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That done, the software was then tested using a second set of samples, this time from 286 breast-cancer patients at Vancouver General Hospital.
We also collected a second set of samples in 2013.
A second set of samples was machined to match the programmed dimensions of the SMP sample set.
Ninety-two percent of SPMs and 77% of indels were validated in a second set of samples adjacent to the discovery set.
A second set of samples was exposed to a UV-C source for different times until complete hydrophilization of the surface was reached.
A second set of samples comprising 29 KC and 38 control samples were collected for performing individual ELISA assays for validation purposes (Table S2).
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A second set of sample cores were collected 1 year later along the same gradient illustrated in Fig. 1.
A third set of samples was collected and kept unfiltered and non-acidified in glass bottles for bacteriological counts.
The ITS tests were also performed on a third set of samples whose loose mixes were subjected to 8, 16, 32, 48, 72 and 100 h oven aging at 135 °C.
In a first set of samples, 300 unfixated cells of each cell type were collected.
After 30 minutes, a first set of samples of 0.8 mL was collected.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com