SpaNCMG: improving spatial domains identification of spatial transcriptomics using neighborhood-complementary mixed-view graph convolutional network.

The advancement of spatial transcriptomics (ST) technology contributes to a more profound comprehension of the spatial properties of gene expression within tissues. However, due to challenges of high dimensionality, pronounced noise and dynamic limitations in ST data, the integration of gene expression and spatial information to accurately identify spatial domains remains challenging. This paper proposes a SpaNCMG algorithm for the purpose of achieving precise spatial domain description and localization based on a neighborhood-complementary mixed-view graph convolutional network. The algorithm enables better adaptation to ST data at different resolutions by integrating the local information from KNN and the global structure from r-radius into a complementary neighborhood graph. It also introduces an attention mechanism to achieve adaptive fusion of different reconstructed expressions, and utilizes KPCA method for dimensionality reduction. The application of SpaNCMG on five datasets from four sequencing platforms demonstrates superior performance to eight existing advanced methods. Specifically, the algorithm achieved highest ARI accuracies of 0.63 and 0.52 on the datasets of the human dorsolateral prefrontal cortex and mouse somatosensory cortex, respectively. It accurately identified the spatial locations of marker genes in the mouse olfactory bulb tissue and inferred the biological functions of different regions. When handling larger datasets such as mouse embryos, the SpaNCMG not only identified the main tissue structures but also explored unlabeled domains. Overall, the good generalization ability and scalability of SpaNCMG make it an outstanding tool for understanding tissue structure and disease mechanisms. Our codes are available at https://github.com/ZhihaoSi/SpaNCMG.

Multi-modal domain adaptation for revealing spatial functional landscape from spatially resolved transcriptomics.

Spatially resolved transcriptomics (SRT) has emerged as a powerful tool for investigating gene expression in spatial contexts, providing insights into the molecular mechanisms underlying organ development and disease pathology. However, the expression sparsity poses a computational challenge to integrate other modalities (e.g. histological images and spatial locations) that are simultaneously captured in SRT datasets for spatial clustering and variation analyses. In this study, to meet such a challenge, we propose multi-modal domain adaption for spatial transcriptomics (stMDA), a novel multi-modal unsupervised domain adaptation method, which integrates gene expression and other modalities to reveal the spatial functional landscape. Specifically, stMDA first learns the modality-specific representations from spatial multi-modal data using multiple neural network architectures and then aligns the spatial distributions across modal representations to integrate these multi-modal representations, thus facilitating the integration of global and spatially local information and improving the consistency of clustering assignments. Our results demonstrate that stMDA outperforms existing methods in identifying spatial domains across diverse platforms and species. Furthermore, stMDA excels in identifying spatially variable genes with high prognostic potential in cancer tissues. In conclusion, stMDA as a new tool of multi-modal data integration provides a powerful and flexible framework for analyzing SRT datasets, thereby advancing our understanding of intricate biological systems.

Accurately deciphering spatial domains for spatially resolved transcriptomics with stCluster.

Spatial transcriptomics provides valuable insights into gene expression within the native tissue context, effectively merging molecular data with spatial information to uncover intricate cellular relationships and tissue organizations. In this context, deciphering cellular spatial domains becomes essential for revealing complex cellular dynamics and tissue structures. However, current methods encounter challenges in seamlessly integrating gene expression data with spatial information, resulting in less informative representations of spots and suboptimal accuracy in spatial domain identification. We introduce stCluster, a novel method that integrates graph contrastive learning with multi-task learning to refine informative representations for spatial transcriptomic data, consequently improving spatial domain identification. stCluster first leverages graph contrastive learning technology to obtain discriminative representations capable of recognizing spatially coherent patterns. Through jointly optimizing multiple tasks, stCluster further fine-tunes the representations to be able to capture complex relationships between gene expression and spatial organization. Benchmarked against six state-of-the-art methods, the experimental results reveal its proficiency in accurately identifying complex spatial domains across various datasets and platforms, spanning tissue, organ, and embryo levels. Moreover, stCluster can effectively denoise the spatial gene expression patterns and enhance the spatial trajectory inference. The source code of stCluster is freely available at https://github.com/hannshu/stCluster.

Spatially contrastive variational autoencoder for deciphering tissue heterogeneity from spatially resolved transcriptomics.

