interactive spindle photoconversion analysis gui matlab 2020b (MathWorks Inc)
MathWorks Inc is a verified supplier 
90
Structured Review
MathWorks Inc
interactive spindle photoconversion analysis gui matlab 2020b
Interactive Spindle Photoconversion Analysis Gui Matlab 2020b, 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/product/interactive+gui/pmc09398449-6-3-8
Average 90 stars, based on 1 article reviews
Interactive Spindle Photoconversion Analysis Gui Matlab 2020b, 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/product/interactive+gui/pmc09398449-6-3-8
Average 90 stars, based on 1 article reviews
interactive spindle photoconversion analysis gui matlab 2020b - by Bioz Stars,
2026-09
90/100 stars
Images
1) Product Images from "Self-organization of kinetochore-fibers in human mitotic spindles"
Article Title: Self-organization of kinetochore-fibers in human mitotic spindles
Journal: eLife
doi: 10.7554/eLife.75458
Figure Legend Snippet: ( A ) Photoactivation experiment showing PA-GFP:alpha-tubulin and SNAP-SIR:centrin immediately preceding photoactivation, 0 s, 30 s, and 60 s after photoactivation with a 750nm femtosecond pulsed laser; 500ms 488nm excitation, 514/30 bandpass emission filter; 300ms 647nm excitation, 647 longpass emission filter; 5s frame rate. ( B ) Line profile generated by averaging the intensity in 15 pixels on either side of the spindle axis in the dotted box shown in A. The intensity is corrected for background from the opposite side of the spindle (see methods). ( C ) Line profiles (shades of green) fit to Gaussian profiles (shades of grey) at 0s, 5s and 25s. Lighter shades are earlier times. The solid line on the fit represents the fit pixels. ( D ) Blue dots: fit position of the line profile peak from the sample cell shown in A, B, and C over time. Black line: linear fit to the central position of the fit peak over time. ( E ) Red dots: fit height of the line profile peak from the sample cell shown in A, B, and C over time. Black line: dual-exponential fit to the fit height of the peak over time. ( F ) Sample ultrastructure from a 3D spindle reconstructed by electron tomography . KMTs are shown in red, non-KMTs yellow. ( G ) Comparison between the mean slow fraction from the photoconversion data (26% ± 2%, n=52 cells, error bars are standard error of the mean) and the fraction of KMTs (25% ± 2%, n=3 cells, error bars are standard error of the mean) from the EM data. The two means are statistically indistinguishable with P =0.86 on a Student’s t-test.
Techniques Used: Generated, Tomography, Comparison
Figure Legend Snippet: ( A ) Sample simulated images and line profiles from a photoconversion simulation using KMT minus end speeds in the nucleate at kinetochore model. ( B ) Comparison of the predicted spatial dependence tubulin flux speed in the nucleate at kinetochore and capture from spindle models. Error bars are standard error of the mean. ( C ) Relative probabilities of hybrid version of the two models.
Techniques Used: Comparison
Figure Legend Snippet: ( A ) Sample simulated images and line profiles from a photoconversion simulation using KMT minus end speeds in the nucleate at kinetochore model. ( B ) Sample simulated images and line profiles from a photoconversion simulation using KMT minus end speeds in the capture from spindle model. ( C ) Comparison of the predicted spatial dependence tubulin speed in the nucleate at kinetochore and capture from spindle models. Error bars are standard error of the mean.
Techniques Used: Comparison
Figure Legend Snippet: Parameters values and sources.
Techniques Used: Electron Microscopy
Figure Legend Snippet:
Techniques Used: Transfection, Construct, Labeling, Retroviral, Plasmid Preparation, Selection, Marker, Software, Control, Imaging, Light Microscopy
Related Articles
other:Article Title: The study of the random evolutionary game model and policy effects of carbon information disclosure by Chinese listed companies. Article Snippet: As global attention to environmental sustainability increases, corporate environmental information disclosure has become a key driver of environmental governance.. Based on public choice theory, this paper constructs a random evolutionary game model for environmental information disclosure by Chinese listed companies, analyzing the interactions and policy effects of the government, enterprises, and the public in the disclosure process.. Public choice theory emphasizes that the behavior of the government, enterprises, and the public is driven by self-interest, and that their interactions through the game process determine the transparency of environmental information. Article Title: A hybrid ARIMA-BP approach for superior accuracy in predicting traffic accident losses. Article Snippet: The BP neural network model for prediction was implemented using Article Title: Supporting Information for Transient Zn2+ deficiency induces replication stress and compromises daughter cell proliferation Article Snippet: All analysis was done in Article Title: Subtle alteration in transcriptional memory governs the lineage-level cell cycle duration heterogeneities of mammalian cells Article Snippet: Article Title: Analysis of Longitudinal Change Patterns in Developing Brain Using Functional and Structural Magnetic Resonance Imaging via Multimodal Fusion. Article Snippet: We conducted preprocessing on the sMRI data using statistical parametric mapping6 within the Article Title: Supporting Information for Transient Zn2+ deficiency induces replication stress and compromises daughter cell proliferation Article Snippet: All analysis was conducted in Software:Article