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Proceedings ArticleDOI

Sample preparation for multiple-reactant bioassays on micro-electrode-dot-array biochips

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TLDR
A generic multiple-reactant sample preparation algorithm that exploits the novel fluidic operations on MEDA biochips and outperforms existing methods in terms of saving reactant cost, minimizing the number of operations, and reducing the amount of waste.
Abstract
Sample preparation, as a key procedure in many biochemical protocols, mixes various samples and/or reagents into solutions that contain the target concentrations. Digital microfluidic biochips (DMFBs) have been adopted as a platform for sample preparation because they provide automatic procedures that require less reactant consumption and reduce human-induced errors. However, traditional DMFBs only utilize the (1:1) mixing model, i.e., only two droplets of the same volume can be mixed at a time, which results in higher completion time and the wastage of valuable reactants. To overcome this limitation, a next-generation micro-electrode-dot-array (MEDA) architecture that provides flexibility of mixing multiple droplets of different volumes in a single operation was proposed. In this paper, we present a generic multiple-reactant sample preparation algorithm that exploits the novel fluidic operations on MEDA biochips. Simulated experiments show that the proposed method outperforms existing methods in terms of saving reactant cost, minimizing the number of operations, and reducing the amount of waste.

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Citations
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Journal ArticleDOI

Multitarget Sample Preparation Using MEDA Biochips

TL;DR: This article presents a generic multiple-reactant sample preparation algorithm that exploits the novel fluidic operations on MEDA biochips and proposes an enhanced algorithm that increases the operation-sharing opportunities when multiple target concentrations are needed, and therefore the usage of reactants can be further reduced.
Journal ArticleDOI

Secure Assay Execution on MEDA Biochips to Thwart Attacks Using Real-Time Sensing

TL;DR: This work proposes a security mechanism that validates assay execution by reconstructing the sequencing graph from the droplet-location maps and comparing it against the golden sequencing graph, and proves that there is a unique (one-to-one) mapping from the set ofDroplet- location maps (over the duration of the assay) to theSet of possible sequencing graphs.
Journal ArticleDOI

Hardware Design and Fault-Tolerant Synthesis for Digital Acoustofluidic Biochips

TL;DR: A hardware design that can efficiently activate/de-activated each IDT, and can fully automate an bio-protocol is presented, and a fault-tolerant synthesis technique that allows us to automatically map biomolecular protocols to acoustofluidic biochips is presented.
Proceedings ArticleDOI

Fault Recovery in Micro-Electrode-Dot-Array Digital Microfluidic Biochips Using an IJTAG NetworkBehaviors

TL;DR: An effective fault- recovery solution based on the homogeneous structure of MEDA is presented, whereby the microelectrode cell (MCs) in a MEDA biochip are identical, and multiplexers are added for reconfigurability, whereby an MC with faulty components can use the hardware resources in a neighboring MC.
Proceedings ArticleDOI

Structural Test and Functional Test for Digital Acoustofluidic Biochips

TL;DR: This paper presents the first approach for testing of an acoustofluidic biochip that includes an array of interdigital transducers (IDTs) and presents structural test techniques to evaluate the pass/fail status of each IDT, and identifies the type of fault if it fails.
References
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