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Journal articles on the topic 'Rapd analysis of E'

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Published: 3 June 2025

Last updated: 31 July 2025

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1

Raddová, J., M. Beránek, I. Oukropec, and M. Vachůn. "RAPD Analysis of peaches within Czech National collection." Czech Journal of Genetics and Plant Breeding 39, No. 4 (2011): 113–19. http://dx.doi.org/10.17221/3728-cjgpb.

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The Random Amplified Polymorphic DNA (RAPD) technique was used to study the genetic diversity and relationships within the collection of the Czech National Plant Genetic Resources (PGR) of peaches (Prunus persica L.). The aim of the work was to elaborate a dendrogram of genetic similarity and to divide collection into clusters. 46 primers were applied to 6 cultivars differing in the place of origin, the fruit shape, the fruit colour, and in some other morphological characteristics. 12 primers were chosen which gave polymorphic repeatable strong and middle strong bands. They were subsequently u

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2

KHATIK, CL, SP SHARMA, SR MALOO, NS DODIYA, A. JOSHI, and RK JAIN. "RAPD Analysis in Opium Poppy (Papaver somniferum L.)." Journal of Medicinal and Aromatic Plant Sciences 38, no. 2 (2016): 43–49. http://dx.doi.org/10.62029/jmaps.v38i2.khatik2.

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The RAPD analysis was carried out with 28 crosses, 8 parents and 2 checks of opium poppy. Purified and isolated DNA was subjected to PCR based marker analysis (RAPD) for assessment of genetic diversity. The quality of DNA was determined by calculating ratio between A260 and A280 observed between 1.857 to 2.167 which indicated a good quality of plant DNA. The concentration of DNA ranged between 123 μg/μl (UOP-60 x UOP- 99) to 750 μg/μl (UOP-79 x UOP- 80). In the RAPD analysis 12 primers gave good amplified products with template DNA. Polymorphism shown by 12 primers ranged between 50 per cent (

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3

Gawel, Nick J., Rory Mellinger, Eric Stout, and R. Sauve. "RAPD Analysis of Acer." HortScience 30, no. 4 (1995): 813F—813. http://dx.doi.org/10.21273/hortsci.30.4.813f.

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DNA from 27 Acer species was used for RAPD analysis. A relatively high number of phylogenically informative polymorphisms were detected, as would be expected in intraspecific comparisons. Principle coordinates analysis was used to discern groupings among the species and a RAPD-based phylogeny was constructed. As expected when making comparisons among species, very high levels of polymorphism were found. Cultivars that grouped together in the principle components analysis also grouped together in the phylogenic analysis. Parts of the phylogenic analysis do not agree with morphology-based phylog

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4

Vlastníková, H., K. Moravcová, and M. Pidra. "The RAPD analysis of several cultivars of grapevine (Vitis viniferaL.) and their clones." Horticultural Science 31, No. 4 (2011): 136–39. http://dx.doi.org/10.17221/3807-hortsci.

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Nine identification RAPD markers (Moravcov&aacute; et al. 2003) were used to distinguish 24 clones and grapevine cultivars. No polymorphism was detected among all the tested clones of Chardonnay, Pinot gris and Zweigeltrebe from Pole&scaron;ovice. Pinot noir, Pinot gris, Pinot blanc and Pinot Meunier were indistinguishable within clones, they also showed the identical RAPD profile within cultivars (except discussed sample No. 26). On the other hand, Auxerrois as a relative to cultivars of Pinot group showed unique patterns and may be classified as a different cultivar. Some irregularit

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5

Ozbey, G., Ertas HB, and A. Muz. "Random amplified polymorphic DNA (RAPD) analysis of Ornithobacterium rhinotracheale strains isolated from chickens in Turkey." Veterinární Medicína 50, No. 12 (2012): 526–30. http://dx.doi.org/10.17221/5660-vetmed.

