Circos Plot (Genomics)

In [1]:

# %pip install pycirclize

# %pip install pycirclize

1. Enterobacteria phage¶

In [2]:

from pycirclize import Circos
from pycirclize.parser import Gff
from pycirclize.utils import load_prokaryote_example_file

# Load GFF file
gff_file = load_prokaryote_example_file("enterobacteria_phage.gff")
gff = Gff(gff_file)

circos = Circos(sectors={gff.name: gff.range_size})
circos.text("Enterobacteria phage\n(NC_000902)", size=15)

sector = circos.sectors[0]
cds_track = sector.add_track((90, 100))
cds_track.axis(fc="#EEEEEE", ec="none")

# Plot forward & reverse CDS
f_cds_feats = gff.extract_features("CDS", target_strand=1)
cds_track.genomic_features(f_cds_feats, plotstyle="arrow", r_lim=(95, 100), fc="salmon")
r_cds_feats = gff.extract_features("CDS", target_strand=-1)
cds_track.genomic_features(r_cds_feats, plotstyle="arrow", r_lim=(90, 95), fc="skyblue")

# Extract CDS product labels
pos_list, labels = [], []
for feat in gff.extract_features("CDS"):
    start, end = int(str(feat.location.end)), int(str(feat.location.start))
    pos = (start + end) / 2
    label = feat.qualifiers.get("product", [""])[0]
    if label == "" or label.startswith("hypothetical"):
        continue
    if len(label) > 20:
        label = label[:20] + "..."
    pos_list.append(pos)
    labels.append(label)

# Plot CDS product labels on outer position
cds_track.xticks(
    pos_list,
    labels,
    label_orientation="vertical",
    show_bottom_line=True,
    label_size=6,
    line_kws=dict(ec="grey"),
)
# Plot xticks & intervals on inner position
cds_track.xticks_by_interval(
    interval=5000,
    outer=False,
    show_bottom_line=True,
    label_formatter=lambda v: f"{v/ 1000:.1f} Kb",
    label_orientation="vertical",
    line_kws=dict(ec="grey"),
)

fig = circos.plotfig()

from pycirclize import Circos from pycirclize.parser import Gff from pycirclize.utils import load_prokaryote_example_file # Load GFF file gff_file = load_prokaryote_example_file("enterobacteria_phage.gff") gff = Gff(gff_file) circos = Circos(sectors={gff.name: gff.range_size}) circos.text("Enterobacteria phage\n(NC_000902)", size=15) sector = circos.sectors[0] cds_track = sector.add_track((90, 100)) cds_track.axis(fc="#EEEEEE", ec="none") # Plot forward & reverse CDS f_cds_feats = gff.extract_features("CDS", target_strand=1) cds_track.genomic_features(f_cds_feats, plotstyle="arrow", r_lim=(95, 100), fc="salmon") r_cds_feats = gff.extract_features("CDS", target_strand=-1) cds_track.genomic_features(r_cds_feats, plotstyle="arrow", r_lim=(90, 95), fc="skyblue") # Extract CDS product labels pos_list, labels = [], [] for feat in gff.extract_features("CDS"): start, end = int(str(feat.location.end)), int(str(feat.location.start)) pos = (start + end) / 2 label = feat.qualifiers.get("product", [""])[0] if label == "" or label.startswith("hypothetical"): continue if len(label) > 20: label = label[:20] + "..." pos_list.append(pos) labels.append(label) # Plot CDS product labels on outer position cds_track.xticks( pos_list, labels, label_orientation="vertical", show_bottom_line=True, label_size=6, line_kws=dict(ec="grey"), ) # Plot xticks & intervals on inner position cds_track.xticks_by_interval( interval=5000, outer=False, show_bottom_line=True, label_formatter=lambda v: f"{v/ 1000:.1f} Kb", label_orientation="vertical", line_kws=dict(ec="grey"), ) fig = circos.plotfig()

2. Escherichia coli¶

In [3]:

from pycirclize import Circos
from pycirclize.parser import Genbank
from pycirclize.utils import load_prokaryote_example_file
import numpy as np
from matplotlib.patches import Patch
from matplotlib.lines import Line2D

# Load Genbank file
gbk_file = load_prokaryote_example_file("escherichia_coli.gbk.gz")
gbk = Genbank(gbk_file)

circos = Circos(sectors={gbk.name: gbk.range_size})
circos.text("Escherichia coli\n(NC_000913)", size=12, r=20)
sector = circos.get_sector(gbk.name)

