71 research outputs found

    Quality and Quantity in Robustness-Checking Using Formal Techniques

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    Fault tolerance is one of the main challenges for future technology scaling to tolerate transient faults. Various techniques at design level are available to catch and handle transient faults, e.g., Triple Modular Redundancy. An important but missing step is to verify the implementation of those techniques since the implementation might be buggy itself. The thesis is focusing on formally verifying digital circuits with respect to fault-tolerant aspects. It considers transient faults and basically checks whether these faults can influence the output behavior of sequential circuits for any kind of scenarios. As a result the designer is pin-pointed directly to critical parts of the design and gets a prove about the absence of faulty behavior for non-critical parts. The focus of the verification is completeness with respect to the analysis. Three issues need to be adequately addressed: 1) cover all input stimuli, 2) all possible transient faults, and, 3) all possibly exponential long (wrt. to number of state bits) propagation paths. All three issues are addressed in different engines. A tool called RobuCheck has been implemented and evaluated on different academic benchmarks from ITC'99 and industrial benchmarks from IBM

    ATPG for Reversible Circuits Using Simulation, Boolean Satisfiability, and Pseudo Boolean Optimization

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    Abstract—Research in the domain of reversible circuits found significant interest in the last years – not least because of the promising applications e.g. in quantum computation and low-power design. First physical realizations are already available, motivating the development of efficient testing methods for this kind of circuits. In this paper, complementary approaches for automatic test pattern generation for reversible circuits are introduced and evaluated. Besides a simulation-based technique, methods based on Boolean satisfiability and pseudo-Boolean optimization are thereby applied. Experiments on large reversible circuits show the suitability of the proposed approaches with re-spect to different application scenarios and test goals, respectively. I

    Compressed Skewed-Load Delay Test Generation Based on Evolution and Deterministic Initialization of Populations

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    The current design and manufacturing semiconductor technologies require to test the products against delay related defects. However, complex acpSOC require low-overhead testability methods to keep the test cost at an acceptable level. Skewed-load tests seem to be the appropriate way to test delay faults in these acpSOC because the test application requires only one storage element per scan cell. Compressed skewed-load test generator based on genetic algorithm is proposed for wrapper-based logic cores of acpSOC. Deterministic population initialization is used to ensure the highest achievable aclTDF coverage for the given wrapper and scan cell order. The developed method performs test data compression by generating test vectors containing already overlapped test vector pairs. The experimental results show high fault coverages, decreased test lengths and better scalability in comparison to recent methods

    Application of Logic Synthesis Toward the Inference and Control of Gene Regulatory Networks

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    In the quest to understand cell behavior and cure genetic diseases such as cancer, the fundamental approach being taken is undergoing a gradual change. It is becoming more acceptable to view these diseases as an engineering problem, and systems engineering approaches are being deployed to tackle genetic diseases. In this light, we believe that logic synthesis techniques can play a very important role. Several techniques from the field of logic synthesis can be adapted to assist in the arguably huge effort of modeling cell behavior, inferring biological networks, and controlling genetic diseases. Genes interact with other genes in a Gene Regulatory Network (GRN) and can be modeled as a Boolean Network (BN) or equivalently as a Finite State Machine (FSM). As the expression of genes deter- mine cell behavior, important problems include (i) inferring the GRN from observed gene expression data from biological measurements, and (ii) using the inferred GRN to explain how genetic diseases occur and determine the ”best” therapy towards treatment of disease. We report results on the application of logic synthesis techniques that we have developed to address both these problems. In the first technique, we present Boolean Satisfiability (SAT) based approaches to infer the predictor (logical support) of each gene that regulates melanoma, using gene expression data from patients who are suffering from the disease. From the output of such a tool, biologists can construct targeted experiments to understand the logic functions that regulate a particular target gene. Our second technique builds upon the first, in which we use a logic synthesis technique; implemented using SAT, to determine gene regulating functions for predictors and gene expression data. This technique determines a BN (or family of BNs) to describe the GRN and is validated on a synthetic network and the p53 network. The first two techniques assume binary valued gene expression data. In the third technique, we utilize continuous (analog) expression data, and present an algorithm to infer and rank predictors using modified Zhegalkin polynomials. We demonstrate our method to rank predictors for genes in the mutated mammalian and melanoma networks. The final technique assumes that the GRN is known, and uses weighted partial Max-SAT (WPMS) towards cancer therapy. In this technique, the GRN is assumed to be known. Cancer is modeled using a stuck-at fault model, and ATPG techniques are used to characterize genes leading to cancer and select drugs to treat cancer. To steer the GRN state towards a desirable healthy state, the optimal selection of drugs is formulated using WPMS. Our techniques can be used to find a set of drugs with the least side-effects, and is demonstrated in the context of growth factor pathways for colon cancer
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