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Six field strains of Ornithobacterium rhinotracheale isolated from chickens in Elazig province located in the East of Turkey were typed by serotyping and random amplified polymorphic DNA assay using a random primer (OPG-11). Using the AGP test used for serotyping, serotype A was found to be the predominant serotype, only one strain was serotyped as serotype B. By RAPD assay, the tested ORT strains were found to have different RAPD profiles. In addition, the RAPD assay showed almost similar DNA profiles among the tested strains of the serotypes A, B, D and E. The strain of serotype C did give a

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6

Scott, Michelle Pellissier, Kenneth M. Haymes, and Scott M. Williams. "Parentage analysis using RAPD PCR." Nucleic Acids Research 20, no. 20 (1992): 5493. http://dx.doi.org/10.1093/nar/20.20.5493.

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7

Rasmussen, H. N., J. E. Olsen, and O. F. Rasmussen. "RAPD analysis of Yersinia enterocolitica." Letters in Applied Microbiology 19, no. 5 (1994): 359–62. http://dx.doi.org/10.1111/j.1472-765x.1994.tb00475.x.

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8

Miyata, M., T. Aoki, V. Inglis, T. Yoshida, and M. Endo. "RAPD analysis ofAeromonas salmonicidaandAeromonas hydrophila." Journal of Applied Bacteriology 79, no. 2 (1995): 181–85. http://dx.doi.org/10.1111/j.1365-2672.1995.tb00933.x.

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9

Säull, T., C. Lind-Halldén, and C. Halldén. "Primer Mixtures in RAPD Analysis." Hereditas 132, no. 3 (2004): 203–8. http://dx.doi.org/10.1111/j.1601-5223.2000.00203.x.

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10

Tigano, Myrian S., and Salah Aljanabi. "RAPD Analysis of Nomuraea rileyi." Journal of Invertebrate Pathology 75, no. 3 (2000): 240–42. http://dx.doi.org/10.1006/jipa.1999.4920.

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11

Kiryanova, O. Yu, R. R. Garafutdinov, D. A. Chemeris, Yu R. Giniyatov, I. M. Gubaidullin, and A. V. Chemeris. "DNA polymorphism of dogs (Canis familiaris L.). II. RAPD-analysis." Biomics 13, no. 3 (2021): 309–20. http://dx.doi.org/10.31301/2221-6197.bmcs.2021-22.

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A rather simple method of detecting DNA polymorphism in dogs in the form of amplification of random fragments of the genome using RAPD analysis with primers with arbitrary nucleotide sequences, which does not require prior knowledge of the sequences of nitrogenous bases of the detected DNA fragments, is considered. However, information about the complete genomes of the investigating species of organisms and, dogs in particular, allows with a preliminary in silico RAPD analysis to predict the expected results for each primer and their multiplex composition, which makes it possible at this stage

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12

Baleiras Couto, M. M., J. M. B. M. van der Vossen, H. Hofstra, and J. H. J. Huis in 't Veld. "RAPD analysis: a rapid technique for differentiation of spoilage yeasts." International Journal of Food Microbiology 24, no. 1-2 (1994): 249–60. http://dx.doi.org/10.1016/0168-1605(94)90123-6.

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13

Okatani, Alexandre Tomomitsu, Hideki Hayashidani, Toshio Takahashi, Takahide Taniguchi, Masuo Ogawa, and Ken-ichi Kaneko. "Randomly Amplified Polymorphic DNA Analysis ofErysipelothrix spp." Journal of Clinical Microbiology 38, no. 12 (2000): 4332–36. http://dx.doi.org/10.1128/jcm.38.12.4332-4336.2000.