# Plot outer track with xticks
major_ticks_interval = 500000
minor_ticks_interval = 100000
outer_track = sector.add_track((98, 100))
outer_track.axis(fc="lightgrey")
outer_track.xticks_by_interval(
    major_ticks_interval, label_formatter=lambda v: f"{v/ 10 ** 6:.1f} Mb"
)
outer_track.xticks_by_interval(minor_ticks_interval, tick_length=1, show_label=False)

# Plot Forward CDS, Reverse CDS, rRNA, tRNA
f_cds_track = sector.add_track((90, 97), r_pad_ratio=0.1)
f_cds_track.genomic_features(gbk.extract_features("CDS", target_strand=1), fc="red")

r_cds_track = sector.add_track((83, 90), r_pad_ratio=0.1)
r_cds_track.genomic_features(gbk.extract_features("CDS", target_strand=-1), fc="blue")

rrna_track = sector.add_track((76, 83), r_pad_ratio=0.1)
rrna_track.genomic_features(gbk.extract_features("rRNA"), fc="green")

trna_track = sector.add_track((69, 76), r_pad_ratio=0.1)
trna_track.genomic_features(gbk.extract_features("tRNA"), color="magenta", lw=0.1)

# Plot GC content
gc_content_track = sector.add_track((50, 65))

pos_list, gc_contents = gbk.calc_gc_content()
gc_contents = gc_contents - gbk.calc_genome_gc_content()
positive_gc_contents = np.where(gc_contents > 0, gc_contents, 0)
negative_gc_contents = np.where(gc_contents < 0, gc_contents, 0)
abs_max_gc_content = np.max(np.abs(gc_contents))
vmin, vmax = -abs_max_gc_content, abs_max_gc_content
gc_content_track.fill_between(
    pos_list, positive_gc_contents, 0, vmin=vmin, vmax=vmax, color="black"
)
gc_content_track.fill_between(
    pos_list, negative_gc_contents, 0, vmin=vmin, vmax=vmax, color="grey"
)

# Plot GC skew
gc_skew_track = sector.add_track((35, 50))

pos_list, gc_skews = gbk.calc_gc_skew()
positive_gc_skews = np.where(gc_skews > 0, gc_skews, 0)
negative_gc_skews = np.where(gc_skews < 0, gc_skews, 0)
abs_max_gc_skew = np.max(np.abs(gc_skews))
vmin, vmax = -abs_max_gc_skew, abs_max_gc_skew
gc_skew_track.fill_between(
    pos_list, positive_gc_skews, 0, vmin=vmin, vmax=vmax, color="olive"
)
gc_skew_track.fill_between(
    pos_list, negative_gc_skews, 0, vmin=vmin, vmax=vmax, color="purple"
)

fig = circos.plotfig()

# Add legend
handles = [
    Patch(color="red", label="Forward CDS"),
    Patch(color="blue", label="Reverse CDS"),
    Patch(color="green", label="rRNA"),
    Patch(color="magenta", label="tRNA"),
    Line2D([], [], color="black", label="Positive GC Content", marker="^", ms=6, ls="None"),
    Line2D([], [], color="grey", label="Negative GC Content", marker="v", ms=6, ls="None"),
    Line2D([], [], color="olive", label="Positive GC Skew", marker="^", ms=6, ls="None"),
    Line2D([], [], color="purple", label="Negative GC Skew", marker="v", ms=6, ls="None"),
]
_ = circos.ax.legend(handles=handles, bbox_to_anchor=(0.5, 0.475), loc="center", fontsize=8)