Recent advances in spatially resolved transcriptomics (SRT) have brought ever-increasing opportunities to characterize expression landscape in the context of tissue spatiality. Nevertheless, there still exist multiple challenges to accurately detect spatial functional regions in tissue. Here, we present a novel contrastive learning framework, SPAtially Contrastive variational AutoEncoder (SpaCAE), which contrasts transcriptomic signals of each spot and its spatial neighbors to achieve fine-grained tissue structures detection. By employing a graph embedding variational autoencoder and incorporating a deep contrastive strategy, SpaCAE achieves a balance between spatial local information and global information of expression, enabling effective learning of representations with spatial constraints. Particularly, SpaCAE provides a graph deconvolutional decoder to address the smoothing effect of local spatial structure on expression's self-supervised learning, an aspect often overlooked by current graph neural networks. We demonstrated that SpaCAE could achieve effective performance on SRT data generated from multiple technologies for spatial domains identification and data denoising, making it a remarkable tool to obtain novel insights from SRT studies.

A multi-view graph contrastive learning framework for deciphering spatially resolved transcriptomics data.

Spatially resolved transcriptomics data are being used in a revolutionary way to decipher the spatial pattern of gene expression and the spatial architecture of cell types. Much work has been done to exploit the genomic spatial architectures of cells. Such work is based on the common assumption that gene expression profiles of spatially adjacent spots are more similar than those of more distant spots. However, related work might not consider the nonlocal spatial co-expression dependency, which can better characterize the tissue architectures. Therefore, we propose MuCoST, a Multi-view graph Contrastive learning framework for deciphering complex Spatially resolved Transcriptomic architectures with dual scale structural dependency. To achieve this, we employ spot dependency augmentation by fusing gene expression correlation and spatial location proximity, thereby enabling MuCoST to model both nonlocal spatial co-expression dependency and spatially adjacent dependency. We benchmark MuCoST on four datasets, and we compare it with other state-of-the-art spatial domain identification methods. We demonstrate that MuCoST achieves the highest accuracy on spatial domain identification from various datasets. In particular, MuCoST accurately deciphers subtle biological textures and elaborates the variation of spatially functional patterns.

Spatial-MGCN: a novel multi-view graph convolutional network for identifying spatial domains with attention mechanism.

MOTIVATION: Recent advances in spatial transcriptomics technologies have enabled gene expression profiles while preserving spatial context. Accurately identifying spatial domains is crucial for downstream analysis and it requires the effective integration of gene expression profiles and spatial information. While increasingly computational methods have been developed for spatial domain detection, most of them cannot adaptively learn the complex relationship between gene expression and spatial information, leading to sub-optimal performance. RESULTS: To overcome these challenges, we propose a novel deep learning method named Spatial-MGCN for identifying spatial domains, which is a Multi-view Graph Convolutional Network (GCN) with attention mechanism. We first construct two neighbor graphs using gene expression profiles and spatial information, respectively. Then, a multi-view GCN encoder is designed to extract unique embeddings from both the feature and spatial graphs, as well as their shared embeddings by combining both graphs. Finally, a zero-inflated negative binomial decoder is used to reconstruct the original expression matrix by capturing the global probability distribution of gene expression profiles. Moreover, Spatial-MGCN incorporates a spatial regularization constraint into the features learning to preserve spatial neighbor information in an end-to-end manner. The experimental results show that Spatial-MGCN outperforms state-of-the-art methods consistently in several tasks, including spatial clustering and trajectory inference.

Identifying spatial domains of spatially resolved transcriptomics via multi-view graph convolutional networks.

MOTIVATION: Recent advances in spatially resolved transcriptomics (ST) technologies enable the measurement of gene expression profiles while preserving cellular spatial context. Linking gene expression of cells with their spatial distribution is essential for better understanding of tissue microenvironment and biological progress. However, effectively combining gene expression data with spatial information to identify spatial domains remains challenging. RESULTS: To deal with the above issue, in this paper, we propose a novel unsupervised learning framework named STMGCN for identifying spatial domains using multi-view graph convolution networks (MGCNs). Specifically, to fully exploit spatial information, we first construct multiple neighbor graphs (views) with different similarity measures based on the spatial coordinates. Then, STMGCN learns multiple view-specific embeddings by combining gene expressions with each neighbor graph through graph convolution networks. Finally, to capture the importance of different graphs, we further introduce an attention mechanism to adaptively fuse view-specific embeddings and thus derive the final spot embedding. STMGCN allows for the effective utilization of spatial context to enhance the expressive power of the latent embeddings with multiple graph convolutions. We apply STMGCN on two simulation datasets and five real spatial transcriptomics datasets with different resolutions across distinct platforms. The experimental results demonstrate that STMGCN obtains competitive results in spatial domain identification compared with five state-of-the-art methods, including spatial and non-spatial alternatives. Besides, STMGCN can detect spatially variable genes with enriched expression patterns in the identified domains. Overall, STMGCN is a powerful and efficient computational framework for identifying spatial domains in spatial transcriptomics data.

