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Relevant bibliographies by topics / Microfluidic biochips

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Academic literature on the topic 'Microfluidic biochips'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Microfluidic biochips"

1

Roy, Pushpita, and Ansuman Banerjee. "A Framework for Validation of Synthesized MicroElectrode Dot Array Actuations for Digital Microfluidic Biochips." ACM Transactions on Design Automation of Electronic Systems 26, no. 6 (July 30, 2021): 1–36. http://dx.doi.org/10.1145/3460437.

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Digital Microfluidics is an emerging technology for automating laboratory procedures in biochemistry. With more and more complex biochemical protocols getting mapped to biochip devices and microfluidics receiving a wide adoption, it is becoming indispensable to develop automated tools and synthesis platforms that can enable a smooth transformation from complex cumbersome benchtop laboratory procedures to biochip execution. Given an informal/semi-formal assay description and a target microfluidic grid architecture on which the assay has to be implemented, a synthesis tool typically translates the high-level assay operations to low-level actuation sequences that can drive the assay realization on the grid. With more and more complex biochemical assay protocols being taken up for synthesis and biochips supporting a wider variety of operations (e.g., MicroElectrode Dot Arrays (MEDAs)), the task of assay synthesis is getting intricately complex. Errors in the synthesized assay descriptions may have undesirable consequences in assay operations, leading to unacceptable outcomes after execution on the biochips. In this work, we focus on the challenge of examining the correctness of synthesized protocol descriptions, before they are taken up for realization on a microfluidic biochip. In particular, we take up a protocol description synthesized for a MEDA biochip and adopt a formal analysis method to derive correctness proofs or a violation thereof, pointing to the exact operation in the erroneous translation. We present experimental results on a few bioassay protocols and show the utility of our framework for verifiable protocol synthesis.

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Kitagawa, Daiki, Dieu Quang Nguyen, Trung Anh Dinh, and Shigeru Yamashita. "Graph-Covering-Based Architectural Synthesis for Programmable Digital Microfluidic Biochips." International Journal of Biomedical and Clinical Engineering 6, no. 2 (July 2017): 33–45. http://dx.doi.org/10.4018/ijbce.2017070103.

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Digital microfluidic technology has been extensively applied in various biomedical fields. Different from application-specific biochips, a programmable design has several advantages such as dynamic reconfigurability and general applicability. Basically, a programmable biochip divides the chip into several virtual modules. However, in the previous design, a virtual module can execute only one operation at a time. In this paper, the authors propose a new multi-functional module for programmable digital microfluidic biochips, which can execute two operations simultaneously. Moreover, they also propose a binding and scheduling algorithm for programmable biochips, which is motivated from a graph-covering problem. Experiment demonstrates that their algorithm can reduce the completion time of the applications compared with the previous approaches.

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Huang, Xing, Tsung-Yi Ho, Wenzhong Guo, Bing Li, Krishnendu Chakrabarty, and Ulf Schlichtmann. "Computer-aided Design Techniques for Flow-based Microfluidic Lab-on-a-chip Systems." ACM Computing Surveys 54, no. 5 (June 2021): 1–29. http://dx.doi.org/10.1145/3450504.

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As one of the most promising lab-on-a-chip systems, flow-based microfluidic biochips are being increasingly used for automatically executing various laboratory procedures in biology and biochemistry, such as enzyme-linked immunosorbent assay, point-of-care diagnosis, and so on. As manufacturing technology advances, the characteristic dimensions of biochip systems keep shrinking, and tens of thousands of microvalves can now be integrated into a coin-sized microfluidic platform, making the conventional manual-based chip design no longer applicable. Accordingly, computer-aided design (CAD) of microfluidics has attracted considerable research interest in the EDA community over the past decade. This review article presents recent advances in the design automation of biochips, involving CAD techniques for architectural synthesis, wash optimization, testing, fault diagnosis, and fault-tolerant design. With the help of these CAD tools, chip designers can be released from the burden of complex, large-scale design tasks. Meanwhile, new chip architectures can be explored automatically to open new doors to meet requirements from future large-scale biological experiments and medical diagnosis. We discuss key trends and directions for future research that are related to enable microfluidics to reach its full potential, thus further advancing the development and progression of the microfluidics industry.