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The usefulness of randomly amplified polymorphic DNA method (RAPD) to identify each species of genus Erysipelothrix and for epidemiological analysis of this genus was studied. Eighty-one strains and 18 random primers were tested. Among the tested primers, the primers NK51 (GGTGGTGGTATC) and NK6 (CCCGCGCCCC) produced noticeable results. The primer NK51 revealed four species-specific RAPD patterns. Of the 66 strains of E. rhusiopathiae, 64 had the same unique band of 884 bp. Of the 12 strains of E. tonsillarum, 11 produced a 1,265-bp band. In addition, two strains, previously thought to be E. rh

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14

Ling, Jing-Tian, Nick Gawel, and Roger J. Sauve. "RAPD Analysis of Hosta Species and Cultivars." HortScience 30, no. 4 (1995): 811E—811. http://dx.doi.org/10.21273/hortsci.30.4.811e.

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The genus of Hosta (plantain lily) is a shade-loving herbaceous plant with attractive foliage. Confusion exists in the genus regarding nomenclature and taxonomy. In this study, the possibility of application of RAPD markers to characterize Hosta species and cultivars was investigated. DNA was extracted from 28 Hosta species and cultivars. Thirty-six of 37 primers generated RAPD markers. Phylogenic analysis and principal components analysis showed groupings among cultivars. Results indicated that H. plantaginea and H. ventricosa were the most distant from the other tested species and cultivars.

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15

Wu, Y. J., Y. Chen, J. Wang, C. X. Zhu, and B. L. Xu. "RAPD analysis of jasmine rice-specific genomic structure." Genome 49, no. 6 (2006): 716–19. http://dx.doi.org/10.1139/g06-018.

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Total genomic DNA was extracted from 29 samples of rice seed, including jasmine rice Oryza sativa L. subsp indica 'KDML105', 'KDML105'-derived varieties, nonaromatic Thailand rice, and japonica rice. Polymorphism in RAPD profiles was analyzed to explore the genomic structure specific to jasmine rice. The degree of band sharing was used to evaluate genetic distance between varieties and to construct a phylogenetic tree. RD15, CNTLR85033, and CNT87040 were found to be closest to 'KDML105', which was consistent with the true relation among them. Four RAPD fragments that cooperatively distinguishe

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16

Jan, C. H., D. H. Byrne, J. Manhart, and H. Wilson. "Rose Germplasm Analysis with RAPD Markers." HortScience 34, no. 2 (1999): 341–45. http://dx.doi.org/10.21273/hortsci.34.2.341.

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The genus Rosa consists of more than 100 species classified into four subgenera, Eurosa, Platyrhodon, Hesperhodos, and Hulthemia, and distributed widely throughout the northern hemisphere. The subgenus Eurosa includes 11 sections. The other subgenera are monotypic. One hundred and nineteen accessions and 213 markers of 36 rose species that include eight sections of the subgenus Eurosa and one species each from the subgenera Hesperhodos and Platyrhodon were used to calculate a similarity matrix, which was clustered with the unweighted pair group method using arithmetic means (UPGMA). The RAPD m

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17

Mandal, P. K., I. M. Santha, and S. L. Mehta. "RAPD Analysis of Lathyrus sativus Somaclones." Journal of Plant Biochemistry and Biotechnology 5, no. 2 (1996): 83–86. http://dx.doi.org/10.1007/bf03262987.

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18

Noli, Enrico, Silvio Salvi, and Roberto Tuberosa. "Comparative analysis of genetic relationships in barley based on RFLP and RAPD markers." Genome 40, no. 5 (1997): 607–16. http://dx.doi.org/10.1139/g97-080.

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Genetic relationships have seldom been analyzed with different types of molecular markers in order to compare the information provided by each marker class. We investigated genetic relationships among nine barley cultivars using separate cluster analyses based on restriction fragment length polymorphisms (RFLPs) and random amplified polymorphic DNAs (RAPDs). Genomic DNA restricted with three enzymes and hybridized with 68 probes revealed 415 RFLPs (74.2% of all bands). Among the 128 primers used for RAPD analysis, 100 provided a reproducible profile, 89 of which revealed 202 polymorphic and 56

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19

Kazan, Kemal, John M. Manners, and Don F. Cameron. "Inheritance of random amplified polymorphic DNA markers in an interspecific cross in the genus Stylosanthes." Genome 36, no. 1 (1993): 50–56. http://dx.doi.org/10.1139/g93-007.

