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Relevant bibliographies by topics / Folding ADC

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Academic literature on the topic 'Folding ADC'

Author: Grafiati

Published: 4 June 2021

Last updated: 15 February 2022

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Journal articles on the topic "Folding ADC"

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van Valburg, J., and R. J. van de Plassche. "An 8-b 650-MHz folding ADC." IEEE Journal of Solid-State Circuits 27, no. 12 (1992): 1662–66. http://dx.doi.org/10.1109/4.173091.

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Moldsvor, Oystein, and Geir S. Ostrem. "8-bit, 200 MSPS folding and interpolating ADC." Computer Standards & Interfaces 21, no. 2 (June 1999): 103. http://dx.doi.org/10.1016/s0920-5489(99)91940-2.

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Le, Binh Son, Trong Tu Bui, and Duc Hung Le. "A Design of 10-b 100-MS/s Pipelined Folding ADC with Distributed Track-and-Hold Preprocessing." Science and Technology Development Journal 17, no. 1 (March 31, 2014): 39–51. http://dx.doi.org/10.32508/stdj.v17i1.1241.

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This paper presents a 10-b ADC designed in a 0.18-μm CMOS technology. The ADC achieves 10-b resolution by using the cascaded folding technique in both the fine and coarse converters. Folding stages are pipelined to improve the settling time. As a result, this ADC can achieve the sampling rate up to 100MS/s. Moreover, instead of using a costly single track-and-hold circuit, a distributed track-and-hold circuit is used to reduce the chip area and the power consumption. This also allows utilizing the open-loop architecture of the folding technique, thus improving the performance of the system. The simulation results show that with a 49 MHz sine-wave input, the ADC consumes 66 mW and the effective number of bit (ENOB) is 9.28-b. Taking into account of process variations by using a Monte Carlo simulation, the DNL varies from ±0.45LSB to ±0.25LSB. The layout of the ADC occupies 1.2 mm2 die area.

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Kobayashi, Haruo, Toshiya Mizuta, Kenji Uchida, Hiroyuki Matsuura, Akira Miura, Tsuyoshi Yakihara, Sadaharu Oka, and Daisuke Murata. "Design consideration for folding/interpolation ADC with SiGe HBT." Computer Standards & Interfaces 21, no. 2 (June 1999): 115. http://dx.doi.org/10.1016/s0920-5489(99)91988-8.

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Zhang, Yi, Qiao Meng, Changchun Zhang, Ying Zhang, Yufeng Guo, Youtao Zhang, Xiaopeng Li, and Lei Yang. "A 2 GSps, 8-Bit Folding and Interpolation ADC with Foreground Calibration in 90 nm CMOS Technology." Journal of Sensors 2017 (2017): 1–7. http://dx.doi.org/10.1155/2017/3984526.

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A single channel 2 GSps, 8-bit folding and interpolation (F&I) analog-to-digital converter (ADC) with foreground calibration in TSMC 90 nm CMOS technology is presented in this paper. The ADC utilizes cascaded folding, which incorporates an interstage sample-and-hold amplifier between the two stages of folding circuits to enhance the quantization time. A master-slave track-and-hold amplifier (THA) with bootstrapped switch is taken as the front-end circuit to improve ADC’s performance. The foreground digital assisted calibration has also been employed to correct the error of zero-crossing point caused by the circuit offset, thus improving the linearity of the ADC. Chip area of the whole ADC including pads is 930 μm × 930 μm. Postsimulation results demonstrate that, under a single supply of 1.2 volts, the power consumption is 210 mW. For the sampling rate of 2 GSps, the signal to noise and distortion ratio (SNDR) is 45.93 dB for Nyquist input signal.

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Ahn, Cheol-Min, and Young-Sik Kim. "A 8-bit 10-MSample/s Folding & Interpolation ADC using Preamplifier Sharing Method." Journal of IKEEE 17, no. 3 (September 30, 2013): 275–83. http://dx.doi.org/10.7471/ikeee.2013.17.3.275.

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Vorenkamp, Pieter, and Raf Roovers. "12-B, 60-MSample/S cascaded folding and interpolating ADC." Computer Standards & Interfaces 21, no. 2 (June 1999): 105. http://dx.doi.org/10.1016/s0920-5489(99)91948-7.

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van de Grift, R., I. W. J. M. Rutten, and M. van der Veen. "An 8-bit video ADC incorporating folding and interpolation techniques." IEEE Journal of Solid-State Circuits 22, no. 6 (December 1987): 944–53. http://dx.doi.org/10.1109/jssc.1987.1052842.

