24 research outputs found

    Crosstalk Noise Analysis for Nano-Meter VLSI Circuits.

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    Scaling of device dimensions into the nanometer process technology has led to a considerable reduction in the gate delays. However, interconnect delays have not scaled in proportion to gate delays, and global-interconnect delays account for a major portion of the total circuit delay. Also, due to process-technology scaling, the spacing between adjacent interconnect wires keeps shrinking, which leads to an increase in the amount of coupling capacitance between interconnect wires. Hence, coupling noise has become an important issue which must be modeled while performing timing verification for VLSI chips. As delay noise strongly depends on the skew between aggressor-victim input transitions, it is not possible to a priori identify the victim-input transition that results in the worst-case delay noise. This thesis presents an analytical result that would obviate the need to search for the worst-case victim-input transition and simplify the aggressor-victim alignment problem significantly. We also propose a heuristic approach to compute the worst-case aggressor alignment that maximizes the victim receiver-output arrival time with current-source driver models. We develop algorithms to compute the set of top-k aggressors in the circuit, which could be fixed to reduce the delay noise of the circuit. Process variations cause variability in the aggressor-victim alignment which leads to variability in the delay noise. This variability is modeled by deriving closed-form expressions of the mean, the standard deviation and the correlations of the delay-noise distribution. We also propose an approach to estimate the confidence bounds on the path delay-noise distribution. Finally, we show that the interconnect corners obtained without incorporating the effects of coupling noise could lead to significant errors, and propose an approach to compute the interconnect corners considering the impact of coupling noise.Ph.D.Electrical EngineeringUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://deepblue.lib.umich.edu/bitstream/2027.42/64663/1/gravkis_1.pd

    Statistical static timing analysis considering process variations and crosstalk

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    Increasing relative semiconductor process variations are making the prediction of realistic worst-case integrated circuit delay or sign-off yield more difficult. As process geometries shrink, intra-die variations have become dominant and it is imperative to model them to obtain accurate timing analysis results. In addition, intra-die process variations are spatially correlated due to pattern dependencies in the manufacturing process. Any statistical static timing analysis (SSTA) tool is incomplete without a model for signal crosstalk, as critical path delays can increase or decrease depending on the switching of capacitively coupled nets. The coupled signal timing in turn depends on the process variations. This work describes an SSTA tool that models signal crosstalk and spatial correlation in intra-die process variations, along with gradients and inter-die variations

    Network-on-Chip

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    Addresses the Challenges Associated with System-on-Chip Integration Network-on-Chip: The Next Generation of System-on-Chip Integration examines the current issues restricting chip-on-chip communication efficiency, and explores Network-on-chip (NoC), a promising alternative that equips designers with the capability to produce a scalable, reusable, and high-performance communication backbone by allowing for the integration of a large number of cores on a single system-on-chip (SoC). This book provides a basic overview of topics associated with NoC-based design: communication infrastructure design, communication methodology, evaluation framework, and mapping of applications onto NoC. It details the design and evaluation of different proposed NoC structures, low-power techniques, signal integrity and reliability issues, application mapping, testing, and future trends. Utilizing examples of chips that have been implemented in industry and academia, this text presents the full architectural design of components verified through implementation in industrial CAD tools. It describes NoC research and developments, incorporates theoretical proofs strengthening the analysis procedures, and includes algorithms used in NoC design and synthesis. In addition, it considers other upcoming NoC issues, such as low-power NoC design, signal integrity issues, NoC testing, reconfiguration, synthesis, and 3-D NoC design. This text comprises 12 chapters and covers: The evolution of NoC from SoC—its research and developmental challenges NoC protocols, elaborating flow control, available network topologies, routing mechanisms, fault tolerance, quality-of-service support, and the design of network interfaces The router design strategies followed in NoCs The evaluation mechanism of NoC architectures The application mapping strategies followed in NoCs Low-power design techniques specifically followed in NoCs The signal integrity and reliability issues of NoC The details of NoC testing strategies reported so far The problem of synthesizing application-specific NoCs Reconfigurable NoC design issues Direction of future research and development in the field of NoC Network-on-Chip: The Next Generation of System-on-Chip Integration covers the basic topics, technology, and future trends relevant to NoC-based design, and can be used by engineers, students, and researchers and other industry professionals interested in computer architecture, embedded systems, and parallel/distributed systems

    Methoden und Beschreibungssprachen zur Modellierung und Verifikation vonSchaltungen und Systemen: MBMV 2015 - Tagungsband, Chemnitz, 03. - 04. März 2015

