Clock skew is becoming increasingly difficult to control due to variations. Link based non-tree clock distribution is a cost-effective technique for reducing clock skew variations. However, previous works based on this technique were limited to unbuffered clock networks and neglected spatial correlations in the experimental validation. In this work, we overcome these shortcomings and make the link based non-tree approach feasible for realistic designs. The short circuit risk and multi-driver delay issues in buffered non-tree clock networks are investigated. Our approach is validated with SPICE based Monte Carlo simulations, considering spatial correlations among variations. The experimental results show that our approach can reduce the maximal skew by 47%, improve the skew yield from 15% to 73% on average with a decrease on the total wire and buffer capacitance.
Abstract-The realization of functions such as log() and antilog() in hardware is of considerable relevance, due to their importance in several computing applications. In this paper, we present an approach to compute log() and antilog() in hardware. Our approach is based on a table lookup, followed by an interpolation step. The interpolation step is implemented in combinational logic, in a fieldprogrammable gate array (FPGA), resulting in an area-efficient, fast design. The novelty of our approach lies in the fact that we perform interpolation efficiently, without the need to perform multiplication or division, and our method performs both the log() and antilog() operation using the same hardware architecture. We compare our work with existing methods, and show that our approach results in significantly lower memory resource utilization, for the same approximation errors. Also our method scales very well with an increase in the required accuracy, compared to existing techniques.Index Terms-Field-programmable gate arrays (FPGAs), floating point arithmetic, logarithmic arithmetic, VLSI.
High space-bandwidth product with high spatial phase sensitivity is indispensable for a single-shot quantitative phase microscopy (QPM) system. It opens avenue for widespread applications of QPM in the field of biomedical imaging. Temporally low coherence light sources are implemented to achieve high spatial phase sensitivity in QPM at the cost of either reduced temporal resolution or smaller field of view (FOV). In addition, such light sources have low photon degeneracy. On the contrary, high temporal coherence light sources like lasers are capable of exploiting the full FOV of the QPM systems at the expense of less spatial phase sensitivity. In the present work, we demonstrated that use of narrowband partially spatially coherent light source also called pseudo-thermal light source (PTLS) in QPM overcomes the limitations of conventional light sources. The performance of PTLS is compared with conventional light sources in terms of space bandwidth product, phase sensitivity and optical imaging quality. The capabilities of PTLS are demonstrated on both amplitude (USAF resolution chart) and phase (thin optical waveguide, height ~ 8 nm) objects. The spatial phase sensitivity of QPM using PTLS is measured to be equivalent to that for white light source and supports the FOV (18 times more) equivalent to that of laser light source. The high-speed capabilities of PTLS based QPM is demonstrated by imaging live sperm cells that is limited by the camera speed and large FOV is demonstrated by imaging histopathology human placenta tissue samples. Minimal invasive, high-throughput, spatially sensitive and single-shot QPM based on PTLS will enable wider penetration of QPM in life sciences and clinical applications.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.