Source code for lineage.visualization

""" Chromosome plotting functions.

Notes
-----
Adapted from Ryan Dale's GitHub Gist for plotting chromosome features. [#Dale]_

References
----------
.. [#Dale] Ryan Dale, GitHub Gist,
   https://gist.github.com/daler/c98fc410282d7570efc3#file-ideograms-py

"""

"""
The MIT License (MIT)

Copyright (c) 2016 Ryan Dale

Permission is hereby granted, free of charge, to any person obtaining a copy
of this software and associated documentation files (the "Software"), to deal
in the Software without restriction, including without limitation the rights
to use, copy, modify, merge, publish, distribute, sublicense, and/or sell
copies of the Software, and to permit persons to whom the Software is
furnished to do so, subject to the following conditions:

The above copyright notice and this permission notice shall be included in all
copies or substantial portions of the Software.

THE SOFTWARE IS PROVIDED "AS IS", WITHOUT WARRANTY OF ANY KIND, EXPRESS OR
IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF MERCHANTABILITY,
FITNESS FOR A PARTICULAR PURPOSE AND NONINFRINGEMENT. IN NO EVENT SHALL THE
AUTHORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY CLAIM, DAMAGES OR OTHER
LIABILITY, WHETHER IN AN ACTION OF CONTRACT, TORT OR OTHERWISE, ARISING FROM,
OUT OF OR IN CONNECTION WITH THE SOFTWARE OR THE USE OR OTHER DEALINGS IN THE
SOFTWARE.

"""

"""
MIT License

Copyright (c) 2017 Andrew Riha

Permission is hereby granted, free of charge, to any person obtaining a copy
of this software and associated documentation files (the "Software"), to deal
in the Software without restriction, including without limitation the rights
to use, copy, modify, merge, publish, distribute, sublicense, and/or sell
copies of the Software, and to permit persons to whom the Software is
furnished to do so, subject to the following conditions:

The above copyright notice and this permission notice shall be included in all
copies or substantial portions of the Software.

THE SOFTWARE IS PROVIDED "AS IS", WITHOUT WARRANTY OF ANY KIND, EXPRESS OR
IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF MERCHANTABILITY,
FITNESS FOR A PARTICULAR PURPOSE AND NONINFRINGEMENT. IN NO EVENT SHALL THE
AUTHORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY CLAIM, DAMAGES OR OTHER
LIABILITY, WHETHER IN AN ACTION OF CONTRACT, TORT OR OTHERWISE, ARISING FROM,
OUT OF OR IN CONNECTION WITH THE SOFTWARE OR THE USE OR OTHER DEALINGS IN THE
SOFTWARE.

"""
import logging
import os

from atomicwrites import atomic_write
import pandas as pd
import numpy as np
import matplotlib

matplotlib.use("Agg")
from matplotlib import pyplot as plt
from matplotlib.collections import BrokenBarHCollection
from matplotlib import patches

logger = logging.getLogger(__name__)


