Search

Your search keyword '"This paper is part of the PhD of CL. The work was supported by ANRt funding under CIFRE PhD program to CL. Financial support to Invenio for this project was provided by the Conseil Régional d’Aquitaine for CL PhD work, as part of the REGINA project, and for BL work (Grant Number 2018-1R20204 project DIGIE 'chestnut dieback: vulnerability and genetic determinism of ink disease resistance'). SNP development and genotyping were performed at the Genome Transcriptome Facility of Bordeaux (Grants from the Conseil Régional d’Aquitaine No. 20030304002FA and 20040305003FA, from the European Union FEDER No. 2003227 and from Investissements d’Avenir ANR-10-EQPX-16-01)"' showing total 1 results
Start Over Author "This paper is part of the PhD of CL. The work was supported by ANRt funding under CIFRE PhD program to CL. Financial support to Invenio for this project was provided by the Conseil Régional d’Aquitaine for CL PhD work, as part of the REGINA project, and for BL work (Grant Number 2018-1R20204 project DIGIE 'chestnut dieback: vulnerability and genetic determinism of ink disease resistance'). SNP development and genotyping were performed at the Genome Transcriptome Facility of Bordeaux (Grants from the Conseil Régional d’Aquitaine No. 20030304002FA and 20040305003FA, from the European Union FEDER No. 2003227 and from Investissements d’Avenir ANR-10-EQPX-16-01)"
1 results on '"This paper is part of the PhD of CL. The work was supported by ANRt funding under CIFRE PhD program to CL. Financial support to Invenio for this project was provided by the Conseil Régional d’Aquitaine for CL PhD work, as part of the REGINA project, and for BL work (Grant Number 2018-1R20204 project DIGIE 'chestnut dieback: vulnerability and genetic determinism of ink disease resistance'). SNP development and genotyping were performed at the Genome Transcriptome Facility of Bordeaux (Grants from the Conseil Régional d’Aquitaine No. 20030304002FA and 20040305003FA, from the European Union FEDER No. 2003227 and from Investissements d’Avenir ANR-10-EQPX-16-01)"'

1. Development of highly validated SNP markers for genetic analyses of chestnut species

Author

Clément Larue, Erwan Guichoux, Benoît Laurent, Teresa Barreneche, Cécile Robin, Marie Massot, Adline Delcamp, Rémy J. Petit, Biodiversité, Gènes & Communautés (BioGeCo), Université de Bordeaux (UB)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Fruits et Légumes d'Aquitaine (INVENIO), Biologie du fruit et pathologie (BFP), This paper is part of the PhD of CL. The work was supported by ANRt funding under CIFRE PhD program to CL. Financial support to Invenio for this project was provided by the Conseil Régional d’Aquitaine for CL PhD work, as part of the REGINA project, and for BL work (Grant Number 2018-1R20204 project DIGIE 'chestnut dieback: vulnerability and genetic determinism of ink disease resistance'). SNP development and genotyping were performed at the Genome Transcriptome Facility of Bordeaux (Grants from the Conseil Régional d’Aquitaine No. 20030304002FA and 20040305003FA, from the European Union FEDER No. 2003227 and from Investissements d’Avenir ANR-10-EQPX-16-01), and ANR-10-EQPX-0016,XYLOFOREST,Plateforme d'Innovation ' Forêt-Bois-Fibre-Biomasse du Futur '(2010)

Subjects
0106 biological sciences, 0303 health sciences, MassARRAY, [SDV]Life Sciences [q-bio], Fagaceae, 01 natural sciences, Single nucleotide polymorphism, 03 medical and health sciences, [SDV.BV.AP]Life Sciences [q-bio]/Vegetal Biology/Plant breeding, Genetics, [SDV.BV]Life Sciences [q-bio]/Vegetal Biology, Castanea sp, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, 010606 plant biology & botany
Abstract

International audience; To better study and manage chestnut trees and species, we identified nuclear single nucleotide polymorphism (SNP) markers using restriction-associated DNA sequencing. Out of 343 loci tested, 68 SNP markers were selected that withhold stringent quality criteria such as quasi-systematic amplification across species and Mendelian segregation in both purebred and hybrid individuals. They provide sufficient power for species, hybrids and backcross characterization as well as for clonal identification, as shown by a comparison with single sequenced repeat (SSR) loci.

Published
2021

Catalog

Books, media, physical & digital resources
See catalog results