Relevant bibliographies by topics / PCR5

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'PCR5'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "PCR5"

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Pietkiewicz, Tadeusz. "Fusion of Identification Information from ESM Sensors and Radars Using Dezert–Smarandache Theory Rules." Remote Sensing 15, no. 16 (2023): 3977. http://dx.doi.org/10.3390/rs15163977.

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This paper presents a method of fusion of identification (attribute) information provided by two types of sensors: combined primary and secondary (IFF) surveillance radars and ESMs (electronic support measures). In the first section, the basic taxonomy of attribute identification is adopted in accordance with the standards of STANAG 1241 ed. 5 and STANAG 1241 ed. 6 (draft). These standards provide the following basic values of the attribute identifications: FRIEND; HOSTILE; NEUTRAL; UNKNOWN; and additional values, namely ASSUMED FRIEND and SUSPECT. The basis of theoretical considerations is De
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Yang, Hongjing, Zhiying Shan, Jaewha Kim, et al. "Regulatory Role of PopN and Its Interacting Partners in Type III Secretion of Pseudomonas aeruginosa." Journal of Bacteriology 189, no. 7 (2007): 2599–609. http://dx.doi.org/10.1128/jb.01680-06.

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ABSTRACT The type III secretion system (T3SS) of Pseudomonas aeruginosa plays a significant role in pathogenesis. We have previously identified type III secretion factor (TSF), which is required for effective secretion of the type III effector molecules, in addition to the low calcium signal. TSF includes many low-affinity high-capacity calcium binding proteins, such as serum albumin and casein. A search for the TSF binding targets on the bacterial outer membrane resulted in identification of PopN, a component of the T3SS that is readily detectable on the bacterial cell surface. PopN specifica
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关, 欣. "NP-PCR5 Fusion Algorithm and Application." Journal of Sensor Technology and Application 07, no. 02 (2019): 13–18. http://dx.doi.org/10.12677/jsta.2019.72002.

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Bröms, Jeanette E., Petra J. Edqvist, Katrin E. Carlsson, Åke Forsberg, and Matthew S. Francis. "Mapping of a YscY Binding Domain within the LcrH Chaperone That Is Required for Regulation of Yersinia Type III Secretion." Journal of Bacteriology 187, no. 22 (2005): 7738–52. http://dx.doi.org/10.1128/jb.187.22.7738-7752.2005.

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ABSTRACT Type III secretion systems are used by many animal and plant interacting bacteria to colonize their host. These systems are often composed of at least 40 genes, making their temporal and spatial regulation very complex. Some type III chaperones of the translocator class are important regulatory molecules, such as the LcrH chaperone of Yersinia pseudotuberculosis. In contrast, the highly homologous PcrH chaperone has no regulatory effect in native Pseudomonas aeruginosa or when produced in Yersinia. In this study, we used LcrH-PcrH chaperone hybrids to identify a discrete region in the
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Asthana, M., K. P. Maheshwari, and M. S. Sodha. "Nonlinear relativistic self-focusing of laser radiation in plasmas: Arbitrary intensity." Laser and Particle Beams 12, no. 4 (1994): 623–32. http://dx.doi.org/10.1017/s0263034600008508.

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A paraxial theory of relativistic self-focusing of a Gaussian laser beam in plasmas, when the nonlinear part of the effective dielectric constant is arbitrarily large, is presented. The plasma is taken to be homogeneous without any density fluctuations being necessary. The approach of Akhmanov et al. based on the WKB and paraxial ray approximations has been followed. It is seen that the saturating nature of nonlinearity leads to two values of critical power of the beam (Pcrl and Pcr2) for self-focusing. When the power of the beam P lies between the two critical values (i.e., Pcr1 < P < P
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Anguita-Maeso, Manuel, Carmen Haro, Juan A. Navas-Cortés, and Blanca B. Landa. "Primer Choice and Xylem-Microbiome-Extraction Method Are Important Determinants in Assessing Xylem Bacterial Community in Olive Trees." Plants 11, no. 10 (2022): 1320. http://dx.doi.org/10.3390/plants11101320.

