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Relevant bibliographies by topics / Deoxyribonucleic acid (DNA)

Academic literature on the topic 'Deoxyribonucleic acid (DNA)'

Author: Grafiati

Published: 4 June 2021

Last updated: 19 February 2023

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Journal articles on the topic "Deoxyribonucleic acid (DNA)"

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Grote, James G., Darnell E. Diggs, Robert L. Nelson, John S. Zetts, F. Kenneth Hopkins, Naoya Ogata, Joshua A. Hagen, et al. "DNA Photonics [Deoxyribonucleic Acid]." Molecular Crystals and Liquid Crystals 426, no. 1 (March 2005): 3–17. http://dx.doi.org/10.1080/15421400590890615.

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Sagar, Adithya, and Karl Oberholser. "Proteopedia Entry: Deoxyribonucleic Acid (DNA)*." Biochemistry and Molecular Biology Education 40, no. 1 (December 7, 2011): 74. http://dx.doi.org/10.1002/bmb.20566.

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Khalaf, Narges, Amal Mohammed, and Ali Rahim. "The Correlation Between Sperm DNA Integrity and Conventional Semen Parameters." Iraqi Journal of Embryos and Infertility Researches 11, no. 1 (August 17, 2022): 1–11. http://dx.doi.org/10.28969/ijeir.v11.i1.r1.

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The integrity of sperm deoxyribonucleic acid (DNA) and chromatin is very important for genetic material transmission into offspring. Therefore, the aim of the present study was to investigate the correlation between sperm deoxyribonucleic acid integrity and sperm parameters. The current study was conducted on 96 semen samples. This study was done at the High Institute for Infertility Diagnosis and Assisted Reproductive Technologies, Al-Nahrain University for the period between November 2020 and May 2021. The samples were collected, and seminal fluid analysis was performed according to World Health Organization guidelines. Sperm Chromatin Dispersion test was performed. The results showed that the deoxyribonucleic acid fragmentation of sperms in infertile men in this study was higher than reported in fertile men in previous studies indicating that deoxyribonucleic acid fragmentation (DNA) is actively contributing at least partially to male infertility. In terms of enrolled men, sperm deoxyribonucleic acid fragmentation (SDF) showed significant positive correlation with round cell count.

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Nur’aini, Siti, Arnia Sari Mukaromah, and Siti Muhlisoh. "Pengenalan Deoxyribonucleic Acid (DNA) Dengan Marker-Based Augmented Reality." Walisongo Journal of Information Technology 1, no. 2 (December 20, 2019): 91. http://dx.doi.org/10.21580/wjit.2019.1.2.4531.

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<p>Proses belajar yang baik harus memuat aspek interaktif, memotivasi, menyenangkan dan memberikan ruang bagi siswa untuk dapat mengembangkan kreativitas dan kemandirian. Siswa kadangkala merasa kesulitan pada saat mengillustrasikan isi pembelajaran yang berupa pengetahuan konsep dan prosedur. Dalam pelajaran biologi, materi terkait konsep dasar struktur <em>Deoxyribonucleic Acid</em> (DNA) merupakan materi yang bersifat teoritik dan abstrak. Pemahaman konsep seperti ini memerlukan penggambaran dan modelling yang lebih realistik agar mudah dipahami. Visualisasi dari sumber belajar dan media belajar yang ada sudah dapat membantu mempermudah pemahaman konsep, tetapi variasi media yang lebih nyata, menarik, dan kekinian diharapkan dapat lebih meningkatkan minat siswa. Pengembangan aplikasi <em>Augmented Reality </em>dapat menjadi salah satu alternatif media pembelajaran DNA. Aplikasi ini dikembangkan dengan metode ADDIE menggunakan Unity3D dan Vuforia. Hasil pengujian fungsional menunjukkan semua fitur dapat berjalan dengan baik sesuai dengan kebutuhan di berbagai versi sistem operasi android. Sedangkan pengujian usability menunjukkan kepuasan mahasiswa sebanyak 86% yang artinya aplikasi ini dapat membantu mahasiswa dalam memahami materi DNA.</p>

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Jolly, Pawan, Pedro Estrela, and Michael Ladomery. "Oligonucleotide-based systems: DNA, microRNAs, DNA/RNA aptamers." Essays in Biochemistry 60, no. 1 (June 30, 2016): 27–35. http://dx.doi.org/10.1042/ebc20150004.

