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Matlab 2007b

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MATLAB 2007b is a high-performance numerical computing environment and programming language. It provides a wide range of mathematical, engineering, and scientific functions, enabling users to perform data analysis, algorithm development, and visualization tasks.

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17 protocols using matlab 2007b

1

Modeling Peripheral Pressure Changes

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Data collected during the final 10 min of supine rest preceding onset of LBNP was averaged and defined as baseline. Data for each minute during LBNP was averaged and served as model input and output. We constructed LME models describing PP in relation to explanatory variable HR (fixed effect). Subject specific variables (random effects) were included to correct for, subject dependency and the expected variation in HR slope. LME models were computed in R (The R Project, The R Foundation for Statistical Computing, Vienna, Austria) (R Core Team, 2014 ) using the NLME library (Pinheiro et al., 2014 ). We used a crossover design to test model performance. The dataset was split into two groups (A and B). Initially, the data of group A served as model input and the data of group B was used to assess the performance of the acquired model. Then the process was interchanged: the data of group B was used to build a model and data of group A to test it (Figure 2). Absolute model errors determined during both baseline and LBNP were assessed per heartbeat. Median errors from all subjects following completion of the interchanging datasets are reported. Except for the modeling all data processing and statistics were performed in Matlab (Matlab 2007b, The MathWorks Inc., Natick, MA, USA).
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2

Quantitative Image Analysis of Immunofluorescence

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Immunofluorescence relative intensity quantification was assessed using a pixel-wise image analysis app (Matlab Image Processing Toolbox; MatLab 2007b, Mathworks, USA). Briefly, the relative fluorescence intensity (RFI) corresponding to the marker of interest in each picture was calculated as the cumulative sum of the value of each pixel above a pre-determined threshold. The cumulative sum of the given marker of interest of each image was then normalized in respect to the RFI of the staining corresponding to the nucleus following the same procedure. Since the pictures of every independent experiment had the same fluorescent light intensity, acquisition time and exposure for each channel, experimental condition could be compared together. At least 5 to 10 pictures with a magnification of 40X were analyzed per independent experiment for each experimental condition and at least 2 independent experiments were performed. The overall RFU mean (RFI of marker of interest/RFI of the nuclei) was determined as a weighted mean relative to the inverse of the variance of each independent experiment.
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3

SH-SY5Y Neurite Outgrowth Assay

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SH-SY5Y cells were grown to 80% confluence on 6-well plates, washed with sterile PBS and incubated with equimolar concentrations (0, 0.1 or 1 nM) of BMP-9, pBMP-9 and SpBMP-9 in serum-free medium with or without 10 µM RA for 5d. 5–10 representative pictures (magnification: 20X) were taken using an Eclipse TE200-S microscope coupled to a CCD camera (Zeiss AxioCam MRm, Car Zeiss, DE). Pictures were smoothed with a Gaussian filter to remove noise, with a Laplace high-pass filter and then with a median filter to detect and enhance neurites using an image analysis app (MatLab Image Processing Toolbox; MatLab 2007b, Mathworks, USA). The resulting images showing the neurite edges (blue lines) were superimposed on the original phase-contrast images. Original pictures were shrunk to fit within the figure panel. Each experiment was performed at least three times in duplicate.
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4

Audiovisual Integration in Drumming Perception

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The stimuli had previously been used in other studies, and a complete description of them can be found elsewhere (Petrini et al., 2009a (link),b (link); Love et al., 2013 (link)). They comprised dynamic audiovisual movies (3 s) containing the point-light representation of a drummer playing a swing groove at 120 beats per minute, with an accent on the second beat (Figure 1). Audio and visual cues were shifted relative to each other to produce stimuli with different cue onset asynchrony (COA). The video was shifted to begin either after the audio (−333, −267, −200, −133, and −67 ms) or before the audio (+333, +267, +200, +133, and +67 ms), producing a total of 10 asynchronous stimuli to be used in the pre-fMRI experiment. Negative and positive numbers will be used to refer to audio-leading and video-leading COA levels respectively, and 0 COA will refer to the synchronous condition. To prevent participants from having to stay in the MRI scanner for an uncomfortably long time only 4 COA levels were used during the fMRI experiment: two asynchronous (−333, +333 COA) and two “synchronous” (0 COA and the individually defined PSS). The −333, 0 and +333 COA conditions are provided as Supplementary Videos 13, respectively.
Stimuli were presented using MATLAB 2007b (MATHWORKS Inc., Natick, MA) and the Psychophysics Toolbox (Brainard, 1997 (link); Pelli, 1997 (link)).
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5

AV Stimuli Manipulation in Psychophysics

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The AV-SOA of the separate audio and video files was manipulated using Psychophysics Toolbox version 3 (PTB-3) under Matlab 2007b (MathWorks Inc., MA, USA). Visual stimuli (size 8.89° * 7° visual angle) were projected using a CRT monitor (Sony Trinitron, Tokyo, Japan) at refresh rate of 100 Hz, and subjects' heads were stabilized using a chin rest. Auditory stimuli were presented at ~75 dB SPL via headphones.
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6