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Wan, Chaowei, Xiaodao Chen, and Dongbo Liu. "A Multi-Objective-Driven Placement Technique for Digital Microfluidic Biochips." Journal of Circuits, Systems and Computers 28, no. 05 (May 2019): 1950076. http://dx.doi.org/10.1142/s0218126619500762.

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Microfluidic biochips are extensively utilized in biochemistry procedures due to their low cost, high precision and efficiency when compared to traditional laboratory procedures. Recent, computer-aided design (CAD) techniques enable a high performance in digital microfluidic biochip design. A key part in digital microfluidic biochip CAD design is the biochip placement procedure which determines the physical location for biological reactions during the physical design. For the biochip physical design, multiple objects need to be considered, such as the size of the chip and the total operation time. In this paper, a multi-objective optimization is proposed based on Markov decision processes (MDPs). The proposed method is evaluated on a set of standard biochip benchmarks. Compared to existing works, experimental results show that the total operation time, the capacity for routing and the chip size can be optimized simultaneously.

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Ibrahim, Mohamed, and Krishnendu Chakrabarty. "Digital-Microfluidic Biochips." Computer 49, no. 6 (June 2016): 8–9. http://dx.doi.org/10.1109/mc.2016.187.

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Narayanamurthy, Vigneswaran, Tze Lee, Al’aina Khan, Fahmi Samsuri, Khairudin Mohamed, Hairul Hamzah, and Madia Baharom. "Pipette Petri Dish Single-Cell Trapping (PP-SCT) in Microfluidic Platforms: A Passive Hydrodynamic Technique." Fluids 3, no. 3 (July 24, 2018): 51. http://dx.doi.org/10.3390/fluids3030051.

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Microfluidics-based biochips play a vital role in single-cell research applications. Handling and positioning of single cells at the microscale level are an essential need for various applications, including genomics, proteomics, secretomics, and lysis-analysis. In this article, the pipette Petri dish single-cell trapping (PP-SCT) technique is demonstrated. PP-SCT is a simple and cost-effective technique with ease of implementation for single cell analysis applications. In this paper a wide operation at different fluid flow rates of the novel PP-SCT technique is demonstrated. The effects of the microfluidic channel shape (straight, branched, and serpent) on the efficiency of single-cell trapping are studied. This article exhibited passive microfluidic-based biochips capable of vertical cell trapping with the hexagonally-positioned array of microwells. Microwells were 35 μm in diameter, a size sufficient to allow the attachment of captured cells for short-term study. Single-cell capture (SCC) capabilities of the microfluidic-biochips were found to be improving from the straight channel, branched channel, and serpent channel, accordingly. Multiple cell capture (MCC) was on the order of decreasing from the straight channel, branch channel, and serpent channel. Among the three designs investigated, the serpent channel biochip offers high SCC percentage with reduced MCC and NC (no capture) percentage. SCC was around 52%, 42%, and 35% for the serpent, branched, and straight channel biochips, respectively, for the tilt angle, θ values were between 10–15°. Human lung cancer cells (A549) were used for characterization. Using the PP-SCT technique, flow rate variations can be precisely achieved with a flow velocity range of 0.25–4 m/s (fluid channel of 2 mm width and 100 µm height). The upper dish (UD) can be used for low flow rate applications and the lower dish (LD) for high flow rate applications. Passive single-cell analysis applications will be facilitated using this method.

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Alistar, Mirela. "Mobile Microfluidics." Bioengineering 6, no. 1 (January 3, 2019): 5. http://dx.doi.org/10.3390/bioengineering6010005.

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Microfluidics platforms can program small amounts of fluids to execute a bio-protocol, and thus, can automate the work of a technician and also integrate a large part of laboratory equipment. Although most microfluidic systems have considerably reduced the size of a laboratory, they are still benchtop units, of a size comparable to a desktop computer. In this paper, we argue that achieving true mobility in microfluidics would revolutionize the domain by making laboratory services accessible during traveling or even in daily situations, such as sport and outdoor activities. We review the existing efforts to achieve mobility in microfluidics, and we discuss the conditions mobile biochips need to satisfy. In particular, we show how we adapted an existing biochip for mobile use, and we present the results when using it during a train ride. Based on these results and our systematic discussion, we identify the challenges that need to be overcome at technical, usability and social levels. In analogy to the history of computing, we make some predictions on the future of mobile biochips. In our vision, mobile biochips will disrupt how people interact with a wide range of healthcare processes, including medical testing and synthesis of on-demand medicine.