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There are an increasing number of applications that have been developed for oligonucleotide-based biosensing systems in genetics and biomedicine. Oligonucleotide-based biosensors are those where the probe to capture the analyte is a strand of deoxyribonucleic acid (DNA), ribonucleic acid (RNA) or a synthetic analogue of naturally occurring nucleic acids. This review will shed light on various types of nucleic acids such as DNA and RNA (particularly microRNAs), their role and their application in biosensing. It will also cover DNA/RNA aptamers, which can be used as bioreceptors for a wide range of targets such as proteins, small molecules, bacteria and even cells. It will also highlight how the invention of synthetic oligonucleotides such as peptide nucleic acid (PNA) or locked nucleic acid (LNA) has pushed the limits of molecular biology and biosensor development to new perspectives. These technologies are very promising albeit still in need of development in order to bridge the gap between the laboratory-based status and the reality of biomedical applications.

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Yu, Sinuo, Tianshu Chen, Qianqian Zhang, Mengru Zhou, and Xiaoli Zhu. "Application of DNA nanodevices for biosensing." Analyst 145, no. 10 (2020): 3481–89. http://dx.doi.org/10.1039/d0an00159g.

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Zhao, Yue, Ruojie Sha, Yudong Hao, Carina Hernandez, Xinshuai Zhao, David Rusling, Jens J. Birktoft, et al. "Self-assembled three-dimensional deoxyribonucleic acid (DNA) crystals." Acta Crystallographica Section A Foundations and Advances 74, a1 (July 20, 2018): a253. http://dx.doi.org/10.1107/s0108767318097465.

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Zhang, Chun-Ting. "Soliton excitations in deoxyribonucleic acid (DNA) double helices." Physical Review A 35, no. 2 (January 1, 1987): 886–91. http://dx.doi.org/10.1103/physreva.35.886.

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Zhao, Xuezhuang, Jianxia Cui, Zucheng Li, Xiufang Xu, Zhenfeng Shang, Yun Li, Guichang Wang, and Ruifang Li. "Symmetries of deoxyribonucleic acid (DNA) and related molecules." Journal of Mathematical Chemistry 55, no. 1 (July 23, 2016): 1–33. http://dx.doi.org/10.1007/s10910-016-0663-2.

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Hai, Wenhua. "Kink couples in deoxyribonucleic acid (DNA) double helices." Physics Letters A 186, no. 4 (March 1994): 309–16. http://dx.doi.org/10.1016/0375-9601(94)91176-2.

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Dissertations / Theses on the topic "Deoxyribonucleic acid (DNA)"

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Pope, Lisa Helen. "X-ray and neutron fibre diffraction studies of deoxyribonucleic acid." Thesis, Keele University, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.388355.

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Mallinder, Benjamin. "Detection of deoxyribonucleic acid by surface enhanced resonance Raman scattering spectroscopy (SERRS)." Thesis, University of Strathclyde, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.248771.

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Bryson, Kevin. "Molecular simulation of DNA and its interaction with polyamines." Thesis, University of York, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297070.

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Walton-Williams, Laura. "An evaluation of the transfer and persistence of deoxyribonucleic acid (DNA) evidence." Thesis, Staffordshire University, 2016. http://eprints.staffs.ac.uk/2786/.

