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Donglai Wei

Publications and source records attributed to Donglai Wei.

47 records · Page 3Linked to original sources

Developmental Stage Classification of Embryos Using Two-Stream Neural Network with Linear-Chain Conditional Random Field

The developmental process of embryos follows a monotonic order. An embryo can progressively cleave from one cell to multiple cells and finally transform to morula and blastocyst. For time-lapse videos of embryos, most existing developmental stage classification methods conduct per-frame predictions using an image frame at each time step. However, classification using only images suffers from overlapping between cells and imbalance between stages. Temporal information can be valuable in addressing this problem by capturing movements between neighboring frames. In this work, we propose a two-stream model for developmental stage classification. Unlike previous methods, our two-stream model accepts both temporal and image information. We develop a linear-chain conditional random field (CRF) on top of neural network features extracted from the temporal and image streams to make use of both modalities. The linear-chain CRF formulation enables tractable training of global sequential models over multiple frames while also making it possible to inject monotonic development order constraints into the learning process explicitly. We demonstrate our algorithm on two time-lapse embryo video datasets: i) mouse and ii) human embryo datasets. Our method achieves 98.1 % and 80.6 % for mouse and human embryo stage classification, respectively. Our approach will enable more profound clinical and biological studies and suggests a new direction for developmental stage classification by utilizing temporal information.

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AxonEM Dataset: 3D Axon Instance Segmentation of Brain Cortical Regions

Electron microscopy (EM) enables the reconstruction of neural circuits at the level of individual synapses, which has been transformative for scientific discoveries. However, due to the complex morphology, an accurate reconstruction of cortical axons has become a major challenge. Worse still, there is no publicly available large-scale EM dataset from the cortex that provides dense ground truth segmentation for axons, making it difficult to develop and evaluate large-scale axon reconstruction methods. To address this, we introduce the AxonEM dataset, which consists of two 30x30x30 um^3 EM image volumes from the human and mouse cortex, respectively. We thoroughly proofread over 18,000 axon instances to provide dense 3D axon instance segmentation, enabling large-scale evaluation of axon reconstruction methods. In addition, we densely annotate nine ground truth subvolumes for training, per each data volume. With this, we reproduce two published state-of-the-art methods and provide their evaluation results as a baseline. We publicly release our code and data at https://connectomics-bazaar.github.io/proj/AxonEM/index.html to foster the development of advanced methods.

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Consistent Recurrent Neural Networks for 3D Neuron Segmentation

We present a recurrent network for the 3D reconstruction of neurons that sequentially generates binary masks for every object in an image with spatio-temporal consistency. Our network models consistency in two parts: (i) local, which allows exploring non-occluding and temporally-adjacent object relationships with bi-directional recurrence. (ii) non-local, which allows exploring long-range object relationships in the temporal domain with skip connections. Our proposed network is end-to-end trainable from an input image to a sequence of object masks, and, compared to methods relying on object boundaries, its output does not require post-processing. We evaluate our method on three benchmarks for neuron segmentation and achieved state-of-the-art performance on the SNEMI3D challenge.

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Learning Vector Quantized Shape Code for Amodal Blastomere Instance Segmentation

Blastomere instance segmentation is important for analyzing embryos' abnormality. To measure the accurate shapes and sizes of blastomeres, their amodal segmentation is necessary. Amodal instance segmentation aims to recover the complete silhouette of an object even when the object is not fully visible. For each detected object, previous methods directly regress the target mask from input features. However, images of an object under different amounts of occlusion should have the same amodal mask output, which makes it harder to train the regression model. To alleviate the problem, we propose to classify input features into intermediate shape codes and recover complete object shapes from them. First, we pre-train the Vector Quantized Variational Autoencoder (VQ-VAE) model to learn these discrete shape codes from ground truth amodal masks. Then, we incorporate the VQ-VAE model into the amodal instance segmentation pipeline with an additional refinement module. We also detect an occlusion map to integrate occlusion information with a backbone feature. As such, our network faithfully detects bounding boxes of amodal objects. On an internal embryo cell image benchmark, the proposed method outperforms previous state-of-the-art methods. To show generalizability, we show segmentation results on the public KINS natural image benchmark. To examine the learned shape codes and model design choices, we perform ablation studies on a synthetic dataset of simple overlaid shapes. Our method would enable accurate measurement of blastomeres in in vitro fertilization (IVF) clinics, which potentially can increase IVF success rate.

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Automated Measurements of Key Morphological Features of Human Embryos for IVF

A major challenge in clinical In-Vitro Fertilization (IVF) is selecting the highest quality embryo to transfer to the patient in the hopes of achieving a pregnancy. Time-lapse microscopy provides clinicians with a wealth of information for selecting embryos. However, the resulting movies of embryos are currently analyzed manually, which is time consuming and subjective. Here, we automate feature extraction of time-lapse microscopy of human embryos with a machine-learning pipeline of five convolutional neural networks (CNNs). Our pipeline consists of (1) semantic segmentation of the regions of the embryo, (2) regression predictions of fragment severity, (3) classification of the developmental stage, and object instance segmentation of (4) cells and (5) pronuclei. Our approach greatly speeds up the measurement of quantitative, biologically relevant features that may aid in embryo selection.

