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During the monitoring campaign the data were validated to the reference (filter) method using a low-volume sampler (Partisol 2025; Thermo Scientific, Schaumburg, IL, USA), equipped with a PM2.5 sampling inlet at a flow rate of 16.7 L/min.
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However, neither SSCC nor MGIT-TTP data are validated to predict relapse.
Both diagnoses of venous thromboembolism 15 and birth 16 information in HES maternity data are validated to external sources with reasonable accuracy.
Extracted drug characteristic data were validated by a second reviewer to ensure data integrity.
Survey and interview data were validated through cross verification in order to overcome weaknesses and intrinsic biases of individual methods.
The subjects' data were validated.
Data were validated by immunohistology.
The microarray data were validated by qPCR.
These data have been validated to be suitable for the permafrost region on the Tibetan Plateau (Qin et al. 2015).
Data collected was validated, to the extent possible, by using multiple methods and sources.
Co-morbidity information derived from administrative data needs to be validated to allow its regular use.
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