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Zhang, Ling, Jun Jin Mei, Bo Wu Yan, and Qin Gao. "A Test Droplets Dispensing Solution for Digital Microfluidic Biochip Parallel Testing." Key Engineering Materials 609-610 (April 2014): 670–74. http://dx.doi.org/10.4028/www.scientific.net/kem.609-610.670.

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Digital microfluidic Biochips are widely used on safety-critical biomedical applications, and dependability is an essential attribute for them. To reduce dispensing time, a new test droplets dispensing solution for digital microfluidic biochip parallel testing is proposed in the paper, where multiple test droplets are allotted to the limited test dispensing sources to transmit them to the corresponding test target. The goal is minimizing the dispensing time, and then reduces the system testing time. Even thought the problem is shown to be NP-complete, it can be solved exactly for practical instances using integer linear programming (ILP). The experimental results demonstrate that optimal solutions to the test droplets dispensing problem in microfluidic biochip parallel testing are indeed feasible.

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Lee, Moo-Yeal, Aravind Srinivasan, Bosung Ku, and Jonathan S. Dordick. "Multienzyme catalysis in microfluidic biochips." Biotechnology and Bioengineering 83, no. 1 (May 5, 2003): 20–28. http://dx.doi.org/10.1002/bit.10642.

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Chiu, Yi-Lung, Ruchi Ashok Kumar Yadav, Hong-Yuan Huang, Yi-Wen Wang, and Da-Jeng Yao. "Unveiling the Potential of Droplet Generation, Sorting, Expansion, and Restoration in Microfluidic Biochips." Micromachines 10, no. 11 (November 6, 2019): 756. http://dx.doi.org/10.3390/mi10110756.

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Microfluidic biochip techniques are prominently replacing conventional biochemical analyzers by the integration of all functions necessary for biochemical analysis using microfluidics. The microfluidics of droplets offer exquisite control over the size of microliter samples to satisfy the requirements of embryo culture, which might involve a size ranging from picoliter to nanoliter. Polydimethylsiloxane (PDMS) is the mainstream material for the fabrication of microfluidic devices due to its excellent biocompatibility and simplicity of fabrication. Herein, we developed a microfluidic biomedical chip on a PDMS substrate that integrated four key functions—generation of a droplet of an emulsion, sorting, expansion and restoration, which were employed in a mouse embryo system to assess reproductive medicine. The main channel of the designed chip had width of 1200 μm and height of 500 μm. The designed microfluidic chips possessed six sections—cleaved into three inlets and three outlets—to study the key functions with five-day embryo culture. The control part of the experiment was conducted with polystyrene (PS) beads (100 μm), the same size as the murine embryos, for the purpose of testing. The outcomes of our work illustrate that the rate of success of the static droplet culture group (87.5%) is only slightly less than that of a conventional group (95%). It clearly demonstrates that a droplet-based microfluidic system can produce a droplet in a volume range from picoliter to nanoliter.

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Dissertations / Theses on the topic "Microfluidic biochips"

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DIVAKAR, RAMGOPAL. "ROOM TEMPERATURE ADHESIVE BONDING TECHNIQUE FOR MICROFLUIDIC BIOCHIPS." University of Cincinnati / OhioLINK, 2002. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1027950500.

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MYNENI, PHALGUN. "INFRARED BASED THERMOCYCLING SYSTEM FOR MICROFLUIDIC PCR BIOCHIPS." University of Cincinnati / OhioLINK, 2004. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1085756783.

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Guo, Wenpeng, and 郭文鹏. "Enhancing capabilities of microfluidic chip-capillary devices to extend working range, adjust analyte/sample ratio and improve sample/reagent mixing in biomedical analysis." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2011. http://hub.hku.hk/bib/B46589673.

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Cui, Huanchun. "Nonlinear electrophoresis in networked microfluidic chips." Online access for everyone, 2007. http://www.dissertations.wsu.edu/Dissertations/Fall2007/h_cui_110207.pdf.

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Todakar, Onkar. "FPGA-based fault tolerant design and deterministic routing-based synthesis for Digital Microfluidic Biochips." University of Cincinnati / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1447071424.

