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The SAXS intensity data, I(h), were collected with a linear proportional counter.
The EEL spectra data set shown in Fig. 5b (5e) contains 96 × 215 (50 × 130) spectra, and they were collected with a linear spectral density of ~29.1 spectra/nm using 20 ms/pixel dwell time acquisition.
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EMI data were collected with a line spacing of 20 m, resulting in approximately 110,000 processed soundings, which were inverted with a full non-linear algorithm.
If signal x is a K sparse signal, that is, K elements in vector θ are not zero and K is far less than N, the signal x can be collected with a small set of nonadaptive, linear measurements according to compressive sensing theory.
Images were collected with a Zeiss MR camera within the linear dynamic range.
IR images were collected with a PerkinElmer Spotlight 300 system (PerkinElmer Inc., Waltham, MA, USA) in transmission mode with an essentially linear array (16×1) of mercury cadmium telluride detector elements.
Anal samples, collected with a Dracon swab in PreservCyt, were used both for liquid-based cytology and HPV testing by the Linear Array HPV Genotyping Test.
Protein spectra were collected with an accelerating voltage of 20 kV in positive ion linear mode.
Figure 10a and 10b show the PL intensity at 10 K for samples A and B, respectively, where the emission spectra, for each sample type, collected with two linear polarizations, namely: along [ 0 1 ¯ 1 ] and along [011].
In contrast, concentrations of LTB4 in EBC samples collected with ECoScreen2 were in the linear part of the calibration curve of the competitive immunoassay.
Using the DATFIT program, spectra collected from tissue sections were fitted with a linear combination of reference spectra (see standard compounds discussed above).
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