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DNA analysis is now a sufficiently sensitive technique to enable identification of an individual from an extremely small amount of biological material. Exhibits are routinely submitted to forensic laboratories for recovery and analysis of ‘touch DNA’, in order to link an offender to the crime scene. One such exhibit type is spent cartridge cases, where DNA transferred from the handler to the exterior surface of the casing may be the only evidence available for identification of the handler. Alternatively the firearm itself may be recovered, which could also have potential for uncovering the identity of the shooter by means of ‘touch DNA’ profiling. However, the analysis of minute amounts of DNA introduces additional interpretational challenges. The ability to identify the source of a low level DNA sample and the relevance of a recovered DNA profile to the crime scene are not comprehensively understood. The variations in DNA deposition, recovery, transfer and persistence were examined, through a series of controlled laboratory experiments. Volunteers were asked to take part in DNA deposition studies that involved handling items for set periods of time, to determine the variability in the quality of DNA deposited. They were also asked to take part in handshaking studies, where the persistence of DNA, as well as the primary and secondary transfer of DNA, was studied. Additional variables were considered in relation to DNA recovered from spent cartridge cases, including the effect of firing and gunshot residue on DNA quality. DNA was extracted using QIAamp® DNA Mini Kit (Qiagen) and Chelex® (Bio-Rad) protocols and amplified with the AmpFlSTR® SGM Plus® Kit and the AmpFlSTR® Identifiler® Kit (both Applied Biosystems). DNA profiles were analysed on the ABI PRISM™ 310 Genetic Analyser and the ABI PRISM™ 3500 Genetic Analyser (both Applied Biosystems). It was possible to recover a usable DNA profile from a handled item and the quality of DNA deposited after repeated contacts was comparable. The quality of DNA recovered from ‘touch DNA’ samples from different individuals varied, and specific methods for recovery based on surface type were found to increase the likelihood of generating a successful DNA profile. Where an item was handled by more than one individual, the major contributor to the profile was not always that of the final handler. Furthermore, secondary transfer of DNA was observed to some degree in every test sample. This research also highlighted the challenges of interpreting mixed profiles, especially with low levels of DNA present. Identification of the handler of a spent cartridge case was not possible using DNA profiling techniques, due to the increased DNA degradation as a result of conditions experienced during the firing process. However, where a higher yield of DNA was present prior to firing, there was the possibility of recovering an interpretable DNA profile from this type of evidence. The findings of this research should be considered when submitting items for DNA analysis, when considering best practice for recovery of ‘touch DNA’ samples and when attempting to interpret ‘touch DNA’ evidence profiles.

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Williams, Robert Keith. "Molecular conformational studies of deoxyribonucleic acid by potential energy minimization with normal mode analysis." Thesis, Keele University, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.292541.

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Edirisinghe, Pathirannehelage Neranjan S. "Charge Transfer in Deoxyribonucleic Acid (DNA): Static Disorder, Dynamic Fluctuations and Complex Kinetic." Digital Archive @ GSU, 2011. http://digitalarchive.gsu.edu/phy_astr_diss/45.

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The fact that loosely bonded DNA bases could tolerate large structural fluctuations, form a dissipative environment for a charge traveling through the DNA. Nonlinear stochastic nature of structural fluctuations facilitates rich charge dynamics in DNA. We study the complex charge dynamics by solving a nonlinear, stochastic, coupled system of differential equations. Charge transfer between donor and acceptor in DNA occurs via different mechanisms depending on the distance between donor and acceptor. It changes from tunneling regime to a polaron assisted hopping regime depending on the donor-acceptor separation. Also we found that charge transport strongly depends on the feasibility of polaron formation. Hence it has complex dependence on temperature and charge-vibrations coupling strength. Mismatched base pairs, such as different conformations of the G・A mispair, cause only minor structural changes in the host DNA molecule, thereby making mispair recognition an arduous task. Electron transport in DNA that depends strongly on the hopping transfer integrals between the nearest base pairs, which in turn are affected by the presence of a mispair, might be an attractive approach in this regard. I report here on our investigations, via the I –V characteristics, of the effect of a mispair on the electrical properties of homogeneous and generic DNA molecules. The I –V characteristics of DNA were studied numerically within the double-stranded tight-binding model. The parameters of the tight-binding model, such as the transfer integrals and on-site energies, are determined from first-principles calculations. The changes in electrical current through the DNA chain due to the presence of a mispair depend on the conformation of the G・A mispair and are appreciable for DNA consisting of up to 90 base pairs. For homogeneous DNA sequences the current through DNA is suppressed and the strongest suppression is realized for the G(anti)・A(syn) conformation of the G・A mispair. For inhomogeneous (generic) DNA molecules, the mispair result can be either suppression or an enhancement of the current, depending on the type of mispairs and actual DNA sequence.

