Won-Ki Jeong

SeungKyu Kim, Hyun-Jic Oh, Seonghui Min et al.

With the emergence of the Segment Anything Model (SAM) as a foundational model for image segmentation, its application has been extensively studied across various domains, including the medical field. However, its potential in the context of histopathology data, specifically in region segmentation, has received relatively limited attention. In this paper, we evaluate SAM's performance in zero-shot and fine-tuned scenarios on histopathology data, with a focus on interactive segmentation. Additionally, we compare SAM with other state-of-the-art interactive models to assess its practical potential and evaluate its generalization capability with domain adaptability. In the experimental results, SAM exhibits a weakness in segmentation performance compared to other models while demonstrating relative strengths in terms of inference time and generalization capability. To improve SAM's limited local refinement ability and to enhance prompt stability while preserving its core strengths, we propose a modification of SAM's decoder. The experimental results suggest that the proposed modification is effective to make SAM useful for interactive histology image segmentation. The code is available at \url{https://github.com/hvcl/SAM_Interactive_Histopathology}

Hyun-Jic Oh, Won-Ki Jeong

Nuclei segmentation and classification is a significant process in pathology image analysis. Deep learning-based approaches have greatly contributed to the higher accuracy of this task. However, those approaches suffer from the imbalanced nuclei data composition, which shows lower classification performance on the rare nuclei class. In this paper, we propose a realistic data synthesis method using a diffusion model. We generate two types of virtual patches to enlarge the training data distribution, which is for balancing the nuclei class variance and for enlarging the chance to look at various nuclei. After that, we use a semantic-label-conditioned diffusion model to generate realistic and high-quality image samples. We demonstrate the efficacy of our method by experiment results on two imbalanced nuclei datasets, improving the state-of-the-art networks. The experimental results suggest that the proposed method improves the classification performance of the rare type nuclei classification, while showing superior segmentation and classification performance in imbalanced pathology nuclei datasets.

Kyungryun Lee, Won-Ki Jeong

Analysis and visualization of 3D microscopy images pose challenges due to anisotropic axial resolution, demanding volumetric super-resolution along the axial direction. While training a learning-based 3D super-resolution model seems to be a straightforward solution, it requires ground truth isotropic volumes and suffers from the curse of dimensionality. Therefore, existing methods utilize 2D neural networks to reconstruct each axial slice, eventually piecing together the entire volume. However, reconstructing each slice in the pixel domain fails to give consistent reconstruction in all directions leading to misalignment artifacts. In this work, we present a reconstruction framework based on implicit neural representation (INR), which allows 3D coherency even when optimized by independent axial slices in a batch-wise manner. Our method optimizes a continuous volumetric representation from low-resolution axial slices, using a 2D diffusion prior trained on high-resolution lateral slices without requiring isotropic volumes. Through experiments on real and synthetic anisotropic microscopy images, we demonstrate that our method surpasses other state-of-the-art reconstruction methods. The source code is available on GitHub: https://github.com/hvcl/INR-diffusion.

Hyun-Jic Oh, Kanggeun Lee, Won-Ki Jeong

Current state-of-the-art supervised deep learning-based segmentation approaches have demonstrated superior performance in medical image segmentation tasks. However, such supervised approaches require fully annotated pixel-level ground-truth labels, which are labor-intensive and time-consuming to acquire. Recently, Scribble2Label (S2L) demonstrated that using only a handful of scribbles with self-supervised learning can generate accurate segmentation results without full annotation. However, owing to the relatively small size of scribbles, the model is prone to overfit and the results may be biased to the selection of scribbles. In this work, we address this issue by employing a novel multiscale contrastive regularization term for S2L. The main idea is to extract features from intermediate layers of the neural network for contrastive loss so that structures at various scales can be effectively separated. To verify the efficacy of our method, we conducted ablation studies on well-known datasets, such as Data Science Bowl 2018 and MoNuSeg. The results show that the proposed multiscale contrastive loss is effective in improving the performance of S2L, which is comparable to that of the supervised learning segmentation method.

Kyungryun Lee, Won-Ki Jeong

Electron microscopy (EM) images exhibit anisotropic axial resolution due to the characteristics inherent to the imaging modality, presenting challenges in analysis and downstream tasks.In this paper, we propose a diffusion-model-based framework that overcomes the limitations of requiring reference data or prior knowledge about the degradation process. Our approach utilizes 2D diffusion models to consistently reconstruct 3D volumes and is well-suited for highly downsampled data. Extensive experiments conducted on two public datasets demonstrate the robustness and superiority of leveraging the generative prior compared to supervised learning methods. Additionally, we demonstrate our method's feasibility for self-supervised reconstruction, which can restore a single anisotropic volume without any training data.