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Understanding the unique and unexplored microbial environment of xylem sap is starting to be of relevant importance for plant health, as it could include microbes that may protect plants against xylem-limited pathogens, such as Verticillium dahliae and Xylella fastidiosa. In this study, we evaluated the effects that the method for extracting the xylem bacterial communities, the plant age and the PCR primers may have on characterizing the xylem-bacterial-community composition by using an NGS approach. Xylem sap was extracted from xylem vessels by using a Scholander pressure chamber, or by macer
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Asthana, Meenu, M. S. Sodha, and K. P. Maheshwari. "Relativistic self-focusing of laser beams in time-harmonic plane waves: arbitrary intensity." Journal of Plasma Physics 51, no. 1 (1994): 155–62. http://dx.doi.org/10.1017/s002237780001744x.

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This paper presents a paraxial theory of relativistic self-focusing of a Gaussian laser beam in plasma for a time-harmonic plane wave at arbitrary beam intensity. Since the relativistic mechanism is instantaneous, the theory is also applicable to self-focusing of laser pulses. The analysis leads to two values for the critical beam power for self-focusing, Pcr1 and Pcr2. When P < Pcr1 < Pcr2, the beam diverges. When Pcr1 <P <pcr2, it first converges, then diverges, and so on. When P > Pcr2 it first diverges, then converges, and so on.
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Bender, Kelly S., Ching Shang, Romy Chakraborty, Sara M. Belchik, John D. Coates, and Laurie A. Achenbach. "Identification, Characterization, and Classification of Genes Encoding Perchlorate Reductase." Journal of Bacteriology 187, no. 15 (2005): 5090–96. http://dx.doi.org/10.1128/jb.187.15.5090-5096.2005.

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ABSTRACT The reduction of perchlorate to chlorite, the first enzymatic step in the bacterial reduction of perchlorate, is catalyzed by perchlorate reductase. The genes encoding perchlorate reductase (pcrABCD) in two Dechloromonas species were characterized. Sequence analysis of the pcrAB gene products revealed similarity to α- and β-subunits of microbial nitrate reductase, selenate reductase, dimethyl sulfide dehydrogenase, ethylbenzene dehydrogenase, and chlorate reductase, all of which are type II members of the microbial dimethyl sulfoxide (DMSO) reductase family. The pcrC gene product was
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Sodha, M. S., S. Konar, and K. P. Maheshwari. "Steady-state self-focusing of rippled laser beams in plasmas: arbitrary nonlinearity." Journal of Plasma Physics 48, no. 1 (1992): 107–18. http://dx.doi.org/10.1017/s0022377800016408.

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This paper presents an analysis of the self-focusing of a rippled Gaussian laser beam in a plasma when the nonlinear part of the effective dielectric constant is arbitrarily large. Considering the nonlinearity to arise from ponderomotive, collisional or thermal-conduction phenomena and following the approach of Akhmanov, Sukhorukov and Khokhlov (which is based on the WKB and paraxial-ray approximation) the phenomenon of self-focusing of rippled laser beams is studied for arbitrary magnitude of nonlinearity. For ponderomotive and collisional nonlinearities, the present theory leads to two value
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Abbasi, Ibrahim. "Strategy for DNA extraction and detection from insect pests in stored home grain samples RESEARCH." Al-Quds Journal for Academic Research 01, no. 1 (2021): 24–32. http://dx.doi.org/10.47874/2021p3.

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Stored grains are subjected to infestations with more than 60 species of insects, that responsible for millions of dollars’ loss and cause several health problems including allergies and gastrointestinal disorders. Traditional detection techniques are laborious, expensive and not sensitive to detect insect contamination at the egg and larvae stages. Therefore, alternative methods are needed for rapid and sensitive detection. One obvious approach is to develop a molecular approach utilizing genetic information of the potential insect species that infest grains for amplification of specific targ
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Dissertations / Theses on the topic "PCR5"

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Cravello, Laëtitia. "Etudes structurales des protéines par spectrométrie de masse couplée aux échanges hydrogène/deuterium et à la réticulation chimique." Université Joseph Fourier (Grenoble), 2005. https://tel.archives-ouvertes.fr/tel-00009698.