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The inheritance of random amplified polymorphic DNA (RAPD) markers generated via the polymerase chain reaction amplification of genomic DNA sequences in an F2 family of an interspecific cross between Stylosanthes hamata and S. scabra was investigated. An initial comparison between the parental species, S. hamata cv. Verano and S. scabra cv. Fitzroy, demonstrated that 34% of detected RAPD bands were polymorphic. Of 90 primers tested, 35 showed relatively simple and reliably scorable polymorphisms and were used for segregation analysis. Sixty F2 individuals were scored for the segregation of 73

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20

Antolin, Michael F., Christopher F. Bosio, Julie Cotton, William Sweeney, Michael R. Strand, and William C. Black. "Intensive Linkage Mapping in a Wasp (Bracon hebetor) and a Mosquito (Aedes aegypti) With Single-Strand Conformation Polymorphism Analysis of Random Amplified Polymorphic DNA Markers." Genetics 143, no. 4 (1996): 1727–38. http://dx.doi.org/10.1093/genetics/143.4.1727.

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Abstract The use of random amplified polymorphic DNA from the polymerase chain reaction (RAPD-PCR) allows efficient construction of saturated linkage maps. However, when analyzed by agarose gel electrophoresis, most RAPD-PCR markers segregate as dominant alleles, reducing the amount of linkage information obtained. We describe the use of single strand conformation polymorphism (SSCP) analysis of RAPD markers to generate linkage maps in a haplodiploid parasitic wasp Bracon (Habrobracon) hebetor and a diploid mosquito, Aedes aegypti. RAPD-SSCP analysis revealed segregation of codominant alleles

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21

Hasan, Mehfuz, and Mohammad Sharif Raihan. "Genetic Variability in Bangladeshi Aromatic Rice through RAPD Analysis." Turkish Journal of Agriculture - Food Science and Technology 3, no. 3 (2014): 107. http://dx.doi.org/10.24925/turjaf.v3i3.107-111.210.

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Genetic polymorphism and relationships among 30 commercial varieties of Bangladeshi aromatic rice (Oryza sativa L.) were established using random amplified polymorphic DNA (RAPD) primers. Out of fifty 10-mer RAPD primers screened initially, four were chosen and used in a comparative analysis of different varieties of indigenous Bangladeshi aromatic rice. Of the 33 total RAPD fragments amplified, 7 (21.21%) were found to be shared by individuals of all eight varieties. The remaining 26 fragments were found to be polymorphic (78.79%). Pair-wise estimates of similarity ranged from 0.101 to 0.911.

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22

Warghat, Nandkishor, Navin Sharma, Punam Thakur, and Mumtaz Baig. "Genetic Diversity Analysis of Crab Spider (Araneae: Thomisidae) based on RAPD-PCR." Indian Journal of Applied Research 4, no. 8 (2011): 1–5. http://dx.doi.org/10.15373/2249555x/august2014/191.

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23

Tabassum, Nadra, Mahbubah Jannat, and Mohammad Nurul Islam. "Genetic Diversity Analysis of Five Different Species of Riccia." Plant Tissue Culture and Biotechnology 32, no. 2 (2022): 137–44. http://dx.doi.org/10.3329/ptcb.v32i2.63548.

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Five species of the Riccia genus have been investigated by Rapid Amplified Polymorphic DNA (RAPD) analysis. The species is explained and demonstrated with its genetic diversity based on morphological variations. Samples were collected from different parts of the University of Dhaka growing in different habitats around the University campus area. After the study of its morphology, it has been observed that the population of this taxon shows significant variation in plant size, shape, colour, ventral scales, appendages of scales, rhizoids, and the position of male and female receptacles, etc. Th

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24

Swoboda, Ines, and Prem L. Bhalla. "RAPD analysis off genetic variation in the Australian fan flower, Scaevola." Genome 40, no. 5 (1997): 600–606. http://dx.doi.org/10.1139/g97-079.

