Evidence map›Paper›PMID 34564692›Full record

ArticleHeredity2021

Multi-generation genomic prediction of maize yield using parametric and non-parametric sparse selection indices.

Marco Lopez-Cruz, Yoseph Beyene, Manje Gowda, Jose Crossa, Paulino Pérez-Rodríguez, Gustavo de Los Campos

Abstract read
In one paragraph

Article in Heredity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Marco Lopez-CruzDepartment of Plant, Soil and Microbial Sciences, Michigan State University, East Lansing, MI, USA. lopezcru@msu.edu.ORCID http://orcid.org/0000-0002-2548-1766
Yoseph BeyeneGlobal Maize Program, International Maize and Wheat Improvement Center (CIMMYT), Nairobi, Kenya.
Manje GowdaGlobal Maize Program, International Maize and Wheat Improvement Center (CIMMYT), Nairobi, Kenya.ORCID http://orcid.org/0000-0003-4434-6364
Jose CrossaBiometrics and Statistics Unit, International Maize and Wheat Improvement Center (CIMMYT), Mexico, Mexico.ORCID http://orcid.org/0000-0001-9429-5855
Paulino Pérez-RodríguezColegio de Postgraduados, Montecillos, Edo. de México, Mexico.
Gustavo de Los CamposDepartment of Epidemiology and Biostatistics, Michigan State University, East Lansing, MI, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genomic prediction models are often calibrated using multi-generation data. Over time, as data accumulates, training data sets become increasingly heterogeneous. Differences in allele frequency and linkage disequilibrium patterns between the training and prediction genotypes may limit prediction accuracy. This leads to the question of whether all available data or a subset of it should be used to calibrate genomic prediction models. Previous research on training set optimization has focused on identifying a subset of the available data that is optimal for a given prediction set. However, this approach does not contemplate the possibility that different training sets may be optimal for different prediction genotypes. To address this problem, we recently introduced a sparse selection index (SSI) that identifies an optimal training set for each individual in a prediction set. Using additive genomic relationships, the SSI can provide increased accuracy relative to genomic-BLUP (GBLUP). Non-parametric genomic models using Gaussian kernels (KBLUP) have, in some cases, yielded higher prediction accuracies than standard additive models. Therefore, here we studied whether combining SSIs and kernel methods could further improve prediction accuracy when training genomic models using multi-generation data. Using four years of doubled haploid maize data from the International Maize and Wheat Improvement Center (CIMMYT), we found that when predicting grain yield the KBLUP outperformed the GBLUP, and that using SSI with additive relationships (GSSI) lead to 5-17% increases in accuracy, relative to the GBLUP. However, differences in prediction accuracy between the KBLUP and the kernel-based SSI were smaller and not always significant.

Indexed as

Models, GeneticZea maysGenomeGenomicsPhenotypePolymorphism, Single Nucleotide

Identifiers

PMID34564692
PMCPMC8551287

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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.