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Les protéines sont impliquées dans de nombreux processus biologiques. Il est nécessaire pour comprendre en détail leur fonction et leur mode d’action afin d’obtenir des informations sur leur structure et sur leurs interactions éventuelles avec leurs partenaires. Le travail réalisé durant cette thèse a consisté à développer deux méthodes innovantes utilisant la spectrométrie de masse pour étudier la structure des protéines et à appliquer ces méthodes à une problématique biologique. Nous avons optimisé une méthode associant les échanges H/D et la spectrométrie de masse sur une protéine modèle, l
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Caye-Eude, Aurélie. "Génétique et architecture clonale des leucémies myélomonocytaires juvéniles sporadiques et syndromiques." Thesis, Sorbonne Paris Cité, 2018. http://www.theses.fr/2018USPCC173/document.

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La LMMJ est un syndrome myéloprolifératif et myélodysplasique rare du jeune enfant, initiée par des mutations classiquement décrites comme mutuellement exclusives de RAS (NRAS, KRAS) ou de régulateurs de la voie RAS (PTPN11, NF1 ou CBL). Ces mutations, somatiques ou constitutionnelles, entraînent l’hyperactivation de cette voie de signalisation et une hypersensibilité spécifique au GM-CSF. La LMMJ est une hémopathie sévère dont le seul traitement est l’allogreffe de moelle osseuse. Cependant sa présentation et son évolution sont particulièrement hétérogènes puisqu’une transformation en leucémi
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Salgado, Vanessa Riesz. "Desenvolvimento de Reações em Cadeia pela Polimerase (PCRs) para o diagnóstico diferencial das principais espécies de Brucella." Universidade de São Paulo, 2011. http://www.teses.usp.br/teses/disponiveis/10/10134/tde-11102012-115215/.

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A brucelose é uma doença altamente contagiosa, responsável por grandes prejuízos econômicos e de saúde pública. É causada por bactérias do gênero Brucella, cujas espécies e seus biovares costumam ser caracterizados pelo isolamento e identificação de características fenotípicas da colônia. Dificuldades como, o perigo na manipulação dos microrganismos, processos laboriosos de tipificação, demora na obtenção de resultados e a instabilidade de características fenotípicas ou isolamento de linhagens atípicas dificultam a tipificação e encorajaram a busca de técnicas mais sensíveis e específicas, com
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Minnella, Walter Settimo Leonardo. "Development of microfluidic tools for biological applications." Thesis, Bordeaux, 2017. http://www.theses.fr/2017BORD0664.

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Cette thèse traite le développement de dispositifs, basés sur la technologie "laboratoire sur puce"(LOC) qui visent à contrôler l'environnement des systèmes biologiques pour des applications macro et microbiologiques. En effet, les caractéristiques de la microfluidique permettent de manipuler l'environnement cellulaire à un niveau supérieur à celui du degré de contrôle atteignable avec les techniques ordinaires. Dans ce travail de thèse sera explorée la possibilité de profiter de ces fonctions afin de développer des outils de diagnostic peu coûteux et pourtant efficaces. En particulier, on rap
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Chisty, L. T. "PcrA function in plasmid replication." Thesis, University College London (University of London), 2014. http://discovery.ucl.ac.uk/1427879/.

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PcrA is a DNA helicase involved in unwinding plasmi ds as a part of a complex in asymmetric rolling - circle replication of certain plasmids carrying antibiotic resistance genes. PcrA translocates on single stranded DNA by coupling ATP hydrolysis to movement on DNA. Initiator protein, RepD is required to nick supercoiled plasmid site - specifically and open an ssDNA stretch that PcrA can bind. The presence of RepD is needed throughout plasmid unwinding to maintain processivity. Using fluorescent - based techniques, PcrA helicase mechanistic functions and interactions with different components
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Rozales, Franciéli Pedrotti. "Real time-pcr e nested-pcr no diagnóstico da tuberculose pulmonar." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2013. http://hdl.handle.net/10183/72990.

