Cellfinder output visualization
Project description
Cellfinder-visualize User Guide
About
cellfinder-visualize
is a tool for post-cellfinder data visualisation and analysis.
The core aims are to provide:
- Publication quality visualisations of cellfinder experiments for multiple samples
- Standardised publication quality plots of cell counts for different region sets
- Easy toggling of regions of interest
- Matching visualisations to quantifications
- Lateralised views
- Slice views
- Statistical analysis (in progress)
cellfinder-visualize
is a tool developed by Stephen Lenzi in the Margrie Lab, generously supported by the Sainsbury Wellcome Centre.
Installation
conda create -n cellfinder-visualize python
conda activate cellfinder-visualize
git clone https://github.com/brainglobe/cellfinder-visualize.git
cd cellfinder-visualize
pip install -e .
Usage
Simply run from the commandline as follows
conda activate cellfinder-visualize
cellfinder_visualize
This will open a GUI for selecting parameters
experiment dir
should be a directory containing cellfinder output directories. When selected, all subfolders in the selected directory will be displayed and available in the experiment group
section in the GUI where they can be selected and assigned a group for running through the analysis.
experiment group
sample directories shown under experiment group can be selected and assigned to groups for comparative analysis.
Set Group A
when clicked, this button will assign all currently highlighted directories to a single experimental group (group A) for analysis.
Set Group B
when clicked, this button will assign all currently highlighted directories to a single experimental group (group B) for analysis.
output dir
should be a directory for saving any outputs for your sample
Save Settings
when clicked, this button will save the current selected settings to a file called settings.pkl in the output directory that can be loaded again later.
config
select a previously saved settings.pkl file to load previous settings into the GUI.
coronal slice start
if you want to show only a coronal subsection this value is the start in microns
coronal slice end
if you want to show only a coronal subsection this value is the end of that section in microns
root
if checked the whole brain outline will be shown
show reference structures
if checked, several brain regions will be added for reference only
filter cells by structure
if checked, cells displayed will be restricted to the regions listed in region list
hemisphere
whether to display and count cells in left/right/both hemispheres
slice root
if checked, and a subregion is selected (e.g. only one hemisphere, or a coronal section) then all other unselected regions will not be visible
subsample factor
show every nth cell of the number chosen
highlight subregion
outlines will be drawn for subregions that contain the string in this box. i.e. if you wanted to highlight layer 5 in displayed regions, then 5
would achieve this.
region list
each item in this list will be displayed and included in any analysis
colors
color labels that each correspond to items in the region list.
reference region
the region used to normalise cell counts to.
brainrender
if checked, brainrender will run.
barplots
if checked, barplots will be generated of the cell counts.
load additional obj files
if any .obj files are present in the directory given then they will be rendered in the brainrender view.
camera pos
position of the camera in brainrender.
camera viewup
the camera "up" direction for brainrender.
camera clipping range
the range of clipping the brainrender image.
shader style
the shader option to be used in brainrender.
The end result should be bar plots per sample indicating the counts and percentages of cells in each region:
And also a pooled plot indicating the averages for all samples and the individual points:
A boxplot of each experimental group:
Together with a brainrender of the samples and target regions:
Any .obj files in the directory hierarchy will be automatically displayed e.g.:Project details
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