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dc.contributor.authorTavassolian, Iraj
dc.contributor.authorRabiei, Gholmereza
dc.contributor.authorGregory, Davina
dc.contributor.authorMnejja, Mourad
dc.contributor.authorWirthensohn, Michelle G
dc.contributor.authorHunt, Peter W
dc.contributor.authorGibson, John P
dc.contributor.authorFord, Christopher M
dc.contributor.authorSedgley, Margaret
dc.contributor.authorWu, Shu-Biao
dc.contributor.otherProducció Vegetalca
dc.date.accessioned2024-08-12T11:17:51Z
dc.date.available2024-08-12T11:17:51Z
dc.date.issued2010-10-09
dc.identifier.citationTavassolian, Iraj, Gholmereza Rabiei, Davina Gregory, Mourad Mnejja, Michelle G Wirthensohn, Peter W Hunt, John P Gibson, Christopher M Ford, Margaret Sedgley, and Shu-Biao Wu. 2010. “Construction of an Almond Linkage Map in an Australian Population Nonpareil × Lauranne.” BMC Genomics 11 (1): 551. doi: 10.1186/1471-2164-11-551ca
dc.identifier.issn1471-2164ca
dc.identifier.urihttp://hdl.handle.net/20.500.12327/3121
dc.description.abstractBackground: Despite a high genetic similarity to peach, almonds (Prunus dulcis) have a fleshless fruit and edible kernel, produced as a crop for human consumption. While the release of peach genome v1.0 provides an excellent opportunity for almond genetic and genomic studies, well-assessed segregating populations and the respective saturated genetic linkage maps lay the foundation for such studies to be completed in almond. Results: Using an almond intraspecific cross between ‘Nonpareil’ and ‘Lauranne’ (N × L), we constructed a moderately saturated map with SSRs, SNPs, ISSRs and RAPDs. The N × L map covered 591.4 cM of the genome with 157 loci. The average marker distance of the map was 4.0 cM. The map displayed high synteny and colinearity with the Prunus T × E reference map in all eight linkage groups (G1-G8). The positions of 14 mapped gene-anchored SNPs corresponded approximately with the positions of homologous sequences in the peach genome v1.0. Analysis of Mendelian segregation ratios showed that 17.9% of markers had significantly skewed genotype ratios at the level of P < 0.05. Due to the large number of skewed markers in the linkage group 7, the potential existence of deleterious gene(s) was assessed in the group. Integrated maps produced by two different mapping methods using JoinMap® 3 were compared, and their high degree of similarity was evident despite the positional inconsistency of a few markers. Conclusions: We presented a moderately saturated Australian almond map, which is highly syntenic and collinear with the Prunus reference map and peach genome V1.0. Therefore, the well-assessed almond population reported here can be used to investigate the traits of interest under Australian growing conditions, and provides more information on the almond genome for the international community.ca
dc.description.sponsorshipAcknowledgements This research was funded by Australian Research Council Grant No. DP0556459. IT and GR were financially supported by the Ministry of Science, Research and Technology (MSRT) of Iran for their PhD studies in Australiaca
dc.format.extent10ca
dc.language.isoengca
dc.publisherBMCca
dc.relation.ispartofBMC Genomicsca
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleConstruction of an almond linkage map in an Australian population Nonpareil × Lauranneca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.subject.udc575ca
dc.subject.udc633ca
dc.identifier.doihttps://doi.org/10.1186/1471-2164-11-551ca
dc.contributor.groupGenòmica i Biotecnologiaca


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Except where otherwise noted, this item's license is described as http://creativecommons.org/licenses/by/4.0/
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