Seonghui Min, Won-Ki Jeong

Tumor region segmentation is an essential task for the quantitative analysis of digital pathology. Recently presented deep neural networks have shown state-of-the-art performance in various image-segmentation tasks. However, because of the unclear boundary between the cancerous and normal regions in pathology images, despite using modern methods, it is difficult to produce satisfactory segmentation results in terms of the reliability and accuracy required for medical data. In this study, we propose an interactive segmentation method that allows users to refine the output of deep neural networks through click-type user interactions. The primary method is to formulate interactive segmentation as an optimization problem that leverages both user-provided click constraints and semantic information in a feature map using a click-guided attention module (CGAM). Unlike other existing methods, CGAM avoids excessive changes in segmentation results, which can lead to the overfitting of user clicks. Another advantage of CGAM is that the model size is independent of input image size. Experimental results on pathology image datasets indicated that our method performs better than existing state-of-the-art methods.

Jing Wei Tan, Won-Ki Jeong

Contrastive learning has gained popularity due to its robustness with good feature representation performance. However, cosine distance, the commonly used similarity metric in contrastive learning, is not well suited to represent the distance between two data points, especially on a nonlinear feature manifold. Inspired by manifold learning, we propose a novel extension of contrastive learning that leverages geodesic distance between features as a similarity metric for histopathology whole slide image classification. To reduce the computational overhead in manifold learning, we propose geodesic-distance-based feature clustering for efficient contrastive loss evaluation using prototypes without time-consuming pairwise feature similarity comparison. The efficacy of the proposed method is evaluated on two real-world histopathology image datasets. Results demonstrate that our method outperforms state-of-the-art cosine-distance-based contrastive learning methods.

Hyun-Jic Oh, Won-Ki Jeong

In the field of computational pathology, deep learning algorithms have made significant progress in tasks such as nuclei segmentation and classification. However, the potential of these advanced methods is limited by the lack of available labeled data. Although image synthesis via recent generative models has been actively explored to address this challenge, existing works have barely addressed label augmentation and are mostly limited to single-class and unconditional label generation. In this paper, we introduce a novel two-stage framework for multi-class nuclei data augmentation using text-conditional diffusion models. In the first stage, we innovate nuclei label synthesis by generating multi-class semantic labels and corresponding instance maps through a joint diffusion model conditioned by text prompts that specify the label structure information. In the second stage, we utilize a semantic and text-conditional latent diffusion model to efficiently generate high-quality pathology images that align with the generated nuclei label images. We demonstrate the effectiveness of our method on large and diverse pathology nuclei datasets, with evaluations including qualitative and quantitative analyses, as well as assessments of downstream tasks.

Seonghui Min, Hyun-Jic Oh, Won-Ki Jeong

In multi-class histopathology nuclei analysis tasks, the lack of training data becomes a main bottleneck for the performance of learning-based methods. To tackle this challenge, previous methods have utilized generative models to increase data by generating synthetic samples. However, existing methods often overlook the importance of considering the context of biological tissues (e.g., shape, spatial layout, and tissue type) in the synthetic data. Moreover, while generative models have shown superior performance in synthesizing realistic histopathology images, none of the existing methods are capable of producing image-label pairs at the same time. In this paper, we introduce a novel framework for co-synthesizing histopathology nuclei images and paired semantic labels using a context-conditioned joint diffusion model. We propose conditioning of a diffusion model using nucleus centroid layouts with structure-related text prompts to incorporate spatial and structural context information into the generation targets. Moreover, we enhance the granularity of our synthesized semantic labels by generating instance-wise nuclei labels using distance maps synthesized concurrently in conjunction with the images and semantic labels. We demonstrate the effectiveness of our framework in generating high-quality samples on multi-institutional, multi-organ, and multi-modality datasets. Our synthetic data consistently outperforms existing augmentation methods in the downstream tasks of nuclei segmentation and classification.

Jing Wei Tan, SeungKyu Kim, Eunsu Kim et al.