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Sefah, Kwame. "Development of deoxyribonucleic acid (DNA) aptamers as effective molecular probes for cancer study." [Gainesville, Fla.] : University of Florida, 2009. http://purl.fcla.edu/fcla/etd/UFE0041196.

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Yu, Zhou. "Optical Properties of Deoxyribonucleic Acid (DNA) and Its Application in Distributed Feedback (DFB) Laser Device Fabrication." University of Cincinnati / OhioLINK, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1154706431.

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Peters, Dimetrie Leslie. "Evaluation of eukaryotic cultured cells as a model to study extracellular DNA / D.L. Peters." Thesis, North-West University, 2011. http://hdl.handle.net/10394/6929.

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The diagnostic value of extracellular occurring DNA (eoDNA) is limited by our lack of understanding its biological function. eoDNA exists in a number of forms, namely vesicle bound DNA, histone/DNA complexes or nucleosomes and virtosomes. These forms of DNA can also be categorized under the terms circulating DNA, cell free DNA, free DNA and extracellular DNA. The DNA can be released by means of form–specific mechanisms and seem to be governed by cell cycle phases and apoptosis. Active release is supported by evidence of energy dependant release mechanisms and various immunological– and messenger functions. Sequencing has shown that eoDNA sequences present in the nucleome reflects traits and distribution of genome sequences and are regulated by ways of release and/or clearance. eoDNA enables the horizontal transfer of gene sequences from one cell to another, over various distances. The ability of eoDNA to partake in horizontal gene transfer makes it an important facet in the field of epigenetic variation. Clinical implementation of eoDNA diagnostics requires that all of the subgroups of eoDNA be properly investigated. It is suggested that eoDNA is the result of the metabolic fraction of DNA that is released by the cell. Various observations indicate that eoDNA may also be incorporated into the genome of a cell, from where it may affect cell function. Therefore horizontal gene transfer in higher organisms is a real possibility. In this study, variations and increases in eoDNA levels over time correlate with stressors that are subjected to 143B human osteosarcoma cells. It seems viable to assume that a stressor is met by a change in the molecular machinery of a cell, required to neutralise the onset of metabolic instability. This may be done by amplification of necessary cistrons, producing metabolic DNA, that may then be observed after its release as eoDNA. The presence of hydrolysing enzymes gives an updated real time picture of the state of eoDNA. The eogenics hypothesis emanating from this study, suggests that amplification and horizontal transfer of cistrons affect tissue and organ function over long periods of time, in order for an organism to evolve one or more a specialized genomes.
Thesis (M.Sc. (Biochemistry))--North-West University, Potchefstroom Campus, 2011.

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Fehrman, Cory Emily Marie. "Fabrication of a Deoxyribonucleic Acid Polymer Ridge Waveguide Electro-Optic Modulator by Nanoimprint Lithography." University of Dayton / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=dayton1398419640.

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Books on the topic "Deoxyribonucleic acid (DNA)"

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Syväoja, Juhani. Factors involved in deoxyribonucleic acid ligation in Escherichia coli cells. Oulu: University of Oulu, 1987.

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2

Court, Philippines Supreme. A.M. no. 06-11-5-SC rule on DNA evidence: Deoxyribonucleic acid. [Manila: Lexpertbooks, 2007.

