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MOIRE: A software package for the estimation of allele frequencies and effective multiplicity of infection from polyallelic data
Malaria parasite genetic data can provide insight into parasite phenotypes, evolution, and transmission. However, estimating key parameters such as allele frequencies, multiplicity of infection (MOI), and within-host relatedness from genetic data has been challenging, particularly in the presence of...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Cold Spring Harbor Laboratory
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592951/ https://www.ncbi.nlm.nih.gov/pubmed/37873322 http://dx.doi.org/10.1101/2023.10.03.560769 |
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author | Murphy, Maxwell Greenhouse, Bryan |
author_facet | Murphy, Maxwell Greenhouse, Bryan |
author_sort | Murphy, Maxwell |
collection | PubMed |
description | Malaria parasite genetic data can provide insight into parasite phenotypes, evolution, and transmission. However, estimating key parameters such as allele frequencies, multiplicity of infection (MOI), and within-host relatedness from genetic data has been challenging, particularly in the presence of multiple related coinfecting strains. Existing methods often rely on single nucleotide polymorphism (SNP) data and do not account for within-host relatedness. In this study, we introduce a Bayesian approach called MOIRE (Multiplicity Of Infection and allele frequency REcovery), designed to estimate allele frequencies, MOI, and within-host relatedness from genetic data subject to experimental error. Importantly, MOIRE is flexible in accommodating both polyallelic and SNP data, making it adaptable to diverse genotyping panels. We also introduce a novel metric, the effective MOI [Formula: see text] , which integrates MOI and within-host relatedness, providing a robust and interpretable measure of genetic diversity. Using extensive simulations and real-world data from a malaria study in Namibia, we demonstrate the superior performance of MOIRE over naive estimation methods, accurately estimating MOI up to 7 with moderate sized panels of diverse loci (e.g. microhaplotypes). MOIRE also revealed substantial heterogeneity in population mean MOI and mean relatedness across health districts in Namibia, suggesting detectable differences in transmission dynamics. Notably, [Formula: see text] emerges as a portable metric of within-host diversity, facilitating meaningful comparisons across settings, even when allele frequencies or genotyping panels are different. MOIRE represents an important addition to the analysis toolkit for malaria population dynamics. Compared to existing software, MOIRE enhances the accuracy of parameter estimation and enables more comprehensive insights into within-host diversity and population structure. Additionally, MOIRE’s adaptability to diverse data sources and potential for future improvements make it a valuable asset for research on malaria and other organisms, such as other eukaryotic pathogens. MOIRE is available as an R package at https://eppicenter.github.io/moire/. |
format | Online Article Text |
id | pubmed-10592951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-105929512023-11-14 MOIRE: A software package for the estimation of allele frequencies and effective multiplicity of infection from polyallelic data Murphy, Maxwell Greenhouse, Bryan bioRxiv Article Malaria parasite genetic data can provide insight into parasite phenotypes, evolution, and transmission. However, estimating key parameters such as allele frequencies, multiplicity of infection (MOI), and within-host relatedness from genetic data has been challenging, particularly in the presence of multiple related coinfecting strains. Existing methods often rely on single nucleotide polymorphism (SNP) data and do not account for within-host relatedness. In this study, we introduce a Bayesian approach called MOIRE (Multiplicity Of Infection and allele frequency REcovery), designed to estimate allele frequencies, MOI, and within-host relatedness from genetic data subject to experimental error. Importantly, MOIRE is flexible in accommodating both polyallelic and SNP data, making it adaptable to diverse genotyping panels. We also introduce a novel metric, the effective MOI [Formula: see text] , which integrates MOI and within-host relatedness, providing a robust and interpretable measure of genetic diversity. Using extensive simulations and real-world data from a malaria study in Namibia, we demonstrate the superior performance of MOIRE over naive estimation methods, accurately estimating MOI up to 7 with moderate sized panels of diverse loci (e.g. microhaplotypes). MOIRE also revealed substantial heterogeneity in population mean MOI and mean relatedness across health districts in Namibia, suggesting detectable differences in transmission dynamics. Notably, [Formula: see text] emerges as a portable metric of within-host diversity, facilitating meaningful comparisons across settings, even when allele frequencies or genotyping panels are different. MOIRE represents an important addition to the analysis toolkit for malaria population dynamics. Compared to existing software, MOIRE enhances the accuracy of parameter estimation and enables more comprehensive insights into within-host diversity and population structure. Additionally, MOIRE’s adaptability to diverse data sources and potential for future improvements make it a valuable asset for research on malaria and other organisms, such as other eukaryotic pathogens. MOIRE is available as an R package at https://eppicenter.github.io/moire/. Cold Spring Harbor Laboratory 2023-11-07 /pmc/articles/PMC10592951/ /pubmed/37873322 http://dx.doi.org/10.1101/2023.10.03.560769 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Murphy, Maxwell Greenhouse, Bryan MOIRE: A software package for the estimation of allele frequencies and effective multiplicity of infection from polyallelic data |
title | MOIRE: A software package for the estimation of allele frequencies and effective multiplicity of infection from polyallelic data |
title_full | MOIRE: A software package for the estimation of allele frequencies and effective multiplicity of infection from polyallelic data |
title_fullStr | MOIRE: A software package for the estimation of allele frequencies and effective multiplicity of infection from polyallelic data |
title_full_unstemmed | MOIRE: A software package for the estimation of allele frequencies and effective multiplicity of infection from polyallelic data |
title_short | MOIRE: A software package for the estimation of allele frequencies and effective multiplicity of infection from polyallelic data |
title_sort | moire: a software package for the estimation of allele frequencies and effective multiplicity of infection from polyallelic data |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592951/ https://www.ncbi.nlm.nih.gov/pubmed/37873322 http://dx.doi.org/10.1101/2023.10.03.560769 |
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