matlab-based fidvc algorithm (MathWorks Inc)
Structured Review
![Experimental procedure. a. Decellularization of murine embryonic forelimbs allows the visualization of the extracellular matrix in its native conformation using confocal microscopy, after staining for ECM of interest. Decellularized forelimbs are imaged with an inverted confocal microscope while submerged in PBS. Embryo decellularization panels adapted from [12]. b. Volume images obtained before (cyan) and after load (magenta), corresponding to the same area of the digit, are correlated to extract displacements with fast iterative digital volume correlation <t>(FIDVC).</t> Displacements are analyzed and plotted in color as vector fields. Strain is calculated by fitting each set <t>of</t> <t>displacement</t> values to polynomial functions and then calculating their derivatives analytically, indicated by u(x) and u’(x).](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_4413/pmc06874413/pmc06874413__nihms-1525080-f0001.jpg)
Matlab Based Fidvc Algorithm, supplied by MathWorks Inc, 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/result/matlab-based fidvc algorithm/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
Images
1) Product Images from "In situ measurement of native extracellular matrix strain"
Article Title: In situ measurement of native extracellular matrix strain
Journal: Experimental mechanics
doi: 10.1007/s11340-019-00499-y
Figure Legend Snippet: Experimental procedure. a. Decellularization of murine embryonic forelimbs allows the visualization of the extracellular matrix in its native conformation using confocal microscopy, after staining for ECM of interest. Decellularized forelimbs are imaged with an inverted confocal microscope while submerged in PBS. Embryo decellularization panels adapted from [12]. b. Volume images obtained before (cyan) and after load (magenta), corresponding to the same area of the digit, are correlated to extract displacements with fast iterative digital volume correlation (FIDVC). Displacements are analyzed and plotted in color as vector fields. Strain is calculated by fitting each set of displacement values to polynomial functions and then calculating their derivatives analytically, indicated by u(x) and u’(x).
Techniques Used: Confocal Microscopy, Staining, Microscopy, Plasmid Preparation
Figure Legend Snippet: Error quantification and analysis. a. Representative displacement vector field resulting from the fast-iterative digital volume correlation (FIDVC) of the same configuration imaged twice, without the application of load for WGA (top) and FBN2 (bottom). Displacement magnitude (in the order of picometers) is shown with color in the vector field. b. Representative absolute displacement error distribution for fibrin gel compression experiment and FIDVC. c. Displacement fields of the fibrils (top) and the fluorescent particles (bottom) in the fibrin gels generated for FIDVC displacement validation. d. Representative absolute difference between the FIDVC-calculated displacement of fluorescent particles and the adjacent fibrils.
Techniques Used: Plasmid Preparation, Generated
Figure Legend Snippet: Gaussian filtered FIDVC displacement components at 3 representative positions (indicated by different colors) in sample B, including their corresponding polynomial fit. Negative z-displacements are in the direction of the applied load.
Techniques Used:
Figure Legend Snippet: FIDVC absolute displacement error
Techniques Used: