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Fig. 6 Temperature of sample in the final stage of fatigue test.
This pooled-control design presented several advantages, namely reduced repercussion of differential sample DNA degradation, increased sample heterozygosity, and a balancing effect over the number of reads per sample in the final control data, leading to increased data homogeneity.
The calculated amount of initial sample in the final extract was 0.5 g mL−1.
In addition, we included only a small proportion of the total sample in the final analysis, and this sample seemed to differ from the excluded sample in race/ethnicity and type of health insurance.
The resulting 14 fastq files corresponding to a replicate sample from each life stage were entered separately in the mapper.pl module of the mirDeep2 package [ 10, 11], using a config.txt file to track the original sample in the final results.
Of the participants, 39 of 40 (97.5%) completed the full-nut dose (i.e., provided a blood sample in the final month), compared with 32 of 38 (84%) of those taking the half-nut dose and 32 of 39 (82%) on muffins.
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In Fig. 10, we show optical and scanning electron microscope (SEM) images of the samples in the final lithographic steps.
Finally, it has to be considered that the values adopted here for the samples in the final part of the symbol are not unique.
The sample weights, i.e., the proportion of the samples in the final positioning result, are a measure of the merits of the standard sample.
Isopropanol is less volatile than ethanol and, therefore, requires more time to air-dry samples in the final step.
The simplest way to simulate tumor growth is to model the entire branching process and then randomly sample cells from the glands sampled in the final generation.
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