TransST: Transfer Learning Embedded Spatial Factor Modeling of Spatial Transcriptomics Data
- URL: http://arxiv.org/abs/2504.12353v1
- Date: Tue, 15 Apr 2025 22:03:38 GMT
- Title: TransST: Transfer Learning Embedded Spatial Factor Modeling of Spatial Transcriptomics Data
- Authors: Shuo Shuo Liu, Shikun Wang, Yuxuan Chen, Anil K. Rustgi, Ming Yuan, Jianhua Hu,
- Abstract summary: We propose a novel transfer learning framework, referred to as TransST, to adaptively leverage the cell-labeled information from external sources.<n>We show that TransST is both effective and robust in identifying cell subclusters and detecting corresponding driving biomarkers in spatial transcriptomics data.
- Score: 13.71468013489106
- License: http://creativecommons.org/licenses/by/4.0/
- Abstract: Background: Spatial transcriptomics have emerged as a powerful tool in biomedical research because of its ability to capture both the spatial contexts and abundance of the complete RNA transcript profile in organs of interest. However, limitations of the technology such as the relatively low resolution and comparatively insufficient sequencing depth make it difficult to reliably extract real biological signals from these data. To alleviate this challenge, we propose a novel transfer learning framework, referred to as TransST, to adaptively leverage the cell-labeled information from external sources in inferring cell-level heterogeneity of a target spatial transcriptomics data. Results: Applications in several real studies as well as a number of simulation settings show that our approach significantly improves existing techniques. For example, in the breast cancer study, TransST successfully identifies five biologically meaningful cell clusters, including the two subgroups of cancer in situ and invasive cancer; in addition, only TransST is able to separate the adipose tissues from the connective issues among all the studied methods. Conclusions: In summary, the proposed method TransST is both effective and robust in identifying cell subclusters and detecting corresponding driving biomarkers in spatial transcriptomics data.
Related papers
- Multi-modal Spatial Clustering for Spatial Transcriptomics Utilizing High-resolution Histology Images [1.3124513975412255]
spatial transcriptomics (ST) enables transcriptome-wide gene expression profiling while preserving spatial context.
Current spatial clustering methods fail to fully integrate high-resolution histology image features with gene expression data.
We propose a novel contrastive learning-based deep learning approach that integrates gene expression data with histology image features.
arXiv Detail & Related papers (2024-10-31T00:32:24Z) - Revisiting Adaptive Cellular Recognition Under Domain Shifts: A Contextual Correspondence View [49.03501451546763]
We identify the importance of implicit correspondences across biological contexts for exploiting domain-invariant pathological composition.
We propose self-adaptive dynamic distillation to secure instance-aware trade-offs across different model constituents.
arXiv Detail & Related papers (2024-07-14T04:41:16Z) - stEnTrans: Transformer-based deep learning for spatial transcriptomics enhancement [1.3124513975412255]
We present stEnTrans, a deep learning method based on Transformer architecture that provides comprehensive predictions for gene expression in unmeasured areas.
We evaluate stEnTrans on six datasets and the results indicate superior performance in enhancing spots resolution and predicting gene expression in unmeasured areas.
arXiv Detail & Related papers (2024-07-11T06:50:34Z) - Must: Maximizing Latent Capacity of Spatial Transcriptomics Data [41.70354088000952]
This paper introduces Multiple-modality Structure Transformation, named MuST, a novel methodology to tackle the challenge.
It integrates the multi-modality information contained in the ST data effectively into a uniform latent space to provide a foundation for all the downstream tasks.
The results show that it outperforms existing state-of-the-art methods with clear advantages in the precision of identifying and preserving structures of tissues and biomarkers.
arXiv Detail & Related papers (2024-01-15T09:07:28Z) - Single-Cell Deep Clustering Method Assisted by Exogenous Gene
Information: A Novel Approach to Identifying Cell Types [50.55583697209676]
We develop an attention-enhanced graph autoencoder, which is designed to efficiently capture the topological features between cells.
During the clustering process, we integrated both sets of information and reconstructed the features of both cells and genes to generate a discriminative representation.
This research offers enhanced insights into the characteristics and distribution of cells, thereby laying the groundwork for early diagnosis and treatment of diseases.
arXiv Detail & Related papers (2023-11-28T09:14:55Z) - Conditionally Invariant Representation Learning for Disentangling
Cellular Heterogeneity [25.488181126364186]
This paper presents a novel approach that leverages domain variability to learn representations that are conditionally invariant to unwanted variability or distractors.
We apply our method to grand biological challenges, such as data integration in single-cell genomics.
Specifically, the proposed approach helps to disentangle biological signals from data biases that are unrelated to the target task or the causal explanation of interest.
arXiv Detail & Related papers (2023-07-02T12:52:41Z) - Challenging mitosis detection algorithms: Global labels allow centroid
localization [1.7382198387953947]
Mitotic activity is a crucial biomarker for the diagnosis and prognosis of different types of cancers.
In this work, we propose to avoid complex scenarios, and we perform the localization task in a weakly supervised manner, using only image-level labels on patches.
The results obtained on the publicly available TUPAC16 dataset are competitive with state-of-the-art methods, using only one training phase.
arXiv Detail & Related papers (2022-11-30T09:52:26Z) - Superficial White Matter Analysis: An Efficient Point-cloud-based Deep
Learning Framework with Supervised Contrastive Learning for Consistent
Tractography Parcellation across Populations and dMRI Acquisitions [68.41088365582831]
White matter parcellation classifies tractography streamlines into clusters or anatomically meaningful tracts.
Most parcellation methods focus on the deep white matter (DWM), whereas fewer methods address the superficial white matter (SWM) due to its complexity.
We propose a novel two-stage deep-learning-based framework, Superficial White Matter Analysis (SupWMA), that performs an efficient parcellation of 198 SWM clusters from whole-brain tractography.
arXiv Detail & Related papers (2022-07-18T23:07:53Z) - Discriminative Singular Spectrum Classifier with Applications on
Bioacoustic Signal Recognition [67.4171845020675]
We present a bioacoustic signal classifier equipped with a discriminative mechanism to extract useful features for analysis and classification efficiently.
Unlike current bioacoustic recognition methods, which are task-oriented, the proposed model relies on transforming the input signals into vector subspaces.
The validity of the proposed method is verified using three challenging bioacoustic datasets containing anuran, bee, and mosquito species.
arXiv Detail & Related papers (2021-03-18T11:01:21Z) - Weakly-Supervised Cross-Domain Adaptation for Endoscopic Lesions
Segmentation [79.58311369297635]
We propose a new weakly-supervised lesions transfer framework, which can explore transferable domain-invariant knowledge across different datasets.
A Wasserstein quantified transferability framework is developed to highlight widerange transferable contextual dependencies.
A novel self-supervised pseudo label generator is designed to equally provide confident pseudo pixel labels for both hard-to-transfer and easy-to-transfer target samples.
arXiv Detail & Related papers (2020-12-08T02:26:03Z) - Topological Data Analysis of copy number alterations in cancer [70.85487611525896]
We explore the potential to capture information contained in cancer genomic information using a novel topology-based approach.
We find that this technique has the potential to extract meaningful low-dimensional representations in cancer somatic genetic data.
arXiv Detail & Related papers (2020-11-22T17:31:23Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.