Relevant bibliographies by topics / Randomly Amplified Polymorphic DNA (RAPD)

Academic literature on the topic 'Randomly Amplified Polymorphic DNA (RAPD)'

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Published: 4 June 2021
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Journal articles on the topic "Randomly Amplified Polymorphic DNA (RAPD)"

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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. rhusiopathiae, produced the 1,265-bp band, suggesting that they had been misclassified. One strain of E. tonsillarumproduced the 884-bp band, suggesting that it too was E. rhusiopathiae. The E. rhusiopathiae strain of serovar 13 produced a 650-bp band, and the strain of serovar 18 produced a clear 420-bp band as well as three weak bands of 1,265, 918, and 444 bp. The primer NK6 revealed 14 RAPD patterns that were not serovar specific. However, different patterns were produced among strains of the same serovar showing that the RAPD method is able to identify the genetic variations of strains of this genus and can rapidly and easily differentiate strains of the same serovar. Based on these results, we concluded that the RAPD method with primers NK51 and NK6 is a rapid and reliable method to identify the species of this genus; we also concluded that this method might be a useful tool for the epidemiological analysis of the Erysipelothrix species.
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Wong, N. A. C. S., C. J. Linton, H. Jalal, and M. R. Millar. "Randomly amplified polymorphic DNA typing: a useful tool for rapid epidemiological typing ofKlebsiella pneumoniae." Epidemiology and Infection 113, no. 3 (December 1994): 445–54. http://dx.doi.org/10.1017/s095026880006845x.

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SUMMARYDiscriminatory typing methods are invaluable in the investigation of outbreaks of infectious diseases. Single primers were used to generate randomly amplified polymorphic DNA (RAPD) profiles fromKlebsiella pneumoniaeisolates of various serotype andK. pneumoniaeisolates from cases of sepsis at a Malaysian hospital and two English hospitals. RAPD profiles of acceptable reproducibility, a maximum of three minor band variations, were produced using a rapid DNA extraction method. RAPD typing ofK. pneumoniaewas shown to be as discriminatory as restriction fragment length polymorphism analysis using pulsed field gel electrophoresis yet quicker and less costly. The findings suggest that RAPD typing may be a useful tool for the epidemiological typing ofK. pneumoniae.
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Möller, M., and R. Harling. "Randomly amplified polymorphic DNA (RAPD) profiling of Plasmodiophora brassicae." Letters in Applied Microbiology 22, no. 1 (January 1996): 70–75. http://dx.doi.org/10.1111/j.1472-765x.1996.tb01111.x.

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Echt, C. S., L. A. Erdahl, and T. J. McCoy. "Genetic segregation of random amplified polymorphic DNA in diploid cultivated alfalfa." Genome 35, no. 1 (February 1, 1992): 84–87. http://dx.doi.org/10.1139/g92-014.

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Polymerase chain reaction was used, with single 10-mer primers of arbitrary sequence, to amplify random regions of genomic DNA from a diploid cultivated alfalfa backcross population. Segregation of the random amplified polymorphic DNA (RAPD) fragments was analysed to determine if RAPD markers are suitable for use as genetic markers. Of the 19 primers tested, 13 amplified a total of 37 polymorphic fragments, of which 28 (76%) segregated as dominant Mendelian traits. RAPD markers appear useful for the rapid development of genetic information in species like alfalfa where little information currently exists or is difficult to obtain.Key words: random amplified polymorphic DNA, polymerase chain reaction amplification, genome mapping, restriction fragment length polymorphism, Medicago sativa.
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Weir, B. J., R. G. St Pierre, and R. N. Chibbar. "RAPD Marker Polymorphism among Saskatoon Cultivars, Clones, and Seedlings." HortScience 32, no. 6 (October 1997): 1109–13. http://dx.doi.org/10.21273/hortsci.32.6.1109.