from pycirclize import Circos from pycirclize.parser import Genbank from pycirclize.utils import load_prokaryote_example_file import numpy as np from matplotlib.patches import Patch from matplotlib.lines import Line2D # Load Genbank file gbk_file = load_prokaryote_example_file("escherichia_coli.gbk.gz") gbk = Genbank(gbk_file) circos = Circos(sectors={gbk.name: gbk.range_size}) circos.text("Escherichia coli\n(NC_000913)", size=12, r=20) sector = circos.get_sector(gbk.name) # Plot outer track with xticks major_ticks_interval = 500000 minor_ticks_interval = 100000 outer_track = sector.add_track((98, 100)) outer_track.axis(fc="lightgrey") outer_track.xticks_by_interval( major_ticks_interval, label_formatter=lambda v: f"{v/ 10 ** 6:.1f} Mb" ) outer_track.xticks_by_interval(minor_ticks_interval, tick_length=1, show_label=False) # Plot Forward CDS, Reverse CDS, rRNA, tRNA f_cds_track = sector.add_track((90, 97), r_pad_ratio=0.1) f_cds_track.genomic_features(gbk.extract_features("CDS", target_strand=1), fc="red") r_cds_track = sector.add_track((83, 90), r_pad_ratio=0.1) r_cds_track.genomic_features(gbk.extract_features("CDS", target_strand=-1), fc="blue") rrna_track = sector.add_track((76, 83), r_pad_ratio=0.1) rrna_track.genomic_features(gbk.extract_features("rRNA"), fc="green") trna_track = sector.add_track((69, 76), r_pad_ratio=0.1) trna_track.genomic_features(gbk.extract_features("tRNA"), color="magenta", lw=0.1) # Plot GC content gc_content_track = sector.add_track((50, 65)) pos_list, gc_contents = gbk.calc_gc_content() gc_contents = gc_contents - gbk.calc_genome_gc_content() positive_gc_contents = np.where(gc_contents > 0, gc_contents, 0) negative_gc_contents = np.where(gc_contents < 0, gc_contents, 0) abs_max_gc_content = np.max(np.abs(gc_contents)) vmin, vmax = -abs_max_gc_content, abs_max_gc_content gc_content_track.fill_between( pos_list, positive_gc_contents, 0, vmin=vmin, vmax=vmax, color="black" ) gc_content_track.fill_between( pos_list, negative_gc_contents, 0, vmin=vmin, vmax=vmax, color="grey" ) # Plot GC skew gc_skew_track = sector.add_track((35, 50)) pos_list, gc_skews = gbk.calc_gc_skew() positive_gc_skews = np.where(gc_skews > 0, gc_skews, 0) negative_gc_skews = np.where(gc_skews < 0, gc_skews, 0) abs_max_gc_skew = np.max(np.abs(gc_skews)) vmin, vmax = -abs_max_gc_skew, abs_max_gc_skew gc_skew_track.fill_between( pos_list, positive_gc_skews, 0, vmin=vmin, vmax=vmax, color="olive" ) gc_skew_track.fill_between( pos_list, negative_gc_skews, 0, vmin=vmin, vmax=vmax, color="purple" ) fig = circos.plotfig() # Add legend handles = [ Patch(color="red", label="Forward CDS"), Patch(color="blue", label="Reverse CDS"), Patch(color="green", label="rRNA"), Patch(color="magenta", label="tRNA"), Line2D([], [], color="black", label="Positive GC Content", marker="^", ms=6, ls="None"), Line2D([], [], color="grey", label="Negative GC Content", marker="v", ms=6, ls="None"), Line2D([], [], color="olive", label="Positive GC Skew", marker="^", ms=6, ls="None"), Line2D([], [], color="purple", label="Negative GC Skew", marker="v", ms=6, ls="None"), ] _ = circos.ax.legend(handles=handles, bbox_to_anchor=(0.5, 0.475), loc="center", fontsize=8)

3. Mycoplasma alvi¶

In [4]:

from pycirclize import Circos
from pycirclize.parser import Gff, Genbank
from pycirclize.utils import load_prokaryote_example_file
from matplotlib.patches import Patch

# Case1. Load `GFF` contig genomes
# https://github.com/moshi4/pycirclize-data/blob/main/prokaryote/mycoplasma_alvi.gff
gff_file = load_prokaryote_example_file("mycoplasma_alvi.gff")
parser = Gff(gff_file)

# Case2. Load `Genbank` contig genomes
# https://github.com/moshi4/pycirclize-data/blob/main/prokaryote/mycoplasma_alvi.gbk
# gbk_file = load_prokaryote_example_file("mycoplasma_alvi.gbk")
# parser = Genbank(gbk_file)

# Get contig genome seqid & size, features dict
seqid2size = parser.get_seqid2size()
seqid2features = parser.get_seqid2features(feature_type=None)

circos = Circos(seqid2size, space=2)
circos.text(f"Mycoplasma alvi\n({len(circos.sectors)} contigs)", r=5, size=15)
for sector in circos.sectors:
    # Plot outer track
    outer_track = sector.add_track((98, 100))
    outer_track.axis(fc="lightgrey")
    major_interval = 100000
    minor_interval = int(major_interval / 10)
    if sector.size > minor_interval:
        outer_track.xticks_by_interval(major_interval, label_formatter=lambda v: f"{v / 1000:.0f} Kb")
        outer_track.xticks_by_interval(minor_interval, tick_length=1, show_label=False)