Spatially aware self-representation learning for tissue structure characterization and spatial functional genes identification.

Spatially resolved transcriptomics (SRT) enable the comprehensive characterization of transcriptomic profiles in the context of tissue microenvironments. Unveiling spatial transcriptional heterogeneity needs to effectively incorporate spatial information accounting for the substantial spatial correlation of expression measurements. Here, we develop a computational method, SpaSRL (spatially aware self-representation learning), which flexibly enhances and decodes spatial transcriptional signals to simultaneously achieve spatial domain detection and spatial functional genes identification. This novel tunable spatially aware strategy of SpaSRL not only balances spatial and transcriptional coherence for the two tasks, but also can transfer spatial correlation constraint between them based on a unified model. In addition, this joint analysis by SpaSRL deciphers accurate and fine-grained tissue structures and ensures the effective extraction of biologically informative genes underlying spatial architecture. We verified the superiority of SpaSRL on spatial domain detection, spatial functional genes identification and data denoising using multiple SRT datasets obtained by different platforms and tissue sections. Our results illustrate SpaSRL's utility in flexible integration of spatial information and novel discovery of biological insights from spatial transcriptomic datasets.

stAA: adversarial graph autoencoder for spatial clustering task of spatially resolved transcriptomics.

With the development of spatially resolved transcriptomics technologies, it is now possible to explore the gene expression profiles of single cells while preserving their spatial context. Spatial clustering plays a key role in spatial transcriptome data analysis. In the past 2 years, several graph neural network-based methods have emerged, which significantly improved the accuracy of spatial clustering. However, accurately identifying the boundaries of spatial domains remains a challenging task. In this article, we propose stAA, an adversarial variational graph autoencoder, to identify spatial domain. stAA generates cell embedding by leveraging gene expression and spatial information using graph neural networks and enforces the distribution of cell embeddings to a prior distribution through Wasserstein distance. The adversarial training process can make cell embeddings better capture spatial domain information and more robust. Moreover, stAA incorporates global graph information into cell embeddings using labels generated by pre-clustering. Our experimental results show that stAA outperforms the state-of-the-art methods and achieves better clustering results across different profiling platforms and various resolutions. We also conducted numerous biological analyses and found that stAA can identify fine-grained structures in tissues, recognize different functional subtypes within tumors and accurately identify developmental trajectories.

SGCAST: symmetric graph convolutional auto-encoder for scalable and accurate study of spatial transcriptomics.

Recent advances in spatial transcriptomics (ST) have enabled comprehensive profiling of gene expression with spatial information in the context of the tissue microenvironment. However, with the improvements in the resolution and scale of ST data, deciphering spatial domains precisely while ensuring efficiency and scalability is still challenging. Here, we develop SGCAST, an efficient auto-encoder framework to identify spatial domains. SGCAST adopts a symmetric graph convolutional auto-encoder to learn aggregated latent embeddings via integrating the gene expression similarity and the proximity of the spatial spots. This framework in SGCAST enables a mini-batch training strategy, which makes SGCAST memory-efficient and scalable to high-resolution spatial transcriptomic data with a large number of spots. SGCAST improves the overall accuracy of spatial domain identification on benchmarking data. We also validated the performance of SGCAST on ST datasets at various scales across multiple platforms. Our study illustrates the superior capacity of SGCAST on analyzing spatial transcriptomic data.

Hexagonal image segmentation on spatially resolved transcriptomics.

