Sentence examples for detection of section from inspiring English sources

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When signals overlap significantly in the time frequency domain, the time frequency detection of Section "Weak-sparseness-based time frequency detection for source recovery (multisource selection)" is now inappropriate.

Assuming that r i is a Gaussian random vector, the binary hypothesis detection of Section 3.2 in [70] reveals that the pairwise error probability that (mathbf {s}_{Theta _{i}} ') is incorrectly detected by the ith detection is begin{aligned} text{Pr}left[!mathbf{s}_{Theta_{i}} !rightarrow! left.

As previously noted in [ 35], the detection of section boundaries is not a trivial task.

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The detection procedure of Section "Weak-sparseness-based time frequency detection for source recovery (multisource selection)" then makes it possible to avoid this empirical parameter choice, which brings robustness and significant simplification.

More specifically, the weak-sparseness-based time frequency detection procedure of Section "Weak-sparseness-based time frequency detection for source recovery (multisource selection)" can be used as an automatized pre-processing for multisource selection.

As it is known that the cauliflower mosaic virus (CaMV) 35S promoter is widely used in most transgenic plants (Schnurr and Guerra, 2000), we thus design a simple method based on the detection of a section target DNA (DNA-T) from the transgene CaMV 35S promoter.

For detection of IL8, sections were incubated with anti-sheepIL8 (mouse monoclonal, Abcam, Cambridge, UK) overnight at 4°C.

For the detection of CD34, sections were treated for 15 min with proteinase K (20 μg/ml) at room temperature.

For detection of MCT1, sections were incubated with goat-anti-MCT1 (Santa Cruz)[ 7], 1 100 in PAD, overnight at 4°C.

For detection of PrPd, sections were pretreated with 30 min of hydrated autoclaving at 121°C followed by 5 min in 96% formic acid.

A 63× Plan-APO 1.4 NA objective (Carl Zeiss Inc, Thornwood, NY, USA) was used in conjunction with an iris setting of 2.5, which allowed for detection of optical sections of the fluorescence image that were approximately 0.5 μm thick.

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