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Reid, Kamla. Using gel electrophoresis: Guidelines for separating DNA (deoxyribonucleic acid) in high school science laboratories. [Maitland, Ont.]: Science Teachers' Association of Ontario, 2003.

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DNA repair. New York: W.H. Freeman, 1985.

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Council of Europe. Committee of Ministers. The use of analysis of deoxyribonucleic acid (DNA) within the framework of the criminal justice system: Recommendation No. R (92) 1 [of the Committee of Ministers] on 10 February 1992 and explanatory memorandum. Strasbourg: Council of Europe Press, 1993.

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Ministers, Council of Europe Committee of. The use of analysis of deoxyribonucleic acid (DNA) within the framework of the criminal justice system: Recommendation no. R (92) 1 adopted by the Committee of Ministers of the Council of Europe on 10 February 1992 and explanatory memorandum. Strasbourg: Council of Europe, 1993.

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The double helix: A personal account of the discovery of the structure of DNA. London: Weidenfeld & Nicolson, 1997.

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Sylvia, Nasar, ed. The double helix: A personal account of the discovery of the structure of DNA. New York: a Touchstone book, published by Simon & Schuster, 2001.

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9

D, Watson James. The double helix: A personal account of the discovery of the structure of DNA. New York: Scribner, 1998.

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Shuang luo xuan: DNA jie gou fa xian zhe di qing chun gao bai = The double helix. Taibei Shi: Shi bao wen hua chu ban qi yeh gu fen yu xian gong si, 1998.

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Book chapters on the topic "Deoxyribonucleic acid (DNA)"

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Palmer, Rohan, and Martin Hahn. "Deoxyribonucleic Acid (DNA)." In Encyclopedia of Clinical Neuropsychology, 1110–11. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-57111-9_1857.

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Palmer, Rohan, and Martin Hahn. "Deoxyribonucleic Acid (DNA)." In Encyclopedia of Clinical Neuropsychology, 816–17. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-0-387-79948-3_1857.

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Palmer, Rohan, and Martin Hahn. "Deoxyribonucleic Acid (DNA)." In Encyclopedia of Clinical Neuropsychology, 1–2. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-56782-2_1857-2.

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Cumming, Jeffrey M., Bradley J. Sinclair, Charles A. Triplehorn, Yousif Aldryhim, Eduardo Galante, Ma Angeles Marcos-Garcia, Malcolm Edmunds, et al. "Deoxyribonucleic Acid (DNA)." In Encyclopedia of Entomology, 1178. Dordrecht: Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_874.

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Gooch, Jan W. "Deoxyribonucleic Acid (DNA)." In Encyclopedic Dictionary of Polymers, 886. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_13540.

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Pal Chaudhuri, Parimal, Soumyabrata Ghosh, Adip Dutta, and Somshubhro Pal Choudhury. "Cellular Automata Model for Deoxyribonucleic Acid (DNA)." In A New Kind of Computational Biology, 203–89. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-13-1639-5_4.

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Esiobu, Nwadiuto (Diuto), Ifeoma M. Ezeonu, and Francisca Nwaokorie. "Principles and Techniques for Deoxyribonucleic Acid (DNA) Manipulation." In Medical Biotechnology, Biopharmaceutics, Forensic Science and Bioinformatics, 3–32. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003178903-1.

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Moosavi, Sanaz Rahimi, and Arman Izadifar. "End-to-End Security Scheme for E-Health Systems Using DNA-Based ECC." In Silicon Valley Cybersecurity Conference, 77–89. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-96057-5_6.