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Super-BPD: Super Boundary-to-Pixel Direction for Fast Image Segmentation

Image segmentation is a fundamental vision task and a crucial step for many applications. In this paper, we propose a fast image segmentation method based on a novel super boundary-to-pixel direction (super-BPD) and a customized segmentation algorithm with super-BPD. Precisely, we define BPD on each pixel as a two-dimensional unit vector pointing from its nearest boundary to the pixel. In the BPD, nearby pixels from different regions have opposite directions departing from each other, and adjacent pixels in the same region have directions pointing to the other or each other (i.e., around medial points). We make use of such property to partition an image into super-BPDs, which are novel informative superpixels with robust direction similarity for fast grouping into segmentation regions. Extensive experimental results on BSDS500 and Pascal Context demonstrate the accuracy and efficency of the proposed super-BPD in segmenting images. In practice, the proposed super-BPD achieves comparable or superior performance with MCG while running at ~25fps vs. 0.07fps. Super-BPD also exhibits a noteworthy transferability to unseen scenes. The code is publicly available at https://github.com/JianqiangWan/Super-BPD.

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A Topological Nomenclature for 3D Shape Analysis in Connectomics

One of the essential tasks in connectomics is the morphology analysis of neurons and organelles like mitochondria to shed light on their biological properties. However, these biological objects often have tangled parts or complex branching patterns, which make it hard to abstract, categorize, and manipulate their morphology. In this paper, we develop a novel topological nomenclature system to name these objects like the appellation for chemical compounds to promote neuroscience analysis based on their skeletal structures. We first convert the volumetric representation into the topology-preserving reduced graph to untangle the objects. Next, we develop nomenclature rules for pyramidal neurons and mitochondria from the reduced graph and finally learn the feature embedding for shape manipulation. In ablation studies, we quantitatively show that graphs generated by our proposed method align with the perception of experts. On 3D shape retrieval and decomposition tasks, we qualitatively demonstrate that the encoded topological nomenclature features achieve better results than state-of-the-art shape descriptors. To advance neuroscience, we will release a 3D segmentation dataset of mitochondria and pyramidal neurons reconstructed from a 100um cube electron microscopy volume with their reduced graph and topological nomenclature annotations. Code is publicly available at https://github.com/donglaiw/ibexHelper.

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Video Enhancement with Task-Oriented Flow

Many video enhancement algorithms rely on optical flow to register frames in a video sequence. Precise flow estimation is however intractable; and optical flow itself is often a sub-optimal representation for particular video processing tasks. In this paper, we propose task-oriented flow (TOFlow), a motion representation learned in a self-supervised, task-specific manner. We design a neural network with a trainable motion estimation component and a video processing component, and train them jointly to learn the task-oriented flow. For evaluation, we build Vimeo-90K, a large-scale, high-quality video dataset for low-level video processing. TOFlow outperforms traditional optical flow on standard benchmarks as well as our Vimeo-90K dataset in three video processing tasks: frame interpolation, video denoising/deblocking, and video super-resolution.

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Detecting Synapse Location and Connectivity by Signed Proximity Estimation and Pruning with Deep Nets

Synaptic connectivity detection is a critical task for neural reconstruction from Electron Microscopy (EM) data. Most of the existing algorithms for synapse detection do not identify the cleft location and direction of connectivity simultaneously. The few methods that computes direction along with contact location have only been demonstrated to work on either dyadic (most common in vertebrate brain) or polyadic (found in fruit fly brain) synapses, but not on both types. In this paper, we present an algorithm to automatically predict the location as well as the direction of both dyadic and polyadic synapses. The proposed algorithm first generates candidate synaptic connections from voxelwise predictions of signed proximity generated by a 3D U-net. A second 3D CNN then prunes the set of candidates to produce the final detection of cleft and connectivity orientation. Experimental results demonstrate that the proposed method outperforms the existing methods for determining synapses in both rodent and fruit fly brain.

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Parallel Separable 3D Convolution for Video and Volumetric Data Understanding

For video and volumetric data understanding, 3D convolution layers are widely used in deep learning, however, at the cost of increasing computation and training time. Recent works seek to replace the 3D convolution layer with convolution blocks, e.g. structured combinations of 2D and 1D convolution layers. In this paper, we propose a novel convolution block, Parallel Separable 3D Convolution (PmSCn), which applies m parallel streams of n 2D and one 1D convolution layers along different dimensions. We first mathematically justify the need of parallel streams (Pm) to replace a single 3D convolution layer through tensor decomposition. Then we jointly replace consecutive 3D convolution layers, common in modern network architectures, with the multiple 2D convolution layers (Cn). Lastly, we empirically show that PmSCn is applicable to different backbone architectures, such as ResNet, DenseNet, and UNet, for different applications, such as video action recognition, MRI brain segmentation, and electron microscopy segmentation. In all three applications, we replace the 3D convolution layers in state-of-the art models with PmSCn and achieve around 14% improvement in test performance and 40% reduction in model size and on average.

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Understanding Intra-Class Knowledge Inside CNN

Convolutional Neural Network (CNN) has been successful in image recognition tasks, and recent works shed lights on how CNN separates different classes with the learned inter-class knowledge through visualization. In this work, we instead visualize the intra-class knowledge inside CNN to better understand how an object class is represented in the fully-connected layers. To invert the intra-class knowledge into more interpretable images, we propose a non-parametric patch prior upon previous CNN visualization models. With it, we show how different "styles" of templates for an object class are organized by CNN in terms of location and content, and represented in a hierarchical and ensemble way. Moreover, such intra-class knowledge can be used in many interesting applications, e.g. style-based image retrieval and style-based object completion.

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