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We used a simple random sampling method where we randomly selected a subset of individuals from the BIOS.
Of the initial 714 screenshots, we randomly selected a subset of 379, such that the experiment took approximately one hour.
We selected a subset of genes based on GSEA analysis.
We selected a subset of genes for validation by qPCR.
For our experimental validation we selected a subset of 15 proteins to test for subcellular targeting.
The MARS procedure selected a subset of available attributes to optimize the fit to training data.
We selected a subset of probes for our analysis (Figure S3).
We selected a subset of environmental perturbations from the dataset consisting of 35 experiments and 15 stressors.
We then selected a subset of the predicted epitopes with a broad coverage of 20 fully-sequenced WNV strains.
We then selected a subset of 175 predicted epitopes that constitutes broad coverage of 20 WNV strains as described in Materials and Methods.
Among them we selected a subset of 167 genes that appear in at least three published gene lists, as illustrated in Figure 1.
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