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  • Association for Computing Machinery (ACM)  (2)
  • 2010-2014  (2)
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  • Association for Computing Machinery (ACM)  (2)
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  • 2010-2014  (2)
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  • 1
    Online Resource
    Online Resource
    Association for Computing Machinery (ACM) ; 2012
    In:  ACM Journal on Emerging Technologies in Computing Systems Vol. 8, No. 3 ( 2012-08), p. 1-23
    In: ACM Journal on Emerging Technologies in Computing Systems, Association for Computing Machinery (ACM), Vol. 8, No. 3 ( 2012-08), p. 1-23
    Abstract: Potential applications of digital microfluidic (DMF) biochips now include several areas of real-life applications like environmental monitoring, water and air pollutant detection, and food processing to name a few. In order to achieve sufficiently high throughput for these applications, several instances of the same bioassay may be required to be executed concurrently on different samples. As a straightforward implementation, several identical biochips can be integrated on a single substrate as a multichip to execute the assay for various samples concurrently. Controlling individual electrodes of such a chip by independent pins may not be acceptable since it increases the cost of fabrication. Thus, in order to keep the overall pin-count within an acceptable bound, all the respective electrodes of these individual pieces are connected internally underneath the chip so that they can be controlled with a single external control pin. In this article, we present an orientation strategy for layout of a multichip that reduces routing congestion and consequently facilitates wire routing for the electrode array. The electrode structure of the individual pieces of the multichip may be either direct-addressable or pin-constrained. The method also supports a hierarchical approach to wire routing that ensures scalability. In this scheme, the size of the biochip in terms of the total number of electrodes may be increased by a factor of four by increasing the number of routing layers by only one. In general, for a multichip with 4 n identical blocks, ( n + 1) layers are sufficient for wire routing.
    Type of Medium: Online Resource
    ISSN: 1550-4832 , 1550-4840
    Language: English
    Publisher: Association for Computing Machinery (ACM)
    Publication Date: 2012
    detail.hit.zdb_id: 2198029-9
    detail.hit.zdb_id: 2193538-5
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  • 2
    Online Resource
    Online Resource
    Association for Computing Machinery (ACM) ; 2014
    In:  ACM Journal on Emerging Technologies in Computing Systems Vol. 11, No. 1 ( 2014-10-06), p. 1-33
    In: ACM Journal on Emerging Technologies in Computing Systems, Association for Computing Machinery (ACM), Vol. 11, No. 1 ( 2014-10-06), p. 1-33
    Abstract: Digital microfluidic (DMF) biochips are recently being advocated for fast on-chip implementation of biochemical laboratory assays or protocols, and several algorithms for diluting and mixing of reagents have been reported. However, all methods for such automatic sample preparation suffer from a drawback that they assume the availability of input fluids in pure form, that is, each with an extreme concentration factor ( CF ) of 100%. In many real-life scenarios, the stock solutions consist of samples/reagents with multiple CF s. No algorithm is yet known for preparing a target mixture of fluids with a given ratio when its constituents are supplied with random concentrations. An intriguing question is whether or not a given target ratio is feasible to produce from such a general input condition. In this article, we first study the feasibility properties for the generalized mixing problem under the (1:1) mix-split model with an allowable error in the target CF s not exceeding 1 2d, where the integer d is user specified and denotes the desired accuracy level of CF . Next, an algorithm is proposed which produces the desired target ratio of N reagents in ONd mix-split steps, where N ( ≥ 3) denotes the number of constituent fluids in the mixture. The feasibility analysis also leads to the characterization of the total space of input stock solutions from which a given target mixture can be derived, and conversely, the space of all target ratios, which are derivable from a given set of input reagents with arbitrary CF s. Finally, we present a generalized algorithm for diluting a sample S in minimum (1:1) mix-split steps when two or more arbitrary concentrations of S (diluted with the same buffer) are supplied as inputs. These results settle several open questions in droplet-based algorithmic microfluidics and offer efficient solutions for a wider class of on-chip sample preparation problems.
    Type of Medium: Online Resource
    ISSN: 1550-4832 , 1550-4840
    Language: English
    Publisher: Association for Computing Machinery (ACM)
    Publication Date: 2014
    detail.hit.zdb_id: 2198029-9
    detail.hit.zdb_id: 2193538-5
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
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