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A tuberculose (TB) é um importante problema de saúde pública, portanto, é necessário o desenvolvimento de novas ferramentas para a detecção rápida e confiável do Mycobacterium tuberculosis, prevenindo a transmissão da TB. O objetivo deste estudo foi avaliar dois testes moleculares para detecção de bactérias do Complexo Mycobacterium tuberculosis (MTBC) diretamente de amostras clínicas. Foi realizado um estudo transversal, no qual foram selecionadas 124 amostras respiratórias. As amostras foram avaliadas por dois testes moleculares “in house” para detecção do MTBC: NESTED-PCR (NPCR) e Real Time
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Ziebell, Kim. "Evaluation of PCR and PCR-RFLP protocols to identify the Shiga toxins." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape2/PQDD_0026/MQ51107.pdf.

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Hill, Philip John. "PCR based gene engineering." Thesis, University of Nottingham, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317040.

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Costa, Luciana Fachini da [UNESP]. "Avaliação comparativa entre PCR gênero-específica, PCR espécie-específica e nested PCR espécie-específica no diagnóstico da infecção por Brucella ovis." Universidade Estadual Paulista (UNESP), 2010. http://hdl.handle.net/11449/94670.

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Made available in DSpace on 2014-06-11T19:27:17Z (GMT). No. of bitstreams: 0 Previous issue date: 2010-06-29Bitstream added on 2014-06-13T20:08:22Z : No. of bitstreams: 1 costa_lf_me_botfmvz.pdf: 594547 bytes, checksum: 7d609573704d70bd41e6633e86629767 (MD5)<br>Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)<br>Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)<br>O diagnóstico da infecção por Brucella ovis em ovinos usualmente é realizado por meio de exame clínico, testes sorológicos e bacteriologia. Devido às limitações apresentadas pelas técnicas, o diagnós
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Costa, Luciana Fachini da. "Avaliação comparativa entre PCR gênero-específica, PCR espécie-específica e nested PCR espécie-específica no diagnóstico da infecção por Brucella ovis /." Botucatu : [s.n.], 2010. http://hdl.handle.net/11449/94670.

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Resumo: O diagnóstico da infecção por Brucella ovis em ovinos usualmente é realizado por meio de exame clínico, testes sorológicos e bacteriologia. Devido às limitações apresentadas pelas técnicas, o diagnóstico é geralmente obtido mediante aplicação de duas ou mais técnicas para obtenção de um resultado conclusivo. A Reação em Cadeia pela Polimerase (PCR) tem sido utilizada como ferramenta diagnóstica aplicável, pois é sensível, pouco dispendiosa, rápida, simples de ser realizada e permite o diagnóstico específico do agente infectante. Neste trabalho foram realizados dois experimentos. No pri
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Books on the topic "PCR5"

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Domingues, Lucília, ed. PCR. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7060-5.

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Newton, C. R. PCR. BIOS Scientific in association with the Biochemical Society, 1994.

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McPherson, M. J. PCR. BIOS Scientific Publishers, 2000.

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Domingues, Lucília, ed. PCR. Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3358-8.

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A, Graham, ed. PCR. 2nd ed. BIOS Scientific Publishers, 1997.

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D, Siebert Paul, ed. The PCR technique: RT-PCR. Bio-Techniques Books, 1998.

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W, Larrick James, ed. The PCR technique: Quantitative PCR. BioTechniques Books, 1997.

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Sarkar, Gobinda. PCR in Neuroscience: PCR in Neuroscience. Elsevier, 1995.

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White, Bruce A. PCR Protocols. Humana Press, 1993. http://dx.doi.org/10.1385/0896032442.

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Bartlett, John M. S., and David Stirling. PCR Protocols. Humana Press, 2003. http://dx.doi.org/10.1385/1592593844.

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Book chapters on the topic "PCR5"

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Andrus, Alex. "Chemical methods for 5’ non- isotopic labelling of PCR probes and primers." In PCR2. Oxford University PressOxford, 1995. http://dx.doi.org/10.1093/oso/9780199634255.003.0003.