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The use of randomly amplified polymorphic DNA (RAPD) to study genetic variability in Scaevola (family Goodeniaceae), a native Australian species used in ornamental horticulture, is demonstrated. Plants of the genus Scaevola are commonly known as "fan flowers," due to the fan-like shape of the flowers. Nineteen accessions of Scaevola (12 cultivated and 7 wild) were studied using 20 random decamer arbitrary primers. Eight primers gave a distinct reproducible amplification profile of 90 scorable polymorphic fragments, enabling the differentiation of the Scaevola accessions. RAPD amplification of

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25

Rohit, Sharma, and Kumar Sandeep. "MOLECULAR MARKER ASSISTED STUDIES ON GENETIC DIVERSITY IN BRASSICA SPECIES." International Journal of Research -GRANTHAALAYAH 3, no. 7 (2017): 63–71. https://doi.org/10.5281/zenodo.847072.

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Genetic diversity of seven genotypes of Brassica campestris was evaluated by using RAPD primers. A total of 15 DNA bands were revealed wherein 11 polymorphic bands were observed. Highest polymorphism was showed by the primer OPA 7 (87.50%) and lowest by the primer OPA 9 (57.14%). Relatively higher genetic diversity was found among the collected individuals. A maximum similarity based on Jaccard coefficient was showed highest and lowest value (0.750) and (0.364) respectively. The UPGMA cluster analysis revealed three main group of clusters in which one group was found to be sub grouped and othe

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26

Sun, Gen-Lou, Björn Salomon, and Roland von Bothmer. "Analysis of tetraploid Elymus species using wheat microsatellite markers and RAPD markers." Genome 40, no. 6 (1997): 806–14. http://dx.doi.org/10.1139/g97-804.

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An analysis of Amplification fragment polymorphism of DNA from 27 accessions of 19 tetraploid Elymus species was carried out using 18 wheat microsatellite (WMS) primer pairs and 10 decamer primers. Ten WMS primer pairs produced multiple polymorphism on all accessions tested. Two independent phenograms, one based on WMS-PCR and one on RAPDs, separated the 19 tetraploid species into two main groups, viz., the SH genome species group and the SY genome species group. The results coincide with the genomic classification of these species and hence support previous studies showing that Elymus is not

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27

Jung, Guenhwa, Dale T. Lindmen, and Dermot P. Coyne. "660 PB 072 IDENTIFICATION OF GENETIC VARIABILITY AMONG SPECIES AND CULTIVARS OF PENSTEMON USING RANDOM AMPLIFIED POLYMORPHIC DNA (RAPDS)." HortScience 29, no. 5 (1994): 527d—527. http://dx.doi.org/10.21273/hortsci.29.5.527d.

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Eight species and 57 selections/cultivars of Penstemon were compared for genetic variability using Random Amplified Polymorphic DNAs (RAPDs). The RAPD technique was used to help understand the genetic relationships in species and cultivars in the genus Penstemon. Ten RAPD primers (from Operon) were screened to identify polymorphisms among these eight species and 57 selections. More than 100 RAPD polymorphic bands were obtained. A principle component analysis was used to study genetic relationships. Variation among species was greater than variation among selections/cultivars within species. RA

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28

Bayazit, S., B. Imrak, A. Küden, and M. Kemal Güngör. "RAPD analysis of genetic relatedness among selected quince (Cydonia oblonga Mill.) accessions from different parts of Turkey." Horticultural Science 38, No. 4 (2011): 134–41. http://dx.doi.org/10.17221/97/2011-hortsci.

