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As shown in Fig. 3b, c, the mesopore size of the IM-5-S sample was distributed in a wide range and concentrated in 10 20 nm, and the mesopore size of the IM-5-M sample was widely distributed and concentrated in 30 60 nm.
The sample was distributed equally to two 2 mL reaction tubes, if necessary.
In Bushbuckridge the sample was distributed proportional to the number of deliveries in each of the two hospitals.
The global sample was distributed into 12 strata, in principle, in proportion to the number of pupils in each stratum.
The sample was distributed geographically as follows: Baja California contributed 8 informants, Campeche 9, Distrito Federal 5, Michoacán 7 and San Luis Potosí contributed 14 informants.
The sample was distributed proportionally according to the number of registered births in each of the chosen facilities during the previous year.
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Figure 1 shows how the sample is distributed on the neighborhood scale.
Sample were distributed to each of four centers, and one center processed two sets of the 16 samples at different times using different labeling protocols.
Verified SNPs from the Montana sample were distributed among 484 contigs of the combined assembly, and verified SNPs from the Utah sample were distributed among 767 contigs.
Two aliquots of each RNA sample were distributed to each of three centers: Oregon National Primate Research Center, Yerkes National Primate Research Center and the University of Nebraska Medical Center.
On the 48.48CS dynamic array, each DNA sample is distributed into 48 reaction chambers to genotype 48 SNPs.
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