Academic literature on the topic 'MTCMOS'
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Journal articles on the topic "MTCMOS"
JIAO, HAILONG, and VOLKAN KURSUN. "NOISE-AWARE DATA PRESERVING SEQUENTIAL MTCMOS CIRCUITS WITH DYNAMIC FORWARD BODY BIAS." Journal of Circuits, Systems and Computers 20, no. 01 (February 2011): 125–45. http://dx.doi.org/10.1142/s0218126611007116.
Full textPattanaik, Manisha, Balwinder Raj, Shashikant Sharma, and Anjan Kumar. "Diode Based Trimode Multi-Threshold CMOS Technique for Ground Bounce Noise Reduction in Static CMOS Adders." Advanced Materials Research 548 (July 2012): 885–89. http://dx.doi.org/10.4028/www.scientific.net/amr.548.885.
Full textHailong Jiao and V. Kursun. "Ground-Bouncing-Noise-Aware Combinational MTCMOS Circuits." IEEE Transactions on Circuits and Systems I: Regular Papers 57, no. 8 (August 2010): 2053–65. http://dx.doi.org/10.1109/tcsi.2010.2041505.
Full textChen, Shi-Hao, Youn-Long Lin, and Mango C. T. Chao. "Power-Up Sequence Control for MTCMOS Designs." IEEE Transactions on Very Large Scale Integration (VLSI) Systems 21, no. 3 (March 2013): 413–23. http://dx.doi.org/10.1109/tvlsi.2012.2187689.
Full textCalhoun, B. H., F. A. Honore, and A. P. Chandrakasan. "A leakage reduction methodology for distributed MTCMOS." IEEE Journal of Solid-State Circuits 39, no. 5 (May 2004): 818–26. http://dx.doi.org/10.1109/jssc.2004.826335.
Full textDouseki, T., S. Shigematsu, J. Yamada, M. Harada, H. Inokawa, and T. Tsuchiya. "A 0.5-V MTCMOS/SIMOX logic gate." IEEE Journal of Solid-State Circuits 32, no. 10 (1997): 1604–9. http://dx.doi.org/10.1109/4.634672.
Full textSHRIVASTAVA, ANUJ KUMAR, and SHYAM AKASHE. "DESIGN OF LOW POWER 14T FULL ADDER CELL USING DOUBLE GATE MOSFET WITH MTCMOS REDUCTION TECHNIQUE AT 45 NANOMETER TECHNOLOGY." International Journal of Nanoscience 12, no. 06 (December 2013): 1350042. http://dx.doi.org/10.1142/s0219581x13500427.
Full textTada, Akira, Hiromi Notani, Genichi Tanaka, Takashi Ipposhi, Masaaki Iijima, and Masahiro Numa. "Charge recycling in MTCMOS circuits with block dividing." IEICE Electronics Express 4, no. 18 (2007): 562–68. http://dx.doi.org/10.1587/elex.4.562.
Full textZhou, Qiang, Xin Zhao, Yici Cai, and Xianlong Hong. "An MTCMOS technology for low-power physical design." Integration 42, no. 3 (June 2009): 340–45. http://dx.doi.org/10.1016/j.vlsi.2008.09.004.
Full textAnis, M., S. Areibi, and M. Elmasry. "Design and optimization of multithreshold cmos (mtcmos) circuits." IEEE Transactions on Computer-Aided Design of Integrated Circuits and Systems 22, no. 10 (October 2003): 1324–42. http://dx.doi.org/10.1109/tcad.2003.818127.
Full textDissertations / Theses on the topic "MTCMOS"
Gopalan, Ranganath. "Leakage power driven behavioral synthesis of pipelined asics." [Tampa, Fla.] : University of South Florida, 2005. http://purl.fcla.edu/fcla/etd/SFE0001064.
Full textKleist, Anders. "Theory of super power saving circuits and configurations for mixed signal CPU for smartcard application." Thesis, Linköping University, Department of Electrical Engineering, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-2326.
