Energy-Aware Processing Platform Exploration for Embedded Biosignal Analysis

According to the World Health Organization, lifestyle-related diseases, e.g., cardiovascular diseases are the major cause of mortality worldwide. An accurate and continuous medical supervision is highly required for diagnosis and treatment of such diseases. Our traditional healthcare delivery systems, however can’t cope with consequential increasing healthcare costs and medical management needs. Personal health monitoring systems are poised to offer large-scale and cost-effective solutions to this problem. The use of wearable, miniaturized and autonomous wireless sensor nodes, featuring continuous on-node analysis of biosignals, can indeed provide ambulatory long-term and real-time monitoring required by the patients, and enables faster coordination with medical personnel. In such autonomous nodes, due to very limited available energy resources and costly wireless transmission, an ultra-low-power (ULP) on-node processing platform for advanced biosignal analysis is crucial. In this thesis, I explore ULP processing architectures for on-node biosignal analysis applications; where commonly, moderately complex arithmetic manipulations on single- or multiple- input signals are carried out. To achieve energy efficiency while providing sufficient processing capability to apply advanced biosignal analysis, in this thesis near-threshold (near-Vt h ) computing is exploited. Hence, severe performance degradation and reliability issues, occurring at deeply scaled voltages, can be avoided. In Chapter 3, I introduce a near-Vth computing single-core architecture, consisting of a ULP core, an instruction memory (IM) and a data memory (DM). The ULP core features an instruction set architecture (ISA) customized for biosignal applications. I explore that an ISA with minimal instruction set achieves considerable energy savings compared to the state-of-the-art cores, when executing biosignal applications (i.e., up to 54% compared to an established ISA). The proposed single-core architecture accomplishes high energy efficiency for most of single-input biosignal analysis applications, since it fully exploits near-Vth computing. However, the single-core architecture achieves limited voltage scaling, hence reduced energy awareness, for most of multiple-input biosignal analysis applications, where computational workload requirements are such high that the single-core architecture can’t attain these throughputs in near-Vth regime. To alleviate the performance degradation issue that prevents the single-core architecture from exploiting near-Vt h computing typically for multiple-input biosignal analysis, I propose parallel processing of biosignals on multi-core architectures. To this end, In Chapter 4, a multiple instruction, multiple data (MIMD) multi-core architecture is introduced. The MIMD architecture comprises several ULP cores, individual IMs, and a multi-bank DM shared through a lightweight interconnect between the cores and the DM. I prove that parallel processing of