Evidence map›Paper›PMID 30458008›Full record

ArticlePLoS genetics2018

Population sequencing reveals clonal diversity and ancestral inbreeding in the grapevine cultivar Chardonnay.

Michael J Roach, Daniel L Johnson, Joerg Bohlmann, Hennie J J van Vuuren, Steven J M Jones, Isak S Pretorius, Simon A Schmidt, Anthony R Borneman

Abstract read
In one paragraph

Article in PLoS genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing 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

49 citing papers in PubMed.

  1. Article
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  5. Harnessing clonal diversity in grapevine: from genomic insights to modern breeding applications.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2025
    Review
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  16. Frontiers in plant science · 2023
    Article
  17. Article
  18. Review
  19. De novo whole-genome assembly in an interspecific hybrid table grape, 'Shine Muscat'.DNA research : an international journal for rapid publication of reports on genes and genomes · 2022
    Article
  20. Article
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

8 authors.

Michael J RoachThe Australian Wine Research Institute, Glen Osmond, South Australia, Australia.ORCID 0000-0003-1488-5148
Daniel L JohnsonThe Australian Wine Research Institute, Glen Osmond, South Australia, Australia.ORCID 0000-0001-9284-3600
Joerg BohlmannMichael Smith Laboratories, The University of British Columbia, Vancouver, British Columbia, Canada.ORCID 0000-0002-3637-7956
Hennie J J van VuurenMichael Smith Laboratories, The University of British Columbia, Vancouver, British Columbia, Canada.
Steven J M JonesMichael Smith Genome Sciences Centre, British Columbia Cancer Research Centre, Vancouver, British Columbia, Canada.ORCID 0000-0003-3394-2208
Isak S PretoriusChancellery, Macquarie University, Sydney, New South Wales, Australia.ORCID 0000-0001-9127-3175
Simon A SchmidtThe Australian Wine Research Institute, Glen Osmond, South Australia, Australia.ORCID 0000-0003-1411-4263
Anthony R BornemanThe Australian Wine Research Institute, Glen Osmond, South Australia, Australia.ORCID 0000-0001-8491-7235

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chardonnay is the basis of some of the world's most iconic wines and its success is underpinned by a historic program of clonal selection. There are numerous clones of Chardonnay available that exhibit differences in key viticultural and oenological traits that have arisen from the accumulation of somatic mutations during centuries of asexual propagation. However, the genetic variation that underlies these differences remains largely unknown. To address this knowledge gap, a high-quality, diploid-phased Chardonnay genome assembly was produced from single-molecule real time sequencing, and combined with re-sequencing data from 15 different Chardonnay clones. There were 1620 markers identified that distinguish the 15 clones. These markers were reliably used for clonal identification of independently sourced genomic material, as well as in identifying a potential genetic basis for some clonal phenotypic differences. The predicted parentage of the Chardonnay haplomes was elucidated by mapping sequence data from the predicted parents of Chardonnay (Gouais blanc and Pinot noir) against the Chardonnay reference genome. This enabled the detection of instances of heterosis, with differentially-expanded gene families being inherited from the parents of Chardonnay. Most surprisingly however, the patterns of nucleotide variation present in the Chardonnay genome indicate that Pinot noir and Gouais blanc share an extremely high degree of kinship that has resulted in the Chardonnay genome displaying characteristics that are indicative of inbreeding.

Indexed as

Chromosome MappingDNA, PlantGenetic MarkersGenetic VariationGenome, PlantGenomicsInbreedingINDEL MutationMutationPhenotypePhylogenyPlant BreedingPolymorphism, Single NucleotideVitisWineDNA, PlantGenetic Markers

Identifiers

PMID30458008
PMCPMC6279053

What OpenQuestion holds

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LicenceCC BY
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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.