Evidence map›Paper›PMID 25524444›Full record

ArticleBMC plant biology2014

Characterization of a panel of Vietnamese rice varieties using DArT and SNP markers for association mapping purposes.

Nhung Thi Phuong Phung, Chung Duc Mai, Pierre Mournet, Julien Frouin, Gaëtan Droc, Nhung Kim Ta, Stefan Jouannic, Loan Thi Lê, Vinh Nang Do, Pascal Gantet and 1 more

Abstract read
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Article in BMC plant biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
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1 · What the graph read from it

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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

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3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

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  11. A genome-wide association study reveals the quantitative trait locus and candidate genes that regulate phosphate efficiency in a Vietnamese rice collection.Physiology and molecular biology of plants : an international journal of functional plant biology · 2020
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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Nhung Thi Phuong Phung
Chung Duc Mai
Pierre Mournet
Julien Frouin
Gaëtan Droc
Nhung Kim Ta
Stefan Jouannic
Loan Thi Lê
Vinh Nang Do
Pascal Gantet
Brigitte Courtois

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe development of genome-wide association studies (GWAS) in crops has made it possible to mine interesting alleles hidden in gene bank resources. However, only a small fraction of the rice genetic diversity of any given country has been exploited in the studies with worldwide sampling conducted to date. This study presents the development of a panel of rice varieties from Vietnam for GWAS purposes.

resultsThe panel, initially composed of 270 accessions, was characterized for simple agronomic traits (maturity class, grain shape and endosperm type) commonly used to classify rice varieties. We first genotyped the panel using Diversity Array Technology (DArT) markers. We analyzed the panel structure, identified two subpanels corresponding to the indica and japonica sub-species and selected 182 non-redundant accessions. However, the number of usable DArT markers (241 for an initial library of 6444 clones) was too small for GWAS purposes. Therefore, we characterized the panel of 182 accessions with 25,971 markers using genotyping by sequencing. The same indica and japonica subpanels were identified. The indica subpanel was further divided into six populations (I1 to I6) using a model-based approach. The japonica subpanel, which was more highly differentiated, was divided into 4 populations (J1 to J4), including a temperate type (J2). Passport data and phenotypic traits were used to characterize these populations. Some populations were exclusively composed of glutinous types (I3 and J2). Some of the upland rice varieties appeared to belong to indica populations, which is uncommon in this region of the world. Linkage disequilibrium decayed faster in the indica subpanel (r2 below 0.2 at 101 kb) than in the japonica subpanel (r2 below 0.2 at 425 kb), likely because of the strongest differentiation of the japonica subpanel. A matrix adapted for GWAS was built by eliminating the markers with a minor allele frequency below 5% and imputing the missing data. This matrix contained 21,814 markers. A GWAS was conducted on time to flowering to prove the utility of this panel.

conclusionsThis publicly available panel constitutes an important resource giving access to original allelic diversity. It will be used for GWAS on root and panicle traits.

Indexed as

Genome-Wide Association StudyLinkage DisequilibriumPolymorphism, Single NucleotideChromosome MappingGenetic MarkersMolecular Sequence DataOryzaPhylogenyVietnamGenetic Markers

Identifiers

PMID25524444
PMCPMC4279583

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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.