The experiment was set in random order.
The stones in the walls are set in a random pattern, and those used for the rocky arches over the windows, called voussoirs, are made up of several skinny sections, which somehow gives them a threatening air, suggesting witch's fingers.
The controlling parameters are set in a quite random way.
These results suggest that random asynchronous replication is set in the developing mouse around the time of implantation.
The buildings are set in disordered lots, at strange angles — laid out as if at random.
For the results presented here, we set s and t to fixed values, though in principle they could be set to random variates in each forward iteration, reflecting uncertainty around estimates of selection strength and allele age.
In this system, the initial values of depth (Y), height (Z), and texture for each building were set as random numbers in the G-type.
In addition to the above predictor variables set as fixed effects, the identity of the male and female were set as random effects in all models.
In the original Kohonen's SOM, the initial vectorial data were set by random values, but in the BLSOM the initial vectors are set based on the widest scale of the sequence distribution in the oligonucleotide frequency space with the principal component analysis (PCA) [ 13].
In the original SOM method [ 60], the initial weight vectors are set by random values, but in BL-SOM the vectors are initialized by PCA, which is a statistical method that performs linear mapping to extract optimal features from an input distribution in the mean squared error sense.
