Using simulation and both synthetic and traced packet traffic as input, we show that the RR/RR CICQ switch with the block transfer mechanism has a lower delay than an input queued (IQ) switch that internally uses cells.
In Section Stabilization of SAM against changes in methionine input we show how the long-range interactions moderate the effects of changes in methionine input.
Therefore, in the absence of inhibition they display similar spiking probability as mature neurons in response to excitatory inputs, as we show in Figure 2A, B. Thus, despite having different intrinsic properties, their different responses to synaptic inputs are primarily mediated by inhibition.
We propose different decoding algorithms to identify the input and we show both theoretic and simulations' results.
Given this mapping and an input image, we show how to produce a distribution of holes with varied depth that approximates the image well.
In order to extend this deconvolution to arbitrarily long input signals, we show that, under certain circumstances, a finite impulse response (FIR) filter can be build from it.
Using the sub-sampled INPUT-seq data, we show that INPUT-seq generally provides higher genomic coverage at sequencing depth as low as one million reads.
Using biologically plausible learning rules and inputs, we have shown that ILGA can learn to represent affordances for grasping and to select motor parameters appropriate to act on them.
In Table 3, we show inputs and outputs for the season 2013/14 data from the German Stage Association, Deutscher Bühnenverein (2013)—together with respective CCR and BCC efficiencies plus RTS characteristics IRS, CRS, and DRS for these 30 theatres.
When input traffic is bursty, we show that load balancing is very effective in reducing delay, and the average delay of the load balanced Birkhoff von Neumann switch is proven to converge to that of an output-buffered switch under heavy load.