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Randomly amplified polymorphic DNA (RAPD) markers were used to distinguish among 16 cultivars of saskatoon (Amelanchier spp.). Eight 9-base, oligonucleotide primers amplified a total of 98 DNA fragments, of which 29 were useful as reproducible polymorphic markers. Twelve cultivars and two pairs of cultivars were uniquely characterized by these 29 markers. Polymorphism was not detected among five sources of the cv. Thiessen, whereas variability was found among seedlings from self-pollinated `Thiessen'. Samples of the cvs. Regent and Parkhill were indistinguishable from one of two sources, suggesting that the cultivars were mislabelled.
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Lim, Hak-Tae. "Comparative Studies on Hanabusaya asiatica and Its Allied Groups Based on Randomly Amplified Polymorphic DNA (RAPD) Analysis." HortScience 32, no. 3 (June 1997): 482E—482. http://dx.doi.org/10.21273/hortsci.32.3.482e.

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The phylogenetic relationships between Korean endemic, Hanabusaya asiatica, and its allied groups, including four genera and nine species, were investigated at the DNA level using randomly amplified polymorphic DNA (RAPD) method. Ten primers out of 80 primers (10-mer) screened gave rise to very high polymorphism (99%) in all of the tested plants, producing 153 randomly amplified DNA fragments. H. asiatica was differentiated from its allied groups at the 0.62 of similarity index of RAPDs. This results were in accordance with previous classification based on palynological studies. It was confirmed that H. asiatica could be placed into Korean endemic and suggested that RAPD technique be used as an additional method of phylogenetic relationship for plant systematics.
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Picton, Deric D., and Harrison G. Hughes. "Characterization of Alstroemeria Species using Random Amplified Polymorphic DNA (RAPD) Analysis." HortScience 32, no. 3 (June 1997): 482F—482. http://dx.doi.org/10.21273/hortsci.32.3.482f.

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In this study, 11 species, hybrids, and color variants were characterized using randomly amplified polymorphic DNA (RAPD) analysis. Total genomic DNA was extracted using a 2% CTAB extraction buffer using fresh or frozen leaf material. The DNA was amplified using standard RAPD-PCR protocols utilizing 10-mer primers. All primers utilized exhibited a high degree of polymorphism in their banding patterns among the species and hybrids studied. The primers used produced ≈40 reproducible bands. It was possible to identify and uniquely distinguish all species and hybrids investigated using these bands.
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Ronning, C. M., R. J. Schnell, and S. Gazit. "Using Randomly Amplified Polymorphic DNA (RAPD) Markers to Identify Annona Cultivars." Journal of the American Society for Horticultural Science 120, no. 5 (September 1995): 726–29. http://dx.doi.org/10.21273/jashs.120.5.726.

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The native American genus Annona contains many species that are cultivated for their edible fruit, including the custard apple (A. reticuluta L.), soursop (A. muricata L.), cherimoya (A. cherimola L.), sugar apple (A. squamosa L.), and interspecific hybrids, the atemoyas. RAPD analysis of A. cherimola. `Campa' and `Jete,' A. squamosa `Lessard,' and the atemoyas `Ubranitzki,' `Malali,' and `Kaspi' resulted in very distinctive patterns, indicating that RAPD markers, may be an efficient method of fingerprinting genotypes within and between Annona species. All 15 primers used generated repeatable, polymorphic patterns. An F1 population of `Jete' × `Lessard' was analyzed to determine the inheritance of the RAPD banding patterns. Fifty-two polymorphic loci were identified, which segregated in an expected Mendelian fashion.
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Franklin, Rima B., Douglas R. Taylor, and Aaron L. Mills. "Characterization of microbial communities using randomly amplified polymorphic DNA (RAPD)." Journal of Microbiological Methods 35, no. 3 (April 1999): 225–35. http://dx.doi.org/10.1016/s0167-7012(99)00003-2.

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Gidoni, D., M. Rom, T. Kunik, M. Zur, E. Izsak, S. Izhar, and N. Firon. "Strawberry-cultivar Identification using Randomly Amplified Polymorphic DNA (RAPD) Markers." Plant Breeding 113, no. 4 (December 1994): 339–42. http://dx.doi.org/10.1111/j.1439-0523.1994.tb00747.x.

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Dissertations / Theses on the topic "Randomly Amplified Polymorphic DNA (RAPD)"

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Golembiewski, Robert Craig. "Identification and characterization of creeping bentgrass using randomly amplified polymorphic DNA (RAPD) markers /." The Ohio State University, 1997. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487942739809001.

