Transition-Aware Decoupling-Capacitor Allocation in Power Noise Reduction

Abstract-Dynamic power noises may not only degrade the circuit performance but also reduce the noise margin which may result in the functional errors in integrated circuit. Decoupling capacitor (decap) allocation is one of the most effective way in reducing serious dynamic power noises (hotspots). To allocate decap bef ore placement, we observed that not only locations but also rising time of functional cells are required to accurately predict power noises. Compared to a previous work which only takes neighborhood relation into consideration, our method is more efficient in reducing hotspots. Furthermore, to reduce the hotspots af ter placement, instead of only using the empty space as proposed in the previous work, we move out cells in the area with serious power noise area (hot area). The obtained empty space can be used to accommodate decaps to further reduce the hotspots. The experimental result shows, compared to the previous work [1], our estimation function to allocate decap before placement is 23% better in reducing power noises. Moreover, compared to a method which fills decaps to all remaining empty space, our cell move algorithm can almost eliminate all the remaining hot grid nodes and hot cells. In summary, compared to the original circuits (without decap), about 60% of hotspots can be removed using our prediction function before placement, and most of the remaining hotspots are removed by our cell moving step after placement

The 2018 NVIDIA AI City Challenge

The NVIDIA AI City Challenge has been created to accelerate intelligent video analysis that helps make cities smarter and safer. With millions of traffic video cameras acting as sensors around the world, there is a significant opportunity for real-time and batch analysis of these videos to provide actionable insights. These insights will benefit a wide variety of agencies, from traffic control to public safety. The second edition of the NVIDIA AI City Challenge, being organized as a CVPR workshop, provided a forum to more than 70 academic and industrial research teams to compete and solve real-world problems using traffic camera video data. The Challenge was launched with three tracks — speed estimation, anomaly detection, and vehicle re-identification. Each track was chosen in consultation with traffic and public safety officials based on the value of potential solutions. With the largest available dataset for such tasks, and ground truth for each track, the Challenge enabled 22 teams to evaluate their solutions. Given how complex these tasks are, the results are encouraging and reflect increased value addition year over year for the Challenge

A SNP and SSR Based Genetic Map of Asparagus Bean (Vigna. unguiculata ssp. sesquipedialis) and Comparison with the Broader Species

Asparagus bean (Vigna. unguiculata ssp. sesquipedialis) is a distinctive subspecies of cowpea [Vigna. unguiculata (L.) Walp.] that apparently originated in East Asia and is characterized by extremely long and thin pods and an aggressive climbing growth habit. The crop is widely cultivated throughout Asia for the production of immature pods known as ‘long beans’ or ‘asparagus beans’. While the genome of cowpea ssp. unguiculata has been characterized recently by high-density genetic mapping and partial sequencing, little is known about the genome of asparagus bean. We report here the first genetic map of asparagus bean based on SNP and SSR markers. The current map consists of 375 loci mapped onto 11 linkage groups (LGs), with 191 loci detected by SNP markers and 184 loci by SSR markers. The overall map length is 745 cM, with an average marker distance of 1.98 cM. There are four high marker-density blocks distributed on three LGs and three regions of segregation distortion (SDRs) identified on two other LGs, two of which co-locate in chromosomal regions syntenic to SDRs in soybean. Synteny between asparagus bean and the model legume Lotus. japonica was also established. This work provides the basis for mapping and functional analysis of genes/QTLs of particular interest in asparagus bean, as well as for comparative genomics study of cowpea at the subspecies level

Purification and Characterization of a Novel Hypersensitive Response-Inducing Elicitor from Magnaporthe oryzae that Triggers Defense Response in Rice

<div><h3>Background</h3><p><em>Magnaporthe oryzae</em>, the rice blast fungus, might secrete certain proteins related to plant-fungal pathogen interactions.</p> <h3>Methodology/Principal Findings</h3><p>In this study, we report the purification, characterization, and gene cloning of a novel hypersensitive response-inducing protein elicitor (MoHrip1) secreted by <em>M. oryzae</em>. The protein fraction was purified and identified by de novo sequencing, and the sequence matched the genomic sequence of a putative protein from <em>M. oryzae</em> strain 70-15 (GenBank accession No. XP_366602.1). The elicitor-encoding gene <em>mohrip1</em> was isolated; it consisted of a 429 bp cDNA, which encodes a polypeptide of 142 amino acids with a molecular weight of 14.322 kDa and a pI of 4.53. The deduced protein, MoHrip1, was expressed in <em>E. coli</em>. And the expression protein collected from bacterium also forms necrotic lesions in tobacco. MoHrip1 could induce the early events of the defense response, including hydrogen peroxide production, callose deposition, and alkalization of the extracellular medium, in tobacco. Moreover, MoHrip1-treated rice seedlings possessed significantly enhanced systemic resistance to <em>M. oryzae</em> compared to the control seedlings. The real-time PCR results indicated that the expression of some pathogenesis-related genes and genes involved in signal transduction could also be induced by MoHrip1.</p> <h3>Conclusion/Significance</h3><p>The results demonstrate that MoHrip1 triggers defense responses in rice and could be used for controlling rice blast disease.</p> </div

Robust estimation of bacterial cell count from optical density

Optical density (OD) is widely used to estimate the density of cells in liquid culture, but cannot be compared between instruments without a standardized calibration protocol and is challenging to relate to actual cell count. We address this with an interlaboratory study comparing three simple, low-cost, and highly accessible OD calibration protocols across 244 laboratories, applied to eight strains of constitutive GFP-expressing E. coli. Based on our results, we recommend calibrating OD to estimated cell count using serial dilution of silica microspheres, which produces highly precise calibration (95.5% of residuals &lt;1.2-fold), is easily assessed for quality control, also assesses instrument effective linear range, and can be combined with fluorescence calibration to obtain units of Molecules of Equivalent Fluorescein (MEFL) per cell, allowing direct comparison and data fusion with flow cytometry measurements: in our study, fluorescence per cell measurements showed only a 1.07-fold mean difference between plate reader and flow cytometry data

A Re-engineering Approach to Low Power FPGA Design Using SPFD

In this paper, we present a method to re-synthesize Look-Up Table #LUT# based Field Programmable Gate Arrays #FPGAs# for lowpower design after technology mapping, placement and routing are performed. We use Set of Pairs of Functions to be Distinguished #SPFD# to express functional permissibility of each signal. Using di#erent propagations of SPFD to fan-in signals, we change the functionality of a PLB #Programmable Logic Block# which drives large loading into one with low transition density. Experimental results show that our method can reduce on average 12% power consumption compared to the original circuits without affecting placement and routing