Evidence map›Paper›PMID 41688905›Full record

ArticleBMC bioinformatics2026

PyMSQ: a Python package for fast Mendelian sampling (co)variance and haplotype-based similarity in genomic selection.

Abdulraheem Arome Musa, Norbert Reinsch

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Article in BMC bioinformatics, 2026. 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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2 authors.

Abdulraheem Arome MusaResearch Institute for Farm Animal Biology (FBN), Wilhelm-Stahl-Allee 2, 18196, Dummerstorf, Germany.
Norbert ReinschResearch Institute for Farm Animal Biology (FBN), Wilhelm-Stahl-Allee 2, 18196, Dummerstorf, Germany. reinsch@fbn-dummerstorf.de.

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6 · The paper itself

Abstract

backgroundWhile genomic selection boosts rapid genetic gains by leveraging dense marker data for genomic estimated breeding values (GEBVs), prolonged application can reduce haplotype diversity and increase inbreeding. To address these risks, recent studies indicate that selecting on Mendelian sampling variance (MSV) and covariance (MSC) can partly mitigate the loss of genetic variation by exploiting within-family (co)segregation not captured by GEBVs alone. In parallel, theoretical advances have introduced a haplotype-based similarity measure that targets shared heterozygous segments, enabling more direct control over haplotype diversity, either standalone or in combination with conventional coancestry-based and genomic relationship matrices.

resultsWe present PyMSQ, an open-source Python package for estimating Mendelian sampling-related quantities that implements two key developments: (1) a matrix-based approach for computing MSV and MSC in single-trait, multi-trait, and zygotic contexts, and (2) a haplotype-based similarity matrix between parental Mendelian sampling terms. By combining this matrix-based framework with optimized scientific libraries, PyMSQ achieves up to 332-fold faster computations than gamevar, a publicly available alternative, while preserving numerical accuracy. Using a Holstein-Friesian dataset, we demonstrate PyMSQ's effectiveness in deriving MSV and MSC, as well as its novel similarity measure, which complements standard genomic relationship matrices by explicitly quantifying shared heterozygous segments rather than overall allele sharing, thereby providing additional insights for balancing immediate gains with long-term diversity.

conclusionBy facilitating the practical use of MSV, MSC, and a haplotype-based similarity metric, PyMSQ enables breeders and quantitative geneticists to adopt haplotype diversity constraints, whether as a standalone criterion or in synergy with optimal contribution selection. This framework opens new possibilities for preserving key haplotypic segments, ultimately supporting more sustainable genomic selection strategies. PyMSQ is freely available under an MIT License at https://github.com/aromemusa/PyMSQ .

Indexed as

GenomicsHaplotypesSelection, GeneticSoftwareAnimalsGenetic VariationGametic varianceGenetic diversity managementHaplotype similarity matricesMendelian sampling varianceOptimal mating decisions

Identifiers

PMID41688905
PMCPMC12930755

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