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fft analysis method originlab software  (OriginLab corp)


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    OriginLab corp fft analysis method originlab software
    Fft Analysis Method Originlab Software, supplied by OriginLab corp, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fft+software/fft+analysis+method+originlab+software/pm38147575-114-2-5
    Average 90 stars, based on 1 article reviews
    fft analysis method originlab software - by Bioz Stars, 2026-09
    90/100 stars

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    other:

    Article Title: Crosstalk-Free Position Mapping for One-Step Reconstruction of Surface Topological Information via Eigenfrequency-Registered Wearable Interface.
    Article Snippet: Exploring flexible tactile sensors capable of recognizing surface information is significant for the development of virtual reality, artificial intelligence, soft robotics, and human−machine interactions (HMI).. However, it is still a challenge for current tactile sensors to efficiently recognize the surface pattern information while maintaining the simplicity of the overall system.. In this study, cantilever beam-like magnetized micropillars (MMPs) with height gradients are assembled as a position-registered array for rapid recognition of surface pattern information.

    Software:

    Article Title: Floquet spin states in OLEDs
    Article Snippet: .. To find the center values of magnetic field B of the g 2 resonance for each applied RF power P, the data for each spectrum I(B0) was subjected to a 40 data-point smoothing procedure using the Origin Software FFT smoothing method (https://www.originlab.com/doc/Origin-Help/Smoothing). ..



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    Spectral analysis of Candida albicans nanomotion rate at 24 h incubation time after experiment start. (A,B) Fourier transform spectrum for the RMS amplitude of the nanomotion rate. G0-phase yeast cells (A) S/G2-phase yeast cells (B) . The blue rectangle in the figures shows the frequency range of 0.55–1.60 Hz that lies between two Fourier spectrum peaks that is characteristic for all the C. albicans samples studied (about 0.3 and 1.9 Hz). Pale curves represent experimental data, bright colored curves represent the results of the curve smoothing by the <t>FFT</t> filter method. (C) The scheme of the analysis of cell nanomotion data for control (non-irradiated and untreated) and X-ray irradiated cultures. (D) The relative RMS amplitude of cell nanomotion rate averaged over the frequency range of 0.55–1.60 Hz against the relative averaged cell diameter for C. albicans after their exposure to various factors. Relative RMS amplitude was calculated with respect to the median RMS amplitude of the control yeast culture. A is the RMS amplitude of the studied sample, A c is the RMS amplitude of the control (non-irradiated and untreated) sample. Relative cell diameter was assessed using light microscopy images and <t>ImageJ</t> <t>software</t> and calculated with respect to the median cell diameter of the control yeast culture. D is the cell diameter in the studied C. albicans sample, D c is the cell diameter of the control C. albicans culture. The diameter of cells normally having spheroidal shape was assessed as the average of their maximal and minimal sizes. The diameter of budding cells having the shape of two linked together spheroids is roughly approximated as the diameter of spheroidal cell times 1.3. The cell samples were marked using the following numbers and colors: control (1, 1′, green circles), X-ray irradiated (2, 2′, scarlet circles), FLC-treated (3, 3′, orange circles) and FLC-treated and X-ray irradiated (4, 4′, lilac circles), where 1, 2, 3, and 4 (included into light blue oval) represent the data for G0-phase cells, 1′, 2′, 3′, and 4′ (included into violet oval) represent the data for G2/S-phase cells.
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    Spectral analysis of Candida albicans nanomotion rate at 24 h incubation time after experiment start. (A,B) Fourier transform spectrum for the RMS amplitude of the nanomotion rate. G0-phase yeast cells (A) S/G2-phase yeast cells (B) . The blue rectangle in the figures shows the frequency range of 0.55–1.60 Hz that lies between two Fourier spectrum peaks that is characteristic for all the C. albicans samples studied (about 0.3 and 1.9 Hz). Pale curves represent experimental data, bright colored curves represent the results of the curve smoothing by the FFT filter method. (C) The scheme of the analysis of cell nanomotion data for control (non-irradiated and untreated) and X-ray irradiated cultures. (D) The relative RMS amplitude of cell nanomotion rate averaged over the frequency range of 0.55–1.60 Hz against the relative averaged cell diameter for C. albicans after their exposure to various factors. Relative RMS amplitude was calculated with respect to the median RMS amplitude of the control yeast culture. A is the RMS amplitude of the studied sample, A c is the RMS amplitude of the control (non-irradiated and untreated) sample. Relative cell diameter was assessed using light microscopy images and ImageJ software and calculated with respect to the median cell diameter of the control yeast culture. D is the cell diameter in the studied C. albicans sample, D c is the cell diameter of the control C. albicans culture. The diameter of cells normally having spheroidal shape was assessed as the average of their maximal and minimal sizes. The diameter of budding cells having the shape of two linked together spheroids is roughly approximated as the diameter of spheroidal cell times 1.3. The cell samples were marked using the following numbers and colors: control (1, 1′, green circles), X-ray irradiated (2, 2′, scarlet circles), FLC-treated (3, 3′, orange circles) and FLC-treated and X-ray irradiated (4, 4′, lilac circles), where 1, 2, 3, and 4 (included into light blue oval) represent the data for G0-phase cells, 1′, 2′, 3′, and 4′ (included into violet oval) represent the data for G2/S-phase cells.