    # Plot forward/reverse CDS, rRNA, tRNA tracks
    f_cds_track = sector.add_track((88, 95), r_pad_ratio=0.1)
    r_cds_track = sector.add_track((81, 88), r_pad_ratio=0.1)
    rrna_track = sector.add_track((74, 81), r_pad_ratio=0.1)
    trna_track = sector.add_track((67, 74), r_pad_ratio=0.1)
    for feature in seqid2features[sector.name]:
        if feature.type == "CDS":
            if feature.location.strand == 1:
                f_cds_track.genomic_features([feature], fc="tomato")
            else:
                r_cds_track.genomic_features([feature], fc="skyblue")
        elif feature.type == "rRNA":
            rrna_track.genomic_features([feature], fc="lime")
        elif feature.type == "tRNA":
            trna_track.genomic_features([feature], fc="magenta")

fig = circos.plotfig()
_ = circos.ax.legend(
    handles=[
        Patch(color="tomato", label="Forward CDS"),
        Patch(color="skyblue", label="Reverse CDS"),
        Patch(color="lime", label="rRNA"),
        Patch(color="magenta", label="tRNA"),
    ],
    bbox_to_anchor=(0.5, 0.45),
    loc="center",
    ncols=2,
)

from pycirclize import Circos from pycirclize.parser import Gff, Genbank from pycirclize.utils import load_prokaryote_example_file from matplotlib.patches import Patch # Case1. Load `GFF` contig genomes # https://github.com/moshi4/pycirclize-data/blob/main/prokaryote/mycoplasma_alvi.gff gff_file = load_prokaryote_example_file("mycoplasma_alvi.gff") parser = Gff(gff_file) # Case2. Load `Genbank` contig genomes # https://github.com/moshi4/pycirclize-data/blob/main/prokaryote/mycoplasma_alvi.gbk # gbk_file = load_prokaryote_example_file("mycoplasma_alvi.gbk") # parser = Genbank(gbk_file) # Get contig genome seqid & size, features dict seqid2size = parser.get_seqid2size() seqid2features = parser.get_seqid2features(feature_type=None) circos = Circos(seqid2size, space=2) circos.text(f"Mycoplasma alvi\n({len(circos.sectors)} contigs)", r=5, size=15) for sector in circos.sectors: # Plot outer track outer_track = sector.add_track((98, 100)) outer_track.axis(fc="lightgrey") major_interval = 100000 minor_interval = int(major_interval / 10) if sector.size > minor_interval: outer_track.xticks_by_interval(major_interval, label_formatter=lambda v: f"{v / 1000:.0f} Kb") outer_track.xticks_by_interval(minor_interval, tick_length=1, show_label=False) # Plot forward/reverse CDS, rRNA, tRNA tracks f_cds_track = sector.add_track((88, 95), r_pad_ratio=0.1) r_cds_track = sector.add_track((81, 88), r_pad_ratio=0.1) rrna_track = sector.add_track((74, 81), r_pad_ratio=0.1) trna_track = sector.add_track((67, 74), r_pad_ratio=0.1) for feature in seqid2features[sector.name]: if feature.type == "CDS": if feature.location.strand == 1: f_cds_track.genomic_features([feature], fc="tomato") else: r_cds_track.genomic_features([feature], fc="skyblue") elif feature.type == "rRNA": rrna_track.genomic_features([feature], fc="lime") elif feature.type == "tRNA": trna_track.genomic_features([feature], fc="magenta") fig = circos.plotfig() _ = circos.ax.legend( handles=[ Patch(color="tomato", label="Forward CDS"), Patch(color="skyblue", label="Reverse CDS"), Patch(color="lime", label="rRNA"), Patch(color="magenta", label="tRNA"), ], bbox_to_anchor=(0.5, 0.45), loc="center", ncols=2, )

4. Homo sapiens (hg38)¶

hg38 data files are obtained from UCSC Table Browser.