Vision language models (VLM) have achieved success in both natural language comprehension and image recognition tasks. However, their use in pathology report generation for whole slide images (WSIs) is still limited due to the huge size of multi-scale WSIs and the high cost of WSI annotation. Moreover, in most of the existing research on pathology report generation, sufficient validation regarding clinical efficacy has not been conducted. Herein, we propose a novel Patient-level Multi-organ Pathology Report Generation (PMPRG) model, which utilizes the multi-scale WSI features from our proposed multi-scale regional vision transformer (MR-ViT) model and their real pathology reports to guide VLM training for accurate pathology report generation. The model then automatically generates a report based on the provided key features attended regional features. We assessed our model using a WSI dataset consisting of multiple organs, including the colon and kidney. Our model achieved a METEOR score of 0.68, demonstrating the effectiveness of our approach. This model allows pathologists to efficiently generate pathology reports for patients, regardless of the number of WSIs involved.

Kanggeun Lee, Kyungryun Lee, Won-Ki Jeong

Although the advances of self-supervised blind denoising are significantly superior to conventional approaches without clean supervision in synthetic noise scenarios, it shows poor quality in real-world images due to spatially correlated noise corruption. Recently, pixel-shuffle downsampling (PD) has been proposed to eliminate the spatial correlation of noise. A study combining a blind spot network (BSN) and asymmetric PD (AP) successfully demonstrated that self-supervised blind denoising is applicable to real-world noisy images. However, PD-based inference may degrade texture details in the testing phase because high-frequency details (e.g., edges) are destroyed in the downsampled images. To avoid such an issue, we propose self-residual learning without the PD process to maintain texture information. We also propose an order-variant PD constraint, noise prior loss, and an efficient inference scheme (progressive random-replacing refinement ($\text{PR}^3$)) to boost overall performance. The results of extensive experiments show that the proposed method outperforms state-of-the-art self-supervised blind denoising approaches, including several supervised learning methods, in terms of PSNR, SSIM, LPIPS, and DISTS in real-world sRGB images.

Tran Minh Quan, Thanh Nguyen-Duc, Won-Ki Jeong

Compressed Sensing MRI (CS-MRI) has provided theoretical foundations upon which the time-consuming MRI acquisition process can be accelerated. However, it primarily relies on iterative numerical solvers which still hinders their adaptation in time-critical applications. In addition, recent advances in deep neural networks have shown their potential in computer vision and image processing, but their adaptation to MRI reconstruction is still in an early stage. In this paper, we propose a novel deep learning-based generative adversarial model, RefineGAN, for fast and accurate CS-MRI reconstruction. The proposed model is a variant of fully-residual convolutional autoencoder and generative adversarial networks (GANs), specifically designed for CS-MRI formulation; it employs deeper generator and discriminator networks with cyclic data consistency loss for faithful interpolation in the given under-sampled k-space data. In addition, our solution leverages a chained network to further enhance the reconstruction quality. RefineGAN is fast and accurate -- the reconstruction process is extremely rapid, as low as tens of milliseconds for reconstruction of a 256x256 image, because it is one-way deployment on a feed-forward network, and the image quality is superior even for extremely low sampling rate (as low as 10%) due to the data-driven nature of the method. We demonstrate that RefineGAN outperforms the state-of-the-art CS-MRI methods by a large margin in terms of both running time and image quality via evaluation using several open-source MRI databases.

Hyunsoo Son, Jeonghyun Noh, Suemin Jeon et al.

Implicit Neural Representations (INRs) are widely used to encode data as continuous functions, enabling the visualization of large-scale multivariate scientific simulation data with reduced memory usage. However, existing INR-based methods face three main limitations: (1) inflexible representation of complex structures, (2) primarily focusing on single-variable data, and (3) dependence on structured grids. Thus, their performance degrades when applied to complex real-world datasets. To address these limitations, we propose a novel neural network-based framework, MC-INR, which handles multivariate data on unstructured grids. It combines meta-learning and clustering to enable flexible encoding of complex structures. To further improve performance, we introduce a residual-based dynamic re-clustering mechanism that adaptively partitions clusters based on local error. We also propose a branched layer to leverage multivariate data through independent branches simultaneously. Experimental results demonstrate that MC-INR outperforms existing methods on scientific data encoding tasks.

GaYeon Koh, Hyun-Jic Oh, Jeonghyun Noh et al.

