Efficient and accurate segmentation of cellular structures in microscopic data is an essential task in medical imaging. Many state-of-the-art approaches to image segmentation use structured models whose parameters must be carefully chosen for optimal performance. A popular choice is to learn them using a large-margin framework and more specifically structured support vector machines (SSVM). Although SSVMs are appealing, they suffer from certain limitations. First, they are restricted in practice to linear kernels because the more powerful nonlinear kernels cause the learning to become prohibitively expensive. Second, they require iteratively finding the most violated constraints, which is often intractable for the loopy graphical models used in image segmentation. This requires approximation that can lead to reduced quality of learning. In this paper, we propose three novel techniques to overcome these limitations. We first introduce a method to "kernelize" the features so that a linear SSVM framework can leverage the power of nonlinear kernels without incurring much additional computational cost. Moreover, we employ a working set of constraints to increase the reliability of approximate subgradient methods and introduce a new way to select a suitable step size at each iteration. We demonstrate the strength of our approach on both 2-D and 3-D electron microscopic (EM) image data and show consistent performance improvement over state-of-the-art approaches.

Cascade-style approaches to implementing ensemble classifiers can deliver significant speed-ups at test time. While highly effective, they remain challenging to tune and their overall performance depends on the availability of large validation sets to estimate rejection thresholds. These characteristics are often prohibitive and thus limit their applicability. We introduce an alternative approach to speeding-up classifier evaluation which overcomes these limitations. It involves maintaining a probability estimate of the class label at each intermediary response and stopping when the corresponding uncertainty becomes small enough. As a result, the evaluation terminates early based on the sequence of responses observed. Furthermore, it does so independently of the type of ensemble classifier used or the way it was trained. We show through extensive experimentation that our method provides 2 to 10 fold speed-ups, over existing state-of-the-art methods, at almost no loss in accuracy on a number of object classification tasks.

We propose a new approach to detecting irregular curvilinear structures in noisy image stacks. In contrast to earlier approaches that rely on circular models of the cross-sections, ours allows for the arbitrarily-shaped ones that are prevalent in biological imagery. This is achieved by maximizing the image gradient flux along multiple directions and radii, instead of only two with a unique radius as is usually done. This yields a more complex optimization problem for which we propose a computationally efficient solution. We demonstrate the effectiveness of our approach on a wide range of challenging gray scale and color datasets and show that it outperforms existing techniques, especially on very irregular structures.

A common assumption in machine vision is that the training and test samples are drawn from the same distribution. However, there are many problems when this assumption is grossly violated, as in bio-medical applications where different acquisitions can generate drastic variations in the appearance of the data due to changing experimental conditions. This problem is accentuated with 3D data, for which annotation is very time-consuming, limiting the amount of data that can be labeled in new acquisitions for training. In this paper we present a multi-task learning algorithm for domain adaptation based on boosting. Unlike previous approaches that learn task-specific decision boundaries, our method learns a single decision boundary in a shared feature space, common to all tasks. We use the boosting-trick to learn a non-linear mapping of the observations in each task, with no need for specific a-priori knowledge of its global analytical form. This yields a more parameter-free domain adaptation approach that successfully leverages learning on new tasks where labeled data is scarce. We evaluate our approach on two challenging bio-medical datasets and achieve a significant improvement over the state-of-the-art.

We present a new approach for the automated segmentation of synapses in image stacks acquired by electron microscopy (EM) that relies on image features specifically designed to take spatial context into account. These features are used to train a classifier that can effectively learn cues such as the presence of a nearby post-synaptic region. As a result, our algorithm successfully distinguishes synapses from the numerous other organelles that appear within an EM volume, including those whose local textural properties are relatively similar. Furthermore, as a by-product of the segmentation, our method flawlessly determines synaptic orientation, a crucial element in the interpretation of brain circuits. We evaluate our approach on three different datasets, compare it against the state-of-the-art in synapse segmentation and demonstrate our ability to reliably collect shape, density, and orientation statistics over hundreds of synapses.