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Abstract Synthetic oligonucleotides are now accessible to most laboratories conducting molecular biology experiments. The decreases in preparation time, costs, and the expertise required have enabled the annual production and use of several million oligonucleotides (1). PCR undoubtedly consumes more of these sequences than any other application. Many PCR experiments require the covalent attachment (labelling, tagging, conjugation) of small molecules to perform ancillary functions, in addition to base-specific annealing to complementary nucleic acid and 3’ chain extension by polymerase. The lab
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Bagasra, Omar, Lisa E. Bobroski, Muhammed Amjad, Roger J. Pomerantz,, and John Hansen. "Application of in situ PCR techniques to human tissues." In PCR3. Oxford University PressOxford, 1997. http://dx.doi.org/10.1093/oso/9780199636327.003.0007.

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Abstract Since we first reported our findings regarding in situ amplification of the HIV-1 gag gene in an HIV-1-infected cell line in March 1990 (1), there has been an explosion of research in the area of in situ polymerase chain reaction (in situ PCR). There are over 300 publications describing various forms of in situ gene amplifications (reviewed in 2,3,13) , identifying various infectious agents, tumour marker genes, cytokines, growth factors and their receptors, and other genetic elements of interest, in peer-reviewed journals (1–25). The solution-based PCR method for amplifying defined g
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Patterson, Bruce K. "Applications and modifications of PCR in situ hybridization." In PCR3. Oxford University PressOxford, 1997. http://dx.doi.org/10.1093/oso/9780199636327.003.0008.

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Abstract The localization of genes in specific cells and tissues has been instrumental in many disciplines for defining disease pathogenesis. This pursuit has united scientists studying such diverse topics as oncogene expression, viral infections, and plant pathology. In its earliest incarnation, molecular biologists met with pathologists to use large subgenomic probes to detect genes in situ. This process relied on the intrinsic amplification of genes during transcription into mRNA to accumulate enough target to be detected.
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Welsh, John, Manuel Perucho, Miguel Peinado, David Ralph, and Michael Mcclelland. "Fingerprinting of DNA and RNA using arbitrarily primed PCR." In PCR2. Oxford University PressOxford, 1995. http://dx.doi.org/10.1093/oso/9780199634255.003.0011.

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Abstract Arbitrarily primed PCR is a modification of PCR that provides an informationrich fingerprint of genomic DNA. This method is based on the selective amplification of genomic sequences that, by chance, are flanked by adequate matches to an arbitrarily chosen primer. If two template genomic DNA sequences are different, their arbitrarily primed PCR products display different banding patterns. Such differences can be exploited in ways largely analogous to the uses of restriction fragment length polymorphisms, including genetic mapping, taxonomy, phylogenetics, and the detection of mutations
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Kjijo, K. K., and G. Ruano. "Optimizing PCR." In PCR2. Oxford University PressOxford, 1995. http://dx.doi.org/10.1093/oso/9780199634255.003.0001.

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Abstract Although this entire volume is intended to provide explicit, practical guidelines and protocols for PCR in its myriad manifestations, we wish to start with a series of perspectives on various aspects of the several processes that are collectively called the polymerase chain reaction. No individual protocol will be optimal for all PCR reactions, nor will any single, simple set of variables to be optimized necessarily produce a functioning protocol for a specific case. Therefore, in order to optimize PCR, the researcher must have a mental picture of the underlying processes and be able
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Wahlberg, Johan, Thomas Hultman, and Mathias Uhlén. "Solid phase sequencing of PCR products." In PCR2. Oxford University PressOxford, 1995. http://dx.doi.org/10.1093/oso/9780199634255.003.0005.

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Abstract Solid phase methods have proven to be extremely useful for the separation and synthesis of biomolecules. The advantages of solid phase approaches are a combination of good yields and reproducible results. Furthermore, the facilitated separation of the solid phase from the reaction solution allows routine methods suitable for automation to be designed. This chapter describes protocols for the use of magnetic beads in combination with the biotinstreptavidin system for solid phase DNA sequencing of PCR products. The use of a solid support for the preparation of sequencing templates enabl
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Edwards, Jean Baptiste Dumas Milne, Philippe Ravassard, Christine Icard-Liepkalns, and Jacques Mallet. "cDNA cloning by RT-PCR." In PCR2. Oxford University PressOxford, 1995. http://dx.doi.org/10.1093/oso/9780199634255.003.0006.

