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A higher PS α score suggests that more phospholipidosis positive than negative compounds are associated with the target; the numbers of positive and negative compound associations contributing to each target's PS α score are also shown in this Table, which is in.xls format.
If each network were fully independent and had the same probability p of misclassifying a compound, the contingent probability P that k of K networks in an ensemble will mistakenly assign a "negative" compound to the "positive" class or a "positive" compound to the "negative class" would be expected to follow a binomial distribution: P k | K, p = K k p k 1 - p K - k (1).
The electrocochleography revealed negative compound action potentials on both sides; cochlear microphonics could be recorded on both sides starting at 110 dBHL.
In vector shRNA (shControl -transfected cellshControl -transfectedH110 showed a moderate sensitizing effecellshile SH122 dramatically synegative TRAIL-inducompound death in a doSH110pendent manner.
In comparison, even high concentrations of the negative compound SH123 altered neither NF-κB protein redistribution nor NF-κB target genes expression.
Results with Class II compounds were not conclusive due to assay interference (compounds caused a signal increase, which resulted in negative, compound concentration-dependent, percent effects).
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The negatives associated with leveraged ETFs include: –The impact of negative compounding can result in long-term inaccuracy.
A higher PS α score suggests that more phospholipidosis positive than negative compounds are associated with the target.
This data set consists of 351 positive and 589 negative compounds with respect to the chromosome aberration test.
First of all, the applied estimation methods bear uncertainties which may result in false positive or false negative compounds.
We notice that the fraction of positive and negative compounds is different than in the data set use by Arena et al. [5].
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