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    Der Workshop Methoden und Beschreibungssprachen zur Modellierung und Verifikation von Schaltungen und Systemen (MBMV 2015) findet nun schon zum 18. mal statt. Ausrichter sind in diesem Jahr die Professur Schaltkreis- und Systementwurf der Technischen Universität Chemnitz und das Steinbeis-Forschungszentrum Systementwurf und Test. Der Workshop hat es sich zum Ziel gesetzt, neueste Trends, Ergebnisse und aktuelle Probleme auf dem Gebiet der Methoden zur Modellierung und Verifikation sowie der Beschreibungssprachen digitaler, analoger und Mixed-Signal-Schaltungen zu diskutieren. Er soll somit ein Forum zum Ideenaustausch sein. Weiterhin bietet der Workshop eine Plattform für den Austausch zwischen Forschung und Industrie sowie zur Pflege bestehender und zur Knüpfung neuer Kontakte. Jungen Wissenschaftlern erlaubt er, ihre Ideen und Ansätze einem breiten Publikum aus Wissenschaft und Wirtschaft zu präsentieren und im Rahmen der Veranstaltung auch fundiert zu diskutieren. Sein langjähriges Bestehen hat ihn zu einer festen Größe in vielen Veranstaltungskalendern gemacht. Traditionell sind auch die Treffen der ITGFachgruppen an den Workshop angegliedert. In diesem Jahr nutzen zwei im Rahmen der InnoProfile-Transfer-Initiative durch das Bundesministerium für Bildung und Forschung geförderte Projekte den Workshop, um in zwei eigenen Tracks ihre Forschungsergebnisse einem breiten Publikum zu präsentieren. Vertreter der Projekte Generische Plattform für Systemzuverlässigkeit und Verifikation (GPZV) und GINKO - Generische Infrastruktur zur nahtlosen energetischen Kopplung von Elektrofahrzeugen stellen Teile ihrer gegenwärtigen Arbeiten vor. Dies bereichert denWorkshop durch zusätzliche Themenschwerpunkte und bietet eine wertvolle Ergänzung zu den Beiträgen der Autoren. [... aus dem Vorwort

    Multi-level simulation of nano-electronic digital circuits on GPUs

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    Simulation of circuits and faults is an essential part in design and test validation tasks of contemporary nano-electronic digital integrated CMOS circuits. Shrinking technology processes with smaller feature sizes and strict performance and reliability requirements demand not only detailed validation of the functional properties of a design, but also accurate validation of non-functional aspects including the timing behavior. However, due to the rising complexity of the circuit behavior and the steady growth of the designs with respect to the transistor count, timing-accurate simulation of current designs requires a lot of computational effort which can only be handled by proper abstraction and a high degree of parallelization. This work presents a simulation model for scalable and accurate timing simulation of digital circuits on data-parallel graphics processing unit (GPU) accelerators. By providing compact modeling and data-structures as well as through exploiting multiple dimensions of parallelism, the simulation model enables not only fast and timing-accurate simulation at logic level, but also massively-parallel simulation with switch level accuracy. The model facilitates extensions for fast and efficient fault simulation of small delay faults at logic level, as well as first-order parametric and parasitic faults at switch level. With the parallelization on GPUs, detailed and scalable simulation is enabled that is applicable even to multi-million gate designs. This way, comprehensive analyses of realistic timing-related faults in presence of process- and parameter variations are enabled for the first time. Additional simulation efficiency is achieved by merging the presented methods in a unified simulation model, that allows to combine the unique advantages of the different levels of abstraction in a mixed-abstraction multi-level simulation flow to reach even higher speedups. Experimental results show that the implemented parallel approach achieves unprecedented simulation throughput as well as high speedup compared to conventional timing simulators. The underlying model scales for multi-million gate designs and gives detailed insights into the timing behavior of digital CMOS circuits, thereby enabling large-scale applications to aid even highly complex design and test validation tasks

    Celebrating 120 Years of Butantan Institute Contributions for Toxinology

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    This is collection of original and review articles selected in recognition of the contribution of Instituto Butantan to the field of toxinology and its continued and relevant role in this field in the 120 years since its foundation. Congratulations to the Butantan Institute, its house scientists, and collaborators on its 120th anniversary

    Hexavalent Chromium and Cancer Stem Cells: a view to a kill!

