Evidence map›Paper›PMID 39047024›Full record

ArticlePLoS computational biology2024

FedGMMAT: Federated generalized linear mixed model association tests.

Wentao Li, Han Chen, Xiaoqian Jiang, Arif Harmanci

Abstract read
In one paragraph

Article in PLoS computational biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Clarifying the Risk of Lung Disease in SZ Alpha-1 Antitrypsin Deficiency.American journal of respiratory and critical care medicine · 2020
    Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Wentao LiMcWilliams School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, Texas, United States of America.ORCID 0000-0002-6826-6636
Han ChenMcWilliams School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, Texas, United States of America.ORCID 0000-0002-9510-4923
Xiaoqian JiangMcWilliams School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, Texas, United States of America.
Arif HarmanciMcWilliams School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, Texas, United States of America.ORCID 0000-0002-9696-1118

Funding

Open Health Natural Language Processing CollaboratoryU01TR002062 · NCATS · MAYO CLINIC ROCHESTER · PI JIANG, XIAOQIAN, LIU, HONGFANG · 2017 to 2021
$7.6M
Finding Combinatorial Drug Repositioning Therapy For Alzheimer'S Disease And Related DementiasR01AG066749 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI JIANG, XIAOQIAN, ZHENG, WENJIN JIM · 2020 to 2024
$4.4M
Decentralized differentially-private methods for dynamic data release and analysisR01LM013712 · NLM · YALE UNIVERSITY · PI JIANG, XIAOQIAN, OHNO-MACHADO, LUCILA · 2022 to 2025
$2.5M
Secure Outsourcing of Genotype Imputation for Privacy-aware Genomic Analysis (RO1HE21)R01HG012604 · NHGRI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Arif Ozgun Harmanci · 2023 to 2026
$2.2M
NCATS NIH HHS U01 TR002062NHGRI NIH HHS R01 HG012604NIA NIH HHS R01 AG066749NLM NIH HHS R01 LM013712
6 · The paper itself

Abstract

Increasing genetic and phenotypic data size is critical for understanding the genetic determinants of diseases. Evidently, establishing practical means for collaboration and data sharing among institutions is a fundamental methodological barrier for performing high-powered studies. As the sample sizes become more heterogeneous, complex statistical approaches, such as generalized linear mixed effects models, must be used to correct for the confounders that may bias results. On another front, due to the privacy concerns around Protected Health Information (PHI), genetic information is restrictively protected by sharing according to regulations such as Health Insurance Portability and Accountability Act (HIPAA). This limits data sharing among institutions and hampers efforts around executing high-powered collaborative studies. Federated approaches are promising to alleviate the issues around privacy and performance, since sensitive data never leaves the local sites. Motivated by these, we developed FedGMMAT, a federated genetic association testing tool that utilizes a federated statistical testing approach for efficient association tests that can correct for confounding fixed and additive polygenic random effects among different collaborating sites. Genetic data is never shared among collaborating sites, and the intermediate statistics are protected by encryption. Using simulated and real datasets, we demonstrate FedGMMAT can achieve the virtually same results as pooled analysis under a privacy-preserving framework with practical resource requirements.

Indexed as

Information DisseminationComputational BiologyGenetic Association StudiesGenome-Wide Association StudyHumansLinear ModelsSoftware

Identifiers

PMID39047024
PMCPMC11299833

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.