Early prognosis of respiratory virus shedding in humans

被引:3
作者
Aminian, M. [3 ]
Ghosh, T. [2 ]
Peterson, A. [1 ]
Rasmussen, A. L. [4 ,5 ]
Stiverson, S. [1 ]
Sharma, K. [2 ]
Kirby, M. [1 ,2 ]
机构
[1] Colorado State Univ, Dept Math, Ft Collins, CO 80524 USA
[2] Colorado State Univ, Dept Comp Sci, Ft Collins, CO 80524 USA
[3] Calif State Polytech Univ Pomona, Dept Math & Stat, Pomona, CA USA
[4] Univ Saskatchewan, Vaccine & Infect Dis Org Int Vaccine Ctr VIDD Int, Saskatoon, SK, Canada
[5] Georgetown Univ, Med Ctr, Ctr Global Hlth Sci & Secur, Washington, DC 20007 USA
关键词
SUPPORT; CLASSIFICATION; TRANSMISSION;
D O I
10.1038/s41598-021-95293-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
This paper addresses the development of predictive models for distinguishing pre-symptomatic infections from uninfected individuals. Our machine learning experiments are conducted on publicly available challenge studies that collected whole-blood transcriptomics data from individuals infected with HRV, RSV, H1N1, and H3N2. We address the problem of identifying discriminatory biomarkers between controls and eventual shedders in the first 32 h post-infection. Our exploratory analysis shows that the most discriminatory biomarkers exhibit a strong dependence on time over the course of the human response to infection. We visualize the feature sets to provide evidence of the rapid evolution of the gene expression profiles. To quantify this observation, we partition the data in the first 32 h into four equal time windows of 8 h each and identify all discriminatory biomarkers using sparsity-promoting classifiers and Iterated Feature Removal. We then perform a comparative machine learning classification analysis using linear support vector machines, artificial neural networks and Centroid-Encoder. We present a range of experiments on different groupings of the diseases to demonstrate the robustness of the resulting models.
引用
收藏
页数:15
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