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The site-wise ω estimates (and their mean for each locus) derived from this method were compared to clade-specific ω estimates (see below, values available on request) and incorporated into the principal component analysis for site data (see below).
The precision lost due to the settings given here is reflected in our error estimates (see below).
The first assumption is justified by our parameter estimates (see below), which show that λ and μ are several orders of magnitude larger than ν [67].
In turn, this could cause increased rates of selfing and/or inbreeding (i.e. crosses between related plants), explaining the slightly higher FIS estimates (see below for a discussion on FIS estimates).
Nevertheless, the resulting estimates are nearly identical to Wang and Luo's estimates (see below).
Items for the Advanced Access Module did not form a scale, but asked for various numerical estimates (see below).
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This estimate reveals that at a maternal exposure of 1 µg/kg bw/day (which represents a highly conservative estimate; see below in "How can biomonitoring support risk evaluation?"), fetal BPA exposure is 11.8 pM, whereby passage of BPA-glucuronide through the placenta and deconjugation contributes to the exposure with an amount of 0.2%.
Unfortunately, our priori estimate (see below) is only right for the case of (n=1) owing to technical difficulties, so (1.11) is true only for (n=1) in this paper.
4. Estimate (see below) the two-dimensional empirical distribution ρ 1 (C 1 ).
Subsequently, phenotypes of individuals were constructed according to Equation 1 and breeding values were estimated (see below).
We used different numbers of shape PCs to assess the sensitivity of the models to the dimensionality of the subspace, changing both the number of parameters being estimated (see below) and the amount of variation being explained by the subspaces.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com