Sentence examples for each sample were defined from inspiring English sources

DMRs for each sample were defined by comparing methylation levels to wild type in 100 bp bins across the genome.

Finally, the group membership for each sample was defined by applying the threshold of ≥ 0.65 to this matrix.

Each sample was defined as SiMW solar cells (sample A), SiMW solar cells with AZO seed layer (sample B), and SiMW solar cells with ZnO nanorods ARC on AZO seed layer (sample C), respectively.

The tubular differentiation in each sample was defined as the fraction of fields showing tubular differentiation (FTD).

The number of PCR cycles to reach the fluorescence threshold in each sample was defined as the cycle threshold (Ct).

An enrichment score of each gene in each sample was defined as the fold change of log2d RPKM between the pull down sample vs its corresponding input.

The neutralization titer of each sample was defined as the last dilution in which at least half of the monolayer was intact (TCID50).

The difference in the expression of the hRasGRP4 transcripts among each sample was defined as fold changes in mRNA levels by 2-ΔΔCT.

The MIC of each sample was defined as its lowest concentration that prevented this change and then resulted in the complete inhibition of microbial growth.

The enrichment for each sample was defined by dividing read-count normalized IP signal by the read-count normalized WCE control signal.

In our library, each sample was defined by a combination of variable length barcodes at the 5' and 3' ends (found in P1 and P2 reads).