Despite the recognition of hypertension as a major threat to public health in sub-Saharan Africa, epidemiologic research to guide public health approaches to prevent and treat hypertension is limited in scope, sample size, methodology, and generalizability of conclusions [ 7, 8, 12, 14- 16].
The scope, samples and data collected in the GB abattoir and fallen stock surveys have previously been described elsewhere [ 2, 21, 22].
This left an in-scope sample of 1,157.
We saw the FTPT compartment of HPCs contained the higher number of the T-lymphoid/NK-cell precursors than the CB, but it did not reach statistical significance that may be due to a relatively small-scope sampling.
We experimented with a large generic ontology as a basis for automatically generating domain ontologies that fit the scope of sample natural language web pages.
As this research is limited in scope and sample to examining the effect of three (viz., consciousness-raising tasks, input enhancement, and task-essential language) out of eleven FFI techniques on linguistic (viz. the simple present, gerunds, modal auxiliaries, questions, the present perfect and conditionals type II) and pragmatic (viz.
Further research is needed to extend the scope and sample size.
The scope and sample size for each survey used in this paper are detailed in Table 1.
While the techniques are totally different, there is still considerable scope for sample contamination and sequence comparison, Table 2, suggests at least 7% of public data provided by The 1000 Genomes Project may have some Mycoplasma contamination.
Despite the limited scope and sample of the Tanzania study, our findings provide an insight into how living with diabetes in a resource constrained environment has major implications for diabetes health-seeking, often leaving people with few choices that may have severe consequences for their future health.
This study has a number of strengths, including the large geographic scope and sample size of the NBDPS that allows analysis of systematically classified individual CHDs, while limiting analyses to simple, isolated defects to avoid heterogeneity from etiologies of multiple defects.
