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Статті в журналах з теми "Genomic techniques"
Ramzan, Fahad, Adnan Younis, and Ki-Byung Lim. "Application of Genomic In Situ Hybridization in Horticultural Science." International Journal of Genomics 2017 (2017): 1–12. http://dx.doi.org/10.1155/2017/7561909.
Повний текст джерелаXin-Yun Zhang, Fei Chen, Yuan-Ting Zhang, S. C. Agner, M. Akay, Zu-Hong Lu, M. M. Y. Waye, and S. K. W. Tsui. "Signal processing techniques in genomic engineering." Proceedings of the IEEE 90, no. 12 (December 2002): 1822–33. http://dx.doi.org/10.1109/jproc.2002.805308.
Повний текст джерелаDamaj, Mona B., Phillip D. Beremand, Marco T. Buenrostro-Nava, John Ivy, Siva P. Kumpatla, John Jifon, Getu Beyene, Qingyi Yu, Terry L. Thomas, and T. Erik Mirkov. "Isolating promoters of multigene family members from the polyploid sugarcane genome by PCR-based walking in BAC DNA." Genome 53, no. 10 (October 2010): 840–47. http://dx.doi.org/10.1139/g10-064.
Повний текст джерелаMorrison, Carl. "Fluorescent In Situ Hybridization and Array Comparative Genomic Hybridization: Complementary Techniques for Genomic Evaluation." Archives of Pathology & Laboratory Medicine 130, no. 7 (July 1, 2006): 967–74. http://dx.doi.org/10.5858/2006-130-967-fishaa.
Повний текст джерелаvan Oppen, Madeleine J. H., and Melinda A. Coleman. "Advancing the protection of marine life through genomics." PLOS Biology 20, no. 10 (October 17, 2022): e3001801. http://dx.doi.org/10.1371/journal.pbio.3001801.
Повний текст джерелаUpadhyay, Tejal, and Samir Patel. "Identifying Subtypes of Cancer Using Genomic Data by Applying Data Mining Techniques." International Journal of Natural Computing Research 8, no. 3 (July 2019): 55–64. http://dx.doi.org/10.4018/ijncr.2019070104.
Повний текст джерелаKyselová, Jitka, Ladislav Tichý, and Kateřina Jochová. "The role of molecular genetics in animal breeding: A minireview." Czech Journal of Animal Science 66, No. 4 (March 26, 2021): 107–11. http://dx.doi.org/10.17221/251/2020-cjas.
Повний текст джерелаTramontano, Anna. "Comparative Modelling Techniques: Where are we?" Comparative and Functional Genomics 4, no. 4 (2003): 402–5. http://dx.doi.org/10.1002/cfg.306.
Повний текст джерелаAziz, Md Momin Al, Md Nazmus Sadat, Dima Alhadidi, Shuang Wang, Xiaoqian Jiang, Cheryl L. Brown, and Noman Mohammed. "Privacy-preserving techniques of genomic data—a survey." Briefings in Bioinformatics 20, no. 3 (November 7, 2017): 887–95. http://dx.doi.org/10.1093/bib/bbx139.
Повний текст джерелаNusrat, S., T. Harbig, and N. Gehlenborg. "Tasks, Techniques, and Tools for Genomic Data Visualization." Computer Graphics Forum 38, no. 3 (June 2019): 781–805. http://dx.doi.org/10.1111/cgf.13727.
Повний текст джерелаДисертації з теми "Genomic techniques"
Haghighi, Maryam. "Application of Combinatorial Optimization Techniques in Genomic Median Problems." Thèse, Université d'Ottawa / University of Ottawa, 2011. http://hdl.handle.net/10393/20484.
Повний текст джерелаKhanam, Taslima. "Sex determination and genetic management in Nile tilapia using genomic techniques." Thesis, University of Stirling, 2017. http://hdl.handle.net/1893/25285.
Повний текст джерелаRaiford, Douglas W. III. "Algorithmic Techniques Employed in the Isolation of Codon Usage Biases in Prokaryotic Genomes." Wright State University / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=wright1211902424.
Повний текст джерелаBrown, Margaret M. "Application of genomic techniques to development of biomarkers for the aquatic environment." Thesis, Glasgow Caledonian University, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.443169.
Повний текст джерелаSharma, Jason P. (Jason Poonam) 1979. "Classification performance of support vector machines on genomic data utilizing feature space selection techniques." Thesis, Massachusetts Institute of Technology, 2002. http://hdl.handle.net/1721.1/87830.
