Evidence map›Paper›PMID 31440267›Full record

ArticleFrontiers in plant science2019

Single Primer Enrichment Technology (SPET) for High-Throughput Genotyping in Tomato and Eggplant Germplasm.

Lorenzo Barchi, Alberto Acquadro, David Alonso, Giuseppe Aprea, Laura Bassolino, Olivia Demurtas, Paola Ferrante, Pietro Gramazio, Paola Mini, Ezio Portis and 8 more

Abstract read
In one paragraph

Article in Frontiers in plant science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing 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

51 citing papers in PubMed.

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  11. Resolving a century-old enigma: potato 'Bolters' originate from instability of the StCDF1.3 allele.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2025
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  20. A novel tomato interspecific (Horticulture research · 2024
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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

18 authors.

Lorenzo BarchiDISAFA, University of Turin, Turin, Italy.
Alberto AcquadroDISAFA, University of Turin, Turin, Italy.
David AlonsoCOMAV, Universitat Politècnica de Valencia, Valencia, Spain.
Giuseppe ApreaENEA, Italian National Agency for New Technologies, Energy and Sustainable Economic Development, Rome, Italy.
Laura BassolinoCREA-GB, Research Centre for Genomics and Bioinformatics, Montanaso Lombardo, Italy.
Olivia DemurtasENEA, Italian National Agency for New Technologies, Energy and Sustainable Economic Development, Rome, Italy.
Paola FerranteENEA, Italian National Agency for New Technologies, Energy and Sustainable Economic Development, Rome, Italy.
Pietro GramazioCOMAV, Universitat Politècnica de Valencia, Valencia, Spain.
Paola MiniENEA, Italian National Agency for New Technologies, Energy and Sustainable Economic Development, Rome, Italy.
Ezio PortisDISAFA, University of Turin, Turin, Italy.
Davide ScaglioneIGA Technology Services Srl, Udine, Italy.
Laura ToppinoCREA-GB, Research Centre for Genomics and Bioinformatics, Montanaso Lombardo, Italy.
Santiago VilanovaCOMAV, Universitat Politècnica de Valencia, Valencia, Spain.
María José DíezCOMAV, Universitat Politècnica de Valencia, Valencia, Spain.
Giuseppe Leonardo RotinoCREA-GB, Research Centre for Genomics and Bioinformatics, Montanaso Lombardo, Italy.
Sergio LanteriDISAFA, University of Turin, Turin, Italy.
Jaime ProhensCOMAV, Universitat Politècnica de Valencia, Valencia, Spain.
Giovanni GiulianoENEA, Italian National Agency for New Technologies, Energy and Sustainable Economic Development, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single primer enrichment technology (SPET) is a new, robust, and customizable solution for targeted genotyping. Unlike genotyping by sequencing (GBS), and like DNA chips, SPET is a targeted genotyping technology, relying on the sequencing of a region flanking a primer. Its reliance on single primers, rather than on primer pairs, greatly simplifies panel design, and allows higher levels of multiplexing than PCR-based genotyping. Thanks to the sequencing of the regions surrounding the target SNP, SPET allows the discovery of thousands of closely linked, novel SNPs. In order to assess the potential of SPET for high-throughput genotyping in plants, a panel comprising 5k target SNPs, designed both on coding regions and introns/UTRs, was developed for tomato and eggplant. Genotyping of two panels composed of 400 tomato and 422 eggplant accessions, comprising both domesticated material and wild relatives, generated a total of 12,002 and 30,731 high confidence SNPs, respectively, which comprised both target and novel SNPs in an approximate ratio of 1:1.6, and 1:5.5 in tomato and eggplant, respectively. The vast majority of the markers was transferrable to related species that diverged up to 3.4 million years ago (

Indexed as

eggplantgenotypinggermplasmSPETtomato

Identifiers

PMID31440267
PMCPMC6693525

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LicenceCC BY
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Registered trials

None linked

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.