Create image masks for NF1 test data

.pre-commit-config.yaml

@@ -23,7 +23,8 @@ repos:
           (?x)^(
               .*\.lock |
               .*\.json |
-              .*\.ipynb
+              .*\.ipynb |
+              .*\.cppipe
           )$
   - repo: https://github.com/executablebooks/mdformat
     rev: 0.7.17

tests/data/cytotable/NF1_cellpainting_data_shrunken/NF1_plate2_export_masks.cppipe

@@ -0,0 +1,227 @@
+CellProfiler Pipeline: http://www.cellprofiler.org
+Version:5
+DateRevision:424
+GitHash:
+ModuleCount:13
+HasImagePlaneDetails:False
+
+Images:[module_num:1|svn_version:'Unknown'|variable_revision_number:2|show_window:False|notes:['Images module is left blank as we are giving the path to the corrected images in the CLI']|batch_state:array([], dtype=uint8)|enabled:True|wants_pause:False]
+    :
+    Filter images?:Images only
+    Select the rule criteria:and (extension does isimage) (directory doesnot containregexp "[\\\\/]\\.")
+
+Metadata:[module_num:2|svn_version:'Unknown'|variable_revision_number:6|show_window:False|notes:['Extract metadata from file names and folder names using regular expressions.', '', 'The only metadata that will be outputed in the SQLite DB file are:', '', 'Plate', 'Well', 'Site', '', 'The rest of the information is useful to make sure that the expression is working, but can be removed/not necessary.']|batch_state:array([], dtype=uint8)|enabled:True|wants_pause:False]
+    Extract metadata?:Yes
+    Metadata data type:Text
+    Metadata types:{"Channel": "integer", "FileLocation": "text", "Frame": "text", "Plate": "text", "Series": "text", "Site": "integer", "Stain": "float", "Well": "text"}
+    Extraction method count:2
+    Metadata extraction method:Extract from file/folder names
+    Metadata source:File name
+    Regular expression to extract from file name:(?P<Well>[A-Z]{1}[0-9]{1,2})_01_(?P<Channel>[1-3]{1})_(?P<Site>[1-4]{1})_(?P<Stain>DAPI|GFP|RFP)
+    Regular expression to extract from folder name:(?P<Date>[0-9]{4}_[0-9]{2}_[0-9]{2})$
+    Extract metadata from:All images
+    Select the filtering criteria:and (file does contain "")
+    Metadata file location:Elsewhere...|
+    Match file and image metadata:[]
+    Use case insensitive matching?:No
+    Metadata file name:None
+    Does cached metadata exist?:No
+    Metadata extraction method:Extract from file/folder names
+    Metadata source:Folder name
+    Regular expression to extract from file name:^(?P<Plate>.*)_(?P<Well>[A-P][0-9]{2})_s(?P<Site>[0-9])_w(?P<ChannelNumber>[0-9])
+    Regular expression to extract from folder name:Corrected_(?P<Plate>Plate_[0-9]{1})
+    Extract metadata from:All images
+    Select the filtering criteria:and (file does contain "")
+    Metadata file location:Elsewhere...|
+    Match file and image metadata:[]
+    Use case insensitive matching?:No
+    Metadata file name:None
+    Does cached metadata exist?:No
+
+NamesAndTypes:[module_num:3|svn_version:'Unknown'|variable_revision_number:8|show_window:False|notes:['Assign files to their respective channel (only 3):', '', 'DAPI', 'GFP', 'RFP']|batch_state:array([], dtype=uint8)|enabled:True|wants_pause:False]
+    Assign a name to:Images matching rules
+    Select the image type:Grayscale image
+    Name to assign these images:DNA
+    Match metadata:[]
+    Image set matching method:Order
+    Set intensity range from:Image metadata
+    Assignments count:3
+    Single images count:0
+    Maximum intensity:255.0
+    Process as 3D?:No
+    Relative pixel spacing in X:1.0
+    Relative pixel spacing in Y:1.0
+    Relative pixel spacing in Z:1.0
+    Select the rule criteria:and (file does contain "DAPI")
+    Name to assign these images:DAPI
+    Name to assign these objects:Cell
+    Select the image type:Grayscale image
+    Set intensity range from:Image metadata
+    Maximum intensity:255.0
+    Select the rule criteria:and (file does contain "GFP")
+    Name to assign these images:GFP
+    Name to assign these objects:Nucleus
+    Select the image type:Grayscale image
+    Set intensity range from:Image metadata
+    Maximum intensity:255.0
+    Select the rule criteria:and (file does contain "RFP")
+    Name to assign these images:RFP
+    Name to assign these objects:Cytoplasm
+    Select the image type:Grayscale image
+    Set intensity range from:Image metadata
+    Maximum intensity:255.0
+
+Groups:[module_num:4|svn_version:'Unknown'|variable_revision_number:2|show_window:False|notes:['We do not use the Groups module.']|batch_state:array([], dtype=uint8)|enabled:True|wants_pause:False]
+    Do you want to group your images?:No
+    grouping metadata count:1
+    Metadata category:None
+
+IdentifyPrimaryObjects:[module_num:5|svn_version:'Unknown'|variable_revision_number:15|show_window:False|notes:['These are the current best parameters to segment nuclei from the DAPI channel']|batch_state:array([], dtype=uint8)|enabled:True|wants_pause:False]
+    Select the input image:DAPI
+    Name the primary objects to be identified:Nuclei
+    Typical diameter of objects, in pixel units (Min,Max):30,90
+    Discard objects outside the diameter range?:Yes
+    Discard objects touching the border of the image?:Yes
+    Method to distinguish clumped objects:None
+    Method to draw dividing lines between clumped objects:Shape
+    Size of smoothing filter:10
+    Suppress local maxima that are closer than this minimum allowed distance:7.0
+    Speed up by using lower-resolution image to find local maxima?:Yes
+    Fill holes in identified objects?:After both thresholding and declumping
+    Automatically calculate size of smoothing filter for declumping?:Yes
+    Automatically calculate minimum allowed distance between local maxima?:Yes
+    Handling of objects if excessive number of objects identified:Continue
+    Maximum number of objects:500
+    Use advanced settings?:Yes
+    Threshold setting version:12
+    Threshold strategy:Global
+    Thresholding method:Otsu
+    Threshold smoothing scale:1.3488
+    Threshold correction factor:1.0
+    Lower and upper bounds on threshold:0.0,1.0
+    Manual threshold:0.0
+    Select the measurement to threshold with:None
+    Two-class or three-class thresholding?:Three classes
