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Glycogen produced by Synechococcus sp. strain PCC 7002 in this study was converted to ethanol by yeast fermentation (Additional file 3: Figure S3).
In addition, the mouse dose used in Robey et al (2009) study was converted to an equivalent human dose to estimate whether this dose would result in a similar buffering impact.
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In the following section we first describe how the estimates from the HP study are converted to values that can be implemented in policy evaluations and how the WTP estimates of annoyance and health effects can be combined to reflect the total social cost (under the assumption that the WTP does not already reflect to total social cost).
All the RNA samples in the study were converted to cDNA using the same reverse-transcription cocktail and procedure.
Protein IDs in the datasets from each study were converted to gene symbols.
Using the values of reported intracellular buffer concentrations and affinities, the free [Ca2+]i in this study were converted to total cellular [Ca2+]i.
Hazard ratios (HRs) for overall survival (OS) and disease-free survival (DFS) from each study were converted to a regression coefficient corresponding to a continuous representation per 4-week delay of AC.
The proportion of patients who developed coronary aneurysms and the non-responsive rate in each study were converted to odds ratio (OR) and the duration of fever and C-reactive protein (CRP) levels after treatment were expressed with mean±standard deviation (mean±SD).
With the phantom-based calibration just described, the quantitative SBR from the follow-up studies were converted to true striatal SBR before being compared to the lower limits of the normal database.
NSIs reported for all studies were converted to a per year basis.
For comparability, results from other studies were converted to a common metric based on the IQR for gestational exposure for our data set (see Table 1).
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