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Temporal response characterization across individual multiomics profiles of prediabetic and diabetic subjects

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Abstract Longitudinal deep multiomics profiling, which combines biomolecular, physiological, environmental and clinical measures data, shows great promise for precision health. However, integrating and understanding the complexity of such data remains a big challenge. Here we utilize an individual-focused bottom-up approach aimed at first assessing single individuals’ multiomics time series, and using the individual-level responses to assess multi-individual grouping based directly on similarity of their longitudinal deep multiomics profiles. We used this individual-focused approach to analyze profiles from a study profiling longitudinal responses in type 2 diabetes mellitus. After generating periodograms for individual subject omics signals, we constructed within-person omics networks and analyzed personal-level immune changes. The results identified both individual-level responses to immune perturbation, and the clusters of individuals that have similar behaviors in immune response and which were associated to measures of their diabetic status.
Title: Temporal response characterization across individual multiomics profiles of prediabetic and diabetic subjects
Description:
Abstract Longitudinal deep multiomics profiling, which combines biomolecular, physiological, environmental and clinical measures data, shows great promise for precision health.
However, integrating and understanding the complexity of such data remains a big challenge.
Here we utilize an individual-focused bottom-up approach aimed at first assessing single individuals’ multiomics time series, and using the individual-level responses to assess multi-individual grouping based directly on similarity of their longitudinal deep multiomics profiles.
We used this individual-focused approach to analyze profiles from a study profiling longitudinal responses in type 2 diabetes mellitus.
After generating periodograms for individual subject omics signals, we constructed within-person omics networks and analyzed personal-level immune changes.
The results identified both individual-level responses to immune perturbation, and the clusters of individuals that have similar behaviors in immune response and which were associated to measures of their diabetic status.

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