Повний текст джерелаRenard, Meseguer Joan. "Identification of genes related to seed longevity in Arabidopsis thaliana using genomic molecular techniques." Doctoral thesis, Universitat Politècnica de València, 2021. http://hdl.handle.net/10251/170554.
Повний текст джерела[ES] La longevidad de las semillas, o el tiempo durante el cual permanecen las semillas viables, es de gran importancia para la conservación de la biodiversidad, la agricultura y la economía. Además, el estudio de este parámetro puede contribuir a conocer mejor los mecanismos moleculares comunes a todos los organismos para prevenir el envejecimiento. Una de las principales estrategias de las semillas para ralentizar su envejecimiento consiste en detener su metabolismo, a través de su deshidratación. Otros mecanismos moleculares para evitar daños son el aislamiento frente al entorno a través de la cubierta de la semilla, y la producción de antioxidantes y otras moléculas para evitar el daño oxidativo, uno de los principales causantes del envejecimiento de las semillas. Los mecanismos de reparación mitigan parte del daño acumulado. El organismo modelo de plantas Arabidopsis thaliana brinda la oportunidad de la realización de estudios genómicos para el estudio de, en este caso, la longevidad de las semillas para descubrir nuevos factores genéticos y mecanismos moleculares determinantes. Este conocimiento servirá para entender mejor los procesos de deterioro de las semillas y que también será clave para aumentar la longevidad de estas. Mediante el uso de variedades naturales genotipadas de Arabidopsis thaliana y un estudio de asociación del genoma conocido como GWAS, seguido de estudios de genética reversa, se han identificado 12 nuevos genes relacionados con la longevidad de las semillas, relacionados con la protección del embrión, el control del daño oxidativo, y la permeabilidad de la cubierta de la semilla. El desarrollo de la cubierta de la semilla está determinado por factores de transcripción. Plantas mutantes en diversos factores de transcripción involucrados en el desarrollo de la cubierta de la semilla presentan una longevidad alterada. La sobreexpresión de los factores de transcripción AtHB25 y COG1 provoca que las semillas presenten una mayor longevidad debido a una incrementada deposición de poliésteres lipídicos. Estas barreras de poliésteres lipídicos son la cutícula, formada por cutina, y la suberina. Ambas participan positivamente en la protección del embrión frente al ambiente exterior. Estudios genómicos de ambos factores de transcripción han demostrado que AtHB25 regula directamente a enzimas biosintéticos de los monómeros de suberina y cutina, y COG1 regula la expresión de enzimas relacionados con la polimerización de poliésteres lipídicos y lignina. La regulación en la que participa AtHB25 es muy importante debido a la alta conservación de las secuencias genómicas y funciones de AtHB25 en angiospermas, y parece involucrado en la respuesta a bajas temperaturas. Por otra parte, COG1, que está involucrado en la percepción de luz, regula parte del desarrollo del tegumento externo a través de la regulación de AP2, un factor clave en el establecimiento de la identidad de tejido de este tegumento de la cubierta de la semilla, donde se localiza la suberina. AtHB25 y COG1 están involucrados en la adaptación de la longevidad de la semilla a través de señales ambientales como la temperatura y la luz, respectivamente, regulando la deposición de poliésteres lipídicos.