+    Log transform before thresholding?:No
+    Assign pixels in the middle intensity class to the foreground or the background?:Foreground
+    Size of adaptive window:50
+    Lower outlier fraction:0.05
+    Upper outlier fraction:0.05
+    Averaging method:Mean
+    Variance method:Standard deviation
+    # of deviations:2.0
+    Thresholding method:Minimum Cross-Entropy
+
+IdentifySecondaryObjects:[module_num:6|svn_version:'Unknown'|variable_revision_number:10|show_window:False|notes:['These are the current best parameters to segment whole cells using the RFP (actin) channel']|batch_state:array([], dtype=uint8)|enabled:True|wants_pause:False]
+    Select the input objects:Nuclei
+    Name the objects to be identified:Cells
+    Select the method to identify the secondary objects:Propagation
+    Select the input image:RFP
+    Number of pixels by which to expand the primary objects:10
+    Regularization factor:0.05
+    Discard secondary objects touching the border of the image?:Yes
+    Discard the associated primary objects?:No
+    Name the new primary objects:Nuclei
+    Fill holes in identified objects?:Yes
+    Threshold setting version:12
+    Threshold strategy:Global
+    Thresholding method:Otsu
+    Threshold smoothing scale:1.3488
+    Threshold correction factor:1.0
+    Lower and upper bounds on threshold:0.0,1.0
+    Manual threshold:0.0
+    Select the measurement to threshold with:None
+    Two-class or three-class thresholding?:Three classes
+    Log transform before thresholding?:No
+    Assign pixels in the middle intensity class to the foreground or the background?:Foreground
+    Size of adaptive window:50
+    Lower outlier fraction:0.05
+    Upper outlier fraction:0.05
+    Averaging method:Mean
+    Variance method:Standard deviation
+    # of deviations:2.0
+    Thresholding method:Otsu
+
+IdentifyTertiaryObjects:[module_num:7|svn_version:'Unknown'|variable_revision_number:3|show_window:False|notes:['This module creates a third object from the first two where the nuclei is subtracted from the cells to create cytoplasm']|batch_state:array([], dtype=uint8)|enabled:True|wants_pause:False]
+    Select the larger identified objects:Cells
+    Select the smaller identified objects:Nuclei
+    Name the tertiary objects to be identified:Cytoplasm
+    Shrink smaller object prior to subtraction?:Yes
+
+ConvertObjectsToImage:[module_num:8|svn_version:'Unknown'|variable_revision_number:1|show_window:False|notes:[]|batch_state:array([], dtype=uint8)|enabled:True|wants_pause:False]
+    Select the input objects:Nuclei
+    Name the output image:MaskNuclei
+    Select the color format:Binary (black & white)
+    Select the colormap:Default
+
+ConvertObjectsToImage:[module_num:9|svn_version:'Unknown'|variable_revision_number:1|show_window:False|notes:[]|batch_state:array([], dtype=uint8)|enabled:True|wants_pause:False]
+    Select the input objects:Cells
+    Name the output image:MaskCells
+    Select the color format:Binary (black & white)
+    Select the colormap:Default
+
+ConvertObjectsToImage:[module_num:10|svn_version:'Unknown'|variable_revision_number:1|show_window:False|notes:[]|batch_state:array([], dtype=uint8)|enabled:True|wants_pause:False]
+    Select the input objects:Cytoplasm
+    Name the output image:MaskCytoplasm
+    Select the color format:Binary (black & white)
+    Select the colormap:Default
+
+SaveImages:[module_num:11|svn_version:'Unknown'|variable_revision_number:16|show_window:False|notes:[]|batch_state:array([], dtype=uint8)|enabled:True|wants_pause:False]
+    Select the type of image to save:Image
+    Select the image to save:MaskNuclei
+    Select method for constructing file names:From image filename
+    Select image name for file prefix:DAPI
+    Enter single file name:OrigBlue
+    Number of digits:4
+    Append a suffix to the image file name?:Yes
+    Text to append to the image name:_MaskNuclei
+    Saved file format:tiff
+    Output file location:Default Output Folder|
+    Image bit depth:8-bit integer
+    Overwrite existing files without warning?:No
+    When to save:Every cycle
+    Record the file and path information to the saved image?:No
+    Create subfolders in the output folder?:No
+    Base image folder:Elsewhere...|
+    How to save the series:T (Time)
+    Save with lossless compression?:Yes
+
+SaveImages:[module_num:12|svn_version:'Unknown'|variable_revision_number:16|show_window:False|notes:[]|batch_state:array([], dtype=uint8)|enabled:True|wants_pause:False]
+    Select the type of image to save:Image
+    Select the image to save:MaskCells
+    Select method for constructing file names:From image filename
+    Select image name for file prefix:RFP
+    Enter single file name:OrigBlue
+    Number of digits:4
+    Append a suffix to the image file name?:Yes
+    Text to append to the image name:_MaskCells
+    Saved file format:tiff
+    Output file location:Default Output Folder|
+    Image bit depth:8-bit integer
+    Overwrite existing files without warning?:No
+    When to save:Every cycle
+    Record the file and path information to the saved image?:No
+    Create subfolders in the output folder?:No
+    Base image folder:Elsewhere...|
+    How to save the series:T (Time)
+    Save with lossless compression?:Yes
+
+SaveImages:[module_num:13|svn_version:'Unknown'|variable_revision_number:16|show_window:False|notes:[]|batch_state:array([], dtype=uint8)|enabled:True|wants_pause:False]
+    Select the type of image to save:Image
+    Select the image to save:MaskCytoplasm
+    Select method for constructing file names:From image filename
+    Select image name for file prefix:RFP
+    Enter single file name:OrigBlue
+    Number of digits:4
+    Append a suffix to the image file name?:Yes
+    Text to append to the image name:_MaskCytoplasm
+    Saved file format:tiff
+    Output file location:Default Output Folder|
+    Image bit depth:8-bit integer
+    Overwrite existing files without warning?:No
+    When to save:Every cycle
+    Record the file and path information to the saved image?:No
+    Create subfolders in the output folder?:No
+    Base image folder:Elsewhere...|
+    How to save the series:T (Time)
+    Save with lossless compression?:Yes