Full textDesigning an application specific integrated circuit (ASIC) must be starting with careful preparations, otherwise the chip will not be as good as possible. The theoretical studies must cover everything from the chip circuits to the application structure. In mobile applications there is extremely important that the current consumption becomes minimized because the battery power is limited. The power reductions studies must include the most power costing circuits on the chip. When the whole circuit or segments of the circuit is not in use, they must switch fast and simple into another mode that consume nearly none power. This mode is called sleep-mode. If the sleep-mode has very low leakage currents, the lifetime of the application will dramatically increase.
This report studies the most power costing circuits in smartcard application ASIC. The chip should be used to control a LCD display on the smartcard. The circuits that have been investigated are level shifters, charge pumps and LCD drivers, also sleep-mode configuration possibilities have been investigated. Other small preparing work is also included in the thesis.
Araujo, Natália de Souza. "Análise de espécies crípticas do complexo Anastrepha fraterculus (Díptera: Tephritidae) no Brasil através de sequências do gene mitocondrial cytochrome oxidase I." Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-18122012-225903/.
Full textThe Tephritidae family comprises fruit flies species whose larvae feed and develop in fruits, many of which are commercial varieties and thus the species assume economic significance. Anastrepha genus is distributed throughout the Neotropical region and Southern United States. Analyses of biological characteristics and of the internal transcribed spacer (ITS-1) of the nuclear ribosomal DNA allowed the characterization of three cryptic species of the fraterculus complex in Brazil: Anastrepha sp.1 affinis fraterculus, Anastrepha sp.2 aff. fraterculus and Anastrepha sp.3 aff. fraterculus. Mitochondrial markers as gene cytochrome oxidase I (COI) are largely used in phylogenetic analyses because they have maternal inheritance, none or low recombination and high mutation rates compared to the nuclear DNA. Hence, analyses of the complex based in this marker will offer a divergent perspective from nuclear DNA for inferences on the evolutive relationships between different species. Samples from the fraterculus complex (A. sp.1, A. sp.2, A. sp.3) from 15 localities (average of 5 individuals/ locality) in southeastern Brazil, one sample of A. sp.4 from Ecuador and two outgroups (A. grandis and A. striata) were employed and COI sequences of 1139bp were amplified and analyzed. We identified 45 haplotypes: 30 in A. sp.1, 5 in A.sp.2 and 17 in A. sp.3. The mean distance between the haplotypes was 0.021 and mean Fst 0.347, indicating high population structure and low mitochondrial distance. The neutrality tests had significantly neutral values. The selection tests revealed the action of purifying selection with low values of Ka/Ks and significance in the Z-test selection. Phylogenetic analysis showed strong evidences of introgression and did not separate the various entities in distinct clades grouping the three species in a single branch; there was also the formation of another main branch formed almost exclusively by strains of A. sp.1 and only two samples of A. sp.3. The two main groups of haplotypes were also seen in the haplotype network that showed evidence of population expansion. The analysis of the philogenetic tree based on mitochondrial COI showed strong evidence for introgression. No fixed differences between species were found though mtDNA marker shows a lot of polymorphism. When added sequences deposited in databases by other authors the nominal species A. fraterculus presented in its distribution five groups of mitochondrial haplotypes, two of them in Brazil, one with samples from Mexico and Costa Rica, one in Guatemala and Venezuela and one with individuals from Colombia. The Brazilian groups also collected samples from Argentina and Ecuador. Therefore, the COI sequences do not allow the characterization of the entities of the fraterculus complex, although structure among the species is shown. The most likely hypothesis is that introgression has happened in the mitochondrial molecule among the species with further expansion
Moraes, Letícia Aparecida de [UNESP]. "Levantamento de mosca-branca associada às plantas ornamentais e hortaliças e caracterização de seus endossimbiontes." Universidade Estadual Paulista (UNESP), 2017. http://hdl.handle.net/11449/150129.
