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Min Fan, Yike Gao, Yaohui Gao, Zhiping Wu, Hua Liu, and Qixiang Zhang

), pentanucleotide (0.13%, 6), and hexanucleotide repeat motifs (0.09%, 4) ( Table 1 ). Table 1. Summary of expressed sequence tag–simple sequence repeat (EST-SSR) markers identified in the chrysanthemum transcriptome. The frequency distribution of 35 major types

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Karen Harris-Shultz, Melanie Harrison, Phillip A. Wadl, Robert N. Trigiano, and Timothy Rinehart

). Simple sequence repeat markers, or microsatellites, are repeating DNA sequences of one to six nucleotides that are found in coding and non-coding regions of the genome ( Toth et al., 2000 ). SSR markers, including expressed sequence tag markers, have a

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Jian-Feng Geng, Cheng-Song Zhu, Xiao-Wei Zhang, Yan Cheng, Yuan-Ming Zhang, and Xi-Lin Hou

from simple sequence repeat (SSR), which amplifies specifically the region between two microsatellite motifs ( Zietkiewicz et al., 1994 ). Compared with random amplified polymorphic DNA (RAPD), ISSR produces more reliable and reproducible result

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Kwanjai Pipatchartlearnwong, Akarapong Swatdipong, Supachai Vuttipongchaikij, and Somsak Apisitwanich

for genetic diversity of palmyrah ( Borassus flabellifer ) accessions using Inter Simple Sequence Repeat (ISSR) markers Asian Austral. J. Plant Sci. Biotechnol. 3 1 11 15 Whankaew, S. Kanjanawattanawong, S. Phumichai, C. Smith, D.R. Narangajavana, J

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Nina R.F. Castillo, Barbara M. Reed, Julie Graham, Felicidad Fernández-Fernández, and Nahla Victor Bassil

limited number of simple sequence repeats (SSRs) are reported for Rubus , which include the invasive weed R. alceifolius ( Amsellem et al., 2001 ), an Azorean island endemic species R. hochstetterorum ( Lopes et al., 2006 ), and red raspberry ( Graham

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Imen Rekik, Amelia Salimonti, Naziha Grati Kamoun, Innocenzo Muzzalupo, Oliver Lepais, Sophie Gerber, Enzo Perri, and Ahmed Rebai

markers ( Grati Kamoun et al., 2006 ; Taamalli et al., 2006 ) and simple sequence repeat (SSR) markers ( Taamalli et al., 2006 , 2007 ). However, there is still a need for better genetic diversity assessment and varietal identification using high

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Zahra Noormohammadi, Mehdi Hosseini-Mazinani, Isabel Trujillo, Luis Rallo, Angjelina Belaj, and Majid Sadeghizadeh

genotype, screening was performed on 92 olive accessions by using five high polymorphic simple sequence repeat (SSR) markers (ssrOeUA-DCA3,ssrOeUA-DCA9, ssrOeUA-DCA16, ssrOeUA-DCA18, and UDO99-043), which have been shown to be efficient for cultivar

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Barbara S. Gilmore, Nahla V. Bassil, Danny L. Barney, Brian J. Knaus, and Kim E. Hummer

accessions. z Table 3. List of 29 additional simple sequence repeat primers screened for polymorphism in eight Rheum ×rhabarum accessions ‘Crimson Delicious’ (RB7), ‘Coulter MacDonald’ (RB10), Penn. State 3 (RB12), ‘New Zealand’ (RB19), ‘Parson’s Crimson

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Karen R. Harris-Shultz, Brian M. Schwartz, Wayne W. Hanna, and Jeff A. Brady

574, and each F 1 progeny to the sample and confirming the unknown Gap1 (G 1 ) peak was between the control G 1 peaks. Simple sequence repeat generation. DNA was extracted from 118 F 1 field-grown individuals using a PureLink DNA Purification Kit

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Anil Khar, Jernej Jakse, and Michael J. Havey

), yellow ( iiC-llR-, iiC-L-rr , and iiC-llrr ), and light-red to red ( iiC-L-R -) bulb colors, as well as black ( B -) versus brown ( bb ) seeds ( Davis, 1966 ). We scored segregations for simple sequence repeats (SSRs), bulb and seed colors, and single