[docs] def plot_chromosomes(one_chrom_match, two_chrom_match, cytobands, path, title, build): """Plots chromosomes with designated markers. Parameters ---------- one_chrom_match : pandas.DataFrame segments to highlight on the chromosomes representing one shared chromosome two_chrom_match : pandas.DataFrame segments to highlight on the chromosomes representing two shared chromosomes cytobands : pandas.DataFrame cytobands table loaded with Resources path : str path to destination `.png` file title : str title for plot build : {37} human genome build """ # Height of each chromosome chrom_height = 1.25 # Spacing between consecutive chromosomes chrom_spacing = 1 # Decide which chromosomes to use chromosome_list = ["chr%s" % i for i in range(1, 23)] chromosome_list.append("chrY") chromosome_list.append("chrX") # Keep track of the y positions for chromosomes, and the center of each chromosome # (which is where we'll put the ytick labels) ybase = 0 chrom_ybase = {} chrom_centers = {} # Iterate in reverse so that items in the beginning of `chromosome_list` will # appear at the top of the plot for chrom in chromosome_list[::-1]: chrom_ybase[chrom] = ybase chrom_centers[chrom] = ybase + chrom_height / 2.0 ybase += chrom_height + chrom_spacing # Colors for different chromosome stains color_lookup = { "gneg": (202 / 255, 202 / 255, 202 / 255), # background "one_chrom": (0 / 255, 176 / 255, 240 / 255), "two_chrom": (66 / 255, 69 / 255, 121 / 255), "centromere": (1, 1, 1, 0.6), } df = _patch_chromosomal_features(cytobands, one_chrom_match, two_chrom_match) # Add a new column for colors df["colors"] = df["gie_stain"].apply(lambda x: color_lookup[x]) # Width, height (in inches) figsize = (6.5, 9) fig = plt.figure(figsize=figsize) ax = fig.add_subplot(111) # Now all we have to do is call our function for the chromosome data... for collection in _chromosome_collections(df, chrom_ybase, chrom_height): ax.add_collection(collection) # Axes tweaking ax.set_yticks([chrom_centers[i] for i in chromosome_list]) ax.set_yticklabels(chromosome_list) ax.margins(0.01) ax.axis("tight") handles = [] # setup legend if len(one_chrom_match) > 0: one_chrom_patch = patches.Patch( color=color_lookup["one_chrom"], label="One chromosome shared" ) handles.append(one_chrom_patch) if len(two_chrom_match) > 0: two_chrom_patch = patches.Patch( color=color_lookup["two_chrom"], label="Two chromosomes shared" ) handles.append(two_chrom_patch) no_match_patch = patches.Patch(color=color_lookup["gneg"], label="No shared DNA") handles.append(no_match_patch) centromere_patch = patches.Patch( color=(234 / 255, 234 / 255, 234 / 255), label="Centromere" ) handles.append(centromere_patch) plt.legend(handles=handles, loc="lower right", bbox_to_anchor=(0.95, 0.05)) ax.set_title(title, fontsize=14, fontweight="bold") plt.xlabel("Build " + str(build) + " Chromosome Position", fontsize=10) logger.info("Saving {}".format(os.path.relpath(path))) plt.tight_layout() with atomic_write(path, mode="wb", overwrite=True) as f: plt.savefig(f)
def _chromosome_collections(df, y_positions, height, **kwargs): """ Yields BrokenBarHCollection of features that can be added to an Axes object. Parameters ---------- df : pandas.DataFrame Must at least have columns ['chrom', 'start', 'end', 'color']. If no column 'width', it will be calculated from start/end. y_positions : dict Keys are chromosomes, values are y-value at which to anchor the BrokenBarHCollection height : float Height of each BrokenBarHCollection Additional kwargs are passed to BrokenBarHCollection """ del_width = False if "width" not in df.columns: del_width = True df["width"] = df["end"] - df["start"] for chrom, group in df.groupby("chrom"): yrange = (y_positions["chr" + chrom], height) xranges = group[["start", "width"]].values yield BrokenBarHCollection( xranges, yrange, facecolors=group["colors"], **kwargs ) if del_width: del df["width"] def _patch_chromosomal_features(cytobands, one_chrom_match, two_chrom_match): """Highlight positions for each chromosome segment / feature. Parameters ---------- cytobands : pandas.DataFrame cytoband table from UCSC one_chrom_match : pandas.DataFrame segments to highlight on the chromosomes representing one shared chromosome two_chrom_match : pandas.DataFrame segments to highlight on the chromosomes representing two shared chromosomes Returns ------- df : pandas.DataFrame the start and stop positions of particular features on each chromosome """ def concat(df, chrom, start, end, gie_stain): return pd.concat( [ df, pd.DataFrame( { "chrom": [chrom], "start": [start], "end": [end], "gie_stain": [gie_stain], } ), ], ignore_index=True, ) chromosomes = cytobands["chrom"].unique() df = pd.DataFrame() for chromosome in chromosomes: chromosome_length = np.max( cytobands[cytobands["chrom"] == chromosome]["end"].values ) # get all markers for this chromosome one_chrom_match_markers = one_chrom_match.loc[ one_chrom_match["chrom"] == chromosome ] two_chrom_match_markers = two_chrom_match.loc[ two_chrom_match["chrom"] == chromosome ] # background of chromosome df = concat(df, chromosome, 0, chromosome_length, "gneg") # add markers for shared DNA on one chromosome for marker in one_chrom_match_markers.itertuples(): df = concat(df, chromosome, marker.start, marker.end, "one_chrom") # add markers for shared DNA on both chromosomes for marker in two_chrom_match_markers.itertuples(): df = concat(df, chromosome, marker.start, marker.end, "two_chrom") # add centromeres for item in cytobands.loc[ (cytobands["chrom"] == chromosome) & (cytobands["gie_stain"] == "acen") ].itertuples(): df = concat(df, chromosome, item.start, item.end, "centromere") return df