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Abstract The methods available for the characterization of mRNAs have progressed enormously since the mid 1970s. This includes the isolation of RNAs, cloning and bacterial amplification of specific mRNAs, Northern blotting studies, in situ hybridization, and nuclease protection assays that allow the description of mRNA metabolism in cells.
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Mclean, Michael J. "Use of speciality phosphoramidites in PCR." In PCR2. Oxford University PressOxford, 1995. http://dx.doi.org/10.1093/oso/9780199634255.003.0002.

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Abstract In the decade or so since the introduction of automated oligonucleotide synthesizers, the ability to use these machines for the incorporation of unnatural residues into nucleic acids has led to the chemical synthesis of a wide variety of phosphoramidite derivatives. When included in an oligomer synthesis, these entities provide a source of site-specific, stable modifications of the backbone, thus enabling a rigorous determination of their biochemical effects.
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Gosden, John R., Ernst J. M. Speel,, and Yoshiro Shibasaki. "Primed in situ DNA synthesis (PRINS)." In PCR3. Oxford University PressOxford, 1997. http://dx.doi.org/10.1093/oso/9780199636327.003.0006.

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Abstract Techniques for visualizing DNA sequences on chromosomes have come a long way since Pardue and Gall (1,2) and John et al. (3) first showed that repeated sequences could be visualized in nuclei or on chromosomes by isotopic in situ hybridization. In those first experiments, the probe (RNA or DNA) was made radioactive with 3H by growing cells in the presence of labelled precursors, purifying the nucleic acid, and hybridizing it in situ to cytological preparations. Later came the use of Escherichia coli RNA polymerase to make a complementary RNA from a known DNA template (4,5). Refinement
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Stamm, Stefan, and Jurgen Brosius. "Solid phase PCR." In PCR2. Oxford University PressOxford, 1995. http://dx.doi.org/10.1093/oso/9780199634255.003.0004.

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Abstract The method of solid-anchored PCR uses specific oligonucleotides coupled to a solid phase as primers for cDNA synthesis (1) and results in cDNA that is covalently linked to the solid phase. Typical solid phase matrices are agarose (1), acrylamide (1), magnetic (2-4), or latex beads (5). A solid phase with cDNA attached, generated using oligo(dT) as a primer, contains sequence information similar to a cDNA library, that is, it represents a ‘solid phase library’ (1, 3, 4). The cDNA that is attached to the solid phase can be used directly as a template for PCR reactions or can be modified
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Conference papers on the topic "PCR5"

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Mendoza, Ezekiel, Alzter Aquino, Paul Jason Co, Marc Rosales, Maria Theresa De Leon, and John Richard Hizon. "CARE-PCR: A Portable OpenPCR Thermocyler." In TENCON 2024 - 2024 IEEE Region 10 Conference (TENCON). IEEE, 2024. https://doi.org/10.1109/tencon61640.2024.10902898.

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Li, L. J., J. J. Ding, J. J. Lv, and H. B. Xu. "Adaptive fusion algorithm with DST and PCR5." In IET International Radar Conference 2015. Institution of Engineering and Technology, 2015. http://dx.doi.org/10.1049/cp.2015.1009.

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Li, Xinde, Xinhan Huang, Min Wang, Jiansheng Xu, and Hongbo Zhang. "DSmT Coupling with PCR5 for Mobile Robot's Map Reconstruction." In 2006 International Conference on Mechatronics and Automation. IEEE, 2006. http://dx.doi.org/10.1109/icma.2006.257742.

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Lujun Li, Yanhong Duan, Hui Xie, and Changxi Li. "Study on self-adaptive fusion model with DST and PCR5." In 2016 IEEE Advanced Information Management, Communicates, Electronic and Automation Control Conference (IMCEC). IEEE, 2016. http://dx.doi.org/10.1109/imcec.2016.7867203.