Title: Second-Generation (44-Channel) Suprachoroidal Retinal Prosthesis: Surgical Stability and Safety During a 2-Year Clinical Trial. Article Snippet: Colour fundus photography (TRC- 50EX, Topcon Medical Systems, Japan and Clarus 500, Carl Zeiss Meditec AG, Jena, Germany) and near infrared imaging plus OCT (Spectralis OCT, Heidelberg Engineering GmbH, Heidelberg, Germany) were conducted at least every 12 weeks. .. Near infrared images were montage stitched using the manufacturer provided Heyex software, then scaled and rotated to a common reference frame with Article Title: Integrated method for multi-UAV task assignment and trajectory planning with deadlock based on Three-dimensional dubins path. Article Snippet: .. The hardware environment utilised for the simulation comprises an AMD R5 5600 H processor and 16G memory, while the software environment employed is |
![The “Preprocessing” pop-up window is the initial screen of Robin’s Viewer (RV) and has five distinct sections: First, the electroencephalography (EEG)-file selection (see Section “3.1 Loading EEG data”), where the user can load their EEG recording and display selected statistics about the data once it is loaded. Second, the preprocessing settings (see Section “3.2 Preprocessing and visualization settings”), which are used to set a bandpass filter [finite impulse response (FIR) filter with Blackman window] and a custom reference. Third, the bad-channel handling (see Sections “3.2 Preprocessing and visualization settings” and “3.4 Bad-channel marking”), where the user can decide whether to use automatic bad channel detection, and whether to interpolate bad channels. Fourth, the visualization settings (see Section “3.2 Preprocessing and visualization settings”), comprised of downsampling, custom scaling (by default 1e-6 as RV scales data from volts to microvolts for plotting), the gap between traces (by default 40 (μV); setting this to 0 results in butterfly mode where all traces are collapsed on top of each other; values higher than 40 move traces further apart), segment length to plot [by default 60 (seconds)], whether or not to activate the view-slider, and selection of channels to plot. Visualization settings will only be applied to the data for plotting and hence will not be saved in the save-file (in contrast to the preprocessing settings). Fifth, the deep-learning model settings (see Sections “3.2 Preprocessing and visualization settings” and 3.5 Deep-learning model predictions”), where previously saved model output can be loaded and the integrated deep-learning model can be activated to generate predictions. Clicking the “Plot” button at the bottom will close this window and, after a loading screen (which lasts as long as it takes to plot the data), it will open up the main <t>graphical</t> <t>user</t> <t>interface</t> <t>(GUI).</t>](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_1202/pmc09951202/pmc09951202__fninf-16-1025847-g001.jpg)
![(A) The main graphical user interface (GUI) of Robin’s Viewer (RV) with its six subsections highlighted [see Section “3.3 Graphical user interface (GUI)”]: The menu bar ( red ) contains buttons to open pop-up windows for file loading and preprocessing, saving, annotation statistics, power spectrum, help, and shutting down RV, as well as a button to recalculate the deep-learning model’s predictions (if activated) and left and right arrow buttons used to navigate the currently viewed timeframe (if the data is loaded in segments). The taskbar ( light blue ) seen in detail in panel (B) . The labeled buttons ( dark blue ): The first two buttons are used to reset the view, either across the channel- (“Reset channel-axis”) or time-axis (“Reset time-axis”). The third button (“Hide/show bad channels”) allows to hide marked bad channels from the plot. The fourth button (“Highlight model-channels”) only appears when deep-learning predictions are activated and highlights the channels used by the model to make its predictions in blue. The view-slider ( green ) is used to scroll continuously along the time-axis of the signal. The legend ( purple ) shows all available channels. Clicking on any channel in the legend once will hide it from the plot (clicking again reverses this). Double-clicking on a channel will hide all other channels from the plot, except for the selected channel. The plot ( yellow ) shows the traces for all selected channels spread across the vertical axis, and time (in seconds) on the horizontal axis. The user can hover over any given point in the plot in order to display the time (in seconds) and amplitude (in μV if no custom scaling was used) values of the trace under the mouse. The deep-learning predictions, if activated (see Section “3.5 Deep-learning model predictions”), are plotted below the EEG traces. (B) The taskbar hosts ten buttons from left to right: (1) Take a picture of the (annotated) electroencephalography (EEG) signal and download it as a .png file. (2) Select an area to zoom in on. (3) Move view along the channel- or time-axis. (4) Select a channel to mark it as “bad” or select a segment of the data for which to calculate and display the main underlying frequency and power spectrum. (5) Select a segment of the plot to annotate. (6) Delete the currently selected annotation. (7) Zoom in one step. (8) Zoom out one step. (9) Zoom out as much as necessary to show all channels for the entire duration of the recording (or segment). (10) Display a ruler from both axes to the datapoint currently hovered on.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_1202/pmc09951202/pmc09951202__fninf-16-1025847-g002.jpg)