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Tseng, Tsun-Ming [Verfasser], Ulf [Akademischer Betreuer] [Gutachter] Schlichtmann, and Tsung-Yi [Gutachter] Ho. "Design Automation for Continuous-Flow Microfluidic Biochips / Tsun-Ming Tseng ; Gutachter: Ulf Schlichtmann, Tsung-Yi Ho ; Betreuer: Ulf Schlichtmann." München : Universitätsbibliothek der TU München, 2017. http://d-nb.info/1140586548/34.

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Marchington, Robert F. "Applications of microfluidic chips in optical manipulation & photoporation." Thesis, University of St Andrews, 2010. http://hdl.handle.net/10023/1633.

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Integration and miniaturisation in electronics has undoubtedly revolutionised the modern world. In biotechnology, emerging lab-on-a-chip (LOC) methodologies promise all-integrated laboratory processes, to perform complete biochemical or medical synthesis and analysis encapsulated on small microchips. The integration of electrical, optical and physical sensors, and control devices, with fluid handling, is creating a new class of functional chip-based systems. Scaled down onto a chip, reagent and sample consumption is reduced, point-of-care or in-the-field usage is enabled through portability, costs are reduced, automation increases the ease of use, and favourable scaling laws can be exploited, such as improved fluid control. The capacity to manipulate single cells on-chip has applications across the life sciences, in biotechnology, pharmacology, medical diagnostics and drug discovery. This thesis explores multiple applications of optical manipulation within microfluidic chips. Used in combination with microfluidic systems, optics adds powerful functionalities to emerging LOC technologies. These include particle management such as immobilising, sorting, concentrating, and transportation of cell-sized objects, along with sensing, spectroscopic interrogation, and cell treatment. The work in this thesis brings several key applications of optical techniques for manipulating and porating cell-sized microscopic particles to within microfluidic chips. The fields of optical trapping, optical tweezers and optical sorting are reviewed in the context of lab-on-a-chip application, and the physics of the laminar fluid flow exhibited at this size scale is detailed. Microfluidic chip fabrication methods are presented, including a robust method for the introduction of optical fibres for laser beam delivery, which is demonstrated in a dual-beam optical trap chip and in optical chromatography using photonic crystal fibre. The use of a total internal reflection microscope objective lens is utilised in a novel demonstration of propelling particles within fluid flow. The size and refractive index dependency is modelled and experimentally characterised, before presenting continuous passive optical sorting of microparticles based on these intrinsic optical properties, in a microfluidic chip. Finally, a microfluidic system is utilised in the delivery of mammalian cells to a focused femtosecond laser beam for continuous, high throughput photoporation. The optical injection efficiency of inserting a fluorescent dye is determined and the cell viability is evaluated. This could form the basis for ultra-high throughput, efficient transfection of cells, with the advantages of single cell treatment and unrivalled viability using this optical technique.

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Bai, Yunling. "Surface modifications for enhanced immobilization of biomolecules applications in biocatalysts and immuno-biosensor /." Columbus, Ohio : Ohio State University, 2006. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1149085708.

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Gupta, Madhuri N. "Multi-Board Digital Microfluidic Biochip Synthesis with Droplet Crossover Optimization." University of Cincinnati / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1393237106.

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Naudot, Marie. "Caractérisation par imagerie en temps réel de cultures cellulaires hépatiques en biopuces microfluidiques." Phd thesis, Université de Technologie de Compiègne, 2013. http://tel.archives-ouvertes.fr/tel-00965539.

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Le développement de méthodes alternatives à la culture in vivo pour l'évaluation de la toxicité des molécules chimiques s'est accéléré ces dernières années, l'objectif étant de limiter l'utilisation d'animaux. Préconisés par l'OCDE (Organisation de coopération et de développement économiques), ces modèles alternatifs visent à mimer les conditions physiologiques en employant des systèmes in vitro ou in silico. Parmi les différents systèmes développés, les biopuces microfluidiques ont prouvé leur contribution à l'amélioration des fonctions cellulaires, ce qui permet des études toxicologiques pertinentes. Les travaux de ce doctorat sont basés sur l'emploi de ces biopuces pour cultiver des hépatocytes (cellules du foie) et portent sur la mise au point d'une méthode d'analyse d'images issues de ces cultures sous microscope au cours du temps. L'acquisition d'images tout au long de l'expérience permet de suivre, après traitement, l'évolution et le comportement des cellules au contact de molécules chimiques et d'évaluer les réponses toxicologiques. Les premiers résultats de ces travaux ont permis l'amélioration du procédé de culture microfluidique adaptée au matériel d'acquisition d'images, la sélection de sondes fluorescentes, et le choix d'un algorithme de traitement des images sur CellProfiler. Cela nous a permis de quantifier et caractériser certaines fonctions biologiques au sein de la biopuce comme l'activité mitochondriale. Le potentiel de cet outil pour évaluer la toxicité de molécule a été testé grâce à l'emploi d'un toxique connu : la staurosporine. Les résultats obtenus ont révélé l'impact de la mise en culture en dynamique sur le comportement des hépatocytes, et la toxicité de la staurosporine visible en biopuce.