Spatial transcriptomics is a rapidly evolving field that enables researchers to capture comprehensive molecular profiles while preserving information about the physical locations. One major challenge in this research area involves the identification of spatial domains, which are distinct regions characterized by unique gene expression patterns. However, current unsupervised methods have struggled to perform well in this regard due to the presence of high levels of noise and dropout events in spatial transcriptomic profiles. In this paper, we propose a novel hexagonal Convolutional Neural Network (hexCNN) for hexagonal image segmentation on spatially resolved transcriptomics. To address the problem of noise and dropout occurrences within spatial transcriptomics data, we first extend an unsupervised algorithm to a supervised learning method that can identify useful features and reduce noise hindrance. Then, inspired by the classical convolution in convolutional neural networks (CNNs), we designed a regular hexagonal convolution to compensate for the missing gene expression patterns from adjacent spots. We evaluated the performance of hexCNN by applying it to the DLPFC dataset. The results show that hexCNN achieves a classification accuracy of 86.8% and an average Rand index (ARI) of 77.1% (1.4% and 2.5% higher than those of GNNs). The results also demonstrate that hexCNN is capable of removing the noise caused by batch effect while preserving the biological signal differences.

A Novel No-Reference Quality Assessment Metric for Stereoscopic Images with Consideration of Comprehensive 3D Quality Information.

Recently, stereoscopic image quality assessment has attracted a lot attention. However, compared with 2D image quality assessment, it is much more difficult to assess the quality of stereoscopic images due to the lack of understanding of 3D visual perception. This paper proposes a novel no-reference quality assessment metric for stereoscopic images using natural scene statistics with consideration of both the quality of the cyclopean image and 3D visual perceptual information (binocular fusion and binocular rivalry). In the proposed method, not only is the quality of the cyclopean image considered, but binocular rivalry and other 3D visual intrinsic properties are also exploited. Specifically, in order to improve the objective quality of the cyclopean image, features of the cyclopean images in both the spatial domain and transformed domain are extracted based on the natural scene statistics (NSS) model. Furthermore, to better comprehend intrinsic properties of the stereoscopic image, in our method, the binocular rivalry effect and other 3D visual properties are also considered in the process of feature extraction. Following adaptive feature pruning using principle component analysis, improved metric accuracy can be found in our proposed method. The experimental results show that the proposed metric can achieve a good and consistent alignment with subjective assessment of stereoscopic images in comparison with existing methods, with the highest SROCC (0.952) and PLCC (0.962) scores being acquired on the LIVE 3D database Phase I.

Efficient numerical approximation of a non-regular Fokker-Planck equation associated with first-passage time distributions.

In neuroscience, the distribution of a decision time is modelled by means of a one-dimensional Fokker-Planck equation with time-dependent boundaries and space-time-dependent drift. Efficient approximation of the solution to this equation is required, e.g., for model evaluation and parameter fitting. However, the prescribed boundary conditions lead to a strong singularity and thus to slow convergence of numerical approximations. In this article we demonstrate that the solution can be related to the solution of a parabolic PDE on a rectangular space-time domain with homogeneous initial and boundary conditions by transformation and subtraction of a known function. We verify that the solution of the new PDE is indeed more regular than the solution of the original PDE and proceed to discretize the new PDE using a space-time minimal residual method. We also demonstrate that the solution depends analytically on the parameters determining the boundaries as well as the drift. This justifies the use of a sparse tensor product interpolation method to approximate the PDE solution for various parameter ranges. The predicted convergence rates of the minimal residual method and that of the interpolation method are supported by numerical simulations.

Method for fast lipid reconstruction and removal processing in 1 H MRSI of the brain.

PURPOSE: To develop a new rapid spatial filtering method for lipid removal, fast lipid reconstruction and removal processing (FLIP), which selectively isolates and removes interfering lipid signals from outside the brain in a full-FOV 2D MRSI and whole-brain 3D echo planar spectroscopic imaging (EPSI). THEORY AND METHODS: FLIP uses regularized least-squares regression based on spatial prior information from MRI to selectively remove lipid signals originating from the scalp and measure the brain metabolite signals with minimum cross contamination. FLIP is a noniterative approach, thus allowing a rapid processing speed, and uses only spatial information without any spectral priors. The performance of FLIP was compared with the Papoulis-Gerchberg algorithm (PGA), Hankel singular value decomposition (HSVD), and fast image reconstruction with L2 regularization (L2). RESULTS: FLIP in both 2D and 3D MRSI resulted in consistent metabolite quantification in a greater number of voxels with less concentration variation than other algorithms, demonstrating effective and robust lipid-removal performance. The percentage of voxels that met quality criteria with FLIP, PGA, HSVD, and L2 processing were 90%, 57%, 29%, and 42% in 2D MRSI, and 80%, 75%, 76%, and 74% in 3D EPSI, respectively. The quantification results of full-FOV MRSI using FLIP were comparable to those of volume-localized MRSI, while allowing significantly increased spatial coverage. FLIP performed the fastest in 2D MRSI. CONCLUSION: FLIP is a new lipid-removal algorithm that promises fast and effective lipid removal with improved volume coverage in MRSI.

