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Two designs need to be handled separately: repeat and acute exposure and lifetime exposures.
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To determine the repeatability of the PCR + AFM measurement, we separately repeated the 10-plex measurements of Human Reference total RNA, de novo, in triplicate (see Table S6, Supporting Information).
Dance-based suite movements were binary in outline: the first of the two sections, each separately repeated, moved to the dominant key (a fifth above the tonic or principal key) or to the relative key (i.e., a minor third above the tonic in the case of a minor key); the second section, after some modulatory activity (i.e., passing through several key areas), returned to the central key.
Each experiment was separately repeated in triplicate.
The procedure was separately repeated for the coastal and continental stations.
Quantitative analysis was performed for three separately repeated experiments from each control and experimental groups.
The experiment was performed in duplicate, and separately repeated three times.
In order to study the reliability of these parameters, force-velocity tests on cycle ergometer were separately repeated three times in different sessions for each exercise.
We separately repeated our survival analysis to model the effect of the five most common classes of BSI on outcome (Table 5).
These contrasts were initially performed within treatments of egg-producing females and then were separately repeated for arrays from eggless females.
Repeat elements that fall into coding regions and those that do not were separately analyzed: repeat elements detected within 2 kb of a known transcript were treated as 'genic' repeats, others as 'non-genic'.
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