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Books on the topic "Microfluidic biochips"

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Chakrabarty, Krishnendu. Digital microfluidic biochips: Design automation and optimization. Boca Raton: Taylor & Francis, 2010.

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Pop, Paul, Mirela Alistar, Elena Stuart, and Jan Madsen. Fault-Tolerant Digital Microfluidic Biochips. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-23072-6.

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Keszocze, Oliver, Robert Wille, and Rolf Drechsler. Exact Design of Digital Microfluidic Biochips. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-90936-3.

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Tang, Jack, Mohamed Ibrahim, Krishnendu Chakrabarty, and Ramesh Karri. Secure and Trustworthy Cyberphysical Microfluidic Biochips. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-18163-5.

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1982-, Xu Tao, ed. Digital microfluidic biochips: Design automation and optimization. Boca Raton: Taylor & Francis, 2010.

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6

Yang, Zhao. Design and Testing of Digital Microfluidic Biochips. New York, NY: Springer New York, 2013.

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Zhao, Yang, and Krishnendu Chakrabarty. Design and Testing of Digital Microfluidic Biochips. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0370-8.

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Li, Zipeng, Krishnendu Chakrabarty, Tsung-Yi Ho, and Chen-Yi Lee. Micro-Electrode-Dot-Array Digital Microfluidic Biochips. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-02964-7.

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Microfluidic lab-on-a-chip for chemical and biological analysis and discovery. Boca Raton, Fla: Taylor & Francis, 2005.

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Hu, Kai, Krishnendu Chakrabarty, and Tsung-Yi Ho. Computer-Aided Design of Microfluidic Very Large Scale Integration (mVLSI) Biochips. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-56255-1.

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Book chapters on the topic "Microfluidic biochips"

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Tang, Jack, Mohamed Ibrahim, Krishnendu Chakrabarty, and Ramesh Karri. "Cyberphysical Microfluidic Biochips." In Secure and Trustworthy Cyberphysical Microfluidic Biochips, 1–17. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-18163-5_1.

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Zhang, C. X., and A. Manz. "Trends in Microfluidic Devices for Analytical Chemistry." In Biochips, 101–34. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05092-7_9.

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Liu, Robin H., Ralf Lenigk, Kenneth R. Luehrsen, Huinan Yu, Haixu Chen, Dale Ganser, Justin Bonanno, and Piotr Grodzinski. "Integrated Microfluidic DNA Array Biochips." In Micro Total Analysis Systems 2001, 465–67. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-1015-3_200.

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Pop, Paul, Mirela Alistar, Elena Stuart, and Jan Madsen. "Synthesis of Fault-Tolerant Biochips." In Fault-Tolerant Digital Microfluidic Biochips, 197–207. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-23072-6_13.

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Ugaz, Victor M. "PCR in Integrated Microfluidic Systems." In Integrated Biochips for DNA Analysis, 90–106. New York, NY: Springer New York, 2007. http://dx.doi.org/10.1007/978-0-387-76759-8_7.

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Pop, Paul, Mirela Alistar, Elena Stuart, and Jan Madsen. "Design Methodology for Digital Microfluidic Biochips." In Fault-Tolerant Digital Microfluidic Biochips, 13–28. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-23072-6_2.

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Pop, Paul, Mirela Alistar, Elena Stuart, and Jan Madsen. "Biochip Architecture Model." In Fault-Tolerant Digital Microfluidic Biochips, 29–50. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-23072-6_3.

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Pop, Paul, Mirela Alistar, Elena Stuart, and Jan Madsen. "Introduction." In Fault-Tolerant Digital Microfluidic Biochips, 1–10. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-23072-6_1.

