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The column filtering was set to be 3 kcal/mol and the attenuation factor was set to be 0.3.
The column filtering was set to be 3 kcal/mol to improve the signal noise ratio by omitting those lattices points which energy variation was below this threshold.
To speed up the analysis and reduce noise, column filtering was set at 1.0 kcal/mol so that only those steric and electrostatic energies with values greater than 1.0 kcal/mol are considered in the PLS analysis.
Results of whole genome DNA BLAST search (filtering was set to off) were used to carefully align the whole genomes of FTNF002-00 with either LVS or OSU18 genomes.
No sequence filtering was set.
Mapping quality (MAPQ) filtering was set at 30.
Similar(50)
Minimal number of pixels in the local neighborhood required for performing filtering is set to k=1.
The temperature of quadrupole mass filter was set at 150 °C.
The amplifier internal low-pass eight-pole Bessel filter was set at 10 kHz [3].
The amplifier internal low-pass eight-pole Bessel filter was set at 10 kHz.
An IR cutoff filter was set in the light path to avoid the hyperthermia effect.
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CEO of Professional Science Editing for Scientists @ prosciediting.com