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Myung-Jun Choe, Bang-Sup Song, and K. Bacrania. "An 8-b 100-MSample/s CMOS pipelined folding ADC." IEEE Journal of Solid-State Circuits 36, no. 2 (2001): 184–94. http://dx.doi.org/10.1109/4.902759.

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Gao, Yu Han, Ru Zhang Li, Dong Bing Fu, Yong Lu Wang, and Zheng Ping Zhang. "An Encoder Used in an Ultra High-Speed Folding and Interpolating ADC." Advanced Materials Research 1049-1050 (October 2014): 687–90. http://dx.doi.org/10.4028/www.scientific.net/amr.1049-1050.687.

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High speed encoder is the key element of high speed analog-to-digital converter (ADC). Therefor the type of encoder, the type of code, bubble error suppression and bit synchronization must be taken into careful consideration especially for folding and interpolating ADC. To reduce the bubble error which may resulted from the circuit niose, comparator metastability and other interference, the output of quantizer is first encoded with gray code and then converted to binary code. This high speed encoder is verified in the whole time-interleaved ADC with 0.18 Bi-CMOS technology, the whole ADC can achieve a SNR of 45 dB at the sampling rate of 5GHz and input frequency of 495MHz, meanwhile a bit error rate (BER) of less than 10-16 is ensured by this design.

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Dissertations / Theses on the topic "Folding ADC"

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Hiremath, Vinayashree. "DESIGN OF ULTRA HIGH SPEED FLASH ADC, LOW POWER FOLDING AND INTERPOLATING ADC IN CMOS 90nm TECHNOLOGY." Wright State University / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=wright1291391500.

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Carr, Richard D. "Analog preprocessing in a SNS 2 [mu] low-noise CMOS folding ADC." Thesis, Monterey, Calif. : Springfield, Va. : Naval Postgraduate School ; Available from National Technical Information Service, 1994. http://handle.dtic.mil/100.2/ADA293356.

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Thesis (M.S. in Electrical Engineering) Naval Postgraduate School, December 1994.
"December 1994." Thesis advisor(s): Phillip E. Pace, Douglas J. Fouts. Bibliography: p. 103. Also available online.

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Razzaghi, Alireza. "A single-channel 10b 1GS/s ADC with 2-cycle latency using pipelined cascaded folding architecture." Diss., Restricted to subscribing institutions, 2008. http://proquest.umi.com/pqdweb?did=1566903241&sid=1&Fmt=2&clientId=1564&RQT=309&VName=PQD.

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Carter, Nathan R. "A 12-b 50Msample/s Pipeline Analog to Digital Converter." Digital WPI, 2000. https://digitalcommons.wpi.edu/etd-theses/749.

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This thesis focuses on the performace of pipeline converters and their integration on mixed signal processes. With this in mind, a 12-b 50MHz pipeline ADC has been realized in a 0.6um digital CMOS process. The architecture is based on a 1.5-b per stage structure utilizing digital correction for the first six stages. A differeintial switched capacitor circuit consisting of a cascode gm-c op-amp with 250MHz of bandwidth is used for sampling and amplification in each stage. Comparators with an internal offset voltage are used to implement the decision levels required for the 1.5-b per stage structure. Correction of the pipeline is accomplished by measuring the offset and gain of each of the first six stages using subsequent stages. The measured values are used to calculate digtal values the compensate for the inaccuracies of the analog pipeline. Corrected digital values for each stage are stored in the pipeline and used to create corrected output codes. Errors caused by measuring the first six stages using uncalibrated stages are minimized by using extra switching circuitry during calibration.

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Todorova, Nevena, and Nevena Todorova@rmit edu au. "Molecular modelling of peptide folding, misfolding and aggregation phenomena." RMIT University. Applied Science, 2009. http://adt.lib.rmit.edu.au/adt/public/adt-VIT20091130.111240.

