Patients will be compared with healthy controls (N = 30) who are also tested twice, separated by 6 months, to control for test-retest effects.
The ports of the filled, warm, wet capacitors were soldered shut, dielectric fluid was washed off the outside, and capacitors were sent to quality control for testing.
For the subsequent qPCR experiments significant differences were established using one way ANOVAs with a Fishers post hoc test to control for multiple testing.
The Benjamini-Hochberg (BH) procedure was used to control for multiple testing (i.e. 43 tests per endpoint: 28 genetic and 15 clinical parameter tests) to reduce the risk of finding false-positive associations.
As well as limiting the number of tests performed via specific hypotheses, we propose to use a permutation-based framework to control for multiple testing.
Most of these studies applied the one-tailed binomial test to identify significantly mutated genes, followed by a false discovery rate procedure to control for multiple testing (Benjamini and Hochberg 1995).
Several Mann-Whitney U tests were conducted to find differences in prior performance measures between the two sample populations, and again, Benjamini-Hochberg post hoc corrections were applied to control for multiple testing.
False detection rates helped to control for multiple testing.
To control for multiple testing, we calculated the false discovery rate (FDR) according to Benjamini and Hochberg [25].
