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We used the classical twin study method to decompose variance in the victim-offender overlap into genetic and environmental components.
It was therefore necessary to decompose variance across species by coding the random-effects error structure of GLMM as a hierarchical taxonomic (Order/Family) effect (adjusting the random effect's intercept term) [37], [38].
Because we employ multiple biological replicates (constructed singly) without technical replicates it is difficult to decompose variance attributable to microarray measurement and pooling construction.
In order to handle and quantify this overlap, a method has been presented to decompose variance explained into three parts (unique direct, unique indirect, and joint part).
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This procedure uses the Restricted Maximum Likelihood Method (REML) to decompose variances and allows incorporation of fixed and random effects.
Komorowski et al. [ 31] By decomposing variance into the components from individual reactions, we are able to determine the variability that the model has from each reaction, and therefore we are able to assess and weigh the uncertainty of the model in division into single reactions.
Even remotely related pairs of individuals are excluded so that chance genetic similarity is used as a random effect in a mixed linear maximum likelihood model to decompose phenotypic variance into genetic variance as captured by the additive effects of causal variants in linkage disequilibrium with SNPs genotyped on DNA arrays (Yang et al. 2011b).
This approach was recently recommended to decompose phenotypic variance into a within-subjects variance component (i.e., the variance around the species-specific intercept) and a between-subjects variance component (i.e., the variance between species-specific intercepts).
All existing methods decompose the variance of clinical data into two components: the variance due to additive genetic effects estimated from pedigrees; and the variance due to other effects (residuals).
Using the wavelet transform, we decompose the variance of the underlying process into the variance of its low frequency and of its high frequency components and we design a variance ratio test of no serial correlation in the presence of dependence.
Local AAMs (LAAMs) are trained to model a specific facial area and decompose its variance from the rest of the facial variance.
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