Graphs and statistical analyses utilized Prism (GraphPad).
Data analyses utilized GraphPad Prism 5.00 software (GraphPad, San Diego, CA, USA) and values at P<0.05 were deemed significant.
Statistical analyses utilized GraphPad Prism 4.00 software (GraphPad, San Diego, CA), with Student's paired t tests or ANOVA with the Bonferroni post hoc correction for multiple comparisons along with Spearman's correlation analyses.
Importantly, in addition to ChIP-on-chip approaches, two genome-wide location analyses utilized ChIP-PET and the sensitive ChIP-DSL approaches; all demonstrated no evidence for ERα recruitment to PCNA.
Densitometric analyses utilized TotalLab software (Amersham Biosciences, Freiburg, Germany).
The multilevel analyses utilized 218,589 observations on 31,644 individuals for the cross-sectional analyses examining self-rated health and 181,830 observations on 25,505 participants for the longitudinal analyses.
The MS data were collected for the mass range of m/ z 50−1500, and MS/MS data analyses utilized Micromass software (MassLynx) version 3.5.
This hypothesis is derived from cladistic analyses utilizing 18S rDNA sequences [ 2- 4].
All analyses utilized a significance level of P < 0.05 and were performed using Prism (GraphPad).
All analyses utilized SAS v9.2 statistical software (SAS Institute Inc Cary, NC, USA).
All analyses utilized a two-sided P-value of 0.05 for significance.