Dataset Repository:
https://github.com/moshi4/pycirclize-data/tree/main/eukaryote/hg38

4-1. Ideograms¶

In [5]:

from pycirclize import Circos
from pycirclize.utils import load_eukaryote_example_dataset

# Load hg38 dataset (https://github.com/moshi4/pycirclize-data/tree/main/eukaryote/hg38)
chr_bed_file, cytoband_file, _ = load_eukaryote_example_dataset("hg38")

# Initialize Circos from BED chromosomes
circos = Circos.initialize_from_bed(chr_bed_file, space=3)
circos.text("Homo sapiens (hg38)", size=15)

# Add cytoband tracks from cytoband file
circos.add_cytoband_tracks((95, 100), cytoband_file)

# Plot chromosome name
for sector in circos.sectors:
    sector.text(sector.name, size=10)

fig = circos.plotfig()

from pycirclize import Circos from pycirclize.utils import load_eukaryote_example_dataset # Load hg38 dataset (https://github.com/moshi4/pycirclize-data/tree/main/eukaryote/hg38) chr_bed_file, cytoband_file, _ = load_eukaryote_example_dataset("hg38") # Initialize Circos from BED chromosomes circos = Circos.initialize_from_bed(chr_bed_file, space=3) circos.text("Homo sapiens (hg38)", size=15) # Add cytoband tracks from cytoband file circos.add_cytoband_tracks((95, 100), cytoband_file) # Plot chromosome name for sector in circos.sectors: sector.text(sector.name, size=10) fig = circos.plotfig()

4-2. Segmental Dups Link¶

In [6]:

from pycirclize import Circos
from pycirclize.utils import ColorCycler, load_eukaryote_example_dataset

# Load hg38 dataset (https://github.com/moshi4/pycirclize-data/tree/main/eukaryote/hg38)
chr_bed_file, cytoband_file, chr_links = load_eukaryote_example_dataset("hg38")

# Initialize Circos from BED chromosomes
circos = Circos.initialize_from_bed(chr_bed_file, space=3)
circos.text("Homo sapiens\n(hg38)", deg=315, r=150, size=12)

# Add cytoband tracks from cytoband file
circos.add_cytoband_tracks((95, 100), cytoband_file)

# Create chromosome color dict
ColorCycler.set_cmap("hsv")
chr_names = [s.name for s in circos.sectors]
colors = ColorCycler.get_color_list(len(chr_names))
chr_name2color = {name: color for name, color in zip(chr_names, colors)}

# Plot chromosome name & xticks
for sector in circos.sectors:
    sector.text(sector.name, r=120, size=10, color=chr_name2color[sector.name])
    sector.get_track("cytoband").xticks_by_interval(
        40000000,
        label_size=8,
        label_orientation="vertical",
        label_formatter=lambda v: f"{v / 1000000:.0f} Mb",
    )

# Plot chromosome link
for link in chr_links:
    region1 = (link.query_chr, link.query_start, link.query_end)
    region2 = (link.ref_chr, link.ref_start, link.ref_end)
    color = chr_name2color[link.query_chr]
    if link.query_chr in ("chr1", "chr8", "chr16") and link.query_chr != link.ref_chr:
        circos.link(region1, region2, color=color)

fig = circos.plotfig()

from pycirclize import Circos from pycirclize.utils import ColorCycler, load_eukaryote_example_dataset # Load hg38 dataset (https://github.com/moshi4/pycirclize-data/tree/main/eukaryote/hg38) chr_bed_file, cytoband_file, chr_links = load_eukaryote_example_dataset("hg38") # Initialize Circos from BED chromosomes circos = Circos.initialize_from_bed(chr_bed_file, space=3) circos.text("Homo sapiens\n(hg38)", deg=315, r=150, size=12) # Add cytoband tracks from cytoband file circos.add_cytoband_tracks((95, 100), cytoband_file) # Create chromosome color dict ColorCycler.set_cmap("hsv") chr_names = [s.name for s in circos.sectors] colors = ColorCycler.get_color_list(len(chr_names)) chr_name2color = {name: color for name, color in zip(chr_names, colors)} # Plot chromosome name & xticks for sector in circos.sectors: sector.text(sector.name, r=120, size=10, color=chr_name2color[sector.name]) sector.get_track("cytoband").xticks_by_interval( 40000000, label_size=8, label_orientation="vertical", label_formatter=lambda v: f"{v / 1000000:.0f} Mb", ) # Plot chromosome link for link in chr_links: region1 = (link.query_chr, link.query_start, link.query_end) region2 = (link.ref_chr, link.ref_start, link.ref_end) color = chr_name2color[link.query_chr] if link.query_chr in ("chr1", "chr8", "chr16") and link.query_chr != link.ref_chr: circos.link(region1, region2, color=color) fig = circos.plotfig()