[CAT] La longevitat de les llavors, o el temps que romanen les llavors viables, es de gran importància per la conservació de la biodiversitat, l'agricultura i l'economia. A més a més, l'estudi d'aquest paràmetre pot contribuir a conèixer millor els mecanismes moleculars comuns a tots els organismes per prevenir l'envelliment. Una de les principals estratègies de les llavor per retardar el seu envelliment consisteix detenir el seu metabolisme, mitjançant la seua deshidratació. Altres mecanismes moleculars per evitar danys son el seu aïllament de l'entorn per mitjan de la coberta de la llavor, i la producció d'antioxidants i altres molècules per evitar el dany oxidatiu, un dels principal causants del envelliment de les llavors. Els mecanismes de reparació mitiguen part del dany acumulat. L'organisme model Arabidopsis thaliana brinda la oportunitat de la realització d'estudis genòmics per a l'estudi de, en aquest cas, la longevitat de les llavors per descobrir nous factors genètics y mecanismes moleculars determinants. Aquest coneixement servirà per entendre millor els processos de deteriorament de les llavor i serà clau per augmentar la longevitat d'aquestes. Mitjançant l'ús de varietats naturals genotipades d'Arabidopsis thaliana i un estudi d'associació del genoma conegut com GWAS, seguits d'estudis de genètica inversa, s'han identificat 12 nous gens relacionats amb la longevitat de les llavors, relacionats amb la protecció de l'embrió, el control del dany oxidatiu, y la permeabilitat de la coberta de la llavor. El desenvolupament de la coberta de la llavor està determinada per factors de transcripció. Plantes mutants a diversos factors de transcripció involucrats al desenvolupament de la coberta de les llavors presenten una longevitat alterada. La sobreexpressió dels factors de transcripció AtHB25 i COG1 provoca que les llavors presenten una major longevitat degut a una deposició de polièsters lipídics incrementada. Aquestes barreres de polièsters lipídics son la cutícula, formada per cutina, i la suberina. Ambdues participen positivament la protecció de l'embrió enfront de l'entorn exterior. Estudis genòmics d'ambdós factors de transcripció han demostrat que AtHB25 directament regula a enzims biosintètics dels monòmers de suberina i cutina i COG1 regula enzims relacionats amb la polimerització de polièsters lipídics i lignines. La regulació en la que participa AtHB25 es molt important degut a l'alta conservació de les seqüències genòmiques i funcions de AtHB25 en angiospermes, i parteix estar involucrat en la resposta a baixes temperatures. Per altra banda, COG1, que està involucrat en la percepció de la llum, regula part del desenvolupament del integument extern mitjançant la regulació de AP2, un factor clau en l'establiment de la identitat de teixit de aquest integument de la coberta de la llavor, on es localitza la suberina. AtHB25 i COG1 estan involucrats en l'adaptació de la longevitat de la llavor per mitjan de senyals ambientals com la temperatura i la llum, respectivament, regulant la deposició de polièsters lipídics.
[EN] Seed longevity, or period that seeds remain viable, is important for biodiversity conservation, agriculture and economy. In addition, the study of this parameter could ease the knowledge about molecular mechanisms common to all organisms to prevent aging. One of the main strategies of seeds to reduce their aging consists to stop their metabolism, through drying. Other molecular mechanisms to avoid damages are the isolation from the environment with the seed coat, and the production of antioxidants and other molecules to avoid oxidative damage, one of the main seed aging causes. Repair mechanisms relieve part of the accumulated damage. The model plant Arabidopsis thaliana provides the opportunity to carry out genomic studies for the research of, in this case, seed longevity to discover determinant genetic factors and molecular mechanisms. This will serve to better understand seed deterioration processes and it will be key to increase seed longevity. Using natural genotyped varieties of Arabidopsis thaliana and a genome-wide association study (GWAS) followed by reverse genetic studies, 12 new genes related to seed longevity have been identified. They are related to embryo protection, oxidative damage control, and seed coat permeability. Seed coat development is determined by transcription factors. Mutant plants in some transcription factors involved in the seed coat development present altered seed longevity. The over-expression of the transcription factors AtHB25 and COG1 resulted in seeds with increased longevity due to an increased lipid polyester deposition. These lipid polyesters barriers are the cuticle, formed by cutin, and the suberin layer. Both participate positively in the embryo protection from the external environment. Genomic studies of both transcription factors have revealed that AtHB25 directly regulates biosynthetic enzymes of suberin and cutin monomers, and COG1 regulates the expression of enzymes related to the polymerization of lipid polyesters and lignin. The regulation involving AtHB25 is crucial due to the high conservation of genomic sequences and functions of AtHB25 in angiosperms, and it seems to be involved in the response to low temperatures. On the other hand, COG1, which is involved in light perception, regulates part of the development of the external integument through its regulation by AP2, a key factor in establishing the tissue identity of this seed coat integument, where suberin is located. AtHB25 and COG1 are involved in seed longevity adaptation through environmental signals such as temperature and light, respectively, regulating lipid polyesters deposition.
Agradezco a las instituciones públicas la inversión en investigación. Gracias a ella, los laboratorios, el personal y los distintos equipos se han podido financiar. Gaetano fue quien me ayudó enormemente conseguir la beca FPI del Ministerio de Economía y Competitividad BES-2015-072096, asociada al proyecto de investigación nacional BIO2014-52621-R-AR
Renard Meseguer, J. (2021). Identification of genes related to seed longevity in Arabidopsis thaliana using genomic molecular techniques [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/170554
TESIS
Compendio
Hinojosa, Galisteo Joan Carles 1993. "Exploring the butterfly speciation continuum : A study on butterfly speciation in the transition to genomic techniques." Doctoral thesis, Universitat Pompeu Fabra, 2021. http://hdl.handle.net/10803/672348.