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
Bemisia tabaci (Hemiptera: Aleyrodidae), é um complexo composto por pelo menos 37 espécies crípticas e representa uma das mais importantes pragas agrícolas do mundo, já que é um inseto altamente polifago e considerado um supervector de vírus, uma vez que sozinho é capaz de transmitir mais de 300 espécies, como os begomovírus (gênero Begomovirus, família Geminiviridae) e crinivírus (gênero Crinivirus, família Closteroviridae). Mais de duas décadas depois que a espécie B. tabaci Middle East Asia Menor 1 (MEAM1, biótipo B) invadiu e se estabeleceu no Brasil através de plantas ornamentais, a presença da B. tabaci especie Mediterranean (MED, biótipo Q) foi relatada pela primeira vez no Rio Grande do Sul em 2014, e, recentemente, nos estados de São Paulo e Paraná. Em 2015, espécimes de moscas-brancas coletadas em cultivos comerciais protegidos de begônias, hortênsias, petúnias e poinsettias em São Paulo, bem como de begônias e poinsetias de floriculturas e Capsicum spp. associado a Emilia fosbergii em estufas usadas anteriormente para poinsettia no Paraná, foram todos identificados como pertencentes a espécie MED. Adicionalmente, os endosimbiontes secundários identificados foram Arsenophonus, Hamiltonella e Rickettsia foram detectados por PCR e confirmados por sequenciamento e análise de FISH, divergindo dos encontrados nas moscas MED do Rio Grande do Sul, as quais abrigavam Hamiltonella e Cardinium. Em 2015, portanto, a primeira pesquisa no Estado de São Paulo revelou que a espécie MED estava presente apenas em cultivos protegidos de ornamentais e floriculturas, ou seja, associadas a ornamentais. Em 2016, no entanto, uma segunda e mais extensa pesquisa realizada em São Paulo e Paraná mostraram que MED se espalhou por várias e importantes hortaliças, não somente em estufas, mas também para campos abertos localizados próximos de onde MED foi detectada em plantas ornamentais previamente. Os conjuntos de endossimbiontes, cujos sets foram compostos por Arsenophonus, Hamiltonella, Rickettsia e Wolbachia são diferentes também tanto da MED de São Paulo e Paraná de 2015, como da MED detectada no Rio Grande do Sul em 2014. Através da análise filogenética do gene mtCOI usando o banco de dados global de mosca-branca, os espécimes representam diferentes haplótipos divididos em dois grupos dentro da espécie MED. Além disso, neste trabalho houve o primeiro relato da presença do endossimbionte Arsenophonus infectando B. tabaci MEAM1.
Bemisia tabaci (Hemiptera: Aleyrodidae), it is a complex consisting of at least 37 cryptic species and is one of the most important agricultural pests worldwide, since it is a highly polyphagous insect and considered a virus supervector once it alone transmits more than 300 species, such as begomovirus (genus Begomovirus, Geminiviridae family) and crinivirus (genus Crinivirus, Closteroviridae family). More than two decades after the species B. tabaci Middle East Asia Minor 1 (MEAM1, biotype B) invaded and settled in Brazil through ornamental plants, the presence of B. tabaci Mediterraneann species (MED, biotype Q) was first reported in Rio Grande do Sul in 2014, and recently in São Paulo and Paraná States. In 2015, specimens of whiteflies collected in commercial greenhouses of begonias, hydrangeas, petunias and poinsettias in São Paulo, as well as begonias and poinsettias from flower shops and Capsicum spp. associated with Emilia fosbergii in greenhouses used previously for poinsettia in Paraná, they were all identified as belonging to MED species. In addition, the identified secondary endosymbionts were Arsenophonus, Hamiltonella and Rickettsia were detected by PCR and confirmed by sequencing and FISH analysis, diverging from the set of MED from Rio Grande do Sul, which harbored Hamiltonella and Cardinium. In 2015, therefore, the first research in São Paulo revealed that the MED species was present only in greenhouses of ornamentals and flower shops, associated with ornamental. In 2016, however, a second and more extensive research conducted in São Paulo and Paraná showed that MED has spread to several important vegetables, not only in greenhouses, but also to open fields located close to where MED was detected in ornamental plants previously. The endosymbionts, whose sets were composed of Arsenophonus, Hamiltonella, Rickettsia and Wolbachia are also different from both the MED of São Paulo and Paraná in 2015, and the MED of Rio Grande do Sul in 2014. Through phylogenetic analysis of gene mtCOI using the whitefly global database, specimens has shown to represent different haplotypes divided into two groups within the species MED. In addition, this study was the first report of Arsenophonus endosymbiont present infecting B. tabaci MEAM1.
