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These cells were mounted in the same 90% glycerol solution as used for the calibration sample in section 3.3.
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Then, we describe the normalization of samples in Section 2 and the classifying framework in Section 2, respectively.
We introduce spectrogram feature of HRRP data and analyze its advantages over time domain samples in Section 2. Section 3 briefly reviews the traditional HMMs.
The rest of this article is organized as follows, we first quickly revisit the basic concepts and properties about coprime sampling in Section Theory and properties for coprime sampling.
The four species sampled in section Porphyrochitonium, a section arising ∼ 4.08 mya, display a more than two-fold range in genome sizes (6.21 13.96 pg/2 C).
We can perform inference for this model using MCMC sampling, by extending the sampler in section 5.1 of (Teh et al., 2006) in the following way.
The scattering patterns over the field are not uniform, which may indicate that the light scattering is more similar to the larger microsphere samples in section 3.2.
The genome sizes of the two species sampled in section Polyphyllium (9.17 9.46 pg/2 C) are within 10%% of each other, a variance not greater than within-sample variance (K. Arumuganathan, Flow Cell Core Lab, Benaroya Research Institute, Seattle, WA, USA, pers. commun).
The genome sizes of the two species sampled in section Urospadix (14.32 14.36 pg/2 C) are also within 10%% of each other, but are reported to share the same chromosome count (Table 1, Fig. 1) [see Additional Information].
A Brewster-angle refractometer (Fig. 4(b)) has been used to estimate the n of the solid material composing the phantom (same cubic sample utilized in Section 2.3).
The sample query in Section 4 belongs to a test set that we created to validate the system, which included over 200 queries.
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