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In this thesis we present computer modelling studies that were implemented to investigate protein behavior in various environments causing their folding, unfolding and aggregation. Applications related to two important proteins - insulin and apolipoprotein C-II (ApoC-II) are presented. The use of atomistic simulation methodologies based on empirical force fields has enhanced our understanding of many physical processes governing protein structure and dynamics. However, the force fields used in classical modelling studies are often designed for a particular class of proteins and rely on continuous improvement and validation by comparison of simulations with experimental data. In Chapter 4 we present a comprehensive comparison of five popular force fields for simulation of insulin. The effect of each force field on the conformational evolution and structural properties of the protein is analysed in detail and compared with available experimental data. A fundamental phenomenon in nature is the ability of proteins to fold ab initio to their functional native conformation, also known as their biologically active state. Due to the heterogeneity and dimensionality of the systems involved, it is necessary to employ methodologies capable of accelerating rare events, specifically, configurational changes that involve the crossing of large free energy barriers. In Chapter 5, using the recently developed method BE-META we were able to identify the structural transitions and possible folding pathways of insulin. Another interesting phenomenon is the misfolding of proteins causing their aggregation, that may lead to formation of either amorphous compounds or structures of elongated-unbranched morphology known as amyloid fibrils. The deposition of amyloid fibrils in the human body may cause many debilitating diseases such as Alzheimer's and variant Creutzfeldt-Jakob diseases, thus making this field of research important and urgent. The human plasma protein apoC-II serves important roles in lipid transport, and it has been shown to form amyloid-like aggregates in solution. We have performed computational studies to investigate the effect of mutations, such as Met oxidation and the residue substitutions to hydrophobic Val and hydrophilic Gln, on dynamics of apoC-II(60-70) peptide. The conformation features relevant to the amyloidogenic propensities of the peptide were identified and presented in Chapter 6. The involvement of lipids at the various stages of development of amyloid diseases is becoming more evident in recent research efforts. In particular, micellar and sub-micellar concentrations have showed to have different effect on fibril growth and kinetics of native apoC-II and derived peptides. In Chapter 7 we investigated the influences of phospholipids at various concentrations on the structure of apoC-II(60-70) using MD and umbrella sampling methods. The molecular mechanisms of lipid effects on the peptide conformation and dynamics were identified. In Chapter 8 preliminary results on the structural stability of pre-formed oligomeric composites of apoC-II(60-70) peptide of different sizes and arrangements were also presented. The effects of mutation (oxidised Met, Met60Val and Met60Gln) on the most stable cluster was also investigated. To conclude, several ideas for continuation of research in the protein folding and aggregation field are discussed in the Future Work section of this thesis.

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Bartolo, Natalie Di. "In vitro folding and assembly of the E.Coli ABC transporter BTUCD." Thesis, University of Bristol, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.492472.

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Most studies of membrane protein folding have focused on a-helical monomeric proteins. The next major challenge is to extend these folding studies to incorporate oligomeric membrane proteins, for which there is a paucity of information available on their folding and assembly. The folding of multisubunit proteins is a biologically important and far-reaching area of research since the majority of proteins exist as protein-protein complexes. In order to understand these proteins it is important to be able to recreate their folding and assembly in vitro starting with simple model protein complexes. Work in this thesis takes advantage of the modular organisation of BtuCD and methods are described to prepare the individual building blocks of the protein complex.

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Hart, Troy L. "Analysis and design of CMOS voltage-folding circuits and their use in high speed ADCS." Monterey, Calif. : Springfield, Va. : Naval Postgraduate School ; Available from National Technical Information Service, 1996. http://handle.dtic.mil/100.2/ADA316565.

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Morris, Amie Michelle. "Structure and function of the mammalian small heat shock protein Hsp25." Access electronically Access electronically, 2007. http://www.library.uow.edu.au/adt-NWU/public/adt-NWU20080605.104334/index.html.

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Rossi-Gendron, Caroline. "Dynamic DNA origamis as isothermal supramolecular machines : melting dynamics, photocontrol and isothermal folding." Thesis, Sorbonne université, 2018. http://www.theses.fr/2018SORUS522.