Efficient Optical Sensing Based on Phase Shift of Waves Supported by a One-Dimensional Photonic Crystal.

Interferometric methods of optical sensing based on the phase shift of the Bloch surface waves (BSWs) and guided waves (GWs) supported by a one-dimensional photonic crystal are presented. The photonic crystal, composed of six SiO2/TiO2 bilayers with a termination layer of TiO2, is employed in the Kretschmann configuration. Under resonance condition, an abrupt phase change is revealed, and the corresponding phase shift is measured by interferometric techniques applied in both the spectral and spatial domains. The spectral interferometric technique employing a birefringent quartz crystal is used to obtain interference of projections of p- and s-polarized light waves reflected from the photonic crystal. The phase shifts are retrieved by processing the spectral interferograms recorded for various values of relative humidity (RH) of air, giving the sensitivity to the RH as high as 0.029 rad/%RH and 0.012 rad/%RH for the BSW and GW, respectively. The spatial interferometric technique employs a Wollaston prism and an analyzer to generate an interference pattern, which is processed to retrieve the phase difference, and results are in good agreement with those obtained by sensing the phase shift in the spectral domain. In addition, from the derivative of the spectral phase shifts, the peak positions are obtained, and their changes with the RH give the sensitivities of 0.094 nm/%RH and 0.061 nm/%RH for the BSW and GW, respectively. These experimental results demonstrate an efficient optical sensing with a lot of applications in various research areas.

Stress Classification Using Photoplethysmogram-Based Spatial and Frequency Domain Images.

Stress is subjective and is manifested differently from one person to another. Thus, the performance of generic classification models that classify stress status is crude. Building a person-specific model leads to a reliable classification, but it requires the collection of new data to train a new model for every individual and needs periodic upgrades because stress is dynamic. In this paper, a new binary classification (called stressed and non-stressed) approach is proposed for a subject's stress state in which the inter-beat intervals extracted from a photoplethysomogram (PPG) were transferred to spatial images and then to frequency domain images according to the number of consecutive. Then, the convolution neural network (CNN) was used to train and validate the classification accuracy of the person's stress state. Three types of classification models were built: person-specific models, generic classification models, and calibrated-generic classification models. The average classification accuracies achieved by person-specific models using spatial images and frequency domain images were 99.9%, 100%, and 99.8%, and 99.68%, 98.97%, and 96.4% for the training, validation, and test, respectively. By combining 20% of the samples collected from test subjects into the training data, the calibrated generic models' accuracy was improved and outperformed the generic performance across both the spatial and frequency domain images. The average classification accuracy of 99.6%, 99.9%, and 88.1%, and 99.2%, 97.4%, and 87.6% were obtained for the training set, validation set, and test set, respectively, using the calibrated generic classification-based method for the series of inter-beat interval (IBI) spatial and frequency domain images. The main contribution of this study is the use of the frequency domain images that are generated from the spatial domain images of the IBI extracted from the PPG signal to classify the stress state of the individual by building person-specific models and calibrated generic models.

Spatial dynamics within and between brain functional domains: A hierarchical approach to study time-varying brain function.

The analysis of time-varying activity and connectivity patterns (i.e., the chronnectome) using resting-state magnetic resonance imaging has become an important part of ongoing neuroscience discussions. The majority of previous work has focused on variations of temporal coupling among fixed spatial nodes or transition of the dominant activity/connectivity pattern over time. Here, we introduce an approach to capture spatial dynamics within functional domains (FDs), as well as temporal dynamics within and between FDs. The approach models the brain as a hierarchical functional architecture with different levels of granularity, where lower levels have higher functional homogeneity and less dynamic behavior and higher levels have less homogeneity and more dynamic behavior. First, a high-order spatial independent component analysis is used to approximate functional units. A functional unit is a pattern of regions with very similar functional activity over time. Next, functional units are used to construct FDs. Finally, functional modules (FMs) are calculated from FDs, providing an overall view of brain dynamics. Results highlight the spatial fluidity within FDs, including a broad spectrum of changes in regional associations, from strong coupling to complete decoupling. Moreover, FMs capture the dynamic interplay between FDs. Patients with schizophrenia show transient reductions in functional activity and state connectivity across several FDs, particularly the subcortical domain. Activity and connectivity differences convey unique information in many cases (e.g., the default mode) highlighting their complementarity information. The proposed hierarchical model to capture FD spatiotemporal variations provides new insight into the macroscale chronnectome and identifies changes hidden from existing approaches.

