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The microscopy is based on the vanishing effect and multi-channel photocurrent feedback mechanism of the accuracy improved PSD.
The microscopy is based on the vanishing effect and the multi-channel photocurrent feedback mechanism of the PSD.
High resolution X-ray microscopy is based on X-ray absorption spectroscopy and X-ray absorption near-edge structure analysis (XANES) which provides the chemical information about the specimen.
The mechanism of the microscopy is based on processing 4 photocurrents from 4 input channels A, B, C, and D of the PSD and the developed accurate PSD mapping methodologies.
As opposed to two photon fluorescence microscopy, SHG microscopy is based on a coherent nonlinear optical process of second order that does not require electronic excitation.
In vivo confocal microscopy is based on the acquisition of reflectance images of corneal micro-structures, therefore relying on changes of reflectivity and/or index of refraction of the specimens.
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This high-throughput fluorescence microscopy technique is based on an automated image analysis with simultaneous detection of various phenotypes (multiplexing) across multiple phenotypic parameters (multiparametric).
Second-harmonic generation (SHG) microscopy, which is based on the SHG non-linear optical effect, has emerged as a powerful optical imaging modality.
In its transmission mode of operation, however, the same microscopy platform is based on digital in-line holography to reconstruct transmission images of objects that are placed rather close to the sensor-chip.
A further method, called dual-interference-channel quantitative-phase microscopy (DQPM), is based on a dual-channel interferometric setup that is able to simultaneously obtain two phase-shifted interferograms of the same sample [ 17, 18].
Position-referenced microscopy (PRM) is based on smart sample holders that integrate a position reference pattern (PRP) in their depth, allowing the determination of the lateral coordinates with respect to the sample-holder itself.
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