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Quince (Cydonia oblonga Mill.) is a minor fruit crop, which is primarily used for marmalade, jam, sauce and as rootstocks for pears. Different cultivated and local quince genotypes are grown in almost all parts of Turkey for fruit usage. In this study, randomly amplified polymorphic DNA (RAPD) technology was used to study the genetic relationships among 13 quince accessions selected from different parts of Turkey. Thirty decamer primers were used and 14 of them did not produce any polymorphism. The remaining 16 primers ranged in their amplification fragments between one (P-402, P-437, OPA 10,

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29

Wettasinghe, Ruwanthi C., and Ellen B. Peffley. "Optimizing RAPD Markers for Onion Genomic DNA Analysis." HortScience 30, no. 4 (1995): 877E—877. http://dx.doi.org/10.21273/hortsci.30.4.877e.

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Random amplified polymorphic DNA (RAPD) have potential as genetic markers that may facilitate selection in plant improvement. To obtain clear, reproducible, and repeatable RAPD bands, four DNA extraction protocols and two Taq polymerases were compared. DNA extraction followed modified Tai and Tanksley (PMBR), Dellaporta et al. (PMBR), and Guilllemant et al. (PMBR) protocols, and a plant tissue DNA isolation kit from Gentra Systems was used. The modified Guillemant protocol was selected because of ease of extraction and cost effectiveness. Genotypes studied were TG1015Y (Allium cepa). Polymeras

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30

Wettashinghe, Ruwanthi C., and Ellen B. Peffley. "OPTIMIZING RAPD MARKERS FOR ONION GENOMIC DNA ANALYSIS." HortScience 30, no. 3 (1995): 435a—435. http://dx.doi.org/10.21273/hortsci.30.3.435a.

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Random amplified polymorphic DNA (RAPD) are genetic markers that facilitate selection in plant breeding. To obtain clear reproducible, and repeatable RAPD bands, four DNA extraction protocols and two Taq polymerases were compared using thirteen TG1015Y (Allium cepa) genotypes. Protocols for DNA extraction followed those of a modified Tai and Tanksley, 1989 (PMBR); a modified Dellaporta et al., 1983 (PMBR); a modified Guillemunt et al., 1992 (PMBR); and extracted with a plant tissue DNA isolation kit from Gentra System (Minneapolis). The modified Guillemunt protocol was selected due to ease of

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31

Cheng, Kur-Ta, Borcherng Su, Chien-Tsu Chen, and Chun-Ching Lin. "RAPD Analysis of Astragalus Medicines Marketed in Taiwan." American Journal of Chinese Medicine 28, no. 02 (2000): 273–78. http://dx.doi.org/10.1142/s0192415x00000325.

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The genetic variability of Astragalus medicine materials sold by twenty randomly selected stores in Taiwan was investigated using RAPD analysis in order to obtain available primers which could clearly differentiate among them. Total DNA isolated from the rhizomes of the samples were used as templates, and sixty 10 mer arbitrary primers were used in the analysis. The aim of the present study is to construct an identification model of molecular biotechniques applicable to Chinese herbal medicines in RAPD analysis. Three of the primers, OPT-03, OPT-13, and OPT-17, revealed polymorphic RAPD finger

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Haase, A., A. Melder, H. Smith-Vaughan, D. Kemp, and B. Currie. "RAPD analysis of isolates ofBurkholderia pseudomalleifrom patients with recurrent melioidosis." Epidemiology and Infection 115, no. 1 (1995): 115–21. http://dx.doi.org/10.1017/s0950268800058179.

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SummaryTwenty-seven isolates ofBurholderia pseudomallei(formerlyPseudomonas pseudomallei) from ten patients with recurrent melioidosis were analysed by RAPD. In two cases RAPD patterns in recurrent isolates differed from the original isolates; one was considered a likely reinfection while the other may represent relapse from one of two strains initially infecting the patient. In two cases where a change in antibiotic resistance had occurred between original and relapse isolates, slight changes in RAPD patterns were found with one of the four primers used. In the other six cases the relapse was

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33

Maciuszonek, Anna, Bartosz Grajewski, and Marek Bednarczyk. "RAPD-PCR Analysis of Various Goose Populations." Folia Biologica 53, no. 1 (2005): 83–85. http://dx.doi.org/10.3409/1734916054663384.