tests/data/cytotable/NF1_cellpainting_data_shrunken/create_mask_data.py

@@ -0,0 +1,51 @@
+"""
+Creates image masks for images in
+coSMicQC/tests/data/cytotable/NF1_cellpainting_data (Plate 2)
+
+Note: expects Docker to be installed as a CLI on the system.
+
+This file may be processed using the following command from the root
+of the project repository:
+`poetry run python \
+tests/data/cytotable/NF1_cellpainting_data_shrunken/create_mask_data.py`
+"""
+
+import os
+import pathlib
+import subprocess
+
+# create a dir for segmentation masks
+pathlib.Path("tests/data/cytotable/NF1_cellpainting_data_shrunken/Plate_2_masks").mkdir(
+    exist_ok=True
+)
+
+# define docker command for CellProfiler use with provided pipeline file
+command = [
+    "docker",
+    "run",
+    "--platform",
+    "linux/amd64",
+    "--rm",
+    "-v",
+    f"{os.getcwd()}/tests/data/cytotable/NF1_cellpainting_data_shrunken:/app",
+    "cellprofiler/cellprofiler:4.2.4",
+    "cellprofiler",
+    "-c",
+    "-r",
+    "-p",
+    "/app/NF1_plate2_export_masks.cppipe",
+    "-o",
+    "/app/Plate_2_masks",
+    "-i",
+    "/app/Plate_2_images",
+]
+
+# Run the command and show output
+try:
+    result = subprocess.run(command, check=True, text=True, capture_output=True)
+    print("Command Output:\n", result.stdout)
+    print("Command Error:\n", result.stderr)
+except subprocess.CalledProcessError as e:
+    print("Error:", e)
+    print("Command Output:\n", e.stdout)
+    print("Command Error:\n", e.stderr)