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The structural model describing these relations was modified and tested on a validation sample, and displayed adequate fit statistics.
The number of reads at each position were normalized to the total number of reads for each sample and displayed using the Integrated Genome Viewer from the Broad Institute (Robinson et al., 2011 ).
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In the first stage, a sample is mounted on an XY micro-positioning stage, a vision system captures an image of the sample and displays the size and shape of each entrance hole.
Table 2 shows the main results in terms of perceived quality of care in the full sample and displays both mean scores as well as relative frequencies.
The spectra were similar for all samples and displayed Raman bands characteristic of TiChu in the aluminosilicate framework domain (500 to 1,100 cm-1, Figure 4a; Frost et al. 2007).
Gene ratios were average corrected across experimental samples and displayed according to uncentered correlation algorithm.
The NET-degrading abilities were subsequently measured in all patient samples and displayed over time, starting at study inclusion.
Notably, the CD3+CD8+TM+ cells of the standard samples were located exactly within the gates used to analyze patient samples and displayed a similar scatter pattern.
Data from both the SEFC and green channels was simultaneously sampled and displayed by a personal computer in real-time, using a custom built software (Labview, National Instruments).
Oligonucleotide spacing patterns, summarized as sample parameters and displayed as scatterplots (figs. 6 and 7), provide a further interesting view into the compositional complexity.
All results were adjusted for differences in initial sample weights, and displayed in estimated number of copies (genome equivalents) per mg of tissue.
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