Deep learning-based food image classification enables precise identification of food categories, further facilitating accurate nutritional analysis. However, real-world food images often show a skewed distribution, with some food types being more prevalent than others. This class imbalance can be problematic, causing models to favor the majority (head) classes with overall performance degradation for the less common (tail) classes. Recently, synthetic data augmentation using diffusion-based generative models has emerged as a promising solution to address this issue. By generating high-quality synthetic images, these models can help uniformize the data distribution, potentially improving classification performance. However, existing approaches face challenges: fine-tuning-based methods need a uniformly distributed dataset, while pre-trained model-based approaches often overlook inter-class separation in synthetic data. In this paper, we propose a two-stage synthetic data augmentation framework, leveraging pre-trained diffusion models for long-tailed food classification. We generate a reference set conditioned by a positive prompt on the generation target and then select a class that shares similar features with the generation target as a negative prompt. Subsequently, we generate a synthetic augmentation set using positive and negative prompt conditions by a combined sampling strategy that promotes intra-class diversity and inter-class separation. We demonstrate the efficacy of the proposed method on two long-tailed food benchmark datasets, achieving superior performance compared to previous works in terms of top-1 accuracy.

Jeonghyun Noh, Hyun-Jic Oh, Byungju Chae et al.

Computed tomography (CT) is widely used in clinical diagnosis, but acquiring high-resolution (HR) CT is limited by radiation exposure risks. Deep learning-based super-resolution (SR) methods have been studied to reconstruct HR from low-resolution (LR) inputs. While supervised SR approaches have shown promising results, they require large-scale paired LR-HR volume datasets that are often unavailable. In contrast, zero-shot methods alleviate the need for paired data by using only a single LR input, but typically struggle to recover fine anatomical details due to limited internal information. To overcome these, we propose a novel zero-shot 3D CT SR framework that leverages upsampled 2D X-ray projection priors generated by a diffusion model. Exploiting the abundance of HR 2D X-ray data, we train a diffusion model on large-scale 2D X-ray projection and introduce a per-projection adaptive sampling strategy. It selects the generative process for each projection, thus providing HR projections as strong external priors for 3D CT reconstruction. These projections serve as inputs to 3D Gaussian splatting for reconstructing a 3D CT volume. Furthermore, we propose negative alpha blending (NAB-GS) that allows negative values in Gaussian density representation. NAB-GS enables residual learning between LR and diffusion-based projections, thereby enhancing high-frequency structure reconstruction. Experiments on two datasets show that our method achieves superior quantitative and qualitative results for 3D CT SR.

Hyun-Jic Oh, Junsik Kim, Zhiyi Shi et al.

Multiplex imaging is revolutionizing pathology by enabling the simultaneous visualization of multiple biomarkers within tissue samples, providing molecular-level insights that traditional hematoxylin and eosin (H&E) staining cannot provide. However, the complexity and cost of multiplex data acquisition have hindered its widespread adoption. Additionally, most existing large repositories of H&E images lack corresponding multiplex images, limiting opportunities for multimodal analysis. To address these challenges, we leverage recent advances in latent diffusion models (LDMs), which excel at modeling complex data distributions by utilizing their powerful priors for fine-tuning to a target domain. In this paper, we introduce a novel framework for virtual multiplex staining that utilizes pretrained LDM parameters to generate multiplex images from H&E images using a conditional diffusion model. Our approach enables marker-by-marker generation by conditioning the diffusion model on each marker, while sharing the same architecture across all markers. To tackle the challenge of varying pixel value distributions across different marker stains and to improve inference speed, we fine-tune the model for single-step sampling, enhancing both color contrast fidelity and inference efficiency through pixel-level loss functions. We validate our framework on two publicly available datasets, notably demonstrating its effectiveness in generating up to 18 different marker types with improved accuracy, a substantial increase over the 2-3 marker types achieved in previous approaches. This validation highlights the potential of our framework, pioneering virtual multiplex staining. Finally, this paper bridges the gap between H&E and multiplex imaging, potentially enabling retrospective studies and large-scale analyses of existing H&E image repositories.