FAPESP: 2014/21773-0
Koser, Jaqueline Reginato. "Estrutura populacional e filogeografia de Drosophila antonietae Tidon & Sene." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/17/17135/tde-01072015-091109/.
Full textDrosophila antoneitae is a cactophilic species, ovipositing primarily in the host cacti Cereus hildmaniannus. Both species are found in drained soils or rocky outcrops in the Missiones region - one of the Seasonally Dry Tropical Forest (SDTF) nucleis, and in south Brazilian coast. The Missiones nuclei comprises the basin of the Paraná-Paraguai Rivers and it is a possible area of climatic stability during the Quaternary oscillations. To evaluate the current distribution of the genetic diversity of D. antoneitae and its association with landscape modifications, the following analyses were performed: populational structure, establishment of phylogeographic hypotheses and demographic events, neutrality tests and paleoecological niche modeling. The mitochondrial gene COI and the nuclear gene period were analyzed. The gene period had low genetic diversity and an homogeneity on the distribution of genetic variability. For gene COI analysis we found a high polymorphism and genetic structure among populations, forming three groups: one in Santa Catarina and Rio Grande do Sul, another in Paraná and São Paulo and the third in the midwestern Brazil. The midwestern population is probably the oldest one, coinciding with the most climatically stable area of this study. This group forms a network of separate haplotypes, due to a high structuring and isolation, probably with Paraná River acting as major barrier for gene flow. We suggest that the possible center of dispersion of the remaining populations of D. antonietae is located in southeastern Brazil, and there were several migration events to other regions of its distribution. There is evidence of shared polymorphism due to recent diversification of populations. Both gene clusters exhibit signs of population expansion, especially in border areas at the Missiones nuclei, where the climate seems less stable. The demographic expansion period is recent and coincides with the major expansion of dry vegetation, which can also play a critical role in structuring populations.
Zhang, Xing. "Biogeography and biosystematics of plum curculio, Conotrachelus nenuphar (Herbst)/Wolbachia interactions." Diss., Virginia Tech, 2006. http://hdl.handle.net/10919/25948.
Full textPh. D.
Monteiro, Ana Rita Andril. "Genetic structure of mussel population in NE Atlantic and Mediterranean: connectivity between deep-sea habitats." Master's thesis, Universidade de Aveiro, 2016. http://hdl.handle.net/10773/17460.
Full textSpecies persist over time, due to exchange of individuals between subpopulations. In the marine environment, most benthic organisms have complex life cycles including pelagic larvae that are transported by ocean currents promoting species dispersal. Larval dispersal connects geographically distant populations and determines population structure. The knowledge about this biologic process provides relevant information for conservation of marine populations. This study investigates the genetic structure and connectivity of deep-sea mussel populations between fragmented habitats in the NE Atlantic and Mediterranean. The mitochondrial Cytochrome Oxidase I (mtCOI) gene was used to analyze site-specific genetic diversity and the population structure of two mussel species, Idas modiolaeformis and “Idas” simpsoni. Populations of each species are not geographically isolated. The presence of one dominant haplotype for each species suggests shared ancestral polymorphisms between Mediterranean and NE Atlantic populations. The overall high genetic differentiation observed in I. modiolaeformis indicates that the metapopulation is structured. Distant populations, located in Atlantic and E Mediterranean, revealed low genetic distances, suggesting gene flow between the two regions. Genetic and geographical distances support an island model of I. modiolaeformis population structure. A major drawback of this study is concerned with the discrepant number of individuals among populations. Further research will be needed, using more specimens and other gene markers, to investigate connectivity patterns at different spatial scales.
