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Exact(5)
When selecting drilling modes, we used own data obtained in extensive experimental studies Dudarev et al. (2014) and ensuring high quality of processed holes.
To further decode the growth and/or regrowth mechanisms of the above three modes, we used XRD to investigate the crystal structures of all samples after first- and second-time growths.
Therefore, to establish an assay that can be applied in homogeneous and continuous modes, we used a coupled enzyme, the exopolyphosphatase Ppx1 from Saccharomyces cerevisiae, a cytosolic exopolyphosphatase.
After assigning different epochs to gene duplication modes, we used their Ks distributions only for confirming the order of their relative ages.
If there were multiple modes, we used the mode closest to the median, and if there were two modes equally distant from the median, we chose one at random.
Similar(55)
We employ variational approach to find exciton state in QD and to find cavity modes we use the open source GME code.
For tapping mode we used rectangular silicon cantilevers (nanosensors, 125 μm long, 30 μm wide and 4 μm thick) with a tip radius of about 10 nm, a normal spring constant of 40 N/m and resonance frequency of 339 kHz.
With slow capacitance compensation inactive in voltage-clamp mode, we used responses to a 10 mV hyperpolarisation step to estimate the neuron's membrane resistance (Rm; from the steady holding current at the new voltage) and membrane capacitance (Cm; from the area under the exponentially-decaying current from peak to holding).
Within each mode, we used the relative score formula as described in Section 'Relative scoring'.
Specifically, for the Gene2miR mode, we used >30 large-scale differentially expressed gene profiles that originated from miRNA overexpression experiments.
To investigate the resolution in z-direction for the pulse-echo imaging mode we used a crossed hair phantom as an object.
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