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ILI prevalence can be quickly estimated using rapid telephone surveys, using syndromic surveillance data to determine expected "background" ILI proportion.
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Under this model, given values for cellularity and ploidy, the segment-level parameters can be quickly estimated.
The GMBI includes a small, highly biologically meaningful parameter set that can be relatively easily estimated using expert knowledge, and can therefore be quickly setup to simulate the spread of organisms which have not previously been well characterised.
Transcript abundance was estimated using TPM.
CTF parameters were estimated using CTFFIND435.
Event costs were estimated using National Inpatient Sample data.
1/S' was estimated using BlastPhen.
Confidence intervals were estimated using normal approximation.
RNA concentration was estimated using nanodrop spectrophotometer.
Divergence times were estimated using Multidivtime [52] [54].
Protein concentration was estimated using Coomassie Plus Protein Reagent.
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