用于数字微流控生物芯片的合成微电极点阵列驱动验证框架

Pushpita Roy, A. Banerjee
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引用次数: 0

摘要

数字微流体技术是一种新兴的生物化学实验室自动化技术。随着越来越多复杂的生化方案被映射到生物芯片设备和微流体得到广泛采用,开发自动化工具和合成平台变得必不可少,这些工具和合成平台可以使复杂繁琐的台式实验室程序顺利转换为生物芯片执行。给定非正式/半正式的分析描述和必须在其上实施分析的目标微流体网格结构,合成工具通常将高级分析操作转换为可以在网格上驱动分析实现的低级驱动序列。随着越来越多复杂的生化分析方案被用于合成和支持更广泛操作的生物芯片(例如,微电极点阵列(MEDAs)),分析合成的任务变得错综复杂。合成分析描述中的错误可能在分析操作中产生不良后果,导致在生物芯片上执行后产生不可接受的结果。在这项工作中,我们专注于检查合成方案描述的正确性的挑战,然后在微流控生物芯片上实现它们。特别地,我们针对MEDA生物芯片合成了一个协议描述,并采用形式化分析的方法推导出正确的证明或违反协议的证明,指出错误翻译中的确切操作。我们提出了一些生物测定方案的实验结果,并展示了我们的框架对可验证方案合成的效用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Framework for Validation of Synthesized MicroElectrode Dot Array Actuations for Digital Microfluidic Biochips
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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