Publication:
Plasmodium vivax genetic diversity: microsatellite length matters

dc.contributor.authorBruce Russellen_US
dc.contributor.authorRossarin Suwanarusken_US
dc.contributor.authorUsa Lek-Uthaien_US
dc.contributor.otherMenzies School of Health Researchen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-08-20T07:00:44Z
dc.date.available2018-08-20T07:00:44Z
dc.date.issued2006-09-01en_US
dc.description.abstractThe Plasmodium vivax genome is very diverse but has a relatively low abundance of microsatellites. Leclerc et al. had shown that these di-nucleotide repeats have a low level of polymorphism, suggesting a recent bottleneck event in the evolutionary history of P. vivax. By contrast, in a recent paper, Imwong et al. show that there is a very high level of microsatellite diversity. The difference in these results is probably due to the set array lengths chosen by each group. Longer arrays are more diverse than are shorter ones because slippage mutations become exponentially more common with an increase in array length. These studies highlight the need to consider carefully the application and design of studies involving microsatellites. © 2006 Elsevier Ltd. All rights reserved.en_US
dc.identifier.citationTrends in Parasitology. Vol.22, No.9 (2006), 399-401en_US
dc.identifier.doi10.1016/j.pt.2006.06.013en_US
dc.identifier.issn14714922en_US
dc.identifier.other2-s2.0-33746783035en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/23308
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33746783035&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titlePlasmodium vivax genetic diversity: microsatellite length mattersen_US
dc.typeShort Surveyen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33746783035&origin=inwarden_US

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