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98 protocols using matlab r2010a

1

Temporal Dynamics of Muscle Activity

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The delays in initiation and termination of muscle activity during baseline and post-intervention trials were tested for normal distribution by the univariate Lilliefors test ('lillietest’ in Matlab R2010a, The MathWorks, Inc., USA) for sessions of each tDCS target - M1, cerebellar, sham - pooled from all subjects. Then, a balanced three-way (tDCS target: M1, cerebellar, sham x step-response type: step-up, step-down x subjects) ANOVA ('anovan’ in Matlab R2010a, The MathWorks, Inc., USA) was conducted on the step-response, i.e., the delay in initiation and termination of muscle activity during the baseline trials. Also, a balanced two-way (tDCS target: M1, cerebellar, sham × step-response type: step-up, step-down) ANOVA ('anova2’ in Matlab R2010a, The MathWorks, Inc., USA) was conducted on the normalized delay in initiation and termination of muscle activity during the post-intervention trials. The delay was normalized by subjects’ respective mean baseline delay over their 5 baseline trials. To find which pairs were significantly different, post hoc tests ('multcompare’ in Matlab R2010a, The MathWorks, Inc., USA) were performed with the critical values found from Scheffe’s S procedure.
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2

Transcranial Direct Current Stimulation Effects on Muscle Activation

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The delays in initiation and termination of muscle activity during baseline trials were tested for normal distribution by the univariate Lilliefors test ('lillietest’ in Matlab R2010a, The MathWorks, Inc., USA) for each tDCS group - M1, cerebellar, sham. Then, a balanced two-way (tDCS target: M1, cerebellar, sham x step-response type: step-up, step-down) ANOVA ('anova2’ in Matlab R2010a, The MathWorks, Inc., USA) was conducted on the step-response, i.e., the delay in initiation and termination of muscle activity during the baseline trials.
The normalized response latency and the mean absolute ERROR during the last 5 myoelectric visual pursuit trials (Trial# 2–6) were assessed by fitting the performance with a power law function [33 ] using the Levenberg-Marquardt algorithm ('cftool’ in Matlab R2010a, The MathWorks, Inc., USA). The 95% confidence bounds of the coefficients of the fitted power law function were compared for the tDCS groups: M1, cerebellar, sham.
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3

Confocal Microscopy Analysis of Tissue Antibody Signals

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All observations were carried out and photographs were taken using a confocal laser scanning microscope (CLSM) Olympus BX51 equipped with corresponding software FluoView v. 5.0. (Olympus Corporation, Tokyo, Japan). Representative image sets were selected and edited using the CorelDrawX6 graphics program.
Optical signal density was calculated as the ratio of the total sum of values of pixels from the green channel (fluorescence indicating the presence of the antibody) within the selected region of interest to the pixel area of this region. The regions of interest had rectangular shapes and were selected manually to cover the tissue area below the epidermal layer of cells. CLSM data was analysed using a script written in Matlab R2010a (MathWorks, USA). The data were statistically analyzed using OriginPro 8.5 software (Origin Lab v8.5 Pro, Northampton, USA). For comparisons of the mean values, an analysis of variance (one-way ANOVA) followed by post hoc Tukey’s honestly significant difference test was used. For all analyses, the significance level was estimated at p < 0.05.
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4

Calibrated LED Monitor Display Protocol

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Each surface was displayed on a 24-in. calibrated LED monitor (Viewsonic V3D245) with a linearized gamma. The resolution was set to 1920 × 1080. All stimuli were displayed using Matlab R2010a (The MathWorks Inc., Massachusetts, US) and Psychtoolbox-3 (Brainard, 1997 (link)) that ran on a MAC Pro Quadro-Core Intel Xeon with OSX 10.5.8.
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5

Pupil Sensitivity to Stimulus Contrast

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A control experiment was performed after the end of the study, with the aim of estimating the sensitivity of pupil size measurements to manipulations of stimulus strength. The original set-up was inaccessible at the time of testing, and we replicated the conditions of the main experiment as closely as possible in another set-up, using the same eye-tracker (EyeLink 1000 system, SR Research), similar mirror stereoscope and a computer that ensured equal performance. Specifically, stimuli were generated with the PsychoPhysics Toolbox routines (Brainard, 1997 (link)) and MATLAB (MATLAB r2010a, The MathWorks Inc.) housed in a Mac Pro 4.1, and displayed on a 52.5-cm-wide LCD screen with maximum screen luminance of 108 cd/m2. Instead of using the maximum and minimum screen output, we reduced luminance levels by about a factor of 10 to allow for modulations of stimulus contrast. We set the background luminance to 15 cd/m2 gray and tested six conditions: a no cue and white cued condition in which stimuli where 28 and 2 cd/m2 for the white and black disk, respectively, and four conditions where the Michelson contrast of the white disk stimulus was increased by 25%, 50%, 100% and 150% (luminance values: 33, 40, 63, and 108 cd/m2). Each condition was tested in four trials, and all data were collected over a single session.
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6

