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Biology subjects

Settle, A.

Publications and source records attributed to Settle, A..

2 recordsLinked to original sources

multiTEMPTED: Joint Dimensionality Reduction of Longitudinal Multi-omic Data with Modality-Specific Temporal Dynamics

Longitudinal multi-omic studies profile multiple molecular layers, such as microbiome composition, metabolomics, lipidomics, and proteomics, repeatedly over time. These layers reflect shared subject-level biological processes yet each may exhibit its own temporal dynamics. Most existing methods either integrate multiple omics modalities cross-sectionally or model a single modality longitudinally. The few methods that handle longitudinal multi-omic data assume a shared temporal trajectory across all modalities, limiting their ability to capture modality-specific dynamics, and can be computationally prohibitive at the scale of modern cohort studies. We introduce multiTEMPTED, an extension of the temporal tensor decomposition framework to M>=1 simultaneous omic modalities. The method jointly estimates subject components shared across modalities, modality-specific feature loadings identifying the contributing molecular features, and modality-specific temporal trajectories, while accommodating arbitrary, unaligned sampling schedules across subjects and modalities without imputation. In the MOMS-PI pregnancy cohort, joint analysis of the vaginal microbiome and cervicovaginal cytokines yields clearer separation between preterm and term birth outcomes than microbiome data alone, implicates Lactobacillus-dominant communities as protective, and identifies diverging cytokine trajectories in women who subsequently deliver preterm. In an exercise study profiling four plasma omics modalities, the leading unsupervised subject component from multiTEMPTED is strongly associated with sex, whereas the leading components from MEFISTO show no discernible association with known study phenotypes and appear numerically degenerate. In simulation experiments, multiTEMPTED accurately recovers the underlying component structure across a range of noise levels, outperforms MEFISTO in multiple settings, and runs several orders of magnitude faster. multiTEMPTED is implemented in the open-source R package multi.tempted (https://github.com/loulind/multi.tempted).

bioinformatics↗

Machine-Perception Nanosensor Platform to Detect Cancer Biomarkers

Conventional molecular recognition elements, such as antibodies, present issues for the development of biomolecular assays for use in point-of-care devices, implantable/wearables, and under-resourced settings. Additionally, antibody development and use, especially for highly multiplexed applications, can be slow and costly. We developed a perception-based platform based on an optical nanosensor array that leverages machine learning algorithms to detect multiple protein biomarkers in biofluids. We demonstrated this platform in gynecologic cancers, which are often diagnosed at advanced stages, leading to low survival rates. We investigated the platform for detection in uterine lavage samples, which are enriched with cancer biomarkers compared to blood. We found that the method enables the simultaneous detection of multiple biomarkers in patient samples, with F1-scores of ~0.95 in uterine lavage samples from cancer patients. This work demonstrates the potential of perception-based systems for the development of multiplexed sensors of disease biomarkers without the need for specific molecular recognition elements.

bioengineering↗