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AbstractToday, the amount of data produced and stored in computing Internet of Things (IoT) devices is growing. Massive volumes of sensitive information are exchanged between these devices making it critical to ensure the security of these data. Cryptography is a widely used method for ensuring data security. Many lightweight cryptographic algorithms have been developed to address the limitations of resources on the IoT devices. Such devices have limited processing capabilities in terms of memory, processing power, storage, etc. The primary goal of exploiting cryptographic technique is to send data from the sender to the receiver in the most secure way to prevent eavesdropping of the content of the original data. In this paper, we propose an end-to-end security scheme for IoT system. The proposed scheme consists of (i) a secure and efficient mutual authentication scheme based on the Elliptic Curve Cryptography (ECC) and the Quark lightweight hash design, and (ii) a secure end-to-end communication based on Deoxyribonucleic Acid (DNA) and ECC. DNA Cryptography is the cryptographic technique to encrypt and decrypt the original data using DNA sequences based on its biological processes. It is a novel technique to hide data from unauthorized access with the help of DNA. The security analysis of the proposed scheme reveals that it is secure against the relevant threat models and provides a higher security level than the existing related work in the literature.

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Tahir, M. A., J. Caruso, P. Hamby, and V. K. Sharma. "Deoxyribonucleic Acid (DNA) HLA - DQ α Allele Frequency Distribution in Various Sects of South Indian Population." In Advances in Forensic Haemogenetics, 593–95. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-78782-9_167.

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Tahir, M. A., P. P. Hamby, A. Asghar, J. F. Caruso, and B. Budowle. "Distribution of HLA-DQα Alleles in Deoxyribonucleic Acid (DNA) from Caucasian and Black Populations of Marion County, Indiana, USA." In Advances in Forensic Haemogenetics, 596–98. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-78782-9_168.

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Conference papers on the topic "Deoxyribonucleic acid (DNA)"

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Ouchen, F., G. Subramanyam, H. Zate, J. G. Grote, S. N. Kim, K. Singh, and R. Naik. "Deoxyribonucleic Acid (DNA) based BioTransistors." In 2008 IEEE National Aerospace and Electronics Conference. IEEE, 2008. http://dx.doi.org/10.1109/naecon.2008.4806526.

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Grote, James G., Emily M. Heckman, Joshua A. Hagen, Perry P. Yaney, Guru Subramanyam, Stephen J. Clarson, Darnell E. Diggs, et al. "Deoxyribonucleic acid (DNA)-based optical materials." In European Symposium on Optics and Photonics for Defence and Security, edited by Anthony W. Vere, James G. Grote, and Francois Kajzar. SPIE, 2004. http://dx.doi.org/10.1117/12.573085.

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Grote, James G., Naoya Ogata, Joshua A. Hagen, Emily Heckman, Michael J. Curley, Perry P. Yaney, Morley O. Stone, et al. "Deoxyribonucleic acid (DNA)-based nonlinear optics." In Optical Science and Technology, SPIE's 48th Annual Meeting, edited by A. Todd Yeates, Kevin D. Belfield, Francois Kajzar, and Christopher M. Lawson. SPIE, 2003. http://dx.doi.org/10.1117/12.510909.

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Hagen, Joshua A., James G. Grote, Naoya Ogata, Emily M. Heckman, Perry P. Yaney, Darnell E. Diggs, Gurunathan Subramanyam, et al. "Deoxyribonucleic acid (DNA) photonics for space environments." In Optical Science and Technology, the SPIE 49th Annual Meeting, edited by Edward W. Taylor. SPIE, 2004. http://dx.doi.org/10.1117/12.562138.

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Samoc, Anna, Marek Samoc, James G. Grote, Andrzej Miniewicz, and Barry Luther-Davies. "Optical properties of deoxyribonucleic acid (DNA) polymer host." In Optics/Photonics in Security and Defence, edited by James G. Grote, Francois Kajzar, and Mikael Lindgren. SPIE, 2006. http://dx.doi.org/10.1117/12.691239.

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Grote, James G., Emily M. Heckman, Joshua A. Hagen, Perry P. Yaney, Darnell E. Diggs, Guru Subramanyam, Robert L. Nelson, John S. Zetts, De Yu Zang, and F. K. Hopkins. "Deoxyribonucleic acid (DNA) based photonic materials: current status." In European Symposium on Optics and Photonics for Defence and Security, edited by John C. Carrano, Arturas Zukauskas, Anthony W. Vere, James G. Grote, and François Kajzar. SPIE, 2005. http://dx.doi.org/10.1117/12.632476.

