Affiliation:
1. Duke University, Durham, NC
2. New York University, Brooklyn, NY
Abstract
Digital microfluidic biochips (DMFBs) have emerged as a promising platform for DNA sequencing, clinical chemistry, and point-of-care diagnostics. Recent research has shown that DMFBs are susceptible to various types of malicious attacks. Defenses proposed thus far only offer probabilistic guarantees of security due to the limitation of on-chip sensor resources. A micro-electrode-dot-array (MEDA) biochip is a next-generation DMFB that enables the real-time sensing of on-chip droplet locations, which are captured in the form of a droplet-location map. We propose a security mechanism that validates assay execution by reconstructing the sequencing graph (i.e., the assay specification) from the droplet-location maps and comparing it against the golden sequencing graph. We prove that there is a unique (one-to-one) mapping from the set of droplet-location maps (over the duration of the assay) to the set of possible sequencing graphs. Any deviation in the droplet-location maps due to an attack is detected by this countermeasure because the resulting derived sequencing graph is not isomorphic to the original sequencing graph. We highlight the strength of the security mechanism by simulating attacks on real-life bioassays. We also address the concern that the proposed mechanism may raise false alarms when some fluidic operations are executed on MEDA biochips. To avoid such false alarms, we propose an enhanced sensing technique that provides fine-grained sensing for the security mechanism.
Funder
Army Research Office
National Science Foundation
Publisher
Association for Computing Machinery (ACM)
Subject
Electrical and Electronic Engineering,Computer Graphics and Computer-Aided Design,Computer Science Applications
Cited by
7 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献