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To identify socially structured bacterial taxa within baboon social groups, we utilized a test of spatial autocorrelation, Moran's I, as implemented in the function Moran.I in the R package ape (Paradis et al., 2004).
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We utilized a test set of 23 patients with (n = 8) biopsy-confirmed class III or IV proliferative nephritis, or with either biopsy-confirmed class II nephritis or without significant renal involvement (n = 15), to test accuracy of the prediction model.
(12) d C Ab dt = k − 5 C 1 R : Ab − k 5 C 1 R C Ab (13) d C 1 R : Ab dt = k 5 C 1 R C Ab − k − 5 C 1 R : Ab To examine the effects of both antibody binding affinity and treatment dose, we utilized a test matrix that consists of three antibody K d values (0.1, 1, and 10 nM) and four initial concentrations of the antibody.
The Observed Minus Expected Squared (OMES) approach developed by Kass and Horovitz utilized a χ2 goodness-of-fit test to identify site pairs at which the observed distribution of amino-acid pairs diverged significantly from expectation [10], [11].
Mycobacteriological laboratory methods have traditionally utilized a series of tests based upon growth, microscopic, phenotypic, and biochemical properties in order to segregate the classical members of the MTC [ 10].
In order to identify significant changes in gene expression after IR-induced DNA damage, we utilized a combination of t-test generated p-values and fold change cut-offs (p ≤ 0.05; Fold Change (FC) ≥ ± 1.5) based on global gene expression analysis of 3 WT pre-B cell lines exposed to 0 or 1 Gy IR.
In these tests we utilized a global atlas of mRNA stability in mammalian cells that was recently generated in murine fibroblast and human B cells [ 2, 12].
In addition, one NGO utilized a controlled cooking test, which combined elements of lab- and field-based tests.
To test this, we utilized a murine model of T. cruzi infection.
Germline gene test for FAP utilizes a protein truncation test of APC.
Subsequent in vivo Draize testing utilized a larger size fraction of unground lunar dust that is more relevant to ocular exposures (particles <120 μm; median particle diameter = 50.9 ± 19.8 μm).
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