Evidence map›Paper›PMID 41019386›Full record

ArticleEcology and evolution2025

Pairwise Paternity Assignment With Forward-Backward Simulations: Refining CERVUS Using Trio-Based Likelihood and Locus-Specific Error Rates.

Mahmoud Amiri Roudbar, Seyedeh Fatemeh Mousavi, Mahdi Akbarzadeh, Sabrina H Brounts, Mehdi Momen

Abstract read
In one paragraph

Article in Ecology and evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Mahmoud Amiri RoudbarDepartment of Animal Science Safiabad-Dezful Agricultural and Natural Resources Research and Education Center, Agricultural Research, Education and Extension Organization (AREEO) Dezful Iran.ORCID https://orcid.org/0000-0002-2023-9292
Seyedeh Fatemeh MousaviDepartment of Animal Breeding and Genetics Swedish University of Agricultural Sciences Uppsala Sweden.
Mahdi AkbarzadehCellular and Molecular Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences Tehran Iran.
Sabrina H BrountsDepartment of Surgical Sciences, School of Veterinary Medicine University of Wisconsin-Madison Madison Wisconsin USA.
Mehdi MomenDepartment of Surgical Sciences, School of Veterinary Medicine University of Wisconsin-Madison Madison Wisconsin USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Highly polymorphic markers like microsatellites are extensively utilized in genomic studies to analyze and infer genealogical relationships among individuals in a population. Traditional methods to identify the most likely parent among the potential known candidates rely on a single hypothetical distribution derived from population parameters. Indeed, these methods often make simplifying assumptions, such as a homogeneous genetic structure, consistent typing error rates across all genomic loci, and even random allele substitutions based on allele frequencies, which are frequently violated in practical applications. In this study, we introduce an enhanced likelihood-based approach, called the "Pairwise" algorithm, which builds on the widely used CERVUS method by calculating a trio-specific significance criterion for each father-mother-offspring combination using forward and backward simulations. Our method also accounts for the variable typing errors across genomic loci to enhance the accuracy of paternity analysis. Our findings showed that employing the Pairwise algorithm increases the power of paternity assignments by reducing the number of falsely assigned parents. Furthermore, adjusting likelihood equations to accommodate variable typing errors significantly improves the accuracy of paternity assignments. The developed approach represents a significant advancement in paternity analysis by addressing the limitations of traditional approaches. These improvements have the potential to significantly impact genealogical research and related fields, providing a more robust framework for analyzing complex genetic relationships in the context of parent assignment. Future research should focus on further refining this method and exploring its applications in diverse populations and genetic contexts.

Indexed as

genealogical relationshipsPairwise assignment algorithmpaternity analysisSTR marker

Identifiers

PMID41019386
PMCPMC12475999

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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.