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For statistical analysis, six different substrate fields were measured per sample, and three separate samples were analyzed.
The SEM images of six different substrate fields were measured per sample, and three separate samples were measured for each nanopore surface.
In brief, 18 biomarkers were measured per sample (see list of abbreviations at the end of the manuscript and the online supplement for an overview).
To find out the actual effect caused due to the addition of HAp NPs on nanofiber, the average diameters of nanofibers were calculated from randomly selected individual fibers (100 diameters measured per sample) using the image analyzer software (Innerview 2.0).
A total of 10,000 cells were measured per sample by FACS flow cytometer (Becton Dickinson).
10,000 cells were measured per sample.
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Clonal diversity was measured per taxon and sampling date as: (i) clonal richness R, and (ii) the inverse of the Simpson index.
In order to further improve the number of samples measured per hour, experiments were carried out to optimize sample loop size and flow rate.
In contrast, the GeneChip consists of 11 perfect match (PM) and miss match (MM) 25 mer probes per gene, and a single sample is measured per chip.
This type of information can be used to apportion contributions to the measured PM mass on a per sample basis, along with providing data critical to the assessment and interpretation of health effects associated with individual chemical components of PM.
At least 2 independent samples were measured per gene.
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