Повний текст джерелаLes papallones són un dels animals més ben estudiats però, malgrat els esforços dedicats a la seva recerca, el coneixement que tenim sobre la seva diversitat i sobre els mecanismes que la generen és encara incomplet. Per tal d'entendre com les papallones diversifiquen, s'ha examinat el continu de l'especiació en sis casos mitjançant l'ús de la morfometria i de diverses tècniques genètiques (des de la seqüenciació de marcadors específics fins a la genòmica). L'anàlisi de la variació fenotípica i genètica combinada amb evidències sobre el flux genètic ha permès identificar els estats del continu de l'especiació, i.e. l'estudi de les relacions entre poblacions. Aquesta aproximació s'ha usat com a marc (1) per fer hipòtesis taxonòmiques fonamentades i (2) per extreure pistes sobre els mecanismes que dirigeixen l'especiació. Com a resultat, hem descrit i proposat diversos casos de tàxons que havien passat desapercebuts o que s'havien dividit excessivament. Documentem l'existència de tres tipus de mecanismes productors de diversitat en papallones: deriva, selecció i hibridació. La selecció actuà mitjançant l'adaptació a factors ambientals biòtics, que causaren desplaçament de caràcters reproductius, canvi de planta nutrícia i a\ll ocronia produïda per l'adaptació al període de floració de la planta nutrícia. Addicionalment, les tècniques genètiques emprades són avaluades i els seus avantatges i inconvenients discutits.
Padmanabhan, Babu roshan. "Taxano-genomics, a strategy incorporating genomic data into the taxonomic description of human bacteria." Thesis, Aix-Marseille, 2014. http://www.theses.fr/2014AIXM5056.
Повний текст джерелаMy PhD project was to create a pipeline for taxono-genomics for the comparison of multiple bacterial genomes. Secondly I automated the process of assembly (NGS) and annotation using various open source softwares as well as creating in house scripts for the lab. Finally we incorporated the pipeline in describing several bacterial species from out lab. This thesis is subdivided mainly into Taxono-genomics and Microbiogenomics. The reviews in taxono-genomics section, describes about the technological advances in genomics and metagenomics relevant to the field of medical microbiology and describes the strategy taxono-genomics in detail and how polyphasic strategy along with genomic approaches are reformatting the definition of bacterial taxonomy. The articles describes clinically important bacteria, their whole genome sequencing and the genomic, comparative genomic and taxono-genomic studies of these bacteria
Tanov, Emil Pavlov. "The identification of biologically important secondary structures in disease-causing RNA viruses." University of the Western Cape, 2012. http://hdl.handle.net/11394/4562.
Повний текст джерелаViral genomes consist of either deoxyribonucleic acid (DNA) or ribonucleic acid (RNA). The viral RNA molecules are responsible for two functions, firstly, their sequences contain the genetic code, which encodes the viral proteins, and secondly, they may form structural elements important in the regulation of the viral life-cycle. Using a host of computational and bioinformatics techniques we investigated how predicted secondary structure may influence the evolutionary dynamics of a group of single-stranded RNA viruses from the Picornaviridae family. We detected significant and marginally significant correlations between regions predicted to be structured and synonymous substitution constraints in these regions, suggesting that selection may be acting on those sites to maintain the integrity of certain structures. Additionally, coevolution analysis showed that nucleotides predicted to be base paired, tended to co-evolve with one another in a complimentary fashion in four out of the eleven species examined. Our analyses were then focused on individual structural elements within the genome-wide predicted structures. We ranked the predicted secondary structural elements according to their degree of evolutionary conservation, their associated synonymous substitution rates and the degree to which nucleotides predicted to be base paired coevolved with one another. Top ranking structures coincided with well characterized secondary structures that have been previously described in the literature. We also assessed the impact that genomic secondary structures had on the recombinational dynamics of picornavirus genomes, observing a strong tendency for recombination breakpoints to occur in non-coding regions. However, convincing evidence for the association between the distribution of predicted RNA structural elements and breakpoint clustering was not detected.
Visser, Johan Christiaan. "A study of genomic variation in and the development of detection techniques for potato virus Y in South Africa." Thesis, Stellenbosch : Stellenbosch University, 2008. http://hdl.handle.net/10019.1/21878.