As espécies persistem ao longo do tempo devido à troca de indivíduos entre subpopulações. No ambiente marinho, a maioria dos organismos bentónicos têm ciclos de vida complexos, envolvendo larvas pelágicas que são transportadas por correntes oceânicas contribuindo para dispersão das espécies. A dispersão larvar estabelece conectividade entre populações geograficamente separadas e afeta a estrutura da população. O conhecimento deste processo biológico promove informações importantes para a conservação de populações marinhas. Este estudo investiga a estrutura genética e conectividade de populações de mexilhão de profundidade entre habitats fragmentados no NE Atlântico e Mediterrânico. O gene mitocondrial, Citocromo Oxidase I (mtCOI), foi utilizado para analisar diversidade genética por local e a estrutura populacional de duas espécies de mexilhão, Idas modiolaeformis e "Idas" simpsoni. As populações de cada uma das espécies não se encontram geograficamente isoladas. A presença de um haplótipo dominante para cada espécie sugere a partilha de polimorfismos ancestrais entre populações do Mediterrâneo e do NE Atlântico. As populações de I. modiolaeformis demonstraram uma elevada diferenciação genética, indicando estruturação da metapopulação. Populações distantes umas das outras, localizadas no Atlântico e E Mediterrâneo, revelaram baixas distâncias genéticas, sugerindo fluxo genético entre as duas regiões. Distâncias genéticas e geográficas suportam o modelo de ilha como o modelo para a estrutura populacional de I. modiolaeformis. Uma grande desvantagem deste estudo está relacionada com o número discrepante de indivíduos entre populações. Para investigar os padrões de conectividade em diferentes escalas espaciais serão necessários mais estudos, utilizando mais espécimes e outros marcadores genéticos.
Ally, Hadija Mussa. "Genetic diversity and structure of the superabundant whitefly populations, vectors of viruses causing diseases of cassava in three East African countries (Malawi, Tanzania, and Uganda)." Thesis, La Réunion, 2019. http://www.theses.fr/2019LARE0012.
Full textHigh population of the whitefly, Bemisia tabaci Gennadius, a cryptic species complex had been associated with the vectoring and spread of viruses causing two diseases of cassava in East Africa: the cassava mosaic disease (CMD) and cassava brown streak disease (CBSD). Among the B. tabaci species, sub-Saharan Africa 2 (SSA2) was the vector associated with an epidemic of CMD since the 1990s in Uganda. However, this species is now replaced by the SSA1 and led to development of another epidemic by CBSD since the mid 2000s. The spread of both diseases toward South and West Africa is feared with this new supposed invader. In my thesis I have used ecological data and molecular approaches (mitochondrial and nuclear markers) to better understand the factors driving the presence of the superabundant whitefly populations on cassava in East Africa. We have analyzed: i) species abundance, diversity and distribution (geographic and host plants) along a transect survey over three East African countries: Uganda, Tanzania, Malawi, ii) the genetic diversity and structure of current populations of B. tabaci species, and iii) comparing genetic changes between the old and new populations collected in 1997 and 2017, respectively.This study involving large number of samples provided insights of a more complex picture than expected. SSA1 was found to be the source of the some observed outbreaks although other species, notably IO and sub-group 3 of SSA1 (SSA1-SG3) have also shown this capability. The observed outbreaks are therefore not just related to a single species in East Africa. In addition, we showed that the species community and its genetic diversity differ from one country to another, involving different epidemiological situations, without any clear pattern of invasion detected between the countries. Analysis of old samples did not show the involvement of a new species or the emergence of a new population in 20 years, although the dynamics within the whitefly genetic groups was observed over time. Our results contributed new knowledge on the super abundant populations on cassava in Eastern Africa and help develop targeted control measures for the local populations
原田, 政明, 敬也 山里, 啓. 岡田, 正昭 片山, and 明. 小川. "符号化OFDM通信方式における複数シンボルマッピングによる最大瞬時電力抑圧手法." 電子情報通信学会, 2003. http://hdl.handle.net/2237/12731.
