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In the male fertility study, differences between genotypes were determined using the Kruskal-Wallis analysis with Dunn's post hoc test.
Differences between genotypes were determined by the percent of AQR cells in position 5 using Fisher's Exact Test, and genotypes showing p < 0.05 significance level compared to mab-5 e1751 gof mab-5 e1751 gof in Talone 6 are 7.
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Therefore, the relation between genotypes is determined by the values of s̅g, and the genotype gc which has the minimum value is the fittest genotype.
For each cycle individually, SFR rhythm parameters (time of phase peak, period, PT ratio) were compared between WT and Kcnma1−/− (average±standard error of the mean, s.e.m., or standard deviation, s.d).. Significance of comparison between genotypes was determined by an unpaired, two-tailed t-test, p<0.05.
Statistical analysis between genotypes was determined by unpaired t test with Welch's correction using GraphPad Prism 5.0 (GraphPad Software Inc) statistical software.
Differences between rs1761667 genotypes were determined by Student t tests with significance at P < 0.05 (two-tailed).
The differences between B2BRK genotypes were determined using One-way Analysis of Variance (ANOVA) or Student's two-tailed t test when appropriate (for comparisons between − 9 homozygotes and two other genotypes combined).
After verifying equality of variance, differences between treatments and genotypes were determined using a one-way or a two-way ANOVA.
Associations between clinical and laboratory variables and MBL2 genotypes were determined by Kruskal-Wallis and χ2 tests.
Genotypes were determined by high resolution melt (HRM) analysis [17 19].
Genotypes were determined using the Taqman allelic discrimination assay.
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