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34

Liu, C., and M. Mei. "CLASSIFICATION OF LYCHEE CULTIVARS WITH RAPD ANALYSIS." Acta Horticulturae, no. 665 (January 2005): 149–60. http://dx.doi.org/10.17660/actahortic.2005.665.17.

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35

Takeda, Toshihide, Takehiko Shimada, Keiichi Nomura, et al. "Classification of Apricot Varieties by RAPD Analysis." Engei Gakkai zasshi 67, no. 1 (1998): 21–27. http://dx.doi.org/10.2503/jjshs.67.21.

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36

De la Rosa, R., A. Martin, L. Rallo, A. Angiolillo, C. Guerrero, and L. Baldoni. "RAPD AND AFLP ANALYSIS FOR OLIVE MAPPING." Acta Horticulturae, no. 586 (October 2002): 79–82. http://dx.doi.org/10.17660/actahortic.2002.586.7.

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37

Matsui, Toshiyuki, Yusuke Kosugi, Tomohiro Yanagi, Haruo Suzuki, Pankaj Kumar Bhow, and Sutevee Sukarakarn. "Classification of Oriental Melon by RAPD Analysis." Pakistan Journal of Biological Sciences 5, no. 2 (2002): 208–11. http://dx.doi.org/10.3923/pjbs.2002.208.211.

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38

VANDER KLOET, S. P., and T. A. DICKINSON. "RAPD typification: phenetic analysis of Vaccinium inflorescences." Botanical Journal of the Linnean Society 148, no. 4 (2005): 445–57. http://dx.doi.org/10.1111/j.1095-8339.2005.00429.x.

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Li, Y., H. Liu, and Y. Matsubara. "CULTIVAR IDENTIFICATION BY RAPD ANALYSIS IN EPIDENDRUM." Acta Horticulturae, no. 937 (September 2012): 605–8. http://dx.doi.org/10.17660/actahortic.2012.937.73.

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Ranade, S. A., A. Verma, M. Gupta, and N. Kumar. "RAPD Profile Analysis of Betel Vine Cultivars." Biologia plantarum 45, no. 4 (2002): 523–27. http://dx.doi.org/10.1023/a:1022364823330.

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Bando, Silvia Yumi, Gloria R. F. Valle, Marina B. Martinez, Luiz R. Trabulsi, and Carlos A. Moreira-Filho. "Characterization of enteroinvasiveEscherichia coliandShigellastrains by RAPD analysis." FEMS Microbiology Letters 165, no. 1 (1998): 159–65. http://dx.doi.org/10.1111/j.1574-6968.1998.tb13141.x.

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Ostrowska, Ewa, Morley Muralitharan, Stephen Chandler, et al. "Optimized conditions for rapd analysis inPinus radiata." In Vitro Cellular & Developmental Biology - Plant 34, no. 3 (1998): 225–30. http://dx.doi.org/10.1007/bf02822712.

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43

Ortiz, A., R. Renaud, I. Calzada, and E. Ritter. "Analysis of plum cultivars with RAPD markers." Journal of Horticultural Science 72, no. 1 (1997): 1–9. http://dx.doi.org/10.1080/14620316.1997.11515485.

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Zheng, Z. B., H. J. Luo, S. J. Hu, S. Luo, and C. M. Liu. "IDENTIFICATION OF 'DONGYUAN' LONGAN BY RAPD ANALYSIS." Acta Horticulturae, no. 863 (May 2010): 201–6. http://dx.doi.org/10.17660/actahortic.2010.863.26.

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Makaradze, Elza, Galina Meparishvili, Natela Varshanidze, et al. "RAPD-ANALYSIS OF CYCLAMEN SPP. GENOME POLYMORPHISM." CBU International Conference Proceedings 7 (September 30, 2019): 949–53. http://dx.doi.org/10.12955/cbup.v7.1483.