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Ouchen, Fahima, Benjamin G. Wilson, Perry P. Yaney, Michael M. Salour, and James G. Grote. "Deoxyribonucleic acid (DNA)-Ni-nanostrands composites for EMI shielding." In SPIE Nanoscience + Engineering, edited by Norihisa Kobayashi, Fahima Ouchen, and Ileana Rau. SPIE, 2016. http://dx.doi.org/10.1117/12.2238815.

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Zhang, Gongjian, Lili Wang, Junichi Yoshida, and Naoya Ogata. "Optical and optoelectronic materials derived from biopolymer deoxyribonucleic acid (DNA)." In Asia-Pacific Optical and Wireless Communications Conference and Exhibit, edited by Tien Pei Lee and Qiming Wang. SPIE, 2001. http://dx.doi.org/10.1117/12.444982.

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Samoc, Marek, Anna Samoc, Andrzej Miniewicz, Przemyslaw P. Markowicz, Paras N. Prasad, and James G. Grote. "Cubic nonlinear optical effects in deoxyribonucleic acid (DNA) based materials containing chromophores." In NanoScience + Engineering, edited by Emily M. Heckman, Thokchom B. Singh, and Junichi Yoshida. SPIE, 2007. http://dx.doi.org/10.1117/12.736587.

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Kopacz, Adrian M., Wing K. Liu, and Jae-Hyun Chung. "Design and Optimization of a Nanotip Sensor via Immersed Molecular Electrokinetic Finite Element Method." In ASME 2010 First Global Congress on NanoEngineering for Medicine and Biology. ASMEDC, 2010. http://dx.doi.org/10.1115/nemb2010-13299.

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A critical challenge in the field of medicine is to develop a low cost sensor competent of detecting specific bacterial pathogens via a precise deoxyribonucleic acid (DNA) sequence. In order to identify such biological agents in a patient’s blood or other bodily fluids at the onset of infection, detection of specific pathogen genomic DNA is considered a reliable approach. Current techniques involving multiplex DNA/RNA detection arrays or immunoassays [1] require cumbersome sample preparation, aggressive nucleic acid amplification protocols and must be operated by trained personnel. To overcome the aforementioned obstacles, a time-dependent dielectrophoretic force driven sensor consisting of nanostructured tip is being developed.

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Reports on the topic "Deoxyribonucleic acid (DNA)"

1

Broyde, S., and R. Shapiro. Interactions of carcinogens with DNA (deoxyribonucleic acid). Office of Scientific and Technical Information (OSTI), October 1989. http://dx.doi.org/10.2172/5477407.

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2

Karna, Molly, Govind Mallick, and Shashi P. Karna. Fundamental Interaction Between Au Nanoparticles and Deoxyribonucleic Acid (DNA). Fort Belvoir, VA: Defense Technical Information Center, June 2010. http://dx.doi.org/10.21236/ada522582.

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3

Proctor, Thomas J., and Amethist S. Finch. Method Optimization of Deoxyribonucleic Acid (DNA) Thin Films for Biotronics. Fort Belvoir, VA: Defense Technical Information Center, September 2011. http://dx.doi.org/10.21236/ada549865.

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4

Geacintov, N. Base sequence effects on interactions of aromatic mutagens with DNA (deoxyribonucleic acid). Office of Scientific and Technical Information (OSTI), October 1989. http://dx.doi.org/10.2172/5643342.

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5

Macula, Anthony, Russell Deaton, and Junghuei Chen. A Two-Dimensional Deoxyribonucleic Acid (DNA) Matrix Based Biomolecular Computing and Memory Architecture. Fort Belvoir, VA: Defense Technical Information Center, February 2009. http://dx.doi.org/10.21236/ada494650.

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