Повний текст джерелаENGLISH ABSTRACT: Potato virus Y (PVY) is responsible for considerable yield losses in the South African potato industry. The incidence of this virus has greatly increased over the past few years. Even more worrying is the variation of symptoms observed during PVY infection and the recent appearance of the more virulent PVYNTN strain in local fields. This project aimed to investigate the possible genetic variation within the viral genome and to establish the origin of strains. The project also aimed to establish a dependable, area specific enzyme-linked immunosorbent assay (ELISA) to replace the currently used ELISAs. Currently seed potato certification is done using ELISA kits imported from Europe. These kits were developed for the detection of overseas variants of PVY and the use thereof in South Africa has in the past lead to false negatives. Finally, this project set out to develop, optimize and establish a sensitive and reliable real-time reverse transcriptase polymerase chain reaction (qRT-PCR) detection protocol for PVY. In the first part of the study the coat protein (CP) gene of PVY isolates from plant material obtained from various parts of South Africa was amplified using RT-PCR. The resulting cDNA was then sequenced directly or cloned into a vector and then sequenced. The resulting sequences were aligned in a data matrix with international reference sequences, analyzed and grouped according to strain. Examination of the CP gene within this matrix as well as phylogenetic analysis revealed six main groups of PVY. These six groups included the traditional PVYN and PVYO groups and a recombinant group. Furthermore it also revealed variants of PVYN and PVYO. These mutants and recombinants pose a threat as they may lead to South African strains of PVY expressing coat proteins which vary from those found overseas. This may render the currently used European ELISA method of detection less effective and subsequently result in an increase in viral prevalence. This reinforced the need for a detection method based on local viral strains. Phylogenetic and Simplot analysis also confirmed that a recombinant strain between PVYN and PVYO had evolved and that PVYNTN was such a recombinant. The second part of the study aimed to develop and establish detection methods based on local variants of PVY. This included the development of ELISA and qRT-PCR detection methods of PVY. Previously amplified cDNA of the PVY CP gene was cloned into an expression vector and successfully expressed. Antibodies produced against the recombinant protein, when used in ELISA, however, failed to achieve the required levels of sensitivity. This prompted the development of qRT-PCR detection methods for PVY. Primer combinations for PVY were designed using the previously established CP gene data matrix. A reliable and sensitive SYBR® Green I based qRT-PCR assay was developed for the detection of PVY. The assay effectively detected all known South African variants of PVY. Furthermore, a Taqman® assay was developed for the detection of all variants of PVY. The Taqman® assay was 10 fold less sensitive and does not allow for amplicon verification through melting curve analysis, but it does add more specificity due to the addition of the probe. Although these qRT-PCR detection methods are still too expensive to replace the routine diagnostics done with ELISA, they do offer the opportunity to screen valuable mother material and confirm borderline cases in seed certification.
AFRIKAANSE OPSOMMING: Aartappel virus Y (PVY) is verantwoordelik vir aansienlike opbrengsverliese in die Suid-Afrikaanse aartappelindustrie. Die insidensie van infeksie deur die virus het drasties toegeneem oor die afgelope jare. Wat egter meer kommerwekkend is, is die groter variasie in simptome van PVY infeksie en die onlangse voorkoms ‘n meer virulente ras, PVYNTN. Hierdie projek poog om moontlike genetiese variasie van PVY te ondersoek en om die oorsprong van rasse op te spoor. Die projek het ook gepoog ook om ‘n bruikbare, betroubare en area spesifieke “enzyme-linked immunosorbent assay” (ELISA) toets te ontwikkel om die huidige ingevoerde ELISA te vervang. Hierdie toetse is ontwikkel om oorsese variante van PVY op te spoor en die gebruik daarvan het in die verlede gelei tot vals negatiewes. Verder is daar ook ondersoek ingestel na die ontwikkeling van ‘n sensitiewe en betroubare “real-time reverse transcriptase polymerase chain reaction” (qRT-PCR) protokol vir die opsporing van PVY. In die eerste