Yonghan Shin, SeungKyu Kim, Won-Ki Jeong

Whole slide images (WSIs) in computational pathology (CPath) pose a major computational challenge due to their gigapixel scale, often requiring the processing of tens to hundreds of thousands of high-resolution patches per slide. This results in prohibitive encoding costs, with preprocessing and training times extending to days or even weeks-making WSI encoding the most significant bottleneck in real-world deployment. In this work, we propose WISE-FUSE, an adaptive WSI encoding framework that leverages pathology-domain vision-language models and large language models to address this challenge by selectively processing diagnostically relevant regions. WISE-FUSE first computes similarity scores between low-resolution patches and class-specific textual descriptions using a knowledge distillation mechanism that preserves fine-grained diagnostic features. Based on these similarity scores, we select a small subset of informative regions for the target task, which quickly eliminates irrelevant patches at the coarse level. The corresponding high-resolution patches are then selectively encoded and fused with textual embeddings to reinforce diagnostic context. Extensive experiments demonstrate that WISE-FUSE reduces WSI encoding time by over threefold while achieving diagnostic performance comparable to or surpassing that of exhaustive patch processing, offering a scalable and practical solution for CPath.

JunYoung Choi, Hakjun Lee, Suyeon Kim et al.

Neurons have a polarized structure, including dendrites and axons, and compartment-specific functions can be affected by dwelling mitochondria. It is known that the morphology of mitochondria is closely related to the functions of neurons and neurodegenerative diseases. Even though several deep learning methods have been developed to automatically analyze the morphology of mitochondria, the application of existing methods to actual analysis still encounters several difficulties. Since the performance of pre-trained deep learning model may vary depending on the target data, re-training of the model is often required. Besides, even though deep learning has shown superior performance under a constrained setup, there are always errors that need to be corrected by humans in real analysis. To address these issues, we introduce MitoVis, a novel visualization system for end-to-end data processing and interactive analysis of the morphology of neuronal mitochondria. MitoVis enables interactive fine-tuning of a pre-trained neural network model without the domain knowledge of machine learning, which allows neuroscientists to easily leverage deep learning in their research. MitoVis also provides novel visual guides and interactive proofreading functions so that the users can quickly identify and correct errors in the result with minimal effort. We demonstrate the usefulness and efficacy of the system via a case study conducted by a neuroscientist on a real analysis scenario. The result shows that MitoVis allows up to 15x faster analysis with similar accuracy compared to the fully manual analysis method.

Khoa Tuan Nguyen, Ganghee Jang, Tran Anh Tuan et al.

Segmentation of nanoscale electron microscopy (EM) images is crucial but still challenging in connectomics research. One reason for this is that none of the existing segmentation methods are error-free, so they require proofreading, which is typically implemented as an interactive, semi-automatic process via manual intervention. Herein, we propose a fully automatic proofreading method based on reinforcement learning that mimics the human decision process of detection, classification, and correction of segmentation errors. We systematically design the proposed system by combining multiple reinforcement learning agents in a hierarchical manner, where each agent focuses only on a specific task while preserving dependency between agents. Furthermore, we demonstrate that the episodic task setting of reinforcement learning can efficiently manage a combination of merge and split errors concurrently presented in the input. We demonstrate the efficacy of the proposed system by comparing it with conventional proofreading methods over various testing cases.

Kanggeun Lee, Won-Ki Jeong

With the advent of advances in self-supervised learning, paired clean-noisy data are no longer required in deep learning-based image denoising. However, existing blind denoising methods still require the assumption with regard to noise characteristics, such as zero-mean noise distribution and pixel-wise noise-signal independence; this hinders wide adaptation of the method in the medical domain. On the other hand, unpaired learning can overcome limitations related to the assumption on noise characteristics, which makes it more feasible for collecting the training data in real-world scenarios. In this paper, we propose a novel image denoising scheme, Interdependent Self-Cooperative Learning (ISCL), that leverages unpaired learning by combining cyclic adversarial learning with self-supervised residual learning. Unlike the existing unpaired image denoising methods relying on matching data distributions in different domains, the two architectures in ISCL, designed for different tasks, complement each other and boost the learning process. To assess the performance of the proposed method, we conducted extensive experiments in various biomedical image degradation scenarios, such as noise caused by physical characteristics of electron microscopy (EM) devices (film and charging noise), and structural noise found in low-dose computer tomography (CT). We demonstrate that the image quality of our method is superior to conventional and current state-of-the-art deep learning-based image denoising methods, including supervised learning.

