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This surprising situation is probably due to ancestral haplotype sharing (Hs5) among most populations, indicating ancient dispersal events.
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Previous studies reveal that most HIV-infected infants have genetically homogenous viral populations, indicating that one or a few HIV variants usually initiate infant infection [15].
Indeed, our assessment of genetic variation in Florida populations indicates that most accessions are a mixture of genotypes.
The AMOVA for the eight naturalized populations indicated that most of the genetic diversity occurred within populations and this was true whether hybrids were included or not in the analyses: 93% within and 7% among populations when hybrids were included and 94% within and 6% among when hybrids were excluded (Table 5).
From the data displayed in Table 3, BHIS is the most dominant scheme among the insured population, indicating an almost complete transition from GIS and LIS to BHIS between 1998 and 2003.
Conversely, most of the studies either used random selection or included the complete target population, indicating that the participating HCWs should be representative of the target population.
Although genotypic richness significantly increased the tendency to over-yield, in mixture treatments Dmax was <0, indicating that most populations under-performed compared to outcomes predicted from monoculture responses.
A recent study indicates that most populations do not satisfy this criterion[32].
The M ratio results for TPM and SMM were the same and indicated that most populations have undergone recent bottlenecks.
Indeed, quantitation of standard metrics of local adaptation (Hereford 2009) indicate that most populations were seemingly maladapted for their local environments (meanLA = −0.11, Fig. S10).
The aCGH results indicate that most populations tend to have a higher frequency of the deleted allele than Sub-Saharan Africans.
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