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Regarding memory programming, a tight threshold voltage control is typically realized by using incremental step pulse program [4, 26], i.e., memory cells on the same word-line are recursively programmed.
However, even with such a tight threshold setting, more than 50% of the genes selected from the histone acetylation data were not covered in the gene list obtained from the expression array data.
A tight threshold will in general filter the presence of different phenotypes.
The presence of these feedback loops have been shown to produce switch-like (i.e. bistable) responses to receptor activation, allowing for a tight threshold of cellular response during development [ 50, 51].
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The National Institute for Occupational Safety and Health had recommended a tighter threshold of 1.0.
The analysis was subsequently repeated on a more restricted pool of items those selected for the long scale IONB-QoL through the CTT, and those selected by using a tighter threshold range (0.5÷1.5) considered to be productive for measurement [ 28].
A variable and tight threshold was set to eliminate residual background.
The incremental step pulse programming (ISPP), which is the most widely used programming scheme, was proposed to maintain a tight cell threshold voltage distribution for high reliability[7, 8].
Typically, in the past, random geometric graph analyses involved sophisticated methods from continuum percolation theory; on contrast, our bin-covering approach is discrete and very simple, yet it gives us tight threshold bounds.
Alternatively, given the tight threshold for in vitro cytotoxicity of this drug, it is conceivable that higher doses or a longer treatment schedule (beyond 4 weeks) is required to observe an effect of FP in the PER-403 xenograft.
For theoretical point of view we elaborate on a tighter significance threshold of our two-sample test which is obtained by an expression of the asymptotic distribution.
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