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The light photoirradiation (> 420 nm) was performed using a cutoff filter (Hoya Y44 Tokina Co. Ltd., Saitama, Japan) to eliminate UV light.
SULT1A1 fluorescence was excited at 290 nm and detected above 330 nm using a cutoff filter.
Cy3 fluorophore was excited at 515 nm and its emission was monitored at all wavelengths >570 nm using a cutoff filter (Applied Photophysics).
Raw sequence read data were filtered based on quality scores with the fastq_quality_filter program of FASTXTOOLS (http://hannonlab.cshl.edu/fastx_toolkit/), using a cutoff filter (a minimum 70% of bases must have quality of 20 or greater).
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Acid Orange 7 (and) and methyl orange (MeO): 25 ppm Irradiation time: 240 min for AO7 300 min for MeO visible irradiation: 1000 W halogen lamp short-wavelength components (<420 nm) of the light were cut off using a cutoff glass filter 100%% Dye absorbed on WOx TiO2 surface decolorized and aromatic + aliphatic acid intermediates formed [181] TiO2 0.5 g L−1 Initial conc.
The analyses included high-pass filtering using a cutoff of 1/40 hz to remove high frequency noise4, global intensity normalization and corrections for serial correlations using a first-order autoregressive model (AR(1)).
The analysis included high-pass filtering using a cutoff of 1/128 Hz and serial correlations correction using a first-order autoregressive (or AR [1]) model.
After filtering using a cutoff value of 1.01, 35 and 1493 core and variable LCBs remained, respectively.
An estimate of solubility (LogS) was generated for each compound using QikProp and compounds were filtered using a cutoff of −6.0 for LogS.
These variants were further filtered using a cutoff threshold of p < 0.05 using Fisher's exact test against the 1,000G Project 67 European allele frequencies.
To guarantee the quality of the Mugsy output file, a list of LCBs was further filtered using a cutoff value (score ≤ 1.01).
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