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Woodburn, Mary Alice. "Random amplified polymorphic DNA (RAPD) analysis of Bacillus sphaericus." Thesis, This resource online, 1994. http://scholar.lib.vt.edu/theses/available/etd-07102009-040429/.

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Robert, Florence. "Typage de "Candida albicans" par Random Amplified Polymorphic DNA (RAPD)." Paris 5, 1992. http://www.theses.fr/1992PA05P198.

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Wei, Ling. "Identification of DNA Markers in Triticum aestivum-Aegilops caudata Additions Lines by Randomly Amplified Polymorphic DNA (RAPD) Technology." DigitalCommons@USU, 1995. https://digitalcommons.usu.edu/etd/4543.

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The objective of this study was to identify DNA markers for each of six added C-genome chromosomes in Triticum aestivum L. cv. 'Alceso'-Aegilops caudata L. addition lines using the randomly amplified polymorphic DNA (RAPD) technique. DNA from Ae. caudata, T. aestivum, amphiploid of T. aestivum X Ae. caudata, and six disomic addition lines of wheat having a pair of Ae. caudata chromosomes was used as the template for the amplification of RAPD markers with a total of 58 random 10-mer oligonucleotide primers. Two primers, OPC-08 and OPJ-16, produced one intense band each from the amphiploid of T. aestivum X Ae. caudata and Ae. caudata, which was absent in all six addition lines. Each of these two primers produced a chromosome marker that could be tentatively located to the chromosome CA of Ae. caudata. OPJ-02, OPD-12, OPD-02, OPJ-12, OPD-20, and OPJ-14 produced a marker each for CB, CC, CD, CE, CF, and CG, respectively. OPJ-09 produced C-genome chromosome-specific RAPD markers. Also, OPC-05 and OPJ-19 produced RAPDs from both wheat and Ae. caudata genomes.
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Papadopoulos, Sarantos. "Untersuchungen genomischer Veränderungen von Mammakarzinomzellen mittels Random Amplified Polymorphic DNA." Doctoral thesis, Humboldt-Universität zu Berlin, Medizinische Fakultät - Universitätsklinikum Charité, 2001. http://dx.doi.org/10.18452/14631.

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Im ersten Teil der Arbeit wurde die random amplified polymorphic DNA (RAPD) Methode für die Anwendung humaner DNA optimiert, indem die Konzentrationen der einzelnen Agentien und das thermische Profil der PCR-Reaktion verändert wurden. Des weiteren wurde der Einfluss von Polymerasen und PCR-Maschinen auf die RAPD, insbesondere auf die Erweiterung des Spektrums der Amplimere und die Reproduzierbarkeit der Reaktionen untersucht. Unsere Untersuchungen haben gezeigt, dass die RAPD eine sehr robuste und reproduzierbare Methode ist. Im zweiten Teil wurden qualitative und quantitative Unterschiede zwischen DNA von Brustkrebszellen und DNA von Leukozyten detektiert. Die dazu benutzten Primer basieren auf Sequenzen die in den Mechanismen der Tumorgenese involviert sind. Unsere Studie hat gezeigt, dass random priming in der Abschätzung von genomischen Schäden im Brustkrebs sehr nutzbar sein kann.
In the first part of this work, we have optimized random amplified polymorphic DNA (RAPD) for the use of human DNA in altering the concentration of the reaction components and the steps of the thermal profile in the polymerase chain reaction, by testing a large number of polymerases and multiple combinations with respect to their ability to increase the spectrum of amplimers and by examining the performance of various thermocyclers. We conclude that RAPD is a robust and reproducible method that could prove very useful for scientists and physicians. In the second part we used primers that were designed by choosing sequences involved in the development of DNA mutations, to successfully detect qualitative and quantitative differences between breast cancer DNA/normal DNA pairs. Our study showed that random priming proves very useful for assessing genomic damage in breast cancer.
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Campos, Lázara Pereira. "Genome relationships among Lotus species based on random amplified polymorphic DNA (RAPD)." Thesis, McGill University, 1992. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=56888.

