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The samples were purified using a phenol/chloroform procedure and quantified using a spectrophotometer at a wavelength of 260 nm.
DNA was extracted from EDTA-venous blood samples by a salt extraction procedure and quantified by Picogreen (Invitrogen, Paisley, UK).
DNA was extracted from EDTA-venous blood samples using a salt extraction procedure and quantified by Picogreen.
The strength of association between the query disease and a candidate gene was then assessed by a hypothesis testing procedure and quantified by the corresponding p-value.
Constitutional DNA was extracted from EDTA venous blood samples using a standard salt extraction procedure, and quantified by PicoGreen (Invitrogen, Paisley, UK).
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We check whether or not the known parameters are captured correctly by the estimation procedure and quantify the bias if it exists.
The same authors previously achieved performance in second-order computing, using 2-D wavelets and compression techniques [11,12]; finding, despite the promising results, the limits of the procedure and quantifying its heavy computational cost.
Total proteins were prepared by standard procedures and quantified by the Bradford BSA Protein Assay Kit.
Peripheral blood samples were collected and genomic DNA was extracted by SDS-urea by standard procedures and quantified by nano-drop.
Total RNA was isolated from bacterial cultures using the TRIzol RNA isolation procedure (Invitrogen) and quantified by spectrophotometric methods.
We assess the effects of the transformations based on multiresponse permutation procedures and quantify the enhanced spectral separability between burned areas and other major land cover classes via the Jeffries-Matusita metric.
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