Coarse-Grained Modeling of Collagen Fibrils

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The coordinates of the particles in the coarse‐grained models were created with Matlab R2010a (Mathworks Inc., Natick, MA, USA) based on the full atomistic geometry described previously.32 Visualization of the simulation is performed with visual molecular dynamics (VMD).41 Stress‐strain curves were computed from the box size and the virial‐stress of the particles. The diameter of the fibril was considered constant and equal to 20 nm. The stress‐strain response was divided into five regions to analyze the mechanical response of the fibril (Fig. 2A). The toughness of the fibril is defined as the area under the stress‐strain curve until ultimate strength (gray area in Fig. 2A).
All mineral densities are expressed as weight percentages of the total model.
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7

Mouse Parabiosis Power Analysis

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A power analysis using MATLAB R2010a (MathWorks Inc, Natick, MA) to determine the minimal sample size required to obtain significance levels of α = 0.05 using a one-way analysis of variance across mouse and/or construct pairs determined that three measurements per group would be sufficient to power these assays, and as such we elected to use n = 3 murine pairs per group per time point to ensure adequate statistical precision while minimizing the potential distress that parabiosis creates for the animal subjects. Data are expressed as mean ± standard error of the mean. Statistical analyses were performed using a one-way analysis of variance or unpaired Student t-test. P values ≤0.05 were considered statistically significant.
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8

Neuroimaging Data Processing Pipeline

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Data were processed using Statistical Parametric Mapping software (SPM8) (Wellcome Department of Imaging Neuroscience, London), running in MATLAB R2010a (Mathworks, Sherborn, MA). In SPM8, an image from the control group with no significant atrophy was used as reference to realign images. The images were then segmented into gray matter (GM), white matter (WM), and cerebrospinal fluid (CSF) using the unified segmentation procedure in SPM8 [38 (link)]. The Diffeomorphic Anatomical Registration Through Exponentiated Lie Algebra (DARTEL) algorithm [39 (link)] was then used to spatially normalize the segmented images. These fully normalized images were resliced with trilinear interpolation to a final voxel size of 1.5×1.5×1.5 mm3. An additional “modulation” step was applied, consisting of multiplying each spatially normalized GM image by its relative volume before and after normalization; this ensured that the total amount of GM in each voxel was preserved [40 (link)]. We used the ‘normalize_DARTEL’ matlab script [41 (link),42 (link)] to complete the affine transformation of segmented brain tissues into the MNI space. Finally, the resulting GM images were smoothed using an 8-mm isotropic kernel at full-width half-maximum to ensure a normal distribution of the data, as required by subsequent statistical parametric tests.
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9

Wound Healing Assay Protocol

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Data are expressed as mean ± SEM. Statistical analyses were performed using an unpaired t test. All values of p < 0.05 were considered statistically significant. Matlab R2010a (MathWorks, Inc., Natick, Mass.) was used to perform a power analysis to determine the minimal sample size (independent wound pairs) required to obtain significance levels at each time point. Our analysis determined that three measurements per group would be sufficient to power these assays, and we elected to use n = 3 mice per group per time point to ensure adequate statistical precision.
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10

Voxel-Based Analysis of Fractional Anisotropy in Neuroimaging

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The SPM8 (Statistical Parametric Mapping; http://www.fil.ion.ucl.ac.uk/spm/; University College London, London, UK) software package in Matlab R2010a (Mathworks, Natick, MA, USA) was used for voxelwise group comparisons. The FA images after normalization and smoothing were analyzed using SPM8 within the framework of a General Linear Model. ANCOVA with age and sex as covariates was performed to check the FA differences between the groups. The FA threshold of the mean WM was set at 0.2 to exclude “contaminated voxels” with composition of gray matter or cerebrospinal fluid. The statistical threshold was set at an uncorrected p < 0.005, with a cluster of >200 contiguous voxels. The extended cluster size was arbitrary and was used to putatively detect significant differences between groups with a cluster size <200 voxels, which might not represent reliable findings [25 (link)]. Additionally, multiple comparisons of FA were corrected by AlphaSim (FWE) to control for type I errors [22 (link)–24 (link), 26 (link)] with the threshold at p < 0.05 and cluster size >1871.
The FSL atlas tool (https://www.fmrib.ox.ac.uk/fsl/fslwiki/Atlases) was facilitated for determining the most probable fiber tracts and anatomic location of each significant cluster.
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