deel van die studie is die mantelproteïen geen van PVY isolate vanuit plant materiaal geamplifiseer deur die gebruik van RT-PCR. Hierdie materiaal is vanaf verskeie streke in Suid-Afrika ontvang. ‘n Volgordebepalingsreaksie is uitgevoer op gekloneerde of ongekloneerde cDNA verkry uit die RT-PCR. DNA volgordes is in ‘n data matriks geplaas en vergelyk met internationale volgordes om die plaaslike isolate te analiseer en te groepeer. Deur vergelyking en filogenetiese ontleding kon ses hoofgroepe van PVY geïdentifiseer word, wat tradisionele PVYN en PVYO, sowel as ‘n rekombinante ras en variante binne die tradisionele PVYN en PVYO groepe ingesluit het. Rekombinante en mutante kan veroorsaak dat Suid-Afrikanse rasse van PVY mantelproteïene uitdruk wat afwyk van die oorsese rasse wat tot gevolg mag hê dat die ELISAs van oorsee minder effektief kan wees en kan lei tot verhoogde virus voorkoms. Die realiteit en gevaar versterk die gedagte dat ‘n deteksie metode gebaseer op plaaslike virusse absoluut krities is. Filogenetiese sowel as Simplot analise het bevestig dat ’n mutante ras tussen PVYN en PVYO ontstaan het en dat PVYNTN ’n rekombinante ras is. Die tweede deel van die studie was daarop gemik om deteksie metodes te ontwikkel wat gebaseer was op plaaslike variante van PVY. Dit sluit die ontwikkeling van ELISA sowel as qRT-PCR deteksie van PVY in. Voorheen geamplifiseerde cDNA is in ‘n ekspressievektor gekloneer en suksesvol uitgedruk. Teenliggaampies teen die rekombinante proteïen, indien in ELISA aangewend, kon egter nie die nodige sensitiwiteit oplewer nie. Dit het aanleiding gegee tot ontwikkeling van qRT-PCR deteksie metodes. Inleier kombinasies vir PVY was ontwikkel deur die gebruik van die bestaande mantelproteïen geen data matrikse. ‘n Betroubare en sensitiewe SYBR® Green I qRT-PCR deteksie protokol was ontwikkel vir die effektiewe deteksie van alle bekende Suid-Afrikanse rasse van PVY. Verder is ‘n sogenaamde “Taqman®” protokol ook ontwikkel vir deteksie van alle rasse. Die “Taqman®” protokol was 10 voudiglik minder gevoelig and laat nie bevestiging deur smeltkurwe analise toe nie, maar verleen meer spesifisiteit deur die toevoeging van die “Taqman® probe”. Hierdie qRT-PCR deteksie metodes is tans te duur om as roetine diagnostiese toetse te gebruik en kan dus nie ELISA vervang nie, maar hulle bied wel die geleentheid om waardevolle moeder materiaal te toets en grensgevalle in aartappelsaad sertifisering te bevestig.
Книги з теми "Genomic techniques"
Dassanayake, Ranil S. Genomic and proteomic techniques: In post genomics era. Oxford: Alpha Science International, 2011.
Знайти повний текст джерелаGenomic structural variants: Methods and protocols. New York: Humana Press, 2012.
Знайти повний текст джерелаM, Hernandez Lyla, Institute of Medicine (U.S.). Roundtable on Translating Genomic-Based Research for Health., Institute of Medicine (U.S.). Board on Health Sciences Policy., and National Academies Press (U.S.), eds. Diffusion and use of genomic innovations in health and medicine: Workshop summary. Washington, D.C: National Academies Press, 2008.
Знайти повний текст джерелаSabourin, Marc. Evaluation of DNA extraction techniques for use in plasmid localization and a genomic library for Ophiostoma ulmi (Buisman) Nannf. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1993.
Знайти повний текст джерелаH, Bergman Nicholas, ed. Comparative genomics. Totowa, NJ: Humana Press, 2007.
Знайти повний текст джерелаDeutsche Forschungsgemeinschaft. Senatskommission für Grundsatzfragen der Genforschung., ed. Humangenomforschung: Perspektiven und Konsequenzen. Weinheim: Wiley-VCH, 2000.
Знайти повний текст джерелаDictionary of DNA and genome technology. 3rd ed. Chichester, West Sussex: John Wiley & Sons, 2012.
Знайти повний текст джерелаSensen, C. W. Handbook of genome research: Genomics, proteomics, metabolomics, bioinformatics, ethical, and legal issues. Weinheim: Wiley-VCH, 2005.
Знайти повний текст джерелаMuppalaneni, Naresh Babu, and Vinit Kumar Gunjan, eds. Computational Intelligence Techniques for Comparative Genomics. Singapore: Springer Singapore, 2015. http://dx.doi.org/10.1007/978-981-287-338-5.
Повний текст джерелаGenetics: Analysis of genes and genomes. 8th ed. Sudbury, Mass: Jones & Bartlett Learning, 2012.
Знайти повний текст джерелаЧастини книг з теми "Genomic techniques"
Onuchic, Luiz F., and Gregory G. Germino. "Genomic Libraries." In Techniques in Molecular Medicine, 261–72. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-59811-1_17.
