Evidence map›Paper›PMID 39847531›Full record

ArticleG3 (Bethesda, Md.)2025

Using feedback in pooled experiments augmented with imputation for high genotyping accuracy at reduced cost.

Camille Clouard, Carl Nettelblad

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2025. 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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0citing papers 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

2 authors.

Camille ClouardDivision of Scientific Computing, Department of Information Technology, Uppsala University, Uppsala SE-751 05, Sweden.ORCID 0009-0006-3654-6525
Carl NettelbladDivision of Scientific Computing, Department of Information Technology, Uppsala University, Uppsala SE-751 05, Sweden.ORCID 0000-0003-0458-6902

Funding

Formas 2017-00453NAISSNational Academic Infrastructure for Supercomputing in SwedenSNICUPPMAX SNIC 2022/22-697Uppsala Multidisciplinary Center for Advanced Computational Science
6 · The paper itself

Abstract

Conducting genomic selection (GS) in plant breeding programs can substantially speed up the development of new varieties. GS provides more reliable insights when it is based on dense marker data, in which the rare variants can be particularly informative. Despite the availability of new technologies, the cost of large-scale genotyping remains a major limitation to the implementation of GS. We suggest to combine pooled genotyping with population-based imputation as a cost-effective computational strategy for genotyping SNPs. Pooling saves genotyping tests and has proven to accurately capture the rare variants that are usually missed by imputation. In this study, we investigate adding iterative coupling to a joint model of pooling and imputation that we have previously proposed. In each iteration, the imputed genotype probabilities serve as feedback input for adjusting the per-sample prior genotype probabilities, before running a new imputation based on these adjusted data. This flexible setup indirectly imposes consistency between the imputed genotypes and the pooled observations. We demonstrate that repeated cycles of feedback can take advantage of the strengths in both pooling and imputation when an appropriate set of reference haplotypes is available for imputation. The iterations improve greatly upon the initial genotype predictions, achieving very high genotype accuracy for both low- and high-frequency variants. We enhance the average concordance from 94.5% to 98.4% at limited computational cost and without requiring any additional genotype testing.

Indexed as

Genotyping TechniquesGenotypeHaplotypesModels, GeneticPlant BreedingPolymorphism, Single Nucleotideimputationiterative refinementpoolingSNP array

Identifiers

PMID39847531
PMCPMC11917477

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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.