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To determine if this variation was related to the morphology, we calculated the average pairwise distance between all sequences from a given morph in the same host, and then the average pairwise distance between all sequences from different morphs in the same host (this was not done in I. banksi because the Metacoronympha-morph SSU rRNA was directly sequenced).
For the structural morphology, we calculated tree similarity for both optimisation methods, parsimony (pars) and distance (dist).
Rather than using a single action potential for the local component's morphology, we calculated the local surface component, UEGLS, using the simplest possible model that could incorporate local dispersion of repolarization time.
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To better understand the morphology of dendritic spines, we calculated the breadth-to-length ratio for each spine (F 3,200)=5.663, P<0.001; Figure 3c).
In order to evaluate the degree of resemblance of the morphology of hybrids to each parental line, we calculated the Euclidean distance to the morphological centroid of each parental strain using the shape (PCs) scores of each individual hybrid.
To quantify radial glial morphology in normal and MAM treated brains, we calculated the degree of deviation of radial glial processes as described previously [21], [28], [39].
In order to study the relationship between improvements in renal morphology (GS and IF) with different outcome measures related to renal function, we calculated pair-wise correlations between the SMDs.
We calculated the surface energies of the aragonite {001}, {010}, and {110} surfaces, which are generally expressed in experimental morphology.
We calculated 5000.
We calculated two economic outputs.
We calculated BMI as weight/height2 (kg/m2).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com