Evidence map›Paper›PMID 38187579›Full record

ArticlebioRxiv : the preprint server for biology2023

Matrix Linear Models for connecting metabolite composition to individual characteristics.

Gregory Farage, Chenhao Zhao, Hyo Young Choi, Timothy J Garrett, Katerina Kechris, Marshall B Elam, Śaunak Sen

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Gregory FarageDepartment of Preventive Medicine, Division of Biostatistics, University of Tennessee Health Science Center, Memphis, TN 38163.ORCID 0000-0003-4268-9507
Chenhao ZhaoDepartment of Preventive Medicine, Division of Biostatistics, University of Tennessee Health Science Center, Memphis, TN 38163.ORCID 0000-0001-5607-7443
Hyo Young ChoiDepartment of Preventive Medicine, Division of Biostatistics, University of Tennessee Health Science Center, Memphis, TN 38163.ORCID 0000-0002-7627-8493
Timothy J GarrettDepartment of Pathology, Immunology and Laboratory Medicine, University of Florida, Gainesville, FL 32610.ORCID 0000-0003-1623-009X
Katerina KechrisDepartment of Biostatistics & Informatics, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, CO 80045.ORCID 0000-0002-3725-5459
Marshall B ElamDepartment of Pharmacology and of Medicine, University of Tennessee Health Science Center, Memphis, TN 38163.ORCID 0000-0002-1063-1557
Śaunak SenDepartment of Preventive Medicine, Division of Biostatistics, University of Tennessee Health Science Center Memphis, TN 38163.ORCID 0000-0003-4519-6361

Funding

National Metabolomics Data Repository - nextgen Metabolomics WorkbenchU2CDK119886 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SUBRAMANIAM, SHANKAR · 2018 to 2021
$12.7M
TIM Project NIDA P30 CenterP30DA044223 · NIDA · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI SABA, LAURA MAREN, WILLIAMS, ROBERT W. · 2017 to 2021
$3.9M
A Unified High Performance Web Service for Systems Genetics and Precision MedicineR01GM123489 · NIGMS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI PRINS, PJOTR, SEN, SAUNAK · 2017 to 2024
$3.7M
Biomedical Data Commons Workbench (BDCW)OT2OD030544 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SUBRAMANIAM, SHANKAR · 2020 to 2024
$3.2M
Web Portal CoreU2CDK119889 · NIDDK · UNIVERSITY OF FLORIDA · PI YOST, RICHARD A. · 2018 to 2021
$1.9M
Metabolomics of Statin-induced MyalgiaR21AR074018 · NIAMS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI ELAM, MARSHALL B, RAGHOW, RAJENDRA · 2018 to 2019
$368k
NIAMS NIH HHS R21 AR074018NIDA NIH HHS P30 DA044223NIDDK NIH HHS U2C DK119886NIDDK NIH HHS U2C DK119889NIGMS NIH HHS R01 GM123489NIH HHS OT2 OD030544
6 · The paper itself

Abstract

High-throughput metabolomics data provide a detailed molecular window into biological processes. We consider the problem of assessing how the association of metabolite levels with individual (sample) characteristics such as sex or treatment may depend on metabolite characteristics such as pathway. Typically this is one in a two-step process: In the first step we assess the association of each metabolite with individual characteristics. In the second step an enrichment analysis is performed by metabolite characteristics among significant associations. We combine the two steps using a bilinear model based on the matrix linear model (MLM) framework we have previously developed for high-throughput genetic screens. Our framework can estimate relationships in metabolites sharing known characteristics, whether categorical (such as type of lipid or pathway) or numerical (such as number of double bonds in triglycerides). We demonstrate how MLM offers flexibility and interpretability by applying our method to three metabolomic studies. We show that our approach can separate the contribution of the overlapping triglycerides characteristics, such as the number of double bonds and the number of carbon atoms. The proposed method have been implemented in the open-source Julia package, MatrixLM. Data analysis scripts with example data analyses are also available.

Indexed as

bilinear modelshigh-throughput dataJulia languagelipidomicsmetabolomics

Identifiers

PMID38187579
PMCPMC10769268

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.