Kanggeun Lee, Won-Ki Jeong

With the advent of recent advances in unsupervised learning, efficient training of a deep network for image denoising without pairs of noisy and clean images has become feasible. However, most current unsupervised denoising methods are built on the assumption of zero-mean noise under the signal-independent condition. This assumption causes blind denoising techniques to suffer brightness shifting problems on images that are greatly corrupted by extreme noise such as salt-and-pepper noise. Moreover, most blind denoising methods require a random masking scheme for training to ensure the invariance of the denoising process. In this paper, we propose a dilated convolutional network that satisfies an invariant property, allowing efficient kernel-based training without random masking. We also propose an adaptive self-supervision loss to circumvent the requirement of zero-mean constraint, which is specifically effective in removing salt-and-pepper or hybrid noise where a prior knowledge of noise statistics is not readily available. We demonstrate the efficacy of the proposed method by comparing it with state-of-the-art denoising methods using various examples.

Hyeonsoo Lee, Won-Ki Jeong

Segmentation is a fundamental process in microscopic cell image analysis. With the advent of recent advances in deep learning, more accurate and high-throughput cell segmentation has become feasible. However, most existing deep learning-based cell segmentation algorithms require fully annotated ground-truth cell labels, which are time-consuming and labor-intensive to generate. In this paper, we introduce Scribble2Label, a novel weakly-supervised cell segmentation framework that exploits only a handful of scribble annotations without full segmentation labels. The core idea is to combine pseudo-labeling and label filtering to generate reliable labels from weak supervision. For this, we leverage the consistency of predictions by iteratively averaging the predictions to improve pseudo labels. We demonstrate the performance of Scribble2Label by comparing it to several state-of-the-art cell segmentation methods with various cell image modalities, including bright-field, fluorescence, and electron microscopy. We also show that our method performs robustly across different levels of scribble details, which confirms that only a few scribble annotations are required in real-use cases.

Tuan Tran Anh, Khoa Nguyen-Tuan, Tran Minh Quan et al.

Instance segmentation is one of the actively studied research topics in computer vision in which many objects of interest should be separated individually. While many feed-forward networks produce high-quality segmentation on different types of images, their results often suffer from topological errors (merging or splitting) for segmentation of many objects, requiring post-processing. Existing iterative methods, on the other hand, extract a single object at a time using discriminative knowledge-based properties (shapes, boundaries, etc.) without relying on post-processing, but they do not scale well. To exploit the advantages of conventional single-object-per-step segmentation methods without impairing the scalability, we propose a novel iterative deep reinforcement learning agent that learns how to differentiate multiple objects in parallel. Our reward function for the trainable agent is designed to favor grouping pixels belonging to the same object using a graph coloring algorithm. We demonstrate that the proposed method can efficiently perform instance segmentation of many objects without heavy post-processing.

Inwan Yoo, David G. C. Hildebrand, Willie F. Tobin et al.

The alignment of serial-section electron microscopy (ssEM) images is critical for efforts in neuroscience that seek to reconstruct neuronal circuits. However, each ssEM plane contains densely packed structures that vary from one section to the next, which makes matching features across images a challenge. Advances in deep learning has resulted in unprecedented performance in similar computer vision problems, but to our knowledge, they have not been successfully applied to ssEM image co-registration. In this paper, we introduce a novel deep network model that combines a spatial transformer for image deformation and a convolutional autoencoder for unsupervised feature learning for robust ssEM image alignment. This results in improved accuracy and robustness while requiring substantially less user intervention than conventional methods. We evaluate our method by comparing registration quality across several datasets.

Tran Minh Quan, David G. C. Hildebrand, Won-Ki Jeong

Electron microscopic connectomics is an ambitious research direction with the goal of studying comprehensive brain connectivity maps by using high-throughput, nano-scale microscopy. One of the main challenges in connectomics research is developing scalable image analysis algorithms that require minimal user intervention. Recently, deep learning has drawn much attention in computer vision because of its exceptional performance in image classification tasks. For this reason, its application to connectomic analyses holds great promise, as well. In this paper, we introduce a novel deep neural network architecture, FusionNet, for the automatic segmentation of neuronal structures in connectomics data. FusionNet leverages the latest advances in machine learning, such as semantic segmentation and residual neural networks, with the novel introduction of summation-based skip connections to allow a much deeper network architecture for a more accurate segmentation. We demonstrate the performance of the proposed method by comparing it with state-of-the-art electron microscopy (EM) segmentation methods from the ISBI EM segmentation challenge. We also show the segmentation results on two different tasks including cell membrane and cell body segmentation and a statistical analysis of cell morphology.