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The usefulness of RAPDs (Random Amplified Polymorphic DNA) to distinguish among different taxa of Lotus was evaluated. The following species were included: L. corniculatus, L. tenuis, L. alpinus, L. japonicus, and L. uliginosus. Several accessions for each species were studied. Following DNA extraction, amplification reactions were performed in a Hybaid DNA Thermal Cycler, and the product visualized according to a standard procedure. Twenty primers were used for each species/accession. Clear bands and several polymorphisms were obtained for all primers. A phenogram was drawn based on the genetic distance among the species. L. alpinus appears as the most distant species from L. corniculatus, followed by L. uliginosus, L. tenuis, and L. japonicus. With the exception of L. alpinus, these findings are in agreement with previous experimental studies in the L. corniculatus group. The use of a greater number of primers and increased number of species may provide a greater resolution of the systematics of these taxa.
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Rinaldi, Catherine. "Authentication of the Panax genus plants used in Traditional Chinese Medicine (TCM) using Randomly Amplified Polymorphic DNA (RAPD) analysis." University of Western Australia. Centre for Forensic Science, 2007. http://theses.library.uwa.edu.au/adt-WU2008.0054.

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[Truncated abstract] Traditional medicines are used by millions of people throughout the world as their primary source of medical care. A range of materials are in used traditional medicines including plant and animal parts. Even though the traditional medicine trade is estimated to be worth sixty billion dollars annually the trade remains largely unregulated. Unscrupulous practices by vendors to increase their profit margins such as substituting and adulterating expensive material with cheaper varieties go unchecked. This can be dangerous to consumers because some substitutions involve poisonous material. Also, animal parts from endangered species can find their way into traditional medicines, therefore there needs to be a way to identify them in traditional medicines to prosecute poachers. The traditional techniques used for the identification of material used in Traditional Chinese Medicine (TCM) include, morphological, histological, chemical and immunological analysis. However, these techniques have their limitations. This makes applying multiple techniques essential to provide thorough authentication of the material. DNA profiling provides a technique well suited to analysing material used in TCM. DNA profiling is advantageous over other techniques used to authenticate material used in TCM because it requires only a small sample amount, can determine the cultivator, be used on all forms of TCM and potentially distinguish the components of mixtures. ... Therefore, profiles of different species/individual are different and species? can be distinguished. Commercially sold traditional medicines are processed which is likely to degrade the DNA of the sample making extraction and amplification difficult. Here an organic Phenol:Chloroform extraction technique extracted DNA from commercial dried root samples. The extracted DNA was amplifiable using RAPD primers. The RAPD primers used here produced enough polymorphic bands to distinguish different plant species. They were used to distinguish commercial samples that were sold as three different species within the Panax genus, Panax ginseng, Panax quinquefolium and Panax notoginseng and genetically unrelated plant material; Potato and Eleutherococcus senticosus. Liquid samples and mixtures were also profiled with the RAPD primers to determine whether the RAPD primers provide enough distinguishing ability to analyse these forms of TCM. DNA was extracted from the liquid samples, one a ginseng drink and the other an ginseng extractum. However, there was no reliability in the production of PCR products. The analysis of the mixture samples found that not enough polymorphic bands were produced by the RAPD primers used here to identify Panax species within mixtures of two Panax species. While when P. ginseng was mixed with a genetically unrelated sample there was enough polymorphism to differentiate the two samples in the mixture. The results of this research show that RAPD analysis provides a simple and inexpensive technique to begin analysis of materials used in TCM. Using RAPD analysis it is possible to distinguish Panax plant species from each other. However, the RAPD primers used here did not provide enough reproducibility or polymorphism to analyse liquid and mixtures of Panax species plants.
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Patel, Sushma M. "Ribosomal RNA genes and RAPD for Cryptosporidium species and subspecies discrimination." Thesis, Coventry University, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.389769.

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Hughes, Greta. "Population structure and genetics of the European lobster Homarus gammarus." Thesis, Bangor University, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341219.

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Góis, Plácia Barreto Prata. "Aplicação do RAPD (Randomly Amplified Polymorphic dna) para tipagem molecular de amostras de Salmonella isoladas de diversas fontes da cidade de Aracaju-SE." Universidade Federal de Sergipe, 2006. https://ri.ufs.br/handle/riufs/3673.

