Quantitative analysis of high-throughput biological data

被引:3
|
作者
Juan, Hsueh-Fen [1 ,2 ,3 ]
Huang, Hsuan-Cheng [4 ]
机构
[1] Natl Taiwan Univ, Inst Biomed Elect & Bioinformat, Dept Life Sci, Taipei 106, Taiwan
[2] Natl Taiwan Univ, Ctr Syst Biol, Taipei 106, Taiwan
[3] Taiwan AI Labs, Taipei, Taiwan
[4] Natl Yang Ming Chiao Tung Univ, Inst Biomed Informat, Taipei 112, Taiwan
关键词
biological network; data integration; multiomics data; quantitative analysis; single-cell transcriptomics; MISSING VALUE ESTIMATION; RNA-SEQUENCING DATA; SINGLE-CELL; MASS-SPECTROMETRY; GENE-EXPRESSION; MICROARRAY DATA; PROTEOMICS DATA; COMPUTATIONAL PLATFORM; NORMALIZATION METHODS; INTEGRATIVE ANALYSIS;
D O I
10.1002/wcms.1658
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The study of multiple "omes," such as the genome, transcriptome, proteome, and metabolome has become widespread in biomedical research. High-throughput techniques enable the rapid generation of high-dimensional multiomics data. This multiomics approach provides a more complete perspective to study biological systems compared with traditional methods. However, the quantitative analysis and integration of distinct types of high-dimensional omics data remain a challenge. Here, we provide an up-to-date and comprehensive review of the methods used for omics data quantification and integration. We first review the quantitative analysis of not only bulk but also single-cell transcriptomics data, as well as proteomics data. Current methods for reducing batch effects and integrating heterogeneous high-dimensional data are then introduced. Network analysis on large-scale biomedical data can capture the global properties of drugs, targets, and disease relationships, thus enabling a better understanding of biological systems. Current trends in the applications and methods used to extend quantitative omics data analysis to biological networks are also discussed.This article is categorized under:Data Science > Artificial Intelligence/Machine Learning
引用
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页数:26
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