Peaks were pooled separately and stored at −20°C.
Equal amounts of total RNA from all the time intervals were pooled separately for both the control (700 μg) and infested (350 μg) TN1 plants.
For LCR, ODNs were pooled separately into +/− strands (100 µM).
Briefly, by taking equal amounts of protein from each sample, 10 cancer samples and 10 control samples were pooled separately, with each pool containing 250 µg of proteins.
Therefore, based on examination of operating characteristics of individual sub-cohorts, we pooled separately the two primary care and the two HRA sub-cohorts (Figure 1).
The proportions of mutations for avian isolates of both NCBI and Ottenby sequences were pooled separately, which resulted in six replicates in the NCBI group and five replicates in the Ottenby group.
Hence, data of the blocks with fixation cross and silent movie were pooled separately for each set, resulting in a 5-way ANOVA with factors Chord, Hemisphere, Anterior-Posterior, Set, and Expertise.
We therefore chose to avoid the use of population genetic statistics (such as F-statistics) and focused on general statistics performed on each pool separately: the naturalised rootstocks group versus V. vinifera ssp.
VH, kappa or lambda PCR products were pooled separately.
