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The proportional differences in the COG categories have been analyzed by computing the proportion of each category for the Proteobacteria classes and the other taxonomic phyla, then for each category by computing the difference between the two proportions divided by the proportion seen for the other bacterial phylum.
The proportional differences in the COG categories have been analyzed by computing the proportion of each category for the positively selected genes and all the other genes, then for each category by computing the difference between the two proportions divided by the proportion seen for the genes not positively selected.
According to (28), the optimal weights minimizing (27), can be found by computing the proportion of the noise variance σ2 (E i,Δ t j ) compared to the whole σ2 (E i,Δ t j ) + P ν2 (E i,Δ t j ).
The proposed method detects abrupt scene changes between adjacent frames by computing the proportion of invalid pixels with respect to the total number of pixels in the observed LR frame of size [M × N]: 1 M N ∑ k = 1 M N I ( d k ( t ) ) ≥ T h, w h e r e I ( d k ( t ) ) = 1 i f d k 2 ( t ) > γ. 0 o t h e r w i s e. (15).
We measure the specificity of the predicted blocks by computing the proportion of genes from all reported alignments or clusters that are also located in simulated blocks.
We detected this strategy by computing the proportion of time spent in a 6 cm corridor between the starting point and the center of the safe zone for every trial.
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We characterized the spatial range of the projections of cortical areas by assessing the distances of all afferent and efferent connections to and from each area, by computing the proportions of its projections formed by short (distance 1 and 2) as well as long (distance 4 and 5) connections, respectively.
The excess retention of nodes with property A in the k-core is defined by two steps: (1) computing the proportion of nodes with property A in the whole network (EA = N A/ N) and in the k-core and (2) the excess retention (ER) obtained as.
In computing the proportion of incorrect classification by the ensemble, one should therefore divide not by as in (12), but rather by minus the number of times when the out-of-bag ensembles are empty, which leads to the following modified out-of-bag estimator: (13).
To identify loci at which a systematic change in allele size exists between the Pacific Islander data set and the combined HGDP-CEPH, Native American, Latino, Jewish, Asian Indian, and CGP data set, separately for each locus, we translated the allele sizes of the Pacific Islander data set by a constant c, and we computed the proportion of duplicate pairs that shared 2 alleles IBS (gc,2).
Before testing measurement models, we computed the proportion of disengaged responses by item.
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