Full textZhenghua, Tang. "Synthesis and Energetics of Gold Nanoclusters Tailored by Interfacial Bonding Structure." Digital Archive @ GSU, 2012. http://digitalarchive.gsu.edu/chemistry_diss/67.
Full textBooks on the topic "MTCMOS"
Ajila, J. Lola. HRD, human resources development for a result-oriented civil service: The application of the ministerial training committees system (MTCS). Ikeja [Nigeria]: Index Pub. Co., 1989.
Find full textUnited States. Dept. of Housing and Urban Development. Office of Administration. Request for proposal (RFP) HC-14267 to manage the Multifamily Tenant Characteristics Systems (MTCS) for the Department of Housing and Urban Development. Washington, D.C: U.S. Dept. of Housing and Urban Development, Office of the Assistant Secretary for Administration, 1987.
Find full text1939-, Simon Marvin Kenneth, and Jet Propulsion Laboratory (U.S.), eds. Multiple Trellis Coded Modulation (MTCM). Pasadena, Calif: National Aeronautics and Space Administration, Jet Propulsion Laboratory, California Institute of Technology, 1986.
Find full textMultiple Trellis Coded Modulation (MTCM). Pasadena, Calif: National Aeronautics and Space Administration, Jet Propulsion Laboratory, California Institute of Technology, 1986.
Find full textNational Institute of Standards and Technology (U.S.), ed. A collection of successful interactions between the MTCs and client firms: NIST's Manufacturing Technology Centers program. Gaithersburg, MD: U.S. Dept. of Commerce, National Institute of Standards and Technology, 1993.
Find full textBook chapters on the topic "MTCMOS"
Anis, Mohab, and Mohamed Elmasry. "MTCMOS Sequential Circuits." In Multi-Threshold CMOS Digital Circuits, 135–61. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0391-0_5.
Full textAnis, Mohab, and Mohamed Elmasry. "MTCMOS Dynamic Circuits." In Multi-Threshold CMOS Digital Circuits, 163–93. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0391-0_6.
Full textAnis, Mohab, and Mohamed Elmasry. "Embedded MTCMOS Combinational Circuits." In Multi-Threshold CMOS Digital Circuits, 45–72. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0391-0_3.
Full textAnis, Mohab, and Mohamed Elmasry. "MTCMOS Current-Steering Circuits." In Multi-Threshold CMOS Digital Circuits, 195–214. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0391-0_7.
Full textAnis, Mohab, and Mohamed Elmasry. "MTCMOS Combinational Circuits Using Sleep Transistors." In Multi-Threshold CMOS Digital Circuits, 73–133. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0391-0_4.
Full textAgrawal, Reeya, and Vishal Goyal. "Analysis of MTCMOS Cache Memory Architecture for Processor." In Proceedings of International Conference on Communication and Artificial Intelligence, 81–91. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-33-6546-9_9.
Full textSaraswat, Richa, Shyam Akashe, and Shyam Babu. "Analysis and Simulation of Full Adder Design Using MTCMOS Technique." In Advances in Intelligent Systems and Computing, 189–98. India: Springer India, 2012. http://dx.doi.org/10.1007/978-81-322-1041-2_16.
Full textTripathi, Tripti, D. S. Chauhan, S. K. Singh, and S. V. Singh. "Implementation of Low-Power 6T SRAM Cell Using MTCMOS Technique." In Advances in Computer and Computational Sciences, 475–82. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-3770-2_44.
Full textKushwah, Ankit Singh, and Shyam Akashe. "Power Effective Design of 10T D-FF Using MTCMOS Technique." In Springer Proceedings in Physics, 229–37. New Delhi: Springer India, 2015. http://dx.doi.org/10.1007/978-81-322-2367-2_29.