4-3. Plot Graphs¶

In [7]:

from pycirclize import Circos
from pycirclize.utils import ColorCycler, load_eukaryote_example_dataset
import numpy as np
np.random.seed(0)

# Load hg38 dataset (https://github.com/moshi4/pycirclize-data/tree/main/eukaryote/hg38)
chr_bed_file = load_eukaryote_example_dataset("hg38")[0]

# Initialize Circos from BED chromosomes
circos = Circos.initialize_from_bed(chr_bed_file, start=-80, end=260, space=3, endspace=False)
circos.text("Homo sapiens\n(hg38)", size=15)

# Create chromosome color dict
ColorCycler.set_cmap("gist_rainbow")
chr_names = [s.name for s in circos.sectors]
colors = ColorCycler.get_color_list(len(chr_names))
chr_name2color = {name: color for name, color in zip(chr_names, colors)}

for sector in circos.sectors:
    # Plot chromosome outer track
    sector.text(sector.name.replace("chr", ""))
    color = chr_name2color[sector.name]
    outer_track = sector.add_track((95, 100))
    outer_track.axis(fc=color)
    # Create example x,y plot data
    step = 10000000
    x = np.arange(sector.start + (step / 2), sector.end - (step / 2), step)
    y = np.random.randint(0, 100, size=len(x))
    # Scatter track
    track1 = sector.add_track((80, 90), r_pad_ratio=0.1)
    track1.axis()
    track1.scatter(x, y, s=6, color="red")
    # Line track
    track2 = sector.add_track((65, 75), r_pad_ratio=0.1)
    track2.axis()
    track2.line(x, y, color="blue")
    # Bar track
    track3 = sector.add_track((50, 60), r_pad_ratio=0.1)
    track3.axis()
    track3.bar(x, y, width=step * 0.7, color="olive")
    # Fill between track
    track4 = sector.add_track((35, 45), r_pad_ratio=0.1)
    track4.axis()
    track4.grid()
    track4.fill_between(x, y, color="violet")
    # Plot track labels
    if sector.name == circos.sectors[0].name:
        circos.text("Chr", r=outer_track.r_center, deg=-90)
        circos.text("a", r=track1.r_center, deg=-90, color="red")
        circos.text("b", r=track2.r_center, deg=-90, color="blue")
        circos.text("c", r=track3.r_center, deg=-90, color="olive")
        circos.text("d", r=track4.r_center, deg=-90, color="violet")

fig = circos.plotfig()

from pycirclize import Circos from pycirclize.utils import ColorCycler, load_eukaryote_example_dataset import numpy as np np.random.seed(0) # Load hg38 dataset (https://github.com/moshi4/pycirclize-data/tree/main/eukaryote/hg38) chr_bed_file = load_eukaryote_example_dataset("hg38")[0] # Initialize Circos from BED chromosomes circos = Circos.initialize_from_bed(chr_bed_file, start=-80, end=260, space=3, endspace=False) circos.text("Homo sapiens\n(hg38)", size=15) # Create chromosome color dict ColorCycler.set_cmap("gist_rainbow") chr_names = [s.name for s in circos.sectors] colors = ColorCycler.get_color_list(len(chr_names)) chr_name2color = {name: color for name, color in zip(chr_names, colors)} for sector in circos.sectors: # Plot chromosome outer track sector.text(sector.name.replace("chr", "")) color = chr_name2color[sector.name] outer_track = sector.add_track((95, 100)) outer_track.axis(fc=color) # Create example x,y plot data step = 10000000 x = np.arange(sector.start + (step / 2), sector.end - (step / 2), step) y = np.random.randint(0, 100, size=len(x)) # Scatter track track1 = sector.add_track((80, 90), r_pad_ratio=0.1) track1.axis() track1.scatter(x, y, s=6, color="red") # Line track track2 = sector.add_track((65, 75), r_pad_ratio=0.1) track2.axis() track2.line(x, y, color="blue") # Bar track track3 = sector.add_track((50, 60), r_pad_ratio=0.1) track3.axis() track3.bar(x, y, width=step * 0.7, color="olive") # Fill between track track4 = sector.add_track((35, 45), r_pad_ratio=0.1) track4.axis() track4.grid() track4.fill_between(x, y, color="violet") # Plot track labels if sector.name == circos.sectors[0].name: circos.text("Chr", r=outer_track.r_center, deg=-90) circos.text("a", r=track1.r_center, deg=-90, color="red") circos.text("b", r=track2.r_center, deg=-90, color="blue") circos.text("c", r=track3.r_center, deg=-90, color="olive") circos.text("d", r=track4.r_center, deg=-90, color="violet") fig = circos.plotfig()

5. Mus musculus (mm10)¶

mm10 data files are obtained from UCSC Table Browser.