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The Salmonella infection is a relevant problem in the public health, being one of the most important causes of the world´s enteric pathologies, with 1,3 million ill people, resulting in 600 deaths/year. The Salmonella spp. transmission occurs especially through water consumption and contaminated food. The diagnosis is realized using biochemical, serologic, and molecular tests. The RAPD (Randomly Amplified Polymorphic DNA) test is able to detect the genetic variation present in the isolated Salmonella spp. samples, allowing a molecular typing. This research aimed at achieving molecular typing from Salmonella spp. samples isolated from various resources (oyster, chicken, potable water, blood, and human feces) utilizing the RAPD technique. 33 Salmonella spp. samples, that came from bacteria located at the Laboratório de Virologia Comparada-DMO/CCBS/UFS, and two standard samples were utilized. Six randomized primers were used from the Ready-To-Go System RAPD; the products amplified were submitted to an electrophoretic run in a 5% polyacrilamid gel, and silver dyed. The band standard observed was analyzed by the NTSYS program. After a computational analysis it was possible to discriminate the 35 Salmonella spp. samples, resulting in 35 RAPD individual and distinct patterns, showing that the samples are genetically diversed and that there is an ample genetic biodiversity in the circulating samples in Aracaju-SE. To the grouping the Salmonella spp. samples was observed the epidemiological relationship between human samples and chicken.
A infecção por Salmonella é um relevante problema de saúde pública, sendo uma das mais importantes causas de patologias entéricas do mundo, com 1,3 milhões de doentes, resultando em aproximadamente 16000 hospitalizações e 600 mortes/ano. A transmissão da Salmonella spp. ocorre principalmente através do consumo de água e alimentos contaminados. O diagnóstico é realizado através de testes bioquímicos, sorológicos e moleculares. A técnica de RAPD (Randomly Amplified Polymorfhic DNA) é capaz de detectar as variações genéticas presente nos isolados, permitindo a tipagem molecular. Este estudo teve como objetivo realizar a tipagem molecular das amostras de Salmonella spp. isoladas de diversas fontes (ostra, frango, água residual, sangue e fezes humanas) utilizando a técnica de RAPD. Foram utilizadas 33 amostras de Salmonella spp. da bacterioteca do Laboratório de Virologia Comparada DMO/CCBS/UFS e duas amostras padrões. Foram utilizados seis primers randômicos do Sistema Read-To-Go RAPD, os produtos amplificados foram submetidos à corrida eletroforética em gel de poliacrilamida 5% e corado pela prata. O padrão de bandas observadas foi analisado pelo programa NTSYS. Após análise computacional foi possível discriminar as 35 amostras de Salmonella spp., resultando em 35 padrões de RAPD individuais e distintos, mostrando que as amostras são geneticamente diversas e que existe uma ampla biodiversidade genética nas amostras circulantes em Aracaju-SE. Ao grupar as amostras de Salmonella spp. observou-se o relacionamento epidemiológico entre as amostras humanas e de frango.
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Books on the topic "Randomly Amplified Polymorphic DNA (RAPD)"

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Hilton, Anthony Craig. Randomly amplified polymorphic DNA analysis of salmonella & campylobacter. Birmingham: University of Birmingham, 1996.

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Book chapters on the topic "Randomly Amplified Polymorphic DNA (RAPD)"

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Galvão, Lúcia Maria da Cunha, and Eliane Lages-Silva. "Randomly Amplified Polymorphic DNA (RAPD)." In Springer Protocols Handbooks, 133–47. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-375-6_10.

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Babu, Kantipudi Nirmal, Muliyar Krishna Rajesh, Kukkumgai Samsudeen, Divakaran Minoo, Erinjery Jose Suraby, Kallayan Anupama, and Paul Ritto. "Randomly Amplified Polymorphic DNA (RAPD) and Derived Techniques." In Methods in Molecular Biology, 191–209. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-767-9_10.

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Rafalski, Antoni, Scott Tingey, and John G. K. Williams. "Random amplified polymorphic DNA (RAPD) markers." In Plant Molecular Biology Manual, 423–29. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0511-8_27.