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Pop, Paul, Mirela Alistar, Elena Stuart, and Jan Madsen. "Fault-Tolerant Module-Based Compilation." In Fault-Tolerant Digital Microfluidic Biochips, 137–43. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-23072-6_10.

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Pop, Paul, Mirela Alistar, Elena Stuart, and Jan Madsen. "Compilation for Error Recovery." In Fault-Tolerant Digital Microfluidic Biochips, 145–74. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-23072-6_11.

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Conference papers on the topic "Microfluidic biochips"

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Chakrabarty, Krishnendu. "Digital Microfluidics: Connecting Biochemistry to Electronic System Design." In ASME 2007 5th International Conference on Nanochannels, Microchannels, and Minichannels. ASMEDC, 2007. http://dx.doi.org/10.1115/icnmm2007-30158.

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Microfluidics-based biochips are revolutionizing high-throughput sequencing, parallel immunoassays, blood chemistry for clinical diagnostics, DNA sequencing, and environmental sensing. The complexity of microfluidic devices, also referred to as lab-on-a-chip, is expected to become significant in the near future due to the need for multiple and concurrent biochemical assays on multifunctional and reconfigurable platforms. This paper provides an overview of droplet-based “digital” microfluidic biochips. It presents early work on top-down system-level computer-aided design (CAD) tools for the synthesis, testing and reconfiguration of microfluidic biochips. These CAD techniques allow the biochip to concentrate on the development of the nano- and micro-scale bioassays, leaving assay optimization and implementation details to design automation tools.

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Ho, Tsung-Yi, Krishnendu Chakrabarty, and Paul Pop. "Digital microfluidic biochips." In the seventh IEEE/ACM/IFIP international conference. New York, New York, USA: ACM Press, 2011. http://dx.doi.org/10.1145/2039370.2039422.

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Chakrabarty, Krishnendu, Paul Pop, and Tsung-Yi Ho. "Digital microfluidic biochips." In the seventh IEEE/ACM/IFIP international conference. New York, New York, USA: ACM Press, 2011. http://dx.doi.org/10.1145/2039370.2039430.

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Chakrabarty, Krishnendu. "Digital Microfluidic Biochips." In GLSVLSI '15: Great Lakes Symposium on VLSI 2015. New York, NY, USA: ACM, 2015. http://dx.doi.org/10.1145/2742060.2745701.

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Minot, Michael J., David W. Stowe, Michael A. Detarando, Joseph A. Krans, and Jason L. Kass. "Microfluidic microwell and microcapillary biochips." In Biomedical Optics 2006, edited by Alexander N. Cartwright and Dan V. Nicolau. SPIE, 2006. http://dx.doi.org/10.1117/12.641124.

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Hsieh, Ching-Wei, Zipeng Li, and Tsung-Yi Ho. "Piracy prevention of digital microfluidic biochips." In 2017 22nd Asia and South Pacific Design Automation Conference (ASP-DAC). IEEE, 2017. http://dx.doi.org/10.1109/aspdac.2017.7858374.

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Bhattacharya, Bhargab B. "Digital Microfluidic Biochips: Design and Testing." In 2008 IEEE Region 10 and the Third international Conference on Industrial and Information Systems (ICIIS). IEEE, 2008. http://dx.doi.org/10.1109/iciinfs.2008.4798322.

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Chakrabarty, Krishnendu. "Design and Test of Microfluidic Biochips." In 2007 IEEE Design and Diagnostics of Electronic Circuits and Systems. IEEE, 2007. http://dx.doi.org/10.1109/ddecs.2007.4295247.

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Ibrahim, Mohamed, and Krishnendu Chakrabarty. "Cyberphysical adaptation in digital-microfluidic biochips." In 2016 IEEE Biomedical Circuits and Systems Conference (BioCAS). IEEE, 2016. http://dx.doi.org/10.1109/biocas.2016.7833827.

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Grissom, Daniel, and Philip Brisk. "Path scheduling on digital microfluidic biochips." In the 49th Annual Design Automation Conference. New York, New York, USA: ACM Press, 2012. http://dx.doi.org/10.1145/2228360.2228367.

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Reports on the topic "Microfluidic biochips"

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Ahn, Chong H., Joseph H. Nevin, and Gregory Beaucage. Plastic-Based Structurally Programmable Microfluidic Biochips for Clinical Diagnostics. Fort Belvoir, VA: Defense Technical Information Center, May 2005. http://dx.doi.org/10.21236/ada435658.

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