Dataset Repository:
https://github.com/moshi4/pycirclize-data/tree/main/eukaryote/mm10

5-1. Ideograms¶

In [8]:

from pycirclize import Circos
from pycirclize.utils import load_eukaryote_example_dataset

# Load mm10 dataset (https://github.com/moshi4/pycirclize-data/tree/main/eukaryote/mm10)
chr_bed_file, cytoband_file, _ = load_eukaryote_example_dataset("mm10")

# Initialize Circos from BED chromosomes
circos = Circos.initialize_from_bed(chr_bed_file, space=3)
circos.text("Mus musculus (mm10)", size=15)

# Add cytoband tracks from cytoband file
circos.add_cytoband_tracks((95, 100), cytoband_file)

# Plot chromosome name
for sector in circos.sectors:
    sector.text(sector.name, size=10)

fig = circos.plotfig()

from pycirclize import Circos from pycirclize.utils import load_eukaryote_example_dataset # Load mm10 dataset (https://github.com/moshi4/pycirclize-data/tree/main/eukaryote/mm10) chr_bed_file, cytoband_file, _ = load_eukaryote_example_dataset("mm10") # Initialize Circos from BED chromosomes circos = Circos.initialize_from_bed(chr_bed_file, space=3) circos.text("Mus musculus (mm10)", size=15) # Add cytoband tracks from cytoband file circos.add_cytoband_tracks((95, 100), cytoband_file) # Plot chromosome name for sector in circos.sectors: sector.text(sector.name, size=10) fig = circos.plotfig()

5-2. Segmental Dups Link¶

In [9]:

from pycirclize import Circos
from pycirclize.utils import ColorCycler, load_eukaryote_example_dataset

# Load mm10 dataset (https://github.com/moshi4/pycirclize-data/tree/main/eukaryote/mm10)
chr_bed_file, cytoband_file, chr_links = load_eukaryote_example_dataset("mm10")

# Initialize Circos from BED chromosomes
circos = Circos.initialize_from_bed(chr_bed_file, space=3)
circos.text("Mus musculus\n(mm10)", deg=315, r=150, size=12)

# Add cytoband tracks from cytoband file
circos.add_cytoband_tracks((95, 100), cytoband_file)

# Create chromosome color mapping
ColorCycler.set_cmap("hsv")
chr_names = [s.name for s in circos.sectors]
colors = ColorCycler.get_color_list(len(chr_names))
chr_name2color = {name: color for name, color in zip(chr_names, colors)}

# Plot chromosome name & xticks
for sector in circos.sectors:
    sector.text(sector.name, r=120, size=10, color=chr_name2color[sector.name])
    sector.get_track("cytoband").xticks_by_interval(
        50000000,
        label_size=8,
        label_orientation="vertical",
        label_formatter=lambda v: f"{v / 1000000:.0f} Mb",
    )

# Plot chromosome link
for link in chr_links:
    region1 = (link.query_chr, link.query_start, link.query_end)
    region2 = (link.ref_chr, link.ref_start, link.ref_end)
    color = chr_name2color[link.query_chr]
    if link.query_chr != link.ref_chr:
        circos.link(region1, region2, color=color)

fig = circos.plotfig()

from pycirclize import Circos from pycirclize.utils import ColorCycler, load_eukaryote_example_dataset # Load mm10 dataset (https://github.com/moshi4/pycirclize-data/tree/main/eukaryote/mm10) chr_bed_file, cytoband_file, chr_links = load_eukaryote_example_dataset("mm10") # Initialize Circos from BED chromosomes circos = Circos.initialize_from_bed(chr_bed_file, space=3) circos.text("Mus musculus\n(mm10)", deg=315, r=150, size=12) # Add cytoband tracks from cytoband file circos.add_cytoband_tracks((95, 100), cytoband_file) # Create chromosome color mapping ColorCycler.set_cmap("hsv") chr_names = [s.name for s in circos.sectors] colors = ColorCycler.get_color_list(len(chr_names)) chr_name2color = {name: color for name, color in zip(chr_names, colors)} # Plot chromosome name & xticks for sector in circos.sectors: sector.text(sector.name, r=120, size=10, color=chr_name2color[sector.name]) sector.get_track("cytoband").xticks_by_interval( 50000000, label_size=8, label_orientation="vertical", label_formatter=lambda v: f"{v / 1000000:.0f} Mb", ) # Plot chromosome link for link in chr_links: region1 = (link.query_chr, link.query_start, link.query_end) region2 = (link.ref_chr, link.ref_start, link.ref_end) color = chr_name2color[link.query_chr] if link.query_chr != link.ref_chr: circos.link(region1, region2, color=color) fig = circos.plotfig()