Saliency Detection Based on the Combination of High-Level Knowledge and Low-Level Cues in Foggy Images.

A key issue in saliency detection of the foggy images in the wild for human tracking is how to effectively define the less obvious salient objects, and the leading cause is that the contrast and resolution is reduced by the light scattering through fog particles. In this paper, to suppress the interference of the fog and acquire boundaries of salient objects more precisely, we present a novel saliency detection method for human tracking in the wild. In our method, a combination of object contour detection and salient object detection is introduced. The proposed model can not only maintain the object edge more precisely via object contour detection, but also ensure the integrity of salient objects, and finally obtain accurate saliency maps of objects. Firstly, the input image is transformed into HSV color space, and the amplitude spectrum (AS) of each color channel is adjusted to obtain the frequency domain (FD) saliency map. Then, the contrast of the local-global superpixel is calculated, and the saliency map of the spatial domain (SD) is obtained. We use Discrete Stationary Wavelet Transform (DSWT) to fuse the cues of the FD and SD. Finally, a fully convolutional encoder-decoder model is utilized to refine the contour of the salient objects. Experimental results demonstrate that the presented model can remove the influence of fog efficiently, and the performance is better than 16 state-of-the-art saliency models.

Full L1-regularized Traction Force Microscopy over whole cells.

BACKGROUND: Traction Force Microscopy (TFM) is a widespread technique to estimate the tractions that cells exert on the surrounding substrate. To recover the tractions, it is necessary to solve an inverse problem, which is ill-posed and needs regularization to make the solution stable. The typical regularization scheme is given by the minimization of a cost functional, which is divided in two terms: the error present in the data or data fidelity term; and the regularization or penalty term. The classical approach is to use zero-order Tikhonov or L2-regularization, which uses the L2-norm for both terms in the cost function. Recently, some studies have demonstrated an improved performance using L1-regularization (L1-norm in the penalty term) related to an increase in the spatial resolution and sensitivity of the recovered traction field. In this manuscript, we present a comparison between the previous two regularization schemes (relying in the L2-norm for the data fidelity term) and the full L1-regularization (using the L1-norm for both terms in the cost function) for synthetic and real data. RESULTS: Our results reveal that L1-regularizations give an improved spatial resolution (more important for full L1-regularization) and a reduction in the background noise with respect to the classical zero-order Tikhonov regularization. In addition, we present an approximation, which makes feasible the recovery of cellular tractions over whole cells on typical full-size microscope images when working in the spatial domain. CONCLUSIONS: The proposed full L1-regularization improves the sensitivity to recover small stress footprints. Moreover, the proposed method has been validated to work on full-field microscopy images of real cells, what certainly demonstrates it is a promising tool for biological applications.

Medical image segmentation network based on multi-scale frequency domain filter.

With the development of deep learning, medical image segmentation in computer-aided diagnosis has become a research hotspot. Recently, UNet and its variants have become the most powerful medical image segmentation methods. However, these methods suffer from (1) insufficient sensing field and insufficient depth; (2) computational nonlinearity and redundancy of channel features; and (3) ignoring the interrelationships among feature channels. These problems lead to poor network segmentation performance and weak generalization ability. Therefore, first of all, we propose an effective replacement scheme of UNet base block, Double residual depthwise atrous convolution (DRDAC) block, to effectively improve the deficiency of receptive field and depth. Secondly, a new linear module, the Multi-scale frequency domain filter (MFDF), is designed to capture global information from the frequency domain. The high order multi-scale relationship is extracted by combining the depthwise atrous separable convolution with the frequency domain filter. Finally, a channel attention called Axial selection channel attention (ASCA) is redesigned to enhance the network's ability to model feature channel interrelationships. Further, we design a novel frequency domain medical image segmentation baseline method FDFUNet based on the above modules. We conduct extensive experiments on five publicly available medical image datasets and demonstrate that the present method has stronger segmentation performance as well as generalization ability compared to other state-of-the-art baseline methods.