Evidence map›Paper›PMID 40326704›Full record

ArticleBioinformatics (Oxford, England)2025

Bayesian estimation of allele-specific expression in the presence of phasing uncertainty.

Xue Zou, Zachary W Gomez, Timothy E Reddy, Andrew S Allen, William H Majoros

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Xue ZouDuke Center for Statistical Genetics and Genomics, Duke University, Durham, NC 27710, United States.ORCID 0000-0002-0512-1341
Zachary W GomezIndependent Researcher, Cambridge, Massachusetts, 02139, United States.ORCID 0009-0005-6759-619X
Timothy E ReddyDuke Center for Statistical Genetics and Genomics, Duke University, Durham, NC 27710, United States.ORCID 0000-0002-7629-061X
Andrew S AllenDuke Center for Statistical Genetics and Genomics, Duke University, Durham, NC 27710, United States.ORCID 0000-0002-7232-2143
William H MajorosDuke Center for Statistical Genetics and Genomics, Duke University, Durham, NC 27710, United States.ORCID 0000-0001-7284-9335

Funding

The Duke FUNCTION Center: Pioneering the comprehensive identification of combinatorial noncoding causes of diseaseRM1HG011123 · NHGRI · DUKE UNIVERSITY · PI GREGORY E CRAWFORD, Raluca Gordan · 2020 to 2026
$21.9M
Computational Methods for Investigating the Genetics of Gene RegulationR35GM150404 · NIGMS · DUKE UNIVERSITY · PI William Majoros · 2023 to 2026
$1.5M
NHGRI NIH HHS RM1 HG011123NHGRI NIH HHS RM1HG011123NIGMS NIH HHS R35 GM150404NIGMS NIH HHS RM1HG011123NIH HHS R35GM150404
6 · The paper itself

Abstract

motivationAllele-specific expression (ASE) analyses aim to detect imbalanced expression of maternal versus paternal copies of an autosomal gene. Such allelic imbalance can result from a variety of cis-acting causes, including disruptive mutations within one copy of a gene that impact the stability of transcripts, as well as regulatory variants outside the gene that impact transcription initiation. Current methods for ASE estimation suffer from a number of shortcomings, such as relying on only one variant within a gene, assuming perfect phasing information across multiple variants within a gene, or failing to account for alignment biases and possible genotyping errors.

resultsWe developed BEASTIE, a Bayesian hierarchical model designed for precise ASE quantification at the gene level, based on given genotypes and RNA-Seq data. BEASTIE addresses the complexities of allelic mapping bias, genotyping error, and phasing errors by incorporating empirical phasing error rates derived from Genome-in-a-Bottle individual NA12878. BEASTIE surpasses existing methods in accuracy, especially in scenarios with high phasing errors. This improvement is critical for identifying rare genetic variants often obscured by such errors. Through rigorous validation on simulated data and application to real data from the 1000 Genomes Project, we establish the robustness of BEASTIE. These findings underscore the value of BEASTIE in revealing patterns of ASE across gene sets and pathways. AVAILABILITY AND IMPLEMENTATION: The software is freely available from Github (https://github.com/x811zou/BEASTIE); and Zendo (DOI: 10.5281/zenodo.15062124).

Indexed as

AllelesAllelic ImbalanceBayes TheoremGenotypeHumansSoftwareUncertainty

Identifiers

PMID40326704
PMCPMC12202007

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LicenceCC BY
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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.