2015
DOI: 10.1016/s2095-3119(14)60794-2
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Molecular diversity and genetic structure of 380 sweetpotato accessions as revealed by SSR markers

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Cited by 39 publications
(40 citation statements)
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“…Molecular techniques have been widely adopted as powerful tools for germplasm characterization, cultivar identification, phylogenetic studies, and diversity analysis in many crop plants [8]. In sweet potato studies, molecular markers have been used to evaluate the phylogenetics and germplasm to study the origin of sweet potato and its dissemination [9].…”
Section: Introductionmentioning
confidence: 99%
“…Molecular techniques have been widely adopted as powerful tools for germplasm characterization, cultivar identification, phylogenetic studies, and diversity analysis in many crop plants [8]. In sweet potato studies, molecular markers have been used to evaluate the phylogenetics and germplasm to study the origin of sweet potato and its dissemination [9].…”
Section: Introductionmentioning
confidence: 99%
“…Generally, SSR markers are distributed in both transcribed and non-coding sequences referred to as EST-and genomic-SSRs respectively. With the advantages of being co-dominant, PCR-based, highly polymorphic, chromosome-speci c, reproducible and consistent [42] compared to other molecular markers, SSR markers have been widely used in many genetic and molecular-based studies in sweetpotato including variety identi cation, genetic diversity analysis and construction of linkage maps [19][20][21]. Although several studies have reported the use of SSR markers in sweetpotato, most of them evolved from investigating transcriptome libraries and ESTs.…”
Section: Discussionmentioning
confidence: 99%
“…Nonetheless, SSR analyses may present false-positive results that can cause overlapped SSRs or null alleles [17] and polymerase slippage during DNA replication [18]. In sweetpotato, SSR markers are utilized extensively for the construction of genetic maps, diversity analysis, and variety identi cation [19][20][21]. They are widely distributed in both transcribed and non-coding sequences, generally described as expressed sequence tag (EST)-and genomic-SSRs respectively [22].…”
Section: Development and Characterization Of Simplementioning
confidence: 99%
“…The analysis of RAPD generated polymorphic bands showed variations in the number, length, and intensity of the resulting bands. Yang et al (2015), PCR-RAPD are widely distributed throughout the eukaryotic genomes in coding and non-coding regions. Their random genome distribution and use with low quality DNA have resulted in extensive use in the determination of genetic diversity, germplasm fingerprinting, genetic linkage mapping, and phylogenetic studies of sweet potato.…”
Section: E a Bmentioning
confidence: 99%