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Les origamis d’ADN et les Single Stranded Tiles (SST) semblent être deux des composants les plus prometteurs du domaine des nanotechnologies d’ADN en termes de conceptions et d'applications possibles. Dans cette thèse, nous avons exploré les aspects thermodynamiques et cinétiques sous-jacents à la formation de ces objets, ainsi que de nouvelles méthodes pour construire des nanoobjets programmables dynamiques. Notamment, l'étude du processus de formation a mis en évidence la présence inutile d'ions magnésium ou de molécules tampons dans le milieu, et de nouvelles conditions de formation ont été décrites. Le processus de fusion a été caractérisé à l'aide d'une nouvelle méthode d'électrophorèse sur gel quantifiée mettant en évidence un comportement non monotone et appelant une nouvelle définition de la température de fusion des origamis. De plus, nous avons démontré que la formation et la fusion pouvaient être contrôlées par la lumière en utilisant AzoDiGua, un intercalant d’ADN photosensible mis au point précédemment par notre groupe. Cela nous a permis d'observer pour la première fois un processus d'hybridation/déshybridation contrôlé par la lumière au sein d'origamis individuels à température constante et d'obtenir ainsi un mouvement contrôlé à l'échelle nanométrique. Nous avons également mis au point une méthode originale pour la formation isotherme d’ADN origamis et de SST à température ambiante constante et en l’absence de tout agent dénaturant. Cela nous a permis d'observer pour la première fois et in situ le pliage isotherme d'origamis individuels, démontrant ainsi que l'origami peut atteindre sa forme d'équilibre final en suivant une variété de voies de pliage
DNA origamis and Single Stranded Tiles (SST) appear to be two of the most promising components of the DNA nanotechnology field in terms of possible designs and applications. In this thesis, we explored the thermodynamic and kinetic aspects underlying DNA nanostructures formation as well as new practical ways to build dynamic programmable nano-objects. Notably, the study of the formation process evidenced the unnecessary presence of magnesium ions or buffering molecules in the medium, and new formation conditions have been described. The melting process triggered by temperature elevation was characterised using a new quantified gel electrophoresis method evidencing for the first time a non-monotonous behaviour and calling for a new definition of DNA origami melting temperature. Both formation and melting process were furthermore demonstrated to be controllable by light using AzoDiGua, a photosensitive DNA intercalator previously developed by our group. This allowed us to observe for the first time a light-controlled hybridisation / dehybridisation process within individual origamis at constant temperature and thus achieve a controlled motion at the nanoscale. We also established an original method for the isothermal formation of DNA origamis and SST at constant room temperature and without the presence of any denaturating agent. This allowed us to observe for the first time and in situ the isothermal folding of individual origamis, thus evidencing that origamis can reach their final equilibrium shape following a variety of folding pathways

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Alemany, i. Arias Anna. "Dynamic force spectroscopy and folding kinetics in molecular systems." Doctoral thesis, Universitat de Barcelona, 2014. http://hdl.handle.net/10803/284197.