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Kirchner, Alois, Frederic Dambreville, Francis Celeste, Jean Dezert, and Florentin Smarandache. "Application of probabilistic PCR5 fusion rule for multisensor target tracking." In 2007 10th International Conference on Information Fusion. IEEE, 2007. http://dx.doi.org/10.1109/icif.2007.4408058.

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Dezert, Jean, Albena Tchamova, Florentin Smarandache, and Pavlina Konstantinova. "Target Type Tracking with PCR5 and Dempster's rules: A Comparative Analysis." In 2006 9th International Conference on Information Fusion. IEEE, 2006. http://dx.doi.org/10.1109/icif.2006.301556.

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Qiang Guo, F. Smarandache, Hai-peng Wang, Shi-you Xu, and Xian Li. "A Reasoning Method in Conditional Evidential Networks based on DSm-PCR5." In 6th International Conference on Wireless, Mobile and Multi-Media (ICWMMN 2015). Institution of Engineering and Technology, 2015. http://dx.doi.org/10.1049/cp.2015.0946.

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Jovanović, Snežana. "The good side of the recent pandemic: Improvement of microbiological diagnostics." In Proceedings of the International Congress Public Health - Achievements and Challenges. Institute of Public Health of Serbia "Dr Milan Jovanović Batut", 2024. http://dx.doi.org/10.5937/batutphco24008j.

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Background: On December 31, 2019, the World Health Organization (WHO) warned of pneumonia of unknown etiology in Wuhan, China. Rapid and accurate diagnosis of COVID-19 is crucial for the control of epidemic. Methods: In order to introduce a diagnosis and increase COVID-19 testing capacity, on March 27, 2020, Department of Medical Microbiology, University Clinical Center of Serbia was reorganized in staff and equipment. We started with molecular and serological diagnostics, and months later with tests for detection of SARS-CoV-2 antigen (Ag-RDT). On May 22, 2020, mass molecular testing at the N
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Rangelov, Milena, Heather Dylla, and Nadarajah Sivaneswaran. "Using environmental product declarations for green public procurement and life cycle assessment of concrete pavements." In 12th International Conference on Concrete Pavements. International Society for Concrete Pavements, 2021. http://dx.doi.org/10.33593/8ziapl8i.

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Environmental impacts of concrete production have been evaluated for more than a decade. As a result, a national program for environmental product declarations (EPDs) of concrete has been initiated. The main objective of this paper is to analyze concrete EPDs produced to date and evaluate their applicability for green public procurement (GPP) and life-cycle assessment (LCA) of concrete pavements. EPDs provide transparent and verified quantification of environmental impacts, calculated per predetermined guidelines, known as Product Category Rules (PCRs). PCRs for concrete were developed through
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Marchena Parreira, Daniel, Andrew Petersen, and Michelle Craig. "PCRS-C." In ITICSE '15: Innovation and Technology in Computer Science Education Conference 2015. ACM, 2015. http://dx.doi.org/10.1145/2729094.2754852.

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Reports on the topic "PCR5"

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Montiel Olea, César E., and Leonardo R. Corral. Text Analysis of Project Completion Reports. Inter-American Development Bank, 2021. http://dx.doi.org/10.18235/0003611.

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Project Completion Reports (PCRs) are the main instrument through which different multilateral organizations measure the success of a project once it closes. PCRs are important for development effectiveness as they serve to understand achievements, failures, and challenges within the project cycle they can feed back into the design and execution of new projects. The aim of this paper is to introduce text analysis tools for the exploration of PCR documents. We describe and apply different text analysis tools to explore the content of a sample of PCRs. We seek to illustrate a way in which PCRs c
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Gardner, S., D. Clague, J. Vandersall, G. Hon, and P. Williams. Virtual PCR. Office of Scientific and Technical Information (OSTI), 2006. http://dx.doi.org/10.2172/894750.

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KJ Aitken, KJ Aitken. Demystifying PCR: fostering scientific literacy through hands-on PCR education. Experiment, 2024. http://dx.doi.org/10.18258/69600.

