Each individual sample generated approximate 0.35 billion base data (in 90-bp paired-end raw reads).
Whole genome of each individual sample was amplified and used as the template for further analysis.
Total RNA was extracted, purified, and probed on the Human Genome U95A Array for each individual sample.
In Table 3 sample characteristics, type of test applied and result of the analysis is shown for each individual sample.
Therefore, we reconstructed our model parameter of each individual sample to be linear combination of dictionary elements.
Each bar represents the top ten bacterial species ranked by the relative abundance in each individual sample or group.
Samples were analyzed by flow cytometry, and mean fluorescence intensity (MFI) was decided for each individual sample.
The data were normalized to the level of GAPDH expression in each individual sample.
RNA from each individual sample, plus the reference, were amplified, and used for labeling.
The direction of effect for both variants is consistent across each individual sample set (Table 2).
For each individual sample, the assay was set up in triplicates.