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Codification of genetic information; regulation of gene expression; transport of nutrients inside cells; immune protection against infectious agents; transduction of external signals... These are some of the crucial processes that take place in living organisms at the molecular level. A deep understanding of how these phenomena occur is vital to get a precise knowledge of the laws governing the microscopic world and understand, prevent and even find cures for many illnesses with an origin in the molecular scale. Single-molecule experiments emerge as a powerful and versatile tool to investigate molecular processes at the level of individual molecules and trajectories with unprecedented spatial and temporal resolution. A paradigmatic experimental technique is given by “optical tweezers” (OT), which consist of a laser beam that captures micron-sized plastic beads using light momentum conservation. This instrument makes it possible to manipulate with nanometric precision a biomolecule and exert forces on it in the range of [0-100] pN. The diversity of systems being studied using optical tweezers increases every day. In this thesis, OT are used to unravel the mechanisms of unfolding and folding of several small nucleic acid hairpins and a protein when a force is applied to their ends. Moreover, single antigen-antibody bonds are investigated by qualitatively measuring the correlation between bond affinity and bond elasticity. All single-molecule experiments have in common the relevant role played by thermal fluctuations. These are crucial at the microscopic scale and contain overriding thermodynamic and kinetic information of molecular systems. The study of the characteristic forces at which molecular cooperative transitions occur, such as molecular unfolding or bond dissociation, is known as dynamic force spectroscopy (DFS). In this thesis DFS combined with Markov models are widely used to characterize the unfolding/folding reaction pathway, the transition states present in the molecular free-energy landscape, and the elastic, kinetic and thermodynamic properties of a protein, the antigen-antibody bond and nucleic acid hairpins under different conditions. A general result is that non-equilibrium DFS methods provide an excellent platform to extract thermodynamic properties of molecular states that can only be observed under dynamical conditions (that is, they are never observed in equilibrium at reasonable time scales), such as intermediate or bound configurations. An alternative method to extract thermodynamic properties of molecular systems is the use of fluctuation relations (FR). These are mathematical identities that relate non-equilibrium work measurements to free-energy differences. When an irreversible transformation is mechanically induced in an otherwise full-equilibrated molecular system, a work is performed between an initial and a final state that differs in each independent repetition of the experiment. FR relate a collection of these work measurements to the difference in free energy between the initial and the final states, independently of the molecular reaction pathway. If the system is initially found at a partially equilibrated state, an extended version of FR can be used to measure its free energy of formation. This grants access to the thermodynamic properties of misfolded and intermediate states that are rarely sampled in full equilibrium. Additionally, the extended FR allow us to reconstruct the free-energy branches of molecular states observed during non-equilibrium experiments from irreversible work measurements. Hence, relative stabilities between molecular native, unfolded, misfolded an intermediate states can be compared at different stages of the irreversible experiment. Results in this thesis pave the way to characterize the thermodynamics and kinetics of complex molecular process that occur under partial equilibrium conditions (as is the case in living organisms), using both DFS and FR. Examples are found in many kinetic states related to intermolecular binding or in transient non-equilibrium states occurring in polymerization reactions (e.g. translocating). Hence the influence of the findings and methods developed in this thesis remains to be seen.
La codificació de la informació genètica, la regulació de l'expressió dels gens, el transport de nutrients dins la cèl·lula, la protecció immunològica contra agents infecciosos... Aquests són alguns dels processos moleculars que s'esdevenen en organismes vius i són crucials per la seva supervivència. Entendre el funcionament d'aquests fenòmens és vital per conèixer les lleis que governen l'escala microscòpica i per entendre, preveure, o fins i tot trobar cures de malalties amb origen molecular, com el Parkinson, l'Alzheimer, o alguns càncers. Els experiments amb una única molècula són una eina molt poderosa i versàtil que permet investigar molts processos moleculars a escala de molècula i trajectòria individual, amb una resolució espaio-temporal sense precedents. Una eina paradigmàtica per dur a terme aquest tipus d'estudis són les “pinces òptiques”, consistents en un feix de llum coherent focalitzat capaç d'atrapar partícules de plàstic microscòpiques utilitzant la conservació del moment. Aquest instrument permet manipular una única biomolècula amb precisió nanomètrica, i exercir-hi forces en el rang entre 0 i 100 pN. La diversitat de sistemes estudiats amb les pinces òptiques augmenta cada dia. En aquesta tesi, s'utilitzen per desxifrar els mecanismes del plegament i desplegament d'àcids nucleics i d'una proteïna quan s'hi aplica una força. A més, les propietats d'un únic enllaç entre un antigen i un anticòs s'investiguen de manera qualitativa, mesurant la correlació entre l'afinitat i l'elasticitat de la unió. Els resultats d'aquesta tesi obren la porta a la caracterització termodinàmica i cinètica de processos moleculars complexos que s'esdevenen en condicions d'equilibri parcial (com ocorre en organismes vius) utilitzant l'espectroscòpia dinàmica de forces (és a dir, l'estudi de les forces característiques per induir transicions moleculars) i els teoremes de fluctuació (que proporcionen estimacions de l'energia lliure mitjançant mesures irreversibles). Alguns exemples poden trobar-se en els estats cinètics i metaestables relacionats amb el plegament mecànic -com els estats intermedis i mal plegats-, en la interacció intermolecular, o en estats metaestables que es donen en reaccions de polimerització -com la translocació dels motors moleculars.

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Books on the topic "Folding ADC"

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Memory folding: Add dimensions to your scrapbook pages with this unique paper art. Denver, Colorado: Satellite Press, 1999.

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Analysis and Design of CMOS Voltage-Folding Circuits and Their Use in High Speed ADCS. Storming Media, 1996.

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Book chapters on the topic "Folding ADC"

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Tajalli, Armin, and Yusuf Leblebici. "Scalable Folding and Interpolating ADC Design." In Extreme Low-Power Mixed Signal IC Design, 187–213. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-6478-6_8.

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Oza, Shruti, and N. M. Devashrayee. "Process Corner Analysis for Folding and Interpolating ADC." In Information Technology and Mobile Communication, 33–38. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-20573-6_6.

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Vorenkamp, Pieter, and Raf Roovers. "A 12 bit, 50 MSample/s Cascaded Folding & Interpolating ADC." In Analog Circuit Design, 89–104. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4757-2602-2_5.

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Uyttenhove, Koen, J. Vandenbussche, G. Gielen, and M. Steyaert. "Folding/Interpolating ADCs." In CMOS Telecom Data Converters, 183–211. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4757-3724-0_5.

