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Similarly, there are two samples that target CCND1 with very high level amplification that do not cover either more distal region, however the overall frequency of CCND1 high level amplification is very small (n = 6 with log2 >1.51.5%).
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Furthermore, as pointed out in (26), to get an estimate of the prediction accuracy that we can expect in a target population, we need to perform this estimation using samples from that target population.
The latter result was also reflected in the maps showing for each insular voxel the number of subjects with an above-threshold number of samples to that target (Fig. 7, up).
At step τ the proposed position s i, k ′ of the randomly selected target i is thus sampled from the proposal distribution, which in our case is a Gaussian centered at the value of the last sample for that target, Q ( s i, k ′ | s i, k = N ( s i, k ′ | s i, k , σ q ).
Also, by modifying the composition of standard curve samples, we hypothesized that target ratio estimates can be attained directly without reference to control samples.
Ultimately, RNA was extracted from tomato samples that contained the target bacterial cell densities of about 1×107 CFU/g (symptomless plants) and 1×108 or 1×109 CFU/g (disease index 1, early disease) using the RNeasy Plant Mini Kit (Qiagen, Valencia, CA) including DNaseI treatment according to the manufacturer's instructions.
For example, if comparing a pharmacological approach to a cognitive-behavioral approach we may wish to target 80% power to detect a difference in the effectiveness of each approach, and thus choose a sample size that targets this power.
A key feature of the larger quantitative component was a sampling protocol that targeted an entire community so that data could be collected from both hospitalized and non-hospitalized community-dwelling older adults.
Analyses of 1656 blood glucose measurements during insulin infusion revealed that percentage of samples that showed achievement of target blood glucose level (80 140 mg/dl) was higher under MY (78 ± 15%, n = 870) than EC (57 ± 23%, n = 786, p < 0.0001).
Samples that appear as a target compound in a reaction gain in addition a reaction label which allows the direct assignment of this sample to the reaction and its number.
Then the AAM tracker compares the M face models to find the best set of facial points, F s, from given samples that best match with target face model.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com