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    Tese de doutoramento em Biociências, no ramo de Biologia Molecular e Celular, apresentada ao Departamento de Ciências da Vida da Faculdade de Ciências e Tecnologia da Universidade de CoimbraContornando os avanços científicos feitos nas últimas décadas, o cancro prevalece como um grande problema de saúde pública que afeta milhões de pessoas por todo o mundo. O avanço mais recente feito no campo da oncobiologia foi a descoberta das células estaminais tumorais (CETs) e do seu envolvimento na doença metastática, a principal causa de morte em doentes oncológicos. Subsequentemente ficou demonstrado que as CETs regulam a tumorigenicidade e o grau de diferenciação tumoral, sendo ainda responsáveis pela resistência às terapias convencionais e pelas recidivas. Mais recentemente foram desenvolvidas terapias direcionadas especificamente a estas células que, no entanto, não surtiram o efeito esperado, uma vez as CETs conseguem regenerar- se por dediferenciação a partir de outras células do tumor. Os mecanismos subjacentes ao processo de dediferenciação são ainda desconhecidos, constituindo a sua caracterização parte dos objetivos deste trabalho. O cancro do pulmão é uma das neoplasias mais frequentes. A sua prevalência tem aumentado nos últimos anos, principalmente devido ao acréscimo dos hábitos tabágicos e à acumulação de poluentes atmosféricos. Neste trabalho utilizou-se o crómio hexavalente [Cr(VI)], um agente carcinogénico cujos níveis atmosféricos e relevância ocupacional têm aumentado significativamente nos últimos anos. Para os nossos estudos selecionámos uma linha celular não maligna de epitélio bronquial humano (BEAS-2B), a qual foi malignizada por cultura a baixa densidade na presença de Cr(VI), originando a linha celular RenG2. Em paralelo, uma linha controlo cultivada a baixa densidade na ausência de Cr(VI) (Cont1) foi também estabelecida. Visando aumentar o seu potencial maligno, as células RenG2 foram injetadas em murganhos imunocomprometidos e uma nova linha celular (DRenG2) foi estabelecida a partir do tumor formado. Este processo foi repetido com as células DRenG2, tendo-se obtido as células DDRenG2. Diversas técnicas de biologia celular e molecular foram então utilizadas para caracterizar os vários sistemas celulares, tendo os resultados obtidos sugerido o envolvimento de CETs na malignização das células BEAS-2B. Esta hipótese foi testada usando o ensaio de formação de esferas, no qual se observou a formação de colónias SC-DRenG2 e SC-DDRenG2, apenas nos dois sistemas derivados, DRenG2 e DDRenG2, respetivamente. Os resultados obtidos sugeriram que a formação de CETs na população de RenG2 injetada em murganhos imunocomprometidos decorreu de um processo de dediferenciação, provavelmente orquestrado pelas células do estroma do compartimento subcutâneo do animal. Para testar esta teoria, foram isoladas cirurgicamente células da região lombar de murganhos singénicos aos anteriores, e uma linha primária de fibroblastos (FR) foi estabelecida. A sua subsequente co-cultura com as células RenG2 durante dois meses levou à formação de uma população de CETs no seio das células RenG2 isoladas (iRenG2), cuja posterior caracterização mostrou serem mais semelhantes às DRenG2 e SC-DRenG2 do que às suas progenitoras RenG2. Por fim, o estudo dos meios condicionados das células em co-cultura identificou a Interleucina-6 (IL-6), o Factor estimulador de colónias derivado de granulócitos (G-CSF) e a Activina-A como potenciais mediadores parácrinos do processo de dediferenciação induzido pelas células do estroma do murganho.Bypassing all the research advances made in the last decades, cancer remains as a major public health problem affecting millions of people worldwide. The most recent advance in the tumor biology field was the discovery of cancer stem cells (CSCs) and of their implication in the metastatic disease, the main cause of cancer patients’ mortality. CSCs were shown to drive tumorigenesis and differentiation, contributing to tumors’ heterogeneity and to their chemo- and radiotherapy resistance and eventually relapse. Although targeted therapeutic approaches have been developed to abolish them, CSCs managed to reemerge through dedifferentiation of other tumor cells, condemning these therapies. The mechanisms behind dedifferentiation process are still unclear and were part of the main focus of this project. Lung cancer is one of the most common neoplasias worldwide. Its prevalence is increasing due to the widespread smoking habits and increasing accumulation of atmosphere pollutants. In this work hexavalent chromium [Cr(VI)] was selected as a model for lung carcinogenesis mainly due to is increasing occupational relevance. The nonmalignant human bronchial epithelial airway system 2B (BEAS-2B) was malignantly transformed into the RenG2 cell line using low density culture in the presence of Cr(VI). A parallel control cellular system (Cont1) was produced under the same conditions, though, in the absence of Cr(VI). Two additional derivative cell lines were attained following serial rounds of injection in immunocompromised mice, and named DRenG2 and DDRenG2, respectively. A panoply of techniques was then used to characterize the attained cellular systems leading to the hypothesis of CSCs involvement in Cr(VI)-driven BEAS-2B malignant transformation. The sphere-formation assay tested this hypothesis and allowed the isolation of CSC spheres (SC-DRenG2 and SC-DDRenG2 cells, respectively), but only from the derivative cell lines. These results suggested that a dedifferentiation process featured CSCs’ formation during RenG2 derivation in nude mice. The involvement of the mouse stroma in the dedifferentiation process was uncovered by surgical isolation of lumbar stromal cells (FR fibroblasts) from the subcutaneous compartment and their subsequent co-culture with RenG2 cells. Following two months, RenG2 cells were isolated from the upper compartment (iRenG2) and tested for their ability to form spheres. Gene and protein expression analysis were used to compare iRenG2 cells’ signature with those of RenG2, DRenG2 and SC-DRenG2, showing that iRenG2 cells were no longer similar to RenG2 but rather more close to both DRenG2 and SC-DRenG2. Finally, the study of the conditioned media from co-cultured cells identified interleukin-6 (IL-6), granulocyte colony-stimulating factor (G-CSF) and Activin-A as the potential paracrine orchestrators of this stromal-induced dedifferentiation process.FCT - SFRH/BD/33884/200
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