Quantifying Neurite Lengths in Cell Cultures

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Mean neurite lengths were determined from the normal size high resolution neurite-enhanced pictures taken for morphology analyses (20x magnification) using an image analysis app (Matlab Image Processing Toolbox; MatLab 2007b, Mathworks, USA). Briefly, neurite length was defined as the Euclidean distance in pixels or a combination of Euclidean distances between the cell body and the end of a neurite. The longest path was always chosen when a neurite had several branches. The length in pixels was then calibrated based on the length bar provided by the microscope image treatment software (AxioVision LE, Carl Zeiss, DE). For each experimental condition, 15 to 30 neurites were measured for each picture (4 × 10−3 cm²) and at least 5 pictures were analyzed per condition performed. Those steps were done three independent times in duplicate. The mean neurite length for each picture analyzed within a replicate was weighted by the number of measurement taken. For each independent experiment, the mean was calculated as the weighted mean (relative to the inverse of the variance) of each replicate. Finally, the overall mean was calculated as the weighted mean (relative to the inverse of the variance) of each of the three independent experiments. Overall, a total of at least 300 neurite length measurements were obtained for each experimental condition.
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7

Macroanatomical Landmark Topological Relationships

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Basically, Euclidian distances between given macroanatomical landmarks were used to assess their topological relationship (indicated as “direct distance” in Table 1). Ratios between a set of two given landmark distances were calculated. Specific macroanatomical landmarks used for analyses are depicted in Figure 1. When junctions of sulci and fissures were detected on slice images, they tended to be located beneath the lateral cortical surface. To avoid variability in depth direction, their locations were adjusted to the cortical surface. Macroanatomical structures around the medial cortical surface were projected onto the sagittal plane for analysis. To analyze the height of macroanatomical structures, they were projected onto the coronal plane. Correlation analyses were performed between a given ratio for topological relationship and age of infant (months). All calculations were performed using a numerical processing software package, Matlab 2007b (MathWorks).
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8

Invasive Cardiac Function Assessment

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RV open-chest catheterization was performed using a combined pressure-volume catheter (SPR-869, Millar Instruments, Houston, Texas). Details regarding the RV catheterization can be found online in the Supplemental Material and Methods section. Stroke volume (in relative volume units) obtained from the conductance catheter was calibrated using the echocardiogram stroke volume (in ml). Using custom-made algorithms (programmed in MATLAB 2007b, The MathWorks, Natick, Massachusetts) RV (peak-) systolic pressures and RV end-diastolic pressures were automatically determined from RV catheterization steady-state measurements, as well as arterial elastance (Ea), a measurement of RV afterload (25) (link). From vena cava occlusion, end-systolic elastance (Ees) (RV contractility) and end-diastolic elastance (Eed) (RV stiffness) were determined (13) (link). These parameters represent the slope of end-systolic and end-diastolic pressure-volume relationships, and are considered load-independent measurements for cardiac contractility (Ees) and stiffness (Eed) (26) (link). The ratio Ees/Ea was calculated, and it represents the RV-arterial coupling.
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9

Dichoptic Presentation of Ambiguous Lissajous Figures

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We presented stimuli generated with Psychophysics Toolbox 3 [23 (link)] running under Matlab 2007b (Mathworks inc.) on a 60 Hz Sanyo LCD projector, on which participants viewed alternating blocks of ambiguous and corresponding replay stimulation. In ambiguous blocks, we displayed two identical moving Lissajous figures formed by the intersection of two perpendicular sinusoids (x(t) = sin(3t) and y(t) = sin(6t + δ); with δ increasing from 0 to 2π), separately to the two eyes. In replay blocks, a disambiguated version of the Lissajous figure mimicked the perceptual time-course participants had experienced during the preceding ambiguous block. To this end, the two dichoptically presented Lissajous figures were phase-shifted against each other by an offset of 0.04°. This disparity cue was used to disambiguate the stimulus, biasing participants perceived direction of rotation in the direction of the phase shift. All stimuli subtended 2.05° visual angle.
We achieved dichoptic stimulation by placing a custom build cardboard divider between the mirror attached to the head-coil and the screen at the end of the scanners bore [24 (link)]. Participants wore prism glasses to facilitate fusion between to two eyes. All screens contained a fixation mark at the center and fusion frames surrounding the stimuli.
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10

Functional Neuroimaging Data Preprocessing

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Preprocessing and first-level analyses were carried out using Statistical Parametric Mapping (SPM8, Welcome Department of Cognitive Neurology, London, UK; 2008) implemented in MATLAB 2007b (MathWorks Inc., Sherborn, MA, USA). Preprocessing included unwarping and realignment to the first volume (b-spline interpolation), slice timing correction, coregistration of functional data to each participant’s anatomical image, normalization to the standard brain of the Montreal Neurological Institute, and smoothing with an isotropic three-dimensional Gaussian kernel with a full width at half maximum of 9 mm. Two male participants were excluded from further analyses due to excessive head movements, as described in Wehrum et al. (2013) (link).
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