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Rafalski, Antoni, Scott Tingey, and John G. K. Williams. "Random amplified polymorphic DNA (RAPD) markers." In Plant Molecular Biology, 55–63. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-017-6951-8_3.

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Babu, Kantipudi Nirmal, Thotten Elampilay Sheeja, Divakaran Minoo, Muliyar Krishna Rajesh, Kukkamgai Samsudeen, Erinjery Jose Suraby, and Illathidath Payatatti Vijesh Kumar. "Random Amplified Polymorphic DNA (RAPD) and Derived Techniques." In Methods in Molecular Biology, 219–47. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-0997-2_13.

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Sperisen, Christoph, and Urs Büchler. "Cloning of Random Amplified Polymorphic DNA (RAPD) to Generate Codominant Genetic Markers." In Molecular Tools for Screening Biodiversity, 217–22. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-009-0019-6_43.

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Al-Khalifah, Nasser S., and A. E. Shanavaskhan. "Molecular Identification of Date Palm Cultivars Using Random Amplified Polymorphic DNA (RAPD) Markers." In Methods in Molecular Biology, 185–96. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7159-6_16.

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Modi, Arpan, Bhavesh Gajera, Naraynan Subhash, and Nitish Kumar. "Evaluation of Clonal Fidelity of Micropropagated Date Palm by Random Amplified Polymorphic DNA (RAPD)." In Methods in Molecular Biology, 81–89. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7159-6_8.

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Mergeai, G., I. Vroh Bi, J. P. Baudoin, and P. Du Jardin. "Use of Random Amplified Polymorphic DNA (RAPD) Markers to Assist Wide Hybridization in Cotton." In Biotechnology in Agriculture and Forestry, 121–39. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-80373-4_8.

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Singh, Kamaleshwar P. "Screening of DNA Methylation Changes by Methylation-Sensitive Random Amplified Polymorphic DNA-Polymerase Chain Reaction (MS-RAPD-PCR)." In Molecular Toxicology Protocols, 71–81. Totowa, NJ: Humana Press, 2014. http://dx.doi.org/10.1007/978-1-62703-739-6_6.

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Conference papers on the topic "Randomly Amplified Polymorphic DNA (RAPD)"

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Eriksson, John, Charlotta Löfström, and Peter Rådström. "Randomly amplified polymorphic DNA (RAPD) typing of Salmonella Senftenberg in animal feed production." In Fifth International Symposium on the Epidemiology and Control of Foodborn Pathogens in Pork. Iowa State University, Digital Press, 2003. http://dx.doi.org/10.31274/safepork-180809-538.

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Liu, Haiying, Guie Wang, Xiangying Meng, and Xiuli Wang. "Genetic Variation in Six Oratosquilla oratoria Populations Revealed by Random Amplified Polymorphic DNA (RAPD) Markers." In 2010 4th International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2010. http://dx.doi.org/10.1109/icbbe.2010.5516354.

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Ifah, Arini Al, Endang Yuniastuti, and Parjanto. "Analysis of breadfruit plant diversity (Artocarpus altilis P.) by random amplified polymorphic DNA (RAPD) in DIY." In THE 8TH ANNUAL BASIC SCIENCE INTERNATIONAL CONFERENCE: Coverage of Basic Sciences toward the World’s Sustainability Challanges. Author(s), 2018. http://dx.doi.org/10.1063/1.5062802.

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Darkazanli, Mohamad, Irina Kiseleva, and Kinan Darkazanli. "Genetic diversity of E. coli O157:H7 isolated from Aleppo River water samples using random amplified polymorphic DNA (RAPD) marker." In PHYSICS, TECHNOLOGIES AND INNOVATION (PTI-2019): Proceedings of the VI International Young Researchers’ Conference. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5134359.

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Li, Zi-tong, Guang-xin Yuan, Miao Wang, Li-jun Gao, Li-hua Zhang, Ming-cheng Li, and Jia-mu Niu. "Tortoise shell and falsify random amplified polymorphism DNA (RAPD) appraisal method research." In 2015 International Forum on Energy, Environment Science and Materials. Paris, France: Atlantis Press, 2015. http://dx.doi.org/10.2991/ifeesm-15.2015.188.

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