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Merge pull request #122 from gwaygenomics/sample-images
Adding Code to Visualize Example Images
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1.generate-profiles/4.load-example-cell-painting-image.ipynb
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1.generate-profiles/scripts/nbconverted/4.load-example-cell-painting-image.py
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#!/usr/bin/env python | ||
# coding: utf-8 | ||
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# # Load an Example Image for Approach Figure | ||
# | ||
# Here, I use `skimage` to load, process, and output example images across channels and an example composite image with merged channels. | ||
# | ||
# Note that much of this code was adapted from https://github.com/jr0th/segmentation/blob/master/visualization/CellArt.ipynb and with insights from Marzieh Haghighi. | ||
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# In[1]: | ||
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import os | ||
import sys | ||
import numpy as np | ||
import pandas as pd | ||
import matplotlib.pyplot as plt | ||
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import skimage.io | ||
import skimage.exposure | ||
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from pycytominer.aggregate import AggregateProfiles | ||
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# In[2]: | ||
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sys.path.append("../scripts") | ||
from grabPictures import grabPicture | ||
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# ## Set File Paths | ||
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# In[3]: | ||
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bucket_path = "/home/ubuntu/bucket/projects/2015_07_01_Cell_Health_Vazquez_Cancer_Broad/" | ||
image_path = os.path.join(bucket_path, "CRISPR_PILOT_B1/images/") | ||
sqlite_path = os.path.join(bucket_path, "workspace/backend/CRISPR_PILOT_B1/") | ||
metadata_path = os.path.join("data", "metadata") | ||
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# In[4]: | ||
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plate = "SQ00014613" | ||
sqlite_dir = os.path.join(sqlite_path, plate) | ||
sqlite_file = "sqlite:///{}/{}.sqlite".format(sqlite_dir, plate) | ||
sqlite_file | ||
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# In[5]: | ||
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barcode_file = os.path.join(metadata_path, "barcode_platemap.csv") | ||
platemap_name = pd.read_csv(barcode_file).query("Assay_Plate_Barcode == @plate").Plate_Map_Name.values[0] | ||
platemap_path = os.path.join(metadata_path, "platemap", "{}.csv".format(platemap_name)) | ||
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# ## Process Data and Load Example Images | ||
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# In[6]: | ||
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gene_name = "EMPTY" | ||
pert_name = "EMPTY" | ||
site = 1 | ||
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# In[7]: | ||
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example_image = grabPicture( | ||
bucket_path=bucket_path, | ||
image_path=image_path, | ||
sqlite_path=sqlite_path, | ||
metadata_path=metadata_path, | ||
plate=plate, | ||
aggregate_strata_cols=["Image_Metadata_Plate", "Image_Metadata_Well"], | ||
gene_name=gene_name, | ||
pert_name=pert_name, | ||
site=site, | ||
) | ||
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# In[8]: | ||
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example_image.load_image_table(get_well=True) | ||
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# In[9]: | ||
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# Prep images with a narrow crop | ||
example_image.prep_images(low_prop=0.1, high_prop=0.3) | ||
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# ## Output an Example Image | ||
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# In[10]: | ||
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example_image.plot_images(cropped=True, color=False) | ||
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output_file = os.path.join("figures", "example_images", "greyscale_channel.png") | ||
plt.subplots_adjust(top=0.8) | ||
plt.savefig(output_file, pad_inches=0.2, dpi=500) | ||
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# In[11]: | ||
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example_image.plot_images(cropped=True, color=True) | ||
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output_file = os.path.join("figures", "example_images", "color_channel.png") | ||
plt.subplots_adjust(top=0.8) | ||
plt.savefig(output_file, pad_inches=0.2, dpi=500) | ||
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# In[12]: | ||
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example_image.plot_combined_image() | ||
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output_file = os.path.join("figures", "example_images", "color_merged.png") | ||
plt.savefig(output_file, dpi=500) | ||
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