Повний текст джерелаHamlet, Stephen, Eugen Petcu, and Saso Ivanovski. "Genomic Microarray Analysis." In Handbook of Vascular Biology Techniques, 391–405. Dordrecht: Springer Netherlands, 2015. http://dx.doi.org/10.1007/978-94-017-9716-0_30.
Повний текст джерелаPal, Aruna. "Conventional and Basic Genomic Techniques." In Springer Protocols Handbooks, 1–29. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1818-9_1.
Повний текст джерелаSurzycki, Stefan. "Preparation of Genomic DNA from Bacteria." In Basic Techniques in Molecular Biology, 79–100. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-56968-5_4.
Повний текст джерелаMarlowe, Elizabeth M., and Donna M. Wolk. "Pathogen Detection in the Genomic Era." In Advanced Techniques in Diagnostic Microbiology, 505–23. Boston, MA: Springer US, 2006. http://dx.doi.org/10.1007/0-387-32892-0_28.
Повний текст джерелаBudhlakoti, Neeraj, Sayanti Guha Majumdar, Amar Kant Kushwaha, Chirag Maheshwari, Muzaffar Hasan, D. C. Mishra, Anuj Kumar, Jyotika Bhati, and Anil Rai. "Tools and Techniques for Genomic Imprinting." In Springer Protocols Handbooks, 335–46. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2533-0_18.
Повний текст джерелаSurzycki, Stefan. "Preparation of Genomic DNA from Animal Cells." In Basic Techniques in Molecular Biology, 33–56. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-56968-5_2.
Повний текст джерелаSurzycki, Stefan. "Preparation of Genomic DNA from Plant Cells." In Basic Techniques in Molecular Biology, 57–78. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-56968-5_3.
Повний текст джерелаSobti, RC, Apurav Sharma, and Sanjeev Kumar Soni. "Applications of Biotechnological Techniques in Mitigating Environmental Concerns." In Genomic, Proteomics, and Biotechnology, 249–312. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003220831-17.
Повний текст джерелаJankowicz-Cieslak, Joanna, Ivan L. Ingelbrecht, and Bradley J. Till. "Mutation Detection in Gamma-Irradiated Banana Using Low Coverage Copy Number Variation." In Efficient Screening Techniques to Identify Mutants with TR4 Resistance in Banana, 113–27. Berlin, Heidelberg: Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-64915-2_8.
Повний текст джерелаТези доповідей конференцій з теми "Genomic techniques"
Phogat, Manu, and Dharmender Kumar. "Feature Selection Techniques for Genomic Data." In 2022 International Conference on Machine Learning, Big Data, Cloud and Parallel Computing (COM-IT-CON). IEEE, 2022. http://dx.doi.org/10.1109/com-it-con54601.2022.9850466.
Повний текст джерелаGaldi, Paola, Angela Serra, Dario Greco, and Roberto Tagliaferri. "Effectiveness of projection techniques in genomic data analysis." In 2016 IEEE 2nd International Forum on Research and Technologies for Society and Industry Leveraging a better tomorrow (RTSI). IEEE, 2016. http://dx.doi.org/10.1109/rtsi.2016.7740567.
Повний текст джерелаBhonde, Swati B., and Jayashree R. Prasad. "Deep Learning Techniques in Cancer Prediction Using Genomic Profiles." In 2021 6th International Conference for Convergence in Technology (I2CT). IEEE, 2021. http://dx.doi.org/10.1109/i2ct51068.2021.9417985.
Повний текст джерелаMaheeshanake, S. D. L. H., M. W. A. C. R. Wijesinghe, A. R. Weerasinghe, and M. A. I. Perera. "Unsupervised Techniques for Meta-Analysis of Cancer Genomic Data." In 2020 20th International Conference on Advances in ICT for Emerging Regions (ICTer). IEEE, 2020. http://dx.doi.org/10.1109/icter51097.2020.9325475.
Повний текст джерелаHammad, Muhammed S., Vidan F. Ghoneim, and Mai S. Mabrouk. "Detection of COVID-19 Using Genomic Image Processing Techniques." In 2021 3rd Novel Intelligent and Leading Emerging Sciences Conference (NILES). IEEE, 2021. http://dx.doi.org/10.1109/niles53778.2021.9600525.
Повний текст джерелаPandey, Gaurav, Gowtham Atluri, Gang Fang, Rohit Gupta, Michael Steinbach, and Vipin Kumar. "Association analysis techniques for analyzing complex biological data sets." In 2009 IEEE International Workshop on Genomic Signal Processing and Statistics (GENSIPS). IEEE, 2009. http://dx.doi.org/10.1109/gensips.2009.5174378.
