SpatialCTD: A Large-Scale Tumor Microenvironment Spatial Transcriptomic Dataset to Evaluate Cell Type Deconvolution for Immuno-Oncology.

IF 1.4 4区 生物学 Q4 BIOCHEMICAL RESEARCH METHODS
Journal of Computational Biology Pub Date : 2024-09-01 Epub Date: 2024-08-08 DOI:10.1089/cmb.2024.0532
Jiayuan Ding, Lingxiao Li, Qiaolin Lu, Julian Venegas, Yixin Wang, Lidan Wu, Wei Jin, Hongzhi Wen, Renming Liu, Wenzhuo Tang, Xinnan Dai, Zhaoheng Li, Wangyang Zuo, Yi Chang, Yu Leo Lei, Lulu Shang, Patrick Danaher, Yuying Xie, Jiliang Tang
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引用次数: 0

Abstract

Recent technological advancements have enabled spatially resolved transcriptomic profiling but at a multicellular resolution that is more cost-effective. The task of cell type deconvolution has been introduced to disentangle discrete cell types from such multicellular spots. However, existing benchmark datasets for cell type deconvolution are either generated from simulation or limited in scale, predominantly encompassing data on mice and are not designed for human immuno-oncology. To overcome these limitations and promote comprehensive investigation of cell type deconvolution for human immuno-oncology, we introduce a large-scale spatial transcriptomic deconvolution benchmark dataset named SpatialCTD, encompassing 1.8 million cells and 12,900 pseudo spots from the human tumor microenvironment across the lung, kidney, and liver. In addition, SpatialCTD provides more realistic reference than those generated from single-cell RNA sequencing (scRNA-seq) data for most reference-based deconvolution methods. To utilize the location-aware SpatialCTD reference, we propose a graph neural network-based deconvolution method (i.e., GNNDeconvolver). Extensive experiments show that GNNDeconvolver often outperforms existing state-of-the-art methods by a substantial margin, without requiring scRNA-seq data. To enable comprehensive evaluations of spatial transcriptomics data from flexible protocols, we provide an online tool capable of converting spatial transcriptomic data from various platforms (e.g., 10× Visium, MERFISH, and sci-Space) into pseudo spots, featuring adjustable spot size. The SpatialCTD dataset and GNNDeconvolver implementation are available at https://github.com/OmicsML/SpatialCTD, and the online converter tool can be accessed at https://omicsml.github.io/SpatialCTD/.

SpatialCTD:用于评估免疫肿瘤学细胞类型解旋的大规模肿瘤微环境空间转录组数据集。
最近的技术进步实现了空间分辨率的转录组分析,但其多细胞分辨率更具成本效益。细胞类型解卷积的任务就是要从这种多细胞点中分离出离散的细胞类型。然而,现有的细胞类型解旋基准数据集要么是模拟生成的,要么规模有限,主要包括小鼠数据,并非为人类免疫肿瘤学设计。为了克服这些局限性,促进对人类免疫肿瘤学细胞类型解卷积的全面研究,我们引入了一个名为 SpatialCTD 的大规模空间转录组解卷积基准数据集,其中包括 180 万个细胞和 12,900 个来自肺、肾和肝脏人类肿瘤微环境的伪点。此外,对于大多数基于参考的解卷积方法来说,SpatialCTD 提供了比单细胞 RNA 测序(scRNA-seq)数据更真实的参考。为了利用位置感知的 SpatialCTD 参考,我们提出了一种基于图神经网络的解卷积方法(即 GNNDeconvolver)。广泛的实验表明,GNNDeconvolver 在不需要 scRNA-seq 数据的情况下,往往能大幅超越现有的先进方法。为了能够全面评估来自灵活协议的空间转录组学数据,我们提供了一种在线工具,能够将来自不同平台(如 10× Visium、MERFISH 和 sci-Space)的空间转录组学数据转换成伪斑,其特点是斑的大小可调。SpatialCTD 数据集和 GNNDeconvolver 实现可从 https://github.com/OmicsML/SpatialCTD 获取,在线转换工具可从 https://omicsml.github.io/SpatialCTD/ 访问。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Computational Biology
Journal of Computational Biology 生物-计算机:跨学科应用
CiteScore
3.60
自引率
5.90%
发文量
113
审稿时长
6-12 weeks
期刊介绍: Journal of Computational Biology is the leading peer-reviewed journal in computational biology and bioinformatics, publishing in-depth statistical, mathematical, and computational analysis of methods, as well as their practical impact. Available only online, this is an essential journal for scientists and students who want to keep abreast of developments in bioinformatics. Journal of Computational Biology coverage includes: -Genomics -Mathematical modeling and simulation -Distributed and parallel biological computing -Designing biological databases -Pattern matching and pattern detection -Linking disparate databases and data -New tools for computational biology -Relational and object-oriented database technology for bioinformatics -Biological expert system design and use -Reasoning by analogy, hypothesis formation, and testing by machine -Management of biological databases
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