Evidence map›Paper›PMID 39635923›Full record

ArticleThe plant genome2025

Optimization of high-throughput marker systems for genomic prediction in alfalfa family bulks.

Pablo Sipowicz, Mario Henrique Murad Leite Andrade, Claudio Carlos Fernandes Filho, Juliana Benevenuto, Patricio Muñoz, L Felipe V Ferrão, Marcio F R Resende, C Messina, Esteban F Rios

Abstract read
In one paragraph

Article in The plant genome, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

9 authors.

Pablo SipowiczPlant Breeding Graduate Program, University of Florida, Gainesville, Florida, USA.
Mario Henrique Murad Leite AndradeSchool of Food and Agriculture, University of Maine, Orono, Maine, USA.
Claudio Carlos Fernandes FilhoCentro de Tecnologia Canavieira (CTC), Piracicaba, São Paulo, Brazil.
Juliana BenevenutoHorticultural Sciences Department, University of Florida, Gainesville, Florida, USA.ORCID https://orcid.org/0000-0002-4698-2738
Patricio MuñozHorticultural Sciences Department, University of Florida, Gainesville, Florida, USA.ORCID https://orcid.org/0000-0001-8973-9351
L Felipe V FerrãoHorticultural Sciences Department, University of Florida, Gainesville, Florida, USA.ORCID https://orcid.org/0000-0002-9655-4838
Marcio F R ResendeHorticultural Sciences Department, University of Florida, Gainesville, Florida, USA.ORCID https://orcid.org/0000-0002-2367-0766
C MessinaHorticultural Sciences Department, University of Florida, Gainesville, Florida, USA.
Esteban F RiosAgronomy Department, University of Florida, Gainesville, Florida, USA.ORCID https://orcid.org/0000-0003-3389-7195

Funding

National Institute of Food and Agriculture 2014-67013-22418National Institute of Food and Agriculture Hatch project 7006934
6 · The paper itself

Abstract

Alfalfa (Medicago sativa L.) is a perennial forage legume esteemed for its exceptional quality and dry matter yield (DMY); however, alfalfa has historically exhibited low genetic gain for DMY. Advances in genotyping platforms paved the way for a cost-effective application of genomic prediction in alfalfa family bulks. In this context, the optimization of marker density holds potential to reallocate resources within genomic prediction pipelines. This study aimed to (i) test two genotyping platforms for population structure discrimination and predictive ability (PA) of genomic prediction models (G-BLUP) for DMY, and (ii) explore optimal levels of marker density to predict DMY in family bulks. For this, 160 nondormant alfalfa families were phenotyped for DMY across 11 harvests and genotyped via targeted sequencing using Capture-seq with 17K probes and the DArTag 3K panel. Both platforms discriminated similarly against the population structure and resulted in comparable PA for DMY. For genotyping optimization, different levels of marker density were randomly extracted from each platform. In both cases, a plateau was achieved around 500 markers, yielding similar PA as the full set of markers. For phenotyping optimization, models with 500 markers built with data from five harvests resulted in similar PA compared to the full set of 11 harvests and full set of markers. Altogether, genotyping and phenotyping efforts were optimized in terms of number of markers and harvests. Capture-seq and DArTag yielded similar results and have the flexibility to adjust their panels to meet breeders' needs in terms of marker density.

Indexed as

Genome, PlantGenomicsMedicago sativaGenetic MarkersGenotypeGenotyping TechniquesPhenotypeGenetic Markers

Identifiers

PMID39635923
PMCPMC11726437

What OpenQuestion holds

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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.