Повний текст джерелаKaplan, Roman, Leonid Yavits, and Ran Ginosar. "POSTER: BioSEAL: In-Memory Biological Sequence Alignment Accelerator for Large-Scale Genomic Data." In 2019 28th International Conference on Parallel Architectures and Compilation Techniques (PACT). IEEE, 2019. http://dx.doi.org/10.1109/pact.2019.00044.
Повний текст джерелаKaur, Amandeep, Ajay Pal Singh Chauhan, and Ashwani Kumar Aggarwal. "Machine Learning Based Comparative Analysis of Methods for Enhancer Prediction in Genomic Data." In 2019 2nd International Conference on Intelligent Communication and Computational Techniques (ICCT). IEEE, 2019. http://dx.doi.org/10.1109/icct46177.2019.8969054.
Повний текст джерелаZokaee, Farzaneh, Mingzhe Zhang, and Lei Jiang. "FindeR: Accelerating FM-Index-Based Exact Pattern Matching in Genomic Sequences through ReRAM Technology." In 2019 28th International Conference on Parallel Architectures and Compilation Techniques (PACT). IEEE, 2019. http://dx.doi.org/10.1109/pact.2019.00030.
Повний текст джерелаOcchipinti, Annalisa, and Claudio Angione. "A Computational Model of Cancer Metabolism for Personalised Medicine." In Building Bridges in Medical Science 2021. Cambridge Medicine Journal, 2021. http://dx.doi.org/10.7244/cmj.2021.03.001.3.
Повний текст джерелаЗвіти організацій з теми "Genomic techniques"
Abbott, Albert G., Doron Holland, Douglas Bielenberg, and Gregory Reighard. Structural and Functional Genomic Approaches for Marking and Identifying Genes that Control Chilling Requirement in Apricot and Peach Trees. United States Department of Agriculture, September 2009. http://dx.doi.org/10.32747/2009.7591742.bard.
Повний текст джерелаFluhr, Robert, and Volker Brendel. Harnessing the genetic diversity engendered by alternative gene splicing. United States Department of Agriculture, December 2005. http://dx.doi.org/10.32747/2005.7696517.bard.
Повний текст джерелаWeller, Joel I., Derek M. Bickhart, Micha Ron, Eyal Seroussi, George Liu, and George R. Wiggans. Determination of actual polymorphisms responsible for economic trait variation in dairy cattle. United States Department of Agriculture, January 2015. http://dx.doi.org/10.32747/2015.7600017.bard.
Повний текст джерелаHeifetz, Yael, and Michael Bender. Success and failure in insect fertilization and reproduction - the role of the female accessory glands. United States Department of Agriculture, December 2006. http://dx.doi.org/10.32747/2006.7695586.bard.
Повний текст джерелаWentworth, Jonathan, and David Rapley. Genome edited animals. Parliamentary Office of Science and Technology, November 2022. http://dx.doi.org/10.58248/pb50.
Повний текст джерелаOvcharenko, I. FY06 LDRD Final Report "Development of Computational Techniques For Decoding The Language of Genomes". Office of Scientific and Technical Information (OSTI), January 2007. http://dx.doi.org/10.2172/899447.
Повний текст джерелаEhrlich, Marcelo, John S. Parker, and Terence S. Dermody. Development of a Plasmid-Based Reverse Genetics System for the Bluetongue and Epizootic Hemorrhagic Disease Viruses to Allow a Comparative Characterization of the Function of the NS3 Viroporin in Viral Egress. United States Department of Agriculture, September 2013. http://dx.doi.org/10.32747/2013.7699840.bard.
Повний текст джерелаMishra, Bishnu P., and James M. Reecy. Generation of Bovine Genetic Markers by Representational Difference Analysis: a genome subtraction technique. Ames (Iowa): Iowa State University, January 2004. http://dx.doi.org/10.31274/ans_air-180814-457.
Повний текст джерелаKent, Stephen. Use of Modern Chemical Protein Synthesis and Advanced Fluorescent Assay Techniques to Experimentally Validate the Functional Annotation of Microbial Genomes. Office of Scientific and Technical Information (OSTI), July 2012. http://dx.doi.org/10.2172/1087659.
Повний текст джерелаWeller, Joel, Harris Lewin, Micha Ron, George Wiggans, and Paul VanRaden. A Systematic Genome Search for Genes Affecting Economic Traits Dairy Cattle with the Aid of Genetic Markers. United States Department of Agriculture, April 1999. http://dx.doi.org/10.32747/1999.7695836.bard.
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