The DeSyRe project builds on-demand adaptive and reliable Systems-on-Chips (SoCs). As fabrication technology scales down, chips are becoming less reliable, thereby incurring increased power and performance costs for fault tolerance. To make matters worse, power density is becoming a significant limiting factor in SoC design, in general. In the face of such changes in the technological landscape, current solutions for fault tolerance are expected to introduce excessive overheads in future systems. Moreover, attempting to design and manufacture a totally defect-/fault-free system, would impact heavily, even prohibitively, the design, manufacturing, and testing costs, as well as the system performance and power consumption. In this context, DeSyRe delivers a new generation of systems that are reliable by design at well-balanced power, performance, and design costs. In our attempt to reduce the overheads of fault-tolerance, only a small fraction of the chip is built to be fault-free. This fault-free part is then employed to manage the remaining fault-prone resources of the SoC. The DeSyRe framework is applied to two medical systems with high safety requirements (measured using the IEC 61508 functional safety standard) and tight power and performance constraints.@en

The DeSyRe project builds on-demand adaptive, reliable Systems-on-Chips. In response to the current semiconductor technology trends thatmake chips becoming less reliable, DeSyRe describes a newgeneration of by design reliable systems, at a reduced power and performance cost. This is achieved through the following main contributions. DeSyRe defines a fault-tolerant system architecture built out of unreliable components, rather than aiming at totally fault-free and hence more costly chips. In addition, DeSyRe systems are on-demand adaptive to various types and densities of faults, as well as to other system constraints and application requirements. For leveraging on-demand adaptation/customization and reliability at reduced cost, a new dynamically reconfigurable substrate is designed and combined with runtime system software support. The above define a generic and repeatable design framework, which is applied to two medical SoCs with high reliability constraints and diverse performance and power requirements. One of the main goals of the DeSyRe project is to increase the availability of SoC components in the presence of permanents faults, caused at manufacturing time or due to device aging. A mix of coarse- and fine-grain reconfigurable hardware substrate is designed to isolate and bypass faulty component parts. The flexibility provided by the DeSyRe reconfigurable substrate is exploited at runtime by system optimization heuristics,which decide tomodify component configurationwhen a permanent fault is detected, providing graceful degradation.@en

The Inferior-Olivary nucleus (ION) is a well-charted region of the brain, heavily associated with sensorimotor control of the body. It comprises ION cells with unique properties which facilitate sensory processing and motor-learning skills. Various simulation models of ION-cell networks have been written in an attempt to unravel their mysteries. However, simulations become rapidly intractable when biophysically plausible models and meaningful network sizes (100 cells) are modeled. To overcome this problem, in this work we port a highly detailed ION cell network model, originally coded in Matlab, onto an FPGA chip. It was first converted to ANSI C code and extensively profiled. It was, then, translated to HLS C code for the Xilinx Vivado toolflow and various algorithmic and arithmetic optimizations were applied. The design was implemented in a Virtex 7 (XC7VX485T) device and can simulate a 96-cell network at real-time speed, yielding a speedup of 700 compared to the original Matlab code and 12.5 compared to the reference C implementation running on a Intel Xeon 2.66GHz machine with 20GB RAM. For a 1,056-cell network (non-real-time), an FPGA speedup of 45 against the C code can be achieved, demonstrating the design's usefulness in accelerating neuroscience research. Limited by the available on-chip memory, the FPGA can maximally support a 14,400-cell network (non-real-time) with online parameter configurability for cell state and network size. The maximum throughput of the FPGA IONnetwork accelerator can reach 2.13 GFLOPS.@en

The fast growth of bioinformatics field has attracted the attention of computer scientists in the last few years. At the same time the increasing database sizes require greater efforts to improve the computational performance. From a computer architecture point of view, we intend to investigate how bioinformatics applications can benefit from future multi-core processors. In this paper we present a preliminary study of the Cell BE processor limitations when executing two representative sequence alignment applications (Ssearch and ClustalW). The inherent large parallelism of the targeted algorithms makes them ideal for architectures supporting multiple dimensions of parallelism (TLP and DLP). However, in the case of Cell BE we identified several architectural limitations that need a careful study and quantification.@en