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"Design of a 1.5GSPS 5bit folding and interpolating ADC with distributed S/H folding amplifiers in 90 nm CMOS technology." In Industrial Engineering and Management Science, 75–80. CRC Press, 2014. http://dx.doi.org/10.1201/b17546-18.

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Cappello, Franck, Gilles Fedak, Derrick Kondo, Paul Malecot, and Ala Rezmerita. "Desktop Grids." In Handbook of Research on Scalable Computing Technologies, 31–61. IGI Global, 2010. http://dx.doi.org/10.4018/978-1-60566-661-7.ch003.

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Desktop Grids, literally Grids made of Desktop Computers, are very popular in the context of “Volunteer Computing” for large scale “Distributed Computing” projects like SETI@home and Folding@home. They are very appealing, as “Internet Computing” platforms for scientific projects seeking a huge amount of computational resources for massive high throughput computing, like the EGEE project in Europe. Companies are also interested of using cheap computing solutions that does not add extra hardware and cost of ownership. A very recent argument for Desktop Grids is their ecological impact: by scavenging unused CPU cycles without increasing excessively the power consumption, they reduce the waste of electricity. This book chapter presents the background of Desktop Grid, their principles and essential mechanisms, the evolution of their architectures, their applications and the research tools associated with this technology.

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Conference papers on the topic "Folding ADC"

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van de Plassche and Baltus. "An 8b 100mhz Folding Adc." In 1988 IEEE International Solid-State Circuits Conference. IEEE, 1988. http://dx.doi.org/10.1109/isscc.1988.663701.

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Vun, C. H., and A. B. Premkumar. "RNS encoding based folding ADC." In 2012 IEEE International Symposium on Circuits and Systems - ISCAS 2012. IEEE, 2012. http://dx.doi.org/10.1109/iscas.2012.6272165.

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Chio, U.-Fat, Hou-Lon Choi, Chi-Hang Chan, Si-Seng Wong, Sai-Weng Sin, Seng-Pan U, and R. P. Martins. "Comparator-based successive folding ADC." In Electronics (PrimeAsia). IEEE, 2009. http://dx.doi.org/10.1109/primeasia.2009.5397434.

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Zhen Liu, Song Jia, Yuan Wang, Lijiu Ji, and Xing Zhang. "Efficient encoding scheme for folding ADC." In 2008 9th International Conference on Solid-State and Integrated-Circuit Technology (ICSICT). IEEE, 2008. http://dx.doi.org/10.1109/icsict.2008.4734953.

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Fan, Siqiang, Albert Wang, and Bin Zhao. "Folding and interpolation ADC design methodology." In 2013 IEEE 10th International Conference on ASIC (ASICON 2013). IEEE, 2013. http://dx.doi.org/10.1109/asicon.2013.6811871.

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Oza, Shruti, and N. M. Devashrayee. "Low Voltage, Low Power Folding Amplifier for Folding & Interpolating ADC." In 2009 International Conference on Advances in Recent Technologies in Communication and Computing. IEEE, 2009. http://dx.doi.org/10.1109/artcom.2009.68.

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Mikheev, Roman, and Artem Malygin. "Formalization of folding and interpolating ADC architecture." In 2018 IEEE Conference of Russian Young Researchers in Electrical and Electronic Engineering (EIConRus). IEEE, 2018. http://dx.doi.org/10.1109/eiconrus.2018.8317359.

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Zhen Liu, Yuan Wang, Song Jia, Lijiu Ji, and Xing Zhang. "Low-power CMOS folding and interpolating ADC with a fully-folding technique." In 2007 7th International Conference on ASIC. IEEE, 2007. http://dx.doi.org/10.1109/icasic.2007.4415618.

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Costa, Wendell E. M., Sabiniano A. Rodrigues, Raimundo C. S. Freire, Sebastian Yuri Catunda, and Fernando Rangel de Sousa. "8-bit folding ADC based on switched capacitor." In 2013 IEEE International Instrumentation and Measurement Technology Conference (I2MTC). IEEE, 2013. http://dx.doi.org/10.1109/i2mtc.2013.6555676.

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Qu, Ruoyuan, Zhuohong Du, Ming Zhu, Nan Li, and Hengjing Zhu. "Non-ideality Analysis of Folding and Interpolating ADC." In 2018 IEEE 2nd International Conference on Circuits, System and Simulation (ICCSS). IEEE, 2018. http://dx.doi.org/10.1109/cirsyssim.2018.8525912.

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