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Wild plants form the basis of biological resources both for Georgia and the whole world. A strategic task of any country is to preserve the biological diversity of plants. In the territory of Ajara, a large species diversity of plants grows, among which there are rare, endemic and relict plants. In particular, Cyclamen adzharicum. Modern systematics of wild plants in Georgia is based on classical methods of botany. In this regard, it is relevant to conduct genetic studies of species diversity and genetic polymorphism of species and populations using molecular genetic markers, in particul

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Shim, Young-Hun, Jung-Ho Choi, Chan-Dong Park, Chul-Joo Lim, Jung-Hee Cho, and Hong-Jin Kim. "Molecular differentiation ofPanax species by RAPD analysis." Archives of Pharmacal Research 26, no. 8 (2003): 601–5. http://dx.doi.org/10.1007/bf02976708.

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Maan Hasan Al_yassine. "Molecular characterization of nine grapevine varieties cultivated in Salahaldin, Iraq by using RAPD-PCR marker." Tikrit Journal of Pure Science 22, no. 2 (2023): 13–18. http://dx.doi.org/10.25130/tjps.v22i2.623.

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Grapevine (Vitis vinifera L.) is one of important economic fruit crops found in Salahaldin province \ Iraq. To examine the Molecular characterization and genetic relationships among nine grape varieties by using random amplified polymorphic DNA (RAPD) marker. Fifteen RAPD primers produced polymorphic band (71, 56%), while two RAPD primers yielded monomorphic bands only. The size of the fragment ranged between 250-2700 bp, with an average of 5.47 band/primer. A total of 20 unique and absent bands used to identify seven cultivars. This study has found that genetic distance values ranged from 0.0

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Bandi, C., G. la Rosa, M. G. Bardin, et al. "Random amplified polymorphic DNA fingerprints of the eight taxa of Trichinella and their comparison with allozyme analysis." Parasitology 110, no. 4 (1995): 401–7. http://dx.doi.org/10.1017/s003118200006474x.

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SUMMARYEight taxa have recently been proposed as being encompassed by the genus Trichinella on the basis of allozyme and biological data. In this paper we show that an analogous 8 taxon structure for this genus results from the random amplified polymorphic DNAs (RAPDs). Five 10-mer or 20-mer primers were used under different polymerase chain reaction (PCR) conditions to produce multiband RAPD fingerprints from muscle larvae of 40 isolates of Trichinella spp. The resulting RAPD data were analysed following the numerical taxonomic approach, and the resulting classification was compared to that d

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Besnard, Guillaume, Catherine Breton, Philippe Baradat, Bouchaib Khadari, and André Bervillé. "Cultivar Identification in Olive Based on RAPD Markers." Journal of the American Society for Horticultural Science 126, no. 6 (2001): 668–75. http://dx.doi.org/10.21273/jashs.126.6.668.

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One hundred and thirteen olive (Olea europaea L.) accessions were characterized using randomly amplified polymorphic DNA (RAPD) markers. Forty-five polymorphic RAPD markers were obtained enabling us to distinguish 102 different RAPD profiles. The approximate estimation of the probability of obtaining the same RAPD profile for two different trees was between 6.75 × 10-5 and 4.82 × 10-14. A dendrogram was constructed using Ward's minimum variance algorithm based on chi-square distances. This led to a more clear-cut classification of profiles than the classical approach of unweighted pair group m

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Brummer, E. C., J. H. Bouton, and G. Kochert. "Analysis of annual Medicago species using RAPD markers." Genome 38, no. 2 (1995): 362–67. http://dx.doi.org/10.1139/g95-047.

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Annual species of the genus Medicago have attracted interest as green manure and temporary forage crops. This study was conducted to determine if randomly amplified polymorphic DNA (RAPD) markers could be used to assess the variability within and among species. Several accessions of each six species (M. scutellata Mill., M. disciformis DC, M. murex Willd., M. truncatula Gaertn., M. polymorpha L., and M. rugosa Desr.) were studied. A phylogeny reconstructed with the computer program Phylogenetic Analysis Using Parsimony (PAUP) showed the same relationships as traditional taxonomy. Variation was

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