Evidence map›Paper›PMID 39394173›Full record

ArticleBioData mining2024

PAGER: A novel genotype encoding strategy for modeling deviations from additivity in complex trait association studies.

Philip J Freda, Attri Ghosh, Priyanka Bhandary, Nicholas Matsumoto, Apurva S Chitre, Jiayan Zhou, Molly A Hall, Abraham A Palmer, Tayo Obafemi-Ajayi, Jason H Moore

Abstract read
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Article in BioData mining, 2024. 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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Philip J Freda *Department of Computational Biomedicine, Cedars-Sinai Medical Center, 700 N. San Vincente Blvd., Pacific Design Center, Suite G540, West Hollywood, CA, 90069, USA.
Attri Ghosh *Department of Computational Biomedicine, Cedars-Sinai Medical Center, 700 N. San Vincente Blvd., Pacific Design Center, Suite G540, West Hollywood, CA, 90069, USA.
Priyanka Bhandary *Department of Computational Biomedicine, Cedars-Sinai Medical Center, 700 N. San Vincente Blvd., Pacific Design Center, Suite G540, West Hollywood, CA, 90069, USA.
Nicholas MatsumotoDepartment of Computational Biomedicine, Cedars-Sinai Medical Center, 700 N. San Vincente Blvd., Pacific Design Center, Suite G540, West Hollywood, CA, 90069, USA.
Apurva S ChitreDepartment of Psychiatry, University of California San Diego, 9500 Gilman Dr, La Jolla, CA, 92093-0667, USA.
Jiayan ZhouDepartment of Medicine, Stanford University School of Medicine, 291 Campus Dr., Li Ka Shing Building, Stanford, CA, 94305, USA.
Molly A HallDepartment of Genetics and Institute for Biomedical Informatics, University of Pennsylvania, 3700 Hamilton Walk, Richards Building A301, Philadelphia, PA, 19104, USA.
Abraham A PalmerDepartment of Psychiatry, University of California San Diego, 9500 Gilman Dr, La Jolla, CA, 92093-0667, USA.
Tayo Obafemi-AjayiCooperative Engineering Program, Missouri State University, 901 S. National Ave, Springfield, MO, 65897, USA.
Jason H MooreDepartment of Computational Biomedicine, Cedars-Sinai Medical Center, 700 N. San Vincente Blvd., Pacific Design Center, Suite G540, West Hollywood, CA, 90069, USA. jason.moore@csmc.edu.

Funding

Sequencing CoreP50DA037844 · NIDA · UNIVERSITY OF CHICAGO · PI PALMER, ABRAHAM A · 2014 to 2023
$27.4M
Bioinformatics Strategies for Genome-Wide Association StudiesR01LM010098 · NLM · UNIVERSITY OF PENNSYLVANIA · PI MOORE, JASON H., WILLIAMS, SCOTT MATTHEW · 2009 to 2023
$5.1M
Artificial Intelligence Strategies for Alzheimer's Disease ResearchR01AG066833 · NIA · UNIVERSITY OF PENNSYLVANIA · PI MOORE, JASON H., RITCHIE, MARYLYN D · 2021 to 2021
$1.6M
NIA NIH HHS R01 AG066833NIDA NIH HHS P50 DA037844NIH HHS P50 DA037844NIH HHS R01 LM010098NLM NIH HHS R01 LM010098
6 · The paper itself

Abstract

backgroundThe additive model of inheritance assumes that heterozygotes (Aa) are exactly intermediate in respect to homozygotes (AA and aa). While this model is commonly used in single-locus genetic association studies, significant deviations from additivity are well-documented and contribute to phenotypic variance across many traits and systems. This assumption can introduce type I and type II errors by overestimating or underestimating the effects of variants that deviate from additivity. Alternative genotype encoding strategies have been explored to account for different inheritance patterns, but they often incur significant computational or methodological costs. To address these challenges, we introduce PAGER (Phenotype Adjusted Genotype Encoding and Ranking), an efficient pre-processing method that encodes each genetic variant based on normalized mean phenotypic differences between diallelic genotype classes (AA, Aa, and aa). This approach more accurately reflects each variant's true inheritance model, improving model precision while minimizing the costs associated with alternative encoding strategies.

resultsThrough extensive benchmarking on SNPs simulated with both binary and continuous phenotypes, we demonstrate that PAGER accurately represents various inheritance patterns (including additive, dominant, recessive, and heterosis), achieves levels of statistical power that meet or exceed other encoding strategies, and attains computation speeds up to 55 times faster than a similar method, EDGE. We also apply PAGER to publicly available real-world data and identify a novel, relevant putative QTL associated with body mass index in rats (Rattus norvegicus) that is not detected with the additive model.

conclusionsOverall, we show that PAGER is an efficient genotype encoding approach that can uncover sources of missing heritability and reveal novel insights in the study of complex traits while incurring minimal costs.

Indexed as

Association studiesCase-controlDominanceGeneticsGenotype encodingGWASHeterosisInheritanceQTL analysisQuantitative traits

Identifiers

PMID39394173
PMCPMC11468469

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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.