    Journal: Frontiers in Microbiology

    Article Title: Modulation of the nanoscale motion rate of Candida albicans by X-rays

    doi: 10.3389/fmicb.2023.1133027

    Figure Lengend Snippet: Spectral analysis of Candida albicans nanomotion rate at 24 h incubation time after experiment start. (A,B) Fourier transform spectrum for the RMS amplitude of the nanomotion rate. G0-phase yeast cells (A) S/G2-phase yeast cells (B) . The blue rectangle in the figures shows the frequency range of 0.55–1.60 Hz that lies between two Fourier spectrum peaks that is characteristic for all the C. albicans samples studied (about 0.3 and 1.9 Hz). Pale curves represent experimental data, bright colored curves represent the results of the curve smoothing by the FFT filter method. (C) The scheme of the analysis of cell nanomotion data for control (non-irradiated and untreated) and X-ray irradiated cultures. (D) The relative RMS amplitude of cell nanomotion rate averaged over the frequency range of 0.55–1.60 Hz against the relative averaged cell diameter for C. albicans after their exposure to various factors. Relative RMS amplitude was calculated with respect to the median RMS amplitude of the control yeast culture. A is the RMS amplitude of the studied sample, A c is the RMS amplitude of the control (non-irradiated and untreated) sample. Relative cell diameter was assessed using light microscopy images and ImageJ software and calculated with respect to the median cell diameter of the control yeast culture. D is the cell diameter in the studied C. albicans sample, D c is the cell diameter of the control C. albicans culture. The diameter of cells normally having spheroidal shape was assessed as the average of their maximal and minimal sizes. The diameter of budding cells having the shape of two linked together spheroids is roughly approximated as the diameter of spheroidal cell times 1.3. The cell samples were marked using the following numbers and colors: control (1, 1′, green circles), X-ray irradiated (2, 2′, scarlet circles), FLC-treated (3, 3′, orange circles) and FLC-treated and X-ray irradiated (4, 4′, lilac circles), where 1, 2, 3, and 4 (included into light blue oval) represent the data for G0-phase cells, 1′, 2′, 3′, and 4′ (included into violet oval) represent the data for G2/S-phase cells.

    Article Snippet: The nanomotion cell rate was measured in nm/10 ms. A discrete Fourier transform was performed to the data set ( t,V ) i,j using Fast Fourier Transform (FFT) option of OriginLab software.

    Techniques: Incubation, Control, Irradiation, Light Microscopy, Software