Full textMallidu, Jayashree, and Saroja V. Siddamal. "Crosstalk Noise Reduction in Long Wire Interconnects Using MTCMOS Inverters." In Lecture Notes in Electrical Engineering, 171–77. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-33-4866-0_22.
Full textConference papers on the topic "MTCMOS"
Pakbaznia, Ehsan, Farzan Fallah, and Massoud Pedram. "Charge recycling in MTCMOS circuits." In the 43rd annual conference. New York, New York, USA: ACM Press, 2006. http://dx.doi.org/10.1145/1146909.1146940.
Full textSharroush, Sherif M. "An MTCMOS Subthreshold-Leakage Reduction Algorithm." In 2020 2nd Novel Intelligent and Leading Emerging Sciences Conference (NILES). IEEE, 2020. http://dx.doi.org/10.1109/niles50944.2020.9257933.
Full textYijia Xu and Gary K. Yeap. "An MTCMOS power network design flow." In 2009 1st Asia Symposium on Quality Electronic Design (ASQED 2009). IEEE, 2009. http://dx.doi.org/10.1109/asqed.2009.5206257.
Full textBaek, Seunghan, Sunmean Kim, Youngchang Choi, and Seokhyeong Kang. "MTCMOS-based Ternary to Binary Converter." In 2020 International SoC Design Conference (ISOCC). IEEE, 2020. http://dx.doi.org/10.1109/isocc50952.2020.9333078.
Full textLu, Liang-Ying, Tsung-Yi Wu, Lih-Yih Chiou, and Jing-Wen Shi. "Peak current reduction using an MTCMOS technique." In 2010 2nd Asia Symposium on Quality Electronic Design (ASQED 2010). IEEE, 2010. http://dx.doi.org/10.1109/asqed.2010.5548248.
Full textAkl, Charbel J., and Magdy A. Bayoumi. "Self-Sleep Buffer for Distributed MTCMOS Design." In 21st International Conference on VLSI Design (VLSID 2008). IEEE, 2008. http://dx.doi.org/10.1109/vlsi.2008.24.
Full textDouseki, Takakuni, and Junzo Yamada. "Sub 1-V MTCMOS/SIMOX Circuit Technology." In 1998 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 1998. http://dx.doi.org/10.7567/ssdm.1998.b-7-2.
Full textInukai, Takashi, and Toshiro Hiramoto. "Suppression of Stand-by Tunnel Current in Ultra-Thin Gate Oxide MOSFETs by Dual Oxide Thickness MTCMOS(DOT-MTCMOS)." In 1999 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 1999. http://dx.doi.org/10.7567/ssdm.1999.e-4-1.
Full textHwang, Chanseok, Peng Rong, and Massoud Pedram. "Sleep transistor distribution in row-based MTCMOS designs." In the 17th great lakes symposium. New York, New York, USA: ACM Press, 2007. http://dx.doi.org/10.1145/1228784.1228786.
Full textBo Wang, Jun Zhou, and Tony T. Kim. "Maximization of SRAM energy efficiency utilizing MTCMOS technology." In 2012 4th Asia Symposium on Quality Electronic Design (ASQED 2012). IEEE, 2012. http://dx.doi.org/10.1109/acqed.2012.6320472.
Full textReports on the topic "MTCMOS"
Suenram, Richard, and Richard Suenram. A collection of successful interactions between the MTCs and clients firms. Gaithersburg, MD: National Institute of Standards and Technology, 1993. http://dx.doi.org/10.6028/nist.sp.848.
Full textDooley, James J. Visualizing the Surface Infrastructure Used to Move 2 MtCO2/year from the Dakota Gasification Company to the Weyburn CO2 Enhanced Oil Recovery Project: Version of July 1, 2009. Office of Scientific and Technical Information (OSTI), July 2009. http://dx.doi.org/10.2172/989054.
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