Evidence map›Paper›PMID 33070196›Full record

ArticleBioinformatics (Oxford, England)2021

Unpaired data empowers association tests.

Mingming Gong, Peng Liu, Frank C Sciurba, Petar Stojanov, Dacheng Tao, George C Tseng, Kun Zhang, Kayhan Batmanghelich

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Mingming GongDepartment of Biomedical Informatics, University of Pittsburgh, Pittsburgh, PA 15206, USA.
Peng LiuDepartment of Biomedical Informatics, University of Pittsburgh, Pittsburgh, PA 15206, USA.
Frank C SciurbaDepartment of Biomedical Informatics, University of Pittsburgh, Pittsburgh, PA 15206, USA.
Petar StojanovDepartment of Philosophy, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Dacheng TaoAustralia School of Computer Science, The University of Sydney, Sydney, NSW 2006, Australia.
George C TsengDepartment of Biomedical Informatics, University of Pittsburgh, Pittsburgh, PA 15206, USA.ORCID 0000-0002-5447-1014
Kun ZhangDepartment of Philosophy, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Kayhan BatmanghelichDepartment of Biomedical Informatics, University of Pittsburgh, Pittsburgh, PA 15206, USA.

Funding

Integrating Multi-Modal Data and Biomechanics in COPD: Toward Robust and Interpretable Biomarkers for Disease Subtyping and ProgressionR01HL141813 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Kayhan Batmanghelich · 2018 to 2026
$4.2M
NHLBI NIH HHS R01 HL141813
6 · The paper itself

Abstract

motivationThere is growing interest in the biomedical research community to incorporate retrospective data, available in healthcare systems, to shed light on associations between different biomarkers. Understanding the association between various types of biomedical data, such as genetic, blood biomarkers, imaging, etc. can provide a holistic understanding of human diseases. To formally test a hypothesized association between two types of data in Electronic Health Records (EHRs), one requires a substantial sample size with both data modalities to achieve a reasonable power. Current association test methods only allow using data from individuals who have both data modalities. Hence, researchers cannot take advantage of much larger EHR samples that includes individuals with at least one of the data types, which limits the power of the association test.

resultsWe present a new method called the Semi-paired Association Test (SAT) that makes use of both paired and unpaired data. In contrast to classical approaches, incorporating unpaired data allows SAT to produce better control of false discovery and to improve the power of the association test. We study the properties of the new test theoretically and empirically, through a series of simulations and by applying our method on real studies in the context of Chronic Obstructive Pulmonary Disease. We are able to identify an association between the high-dimensional characterization of Computed Tomography chest images and several blood biomarkers as well as the expression of dozens of genes involved in the immune system. AVAILABILITY AND IMPLEMENTATION: Code is available on https://github.com/batmanlab/Semi-paired-Association-Test. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

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Electronic Health RecordsResearch DesignHumansRetrospective StudiesSample Size

Identifiers

PMID33070196
PMCPMC8098021

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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 OpenQuestion graph.