Robust identification of temporal biomarkers in longitudinal omics studies

Author:

Metwally Ahmed A123ORCID,Zhang Tom4,Wu Si1,Kellogg Ryan15,Zhou Wenyu1,Contrepois Kevin1,Tang Hua1,Snyder Michael1ORCID

Affiliation:

1. Department of Genetics, Stanford University , Stanford, CA 94305, USA

2. Illumina Artificial Intelligence Laboratory, Illumina Inc. , San Diego, CA 92122, USA

3. Systems and Biomedical Engineering Department, Faculty of Engineering, Cairo University , Giza 12613, Egypt

4. Department of Computer Science, Columbia University , New York, NY 10027, USA

5. Department of Bioengineering, Stanford University , Stanford, CA 94305, USA

Abstract

Abstract Motivation Longitudinal studies increasingly collect rich ‘omics’ data sampled frequently over time and across large cohorts to capture dynamic health fluctuations and disease transitions. However, the generation of longitudinal omics data has preceded the development of analysis tools that can efficiently extract insights from such data. In particular, there is a need for statistical frameworks that can identify not only which omics features are differentially regulated between groups but also over what time intervals. Additionally, longitudinal omics data may have inconsistencies, including non-uniform sampling intervals, missing data points, subject dropout and differing numbers of samples per subject. Results In this work, we developed OmicsLonDA, a statistical method that provides robust identification of time intervals of temporal omics biomarkers. OmicsLonDA is based on a semi-parametric approach, in which we use smoothing splines to model longitudinal data and infer significant time intervals of omics features based on an empirical distribution constructed through a permutation procedure. We benchmarked OmicsLonDA on five simulated datasets with diverse temporal patterns, and the method showed specificity greater than 0.99 and sensitivity greater than 0.87. Applying OmicsLonDA to the iPOP cohort revealed temporal patterns of genes, proteins, metabolites and microbes that are differentially regulated in male versus female subjects following a respiratory infection. In addition, we applied OmicsLonDA to a longitudinal multi-omics dataset of pregnant women with and without preeclampsia, and OmicsLonDA identified potential lipid markers that are temporally significantly different between the two groups. Availability and implementation We provide an open-source R package (https://bioconductor.org/packages/OmicsLonDA), to enable widespread use. Supplementary information Supplementary data are available at Bioinformatics online.

Funder

NIH Common Fund Human Microbiome Project

NIH

SCGPM Genome Sequencing Service Center, Stanford Clinical and Translational Science Award

Diabetes Genomics and Analysis Core of the Stanford Diabetes Research Center

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

Reference41 articles.

1. Detection and confirmation of serum lipid biomarkers for preeclampsia using direct infusion mass spectrometry;Anand;J. Lipid Res,2016

2. Eicosanomics: targeted lipidomics of eicosanoids in biological systems;Balazy;Prostaglandins Other Lipid Mediat,2004

3. A multi-tissue type genome-scale metabolic network for analysis of whole-body systems physiology;Bordbar;BMC Syst. Biol,2011

4. Lipid peroxidation and protein oxidation in Alzheimer’s disease brain: potential causes and consequences involving amyloid beta-peptide-associated free radical oxidative stress;Butterfield;Free Radic. Biol. Med,2002

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