unresolved ( Li et al., 2007 ; Ren and Guan, 2008 ). The identification of molecular markers linked to important morphological traits will greatly facilitate maker-assisted breeding aimed at cultivar improvement ( Yu et al., 2000 ). Microsatellite or
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Pan-Hui Huang, Wen-Bin Yu, Jun-Bo Yang, Hong Wang, and Lu Lu
Josh A. Honig, Stacy A. Bonos, and William A. Meyer
., 2003 ). In this report, we describe the development of the first polymorphic microsatellite markers for ongoing molecular genetic research in kentucky bluegrass. Total genomic DNA was extracted from a single plant of the kentucky bluegrass cultivar
Josh A. Honig, Vincenzo Averello, Stacy A. Bonos, and William A. Meyer
Jung, 2004 ) between genetic diversity assessed by RAPD markers and the PTM kentucky bluegrass classification system. In the current study we used microsatellite, or SSR, markers to study the genetic relationships of 247 kentucky bluegrass cultivars and
Ying Wang, Ming Kang, and Hongwen Huang
critical, and a set of molecular markers is also required. Microsatellites or simple sequence repeats (SSRs) are DNA segments containing short sequence repeats (1–6 nucleotides) and have been widely recognized as powerful and informative markers due to
Kahraman Gürcan and Shawn A. Mehlenbacher
variation in chromosome number and genome size among species of the Betulaceae, some degree of microsatellite marker transferability is expected based on results in other plant families. Microsatellites, also known as simple sequence repeats (SSR), are
Nina R.F. Castillo, Barbara M. Reed, Julie Graham, Felicidad Fernández-Fernández, and Nahla Victor Bassil
reliable means for cultivar identification and to assess genetic relatedness and diversity in these collections. Microsatellite markers were only recently developed from an expressed sequence tag library of ‘Merton Thornless’ ( Lewers et al., 2008 ). A
Kuaifei Xia, Xiulin Ye, and Mingyong Zhang
Microsatellites, also known as single sequence repeats (SSRs), are a small array of one to six tandemly arranged bases spread throughout the genomes ( Dietrick et al., 1992 ). The development of SSR-based markers has become increasingly accessible
Yuan Zhang, Chen Wang, HongZheng Ma, and SiLan Dai
-based aneuploid ( Zhang et al., 2013 ), indicating a complicated genetic background. Therefore, the read and data analysis is a major problem for the SSR analysis of chrysanthemums. Fortunately, a powerful method called microsatellite DNA allele counting
Xinwang Wang, Deborah Dean, Phillip Wadl, Denita Hadziabdic, Brian Scheffler, Timothy Rinehart, Raul Cabrera, and Robert Trigiano
. Molecular tools are increasingly used for crape myrtle cultivar identification, parentage comparison, and interspecific hybrid analysis ( Pooler, 2003 ; Pounders et al., 2007 ). We report the development of microsatellites from crape myrtle ‘Natchez’ ( L
Hafid Achtak, Ahmed Oukabli, Mohammed Ater, Sylvain Santoni, Finn Kjellberg, and Bouchaib Khadari
length polymorphism (RFLP), random amplified polymorphic DNA (RAPD), amplified fragment length polymorphism (AFLP), and microsatellites or simple sequence repeat (SSR)]. RAPD and AFLP markers are dominant and present limited reproducibility ( Jones et al