Multiple samples were sent for microbiology and histology.
Multiple samples were tested and analyzed via scanning electron microscopy.
The comparison between two of multiple samples were analyzed using the LSD and SNK tests.
In addition, three multiple samples were simultaneously analysed on a single device.
Multiple samples were collected and stocked at the DNA bank at Southern Cross University, New South wales, Australia under approval of EcoAccess published by the Queensland state government.
Third, DNA extracts of single or multiple samples were pooled prior to profiling in order to test for statistically significant clustering.
HHV-8 DNA was analyzed by PCR in peripheral blood mononuclear cells (PBMC) of 293 patients; in a subgroup multiple samples were analyzed.
In this regard, multiple samples were systematically fabricated to demonstrate that careful selection of process parameters can lead to fabrication of parts with distinctive features and behaviors.
However, multiple samples were collected from each stack at the end of the tests, and these were used as replicates for the estimate of final moisture content, allowing a conclusive evaluation of factor effects.
Second, profiles of single or multiple samples were theoretically averaged to test for statistically significant clustering in order to determine the minimal number of samples to be pooled to achieve representativity.
Multiple samples were sequenced together using barcodes.
