Sentence examples for samples were identified using from inspiring English sources
Both samples were identified using operationalised computer algorithm criteria of DSM-IV major depressive disorder episode (MDD) irrespective of the current clinical diagnosis of the patients.
The differentially expressed genes (DEGs, including both mRNAs and lncRNAs) between ONFH and FNF samples were identified using the edgeR package in R, and were then subjected to enrichment analysis using the BioCloud platform.
Functional groups of DOM samples were identified using FT-IR spectrophotometer (IRPrestige-21, Shimadzu, Japan).
The crystal structures of the samples were identified using an X-ray powder diffractometer (XRD; D8-Advance, Bruker, Karlsruhe, Germany) with a Cu Kα radiation (λ = 1.5406 Å) and a fixed power source (40.0 kV, 40.0 mA).
The crystal structures of samples were identified using X-ray diffractometer (XRD, D/max-2500, Rigaku, Japan) operated at 50.0 kV and 180.0 mA with Cu Kα radiation, and in the range of 10° 50° with a scanning rate of 0.2° min−1.
Gene clusters representing similar expression profiles between uninjured epicardial and muscle control samples were identified using unsupervised, SOM clustering (Radius 7.0) with a maximum of 4500000 iterations.
In this study the salt content of samples was identified using the conventional notation n, where n indicates the number of (C(O)(CH2 5O) PCL repeat units per Mg2+ ion.
The platelet population in these whole blood samples was identified using flow cytometry.
The concentration (pg/mL) of different analytes in the plasma samples was identified using standard curves from the multiplex assays.
The location and identity of all samples is stored using a sample inventory software package, Pro-Curo (Brady Laboratories), and samples are identified using a bar coded label.
Using a screening set of 18 tumor samples (from eight control patients and 10 TF patients), a 47-gene signature discriminating between TF and control samples was identified using cDNA arrays.
