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用于表观遗传学的 ISFET 适配:概述。

Adapting ISFETs for Epigenetics: An Overview.

出版信息

IEEE Trans Biomed Circuits Syst. 2018 Oct;12(5):1186-1201. doi: 10.1109/TBCAS.2018.2838153. Epub 2018 Jul 13.

Abstract

This paper gives an overview of how CMOS design methods can be applied to ion-sensitive field effect transistor (ISFETs) for pH-based DNA methylation and miRNA detection. Design specifications are fundamentally defined by the choice of analysis. As such, the focus for DNA methylation was on developing front-end analogue circuits to carry out Methylation-specific PCR (MSP) for Point-of-Care applications, and sequencing for detailed analysis. The use of MSP prompted the design of an ISFET weak inversion current mirror topology for differential sensing and reduction of drift and temperature sensitivities. The primary limitation in ion-semiconductor sequencing is base calling of repeated nucleotides known as homopolymers. Implementation of a switched current integrator can potentially increase both accuracy and window for detection, within the frequency region of DNA reactions. For quantifying miRNAs, digital back-end processing circuits were considered toward a fully portable platform that can carry out real-time monitoring of DNA amplification reactions. Two systems to evaluate threshold cycles were developed, based on the Derivative method and a new proposed 3-point exponential evaluation aim to reduce detection time simultaneously. Both implementations were tested with datasets from fluorescent qPCR reactions, as well as pH-LAMP experiments that have been optimized for on-chip amplifications. All designs were fabricated in unmodified CMOS with performance assessed based on functionality as well as pH-resolution required in practice.

摘要

本文概述了如何将 CMOS 设计方法应用于离子敏场效应晶体管 (ISFET),用于基于 pH 的 DNA 甲基化和 miRNA 检测。设计规范从根本上由分析选择定义。因此,DNA 甲基化的重点是开发前端模拟电路,以进行即时护理应用中的甲基化特异性聚合酶链反应 (MSP),以及用于详细分析的测序。MSP 的使用促使设计了一种 ISFET 弱反型电流镜拓扑结构,用于差分感测和降低漂移和温度灵敏度。离子半导体测序的主要限制是对称为重复核苷酸的重复核苷酸的碱基调用。开关电流积分器的实现可以在 DNA 反应的频率范围内,潜在地提高准确性和检测窗口。为了定量检测 miRNA,考虑了数字后端处理电路,以实现可进行 DNA 扩增反应实时监测的完全便携式平台。根据导数法和新提出的三点指数评估法,开发了两种评估阈值循环的系统,旨在同时减少检测时间。这两种实现都使用荧光 qPCR 反应的数据集以及已针对芯片上扩增进行了优化的 pH-LAMP 实验进行了测试。所有设计均在未经修改的 CMOS 中制造,并根据功能以及实际所需的 pH 分辨率来评估性能。

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