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基于模型的多个组成型组学数据集的联合可视化

Model-based joint visualization of multiple compositional omics datasets.

作者信息

Hawinkel Stijn, Bijnens Luc, Cao Kim-Anh Lê, Thas Olivier

机构信息

Department of Data Analysis and Mathematical Modelling, Ghent University, 9000 Ghent, Belgium.

Quantitative Sciences, Janssen Pharmaceutical companies of Johnson and Johnson, 2340 Beerse, Belgium.

出版信息

NAR Genom Bioinform. 2020 Jul 21;2(3):lqaa050. doi: 10.1093/nargab/lqaa050. eCollection 2020 Sep.

DOI:10.1093/nargab/lqaa050
PMID:33575602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7671331/
Abstract

The integration of multiple omics datasets measured on the same samples is a challenging task: data come from heterogeneous sources and vary in signal quality. In addition, some omics data are inherently compositional, e.g. sequence count data. Most integrative methods are limited in their ability to handle covariates, missing values, compositional structure and heteroscedasticity. In this article we introduce a flexible model-based approach to data integration to address these current limitations: COMBI. We combine concepts, such as compositional biplots and log-ratio link functions with latent variable models, and propose an attractive visualization through multiplots to improve interpretation. Using real data examples and simulations, we illustrate and compare our method with other data integration techniques. Our algorithm is available in the R-package .

摘要

对同一组样本测量得到的多个组学数据集进行整合是一项具有挑战性的任务

数据来自异质来源,信号质量也各不相同。此外,一些组学数据本质上具有构成性,例如序列计数数据。大多数整合方法在处理协变量、缺失值、构成结构和异方差性方面能力有限。在本文中,我们引入了一种基于灵活模型的数据整合方法来解决这些当前的局限性:COMBI。我们将诸如构成双标图和对数比率链接函数等概念与潜在变量模型相结合,并通过多图提出一种有吸引力的可视化方法以改进解释。使用实际数据示例和模拟,我们阐述并将我们的方法与其他数据整合技术进行比较。我们的算法可在R包中获取。

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本文引用的文献

1
Sequence count data are poorly fit by the negative binomial distribution.序列计数数据不适用于负二项分布。
PLoS One. 2020 Apr 30;15(4):e0224909. doi: 10.1371/journal.pone.0224909. eCollection 2020.
2
Multi-omics of the gut microbial ecosystem in inflammatory bowel diseases.炎症性肠病中的肠道微生物生态系统的多组学研究。
Nature. 2019 May;569(7758):655-662. doi: 10.1038/s41586-019-1237-9. Epub 2019 May 29.
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A unified framework for unconstrained and constrained ordination of microbiome read count data.用于无约束和约束微生物组读计数数据排序的统一框架。
Genes (Basel). 2022 Dec 14;13(12):2362. doi: 10.3390/genes13122362.
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Editorial: Compositional data analysis and related methods applied to genomics-a first special issue from .社论:应用于基因组学的成分数据分析及相关方法——来自……的首个特刊
NAR Genom Bioinform. 2020 Dec 9;2(4):lqaa103. doi: 10.1093/nargab/lqaa103. eCollection 2020 Dec.
PLoS One. 2019 Feb 13;14(2):e0205474. doi: 10.1371/journal.pone.0205474. eCollection 2019.
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DIABLO: an integrative approach for identifying key molecular drivers from multi-omics assays.DIABLO:一种从多组学分析中识别关键分子驱动因素的综合方法。
Bioinformatics. 2019 Sep 1;35(17):3055-3062. doi: 10.1093/bioinformatics/bty1054.
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Analysis of relative abundances with zeros on environmental gradients: a multinomial regression model.基于环境梯度的含零相对丰度分析:多项式回归模型
PeerJ. 2018 Sep 27;6:e5643. doi: 10.7717/peerj.5643. eCollection 2018.
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Intestinal Metaproteomics Reveals Host-Microbiota Interactions in Subjects at Risk for Type 1 Diabetes.肠道宏蛋白质组学揭示 1 型糖尿病风险人群中的宿主-微生物相互作用。
Diabetes Care. 2018 Oct;41(10):2178-2186. doi: 10.2337/dc18-0777. Epub 2018 Aug 12.
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Differential gene expression analysis tools exhibit substandard performance for long non-coding RNA-sequencing data.差异基因表达分析工具在长链非编码 RNA-seq 数据上的表现不佳。
Genome Biol. 2018 Jul 24;19(1):96. doi: 10.1186/s13059-018-1466-5.
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Antibiotic-induced acceleration of type 1 diabetes alters maturation of innate intestinal immunity.抗生素诱导的 1 型糖尿病加速改变固有肠免疫的成熟。
Elife. 2018 Jul 25;7:e37816. doi: 10.7554/eLife.37816.
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Multi-Omics Factor Analysis-a framework for unsupervised integration of multi-omics data sets.多组学因子分析——一种用于无监督整合多组学数据集的框架。
Mol Syst Biol. 2018 Jun 20;14(6):e8124. doi: 10.15252/msb.20178124.
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Microbiome Datasets Are Compositional: And This Is Not Optional.微生物组数据集具有构成性:这并非可有可无。
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