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Hall, E. W., W. C. Riley, and G. J. Sandelli. PC25{trademark} product and manufacturing experience. Office of Scientific and Technical Information (OSTI), 1996. http://dx.doi.org/10.2172/460284.

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Gonzalez Diez, Verónica M., Nayda Ávalos, Ana María Linares, et al. IDB and IIC Project Performance: OVE’s Review of 2016 Project Completion Reports and Expanded Supervision Reports. Inter-American Development Bank, 2017. http://dx.doi.org/10.18235/0010686.

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Assessing the results of individual development operations is essential to learning what works and what does not and thus to increasing the effectiveness of investments in development. The purpose of this independent review is to ensure the accuracy and credibility of the project performance reporting system. This report summarizes the results and findings of OVE’s review of the 30 Expanded Supervision Reports (XSRs) completed by IIC in 2016 for NSG operations that reached early operating maturity in 2015, and for the 21 Project Completion Reports (PCRs) that IDB completed under the 2014 PCR g
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Lam, H. L. Forecasts of Pc5 magnetic pulsations. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1988. http://dx.doi.org/10.4095/122733.

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กุลวิชิต, วันล่า. โครงการ การตรวจหาปริมาณและความหนาแน่นของไวรัสเดงกี ที่ตรวจพบในเม็ดเลือดขาวชนิดต่าง ๆ ในเลือดและในซีรั่มหรือพลาสมา ด้วยวิธี RT-PCR (reverse transcription - polymerase chain reaction) และ real-time PCR. คณะแพทยศาสตร์ จุฬาลงกรณ์มหาวิทยาลัย, 2005. https://doi.org/10.58837/chula.res.2005.21.

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โรคติดเชื้อไวรัสเองกี เป็นปัญหาสาธารณสุขที่สำคัญที่สุดอย่างหนึ่งของประเทศไทย การวินิจฉัยการติดเชื้อทางห้องปฏิบัติการ ยังมีข้อจำกัดอยู่ที่ความจำเป็นต้องเจาะเลือก ผู้ป่วยเด็กมักไม่ใครให้ความร่วมมือดีนัก คณะผู้วิจัยได้ทำการศึกษาความเป็นไปได้ในการใช้สิ่งส่งตรวจในช่องปาก และ/หรือปัสสาวะของผู้ป่วย มาทำการตรวจวินิจฉัยทางห้องปฏิบัติการ จากการศึกษาเบื้องต้น ในผู้ป่วยหลายสิบราย พบว่า สามารถตรวจพบเชื้อไวรัสในน้ำลายได้ โดยวิธี reverse transcription polymerase chain reaction (RT-PCR) ประมาณ 30-50% ของผู้ป่วย และตรวจได้ในปัสสาวะประมาณ 80% แม้จะเป็นสิ่งส่งตรวจในระยะท้าย ๆ ของไข้ ซึ่งนับเป็นอัตราการตรวจพบที่ใ
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McAdams, H. T. PCR+ In Diesel Fuels and Emissions Research. Office of Scientific and Technical Information (OSTI), 2002. http://dx.doi.org/10.2172/814346.

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Shingo Hisakawa, Shingo Hisakawa. Developing dNinja, an open-source digital PCR. Experiment, 2023. http://dx.doi.org/10.18258/51141.

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Gan, Charles, Melissa Pitton, Jolinda de Korne, et al. Wastewater-based poliovirus surveillance using digital PCR. Swiss Federal Institute of Aquatic Science and Technology, Eawag, 2025. https://doi.org/10.55408/eawag:34819.

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Poliovirus is the causative agent of poliomyelitis, a potentially debilitating disease that is a target for global eradication. Vaccination against poliomyelitis is an important tool in the eradication effort, but one of the available vaccines, the oral poliovirus vaccine, contains live, attenuated strains that can revert to virulent forms. Community transmission of so-called vaccine-derived polioviruses (VDPVs) can contribute to outbreaks, including in areas with no recently reported poliomyelitis cases. Wastewater-based surveillance (WBS) is a widely applied method to monitor communities for
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