5-3. Plot Heatmaps¶

In [10]:

from pycirclize import Circos
from pycirclize.utils import ColorCycler, load_eukaryote_example_dataset
import numpy as np
np.random.seed(0)

# Load mm10 dataset (https://github.com/moshi4/pycirclize-data/tree/main/eukaryote/mm10)
chr_bed_file = load_eukaryote_example_dataset("mm10")[0]

# Initialize Circos from BED chromosomes
circos = Circos.initialize_from_bed(chr_bed_file, space=2, start=10, end=350, endspace=False)
circos.text("Mus musculus\n(mm10)", size=12)

heatmap_cmaps = ["bwr", "Spectral", "viridis", "plasma", "Reds", "Blues", "Greens", "Greys"]
ColorCycler.set_cmap("gist_rainbow")
colors = ColorCycler.get_color_list(len(circos.sectors))
for sector, color in zip(circos.sectors, colors):
    sector.text(sector.name.replace("chr", ""), size=10)
    # Plot chromosome outer track
    chr_track = sector.add_track((95, 100))
    chr_track.axis(fc=color)
    # Create random test data for heatmap plot
    window_size = 10_000_000
    data_num = int(sector.size // window_size) + 1
    vmin, vmax = 0, 100
    data = np.random.randint(vmin, vmax, data_num)
    # Plot heatmap tracks with various cmap
    track_r_size, r_interval, r_start = 4, 2, 90
    for idx, cmap in enumerate(heatmap_cmaps):
        r_pos = r_start - (track_r_size + r_interval) * idx
        track_r_lim = (r_pos - track_r_size, r_pos)
        track = sector.add_track(track_r_lim)
        track.axis(ec="grey")
        track.heatmap(data, width=window_size, vmin=vmin, vmax=vmax, cmap=cmap)
        # Plot colormap name on center
        if sector.name == circos.sectors[0].name:
            circos.text(cmap, r=track.r_center, size=8)

fig = circos.plotfig()

from pycirclize import Circos from pycirclize.utils import ColorCycler, load_eukaryote_example_dataset import numpy as np np.random.seed(0) # Load mm10 dataset (https://github.com/moshi4/pycirclize-data/tree/main/eukaryote/mm10) chr_bed_file = load_eukaryote_example_dataset("mm10")[0] # Initialize Circos from BED chromosomes circos = Circos.initialize_from_bed(chr_bed_file, space=2, start=10, end=350, endspace=False) circos.text("Mus musculus\n(mm10)", size=12) heatmap_cmaps = ["bwr", "Spectral", "viridis", "plasma", "Reds", "Blues", "Greens", "Greys"] ColorCycler.set_cmap("gist_rainbow") colors = ColorCycler.get_color_list(len(circos.sectors)) for sector, color in zip(circos.sectors, colors): sector.text(sector.name.replace("chr", ""), size=10) # Plot chromosome outer track chr_track = sector.add_track((95, 100)) chr_track.axis(fc=color) # Create random test data for heatmap plot window_size = 10_000_000 data_num = int(sector.size // window_size) + 1 vmin, vmax = 0, 100 data = np.random.randint(vmin, vmax, data_num) # Plot heatmap tracks with various cmap track_r_size, r_interval, r_start = 4, 2, 90 for idx, cmap in enumerate(heatmap_cmaps): r_pos = r_start - (track_r_size + r_interval) * idx track_r_lim = (r_pos - track_r_size, r_pos) track = sector.add_track(track_r_lim) track.axis(ec="grey") track.heatmap(data, width=window_size, vmin=vmin, vmax=vmax, cmap=cmap) # Plot colormap name on center if sector.name == circos.sectors[0].name: circos.text(cmap, r=track.r_center, size=8) fig = circos.plotfig()