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Studies were evaluated using a quality assessment scale adapted from Jadad scale and Cochrane handbook.
The overall quality of the individual paleointensity determination can be evaluated using a quality factor (q; Coe et al., 1978) based on several statistical parameters such as σ/ǀbǀ, f, and the gap factor (g; Coe et al., 1978).
All sequences were evaluated using a quality control tool (http://www.hiv.lanl.gov/content/sequence/QC/index.html).html
Advertisements were evaluated using a quality checklist based on a review of hypertension management guidelines.
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Genotyping quality was evaluated using a detailed quality control procedure that consisted of a >95%% successful call rate, duplicate calling of genotypes, internal positive control samples and Hardy-Weinberg Equilibrium (HWE) testing.
For the evaluation of the results, the previous work only includes personal comments of the quality achieved, while in the current manuscript, the results are evaluated using a double-stimulus continuous quality scale (DSCQS) methodology for the video quality assessment, which is reproducible and objective.
Images were evaluated using a three-level image quality scoring system.
The results are evaluated using a double-stimulus continuous quality scale methodology, which is reproducible and objective.
Individual experiments are evaluated using a set of data quality criteria, and summary judgments are made across multiple experiments by applying a criterion of rough reproducibility.
RNA was quantified and the quality evaluated using a 2100 Bioanalyzer (Agilent Technologies, Santa Clara, USA).
Evidence level was rated using Oxford Centre for Evidence Based Medicine Levels and quality evaluated using a domain-based risk-of-bias rating.
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