Evidence map›Paper›PMID 34849578›Full record

ArticleBioinformatics (Oxford, England)2022

GPA-Tree: statistical approach for functional-annotation-tree-guided prioritization of GWAS results.

Aastha Khatiwada, Bethany J Wolf, Ayse Selen Yilmaz, Paula S Ramos, Maciej Pietrzak, Andrew Lawson, Kelly J Hunt, Hang J Kim, Dongjun Chung

Open access · greenAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 93% of its field
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.

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 0 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Aastha KhatiwadaDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, SC 29425, USA.
Bethany J WolfDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, SC 29425, USA.
Ayse Selen YilmazDepartment of Biomedical Informatics, The Ohio State University, Columbus, OH 43210, USA.
Paula S RamosDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, SC 29425, USA.
Maciej PietrzakDepartment of Biomedical Informatics, The Ohio State University, Columbus, OH 43210, USA.
Andrew LawsonDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, SC 29425, USA.
Kelly J HuntDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, SC 29425, USA.
Hang J KimDivision of Statistics and Data Science, University of Cincinnati, Cincinnati, OH 45221, USA.
Dongjun ChungDepartment of Biomedical Informatics, The Ohio State University, Columbus, OH 43210, USA.ORCID 0000-0002-8072-5671
Medical University of South Carolina · USThe Ohio State University · USUniversity of Cincinnati · US

Funding

Resource CoreP30AR072582 · NIAMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI JAMES C OATES · 2017 to 2026
$8.5M
The Genetic Basis of Opioid Dependence Vulnerablility in a Rodent ModelU01DA045300 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Christine Cheng, Dongjun Chung · 2018 to 2026
$6.1M
Predictive Biomarkers for disease activity and organ damage in patients with lupusR01AR071947 · NIAMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI OATES, JAMES C, ROVIN, BRAD H · 2018 to 2022
$3.2M
Statistical Models for Genetic Studies, Using Network and Integrative AnalysisR01GM122078 · NIGMS · OHIO STATE UNIVERSITY · PI CHUNG, DONGJUN · 2016 to 2020
$1.9M
Algorithms for Literature-Guided Multi-Platform Identification of Cancer SubtypesR21CA209848 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI CHUNG, DONGJUN, KELEMEN, LINDA E · 2016 to 2017
$358k
NCI NIH HHS R21 CA209848NIAMS NIH HHS P30 AR072582NIAMS NIH HHS R01 AR071947NIDA NIH HHS U01 DA045300NIGMS NIH HHS R01 GM122078
6 · The paper itself

Abstract

motivationIn spite of great success of genome-wide association studies (GWAS), multiple challenges still remain. First, complex traits are often associated with many single nucleotide polymorphisms (SNPs), each with small or moderate effect sizes. Second, our understanding of the functional mechanisms through which genetic variants are associated with complex traits is still limited. To address these challenges, we propose GPA-Tree and it simultaneously implements association mapping and identifies key combinations of functional annotations related to risk-associated SNPs by combining a decision tree algorithm with a hierarchical modeling framework.

resultsFirst, we implemented simulation studies to evaluate the proposed GPA-Tree method and compared its performance with existing statistical approaches. The results indicate that GPA-Tree outperforms existing statistical approaches in detecting risk-associated SNPs and identifying the true combinations of functional annotations with high accuracy. Second, we applied GPA-Tree to a systemic lupus erythematosus (SLE) GWAS and functional annotation data including GenoSkyline and GenoSkylinePlus. The results from GPA-Tree highlight the dysregulation of blood immune cells, including but not limited to primary B, memory helper T, regulatory T, neutrophils and CD8+ memory T cells in SLE. These results demonstrate that GPA-Tree can be a powerful tool that improves association mapping while facilitating understanding of the underlying genetic architecture of complex traits and potential mechanisms linking risk-associated SNPs with complex traits. AVAILABILITY AND IMPLEMENTATION: The GPATree software is available at https://dongjunchung.github.io/GPATree/. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Genome-Wide Association StudySoftwareAlgorithmsComputer SimulationPolymorphism, Single Nucleotide

Identifiers

PMID34849578
PMCPMC10060690
OpenAlexW3171368715

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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.