Evidence map›Paper›PMID 39109055›Full record

ArticleFrontiers in plant science2024

Sparse testing designs for optimizing predictive ability in sugarcane populations.

Julian Garcia-Abadillo, Paul Adunola, Fernando Silva Aguilar, Jhon Henry Trujillo-Montenegro, John Jaime Riascos, Reyna Persa, Julio Isidro Y Sanchez, Diego Jarquín

Erratum issuedAbstract read
In one paragraph

Article in Frontiers in plant science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Optimizing resource allocation inFrontiers in plant science · 2026
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Julian Garcia-AbadilloCentro de Biotecnología y Genómica de Plantas, Universidad Politécnica de Madrid, Madrid, Spain.
Paul AdunolaHorticultural Sciences Department, University of Florida, Gainesville, FL, United States.
Fernando Silva AguilarColombian Sugarcane Research Center, Cenicaña, Cali, Valle del Cauca, Colombia.
Jhon Henry Trujillo-MontenegroColombian Sugarcane Research Center, Cenicaña, Cali, Valle del Cauca, Colombia.
John Jaime RiascosColombian Sugarcane Research Center, Cenicaña, Cali, Valle del Cauca, Colombia.
Reyna PersaAgronomy Department, University of Florida, Gainesville, FL, United States.
Julio Isidro Y SanchezCentro de Biotecnología y Genómica de Plantas, Universidad Politécnica de Madrid, Madrid, Spain.
Diego JarquínAgronomy Department, University of Florida, Gainesville, FL, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sugarcane is a crucial crop for sugar and bioenergy production. Saccharose content and total weight are the two main key commercial traits that compose sugarcane's yield. These traits are under complex genetic control and their response patterns are influenced by the genotype-by-environment (G×E) interaction. An efficient breeding of sugarcane demands an accurate assessment of the genotype stability through multi-environment trials (METs), where genotypes are tested/evaluated across different environments. However, phenotyping all genotype-in-environment combinations is often impractical due to cost and limited availability of propagation-materials. This study introduces the sparse testing designs as a viable alternative, leveraging genomic information to predict unobserved combinations through genomic prediction models. This approach was applied to a dataset comprising 186 genotypes across six environments (6×186=1,116 phenotypes). Our study employed three predictive models, including environment, genotype, and genomic markers as main effects, as well as the G×E to predict saccharose accumulation (SA) and tons of cane per hectare (TCH). Calibration sets sizes varying between 72 (6.5%) to 186 (16.7%) of the total number of phenotypes were composed to predict the remaining 930 (83.3%). Additionally, we explored the optimal number of common genotypes across environments for G×E pattern prediction. Results demonstrate that maximum accuracy for SA (

Indexed as

genomic prediction GPgenomic selection GSoptimizationsparse testing designssugarcane breeding

Identifiers

PMID39109055
PMCPMC11300217

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Registered trials

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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.