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Data are categorized by place of residence.
For the purpose of matching, the data are categorized by the type of sibling pairs and the number of offspring.
The majority of the sequences that we detected are members of the GH32 group 1 subfamily, although a small number of sequences belong to GH32 groups 5,6,8 and 9. Data are categorized by Ecology, and a separate tally is made of sequences belonging to the phylum Ascomycota or Basidiomycota.
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In-depth evaluation was done by means of a qualitative content analysis [44], therefore the data was categorized by three content-related main categories, derived from the interview guide.
These data were categorized by ward and using population figures for LSMC wards as a denominator, the average annual incidence of S. Typhi, S. Paratyphi A and total enteric fever in each of the 22 wards and overall in LSMC was calculated over this four year period and is reported in Table 1.
Data were categorized by HIV and malaria prevalence and then extrapolated by using 2010 population data.
For calculation of summary statistics and graphical display, observed and simulated concentration data were categorized by rounded time after dosing.
Data were categorized by region according to the 10 Agency for Toxic Substances and Disease Registry (ATSDR) regions (5).
The resulting data were categorized by preservational type, geochronologic age and taxonomic affinities, as defined in Sohn et al. [ 32].
In order to estimate the TPF at different FPF, the data were categorized by several discrimination thresholds.
Data were categorized by the type of exercise; heat training, interval training on flat ground and uphill interval training.
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