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 s, group in df.groupby('sample'):
print s
yrange = (y_positions[s], height)
xranges = group[['start', 'width']].values
yield BrokenBarHCollection(xranges,
yrange,
facecolors=group['colors1'],
**kwargs)
yrange = (y_positions[s] - 0.4, height)
yield BrokenBarHCollection(xranges,
yrange,
facecolors=group['colors2'],
**kwargs)
if del_width:
del df['width']
def regions_to_hbar(region_list_chr):
"""Make a MathPlotLIb 'BrokenbarCollection' from upd sites data,
Isodisomy will have one block and one color. Heterodisomy will
be two adjecent bars with two colors. Both plots will have a
transperant middle line for aestetics."""
return_list = []
for i in region_list_chr:
hbar_upper = BrokenBarHCollection(i["xranges"], (0.52, 1),
facecolors=i["upper"],
label=i["chr"])
hbar_lower = BrokenBarHCollection(i["xranges"], (0, 0.48),
facecolors=i["lower"],
label=i["chr"])
return_list.append([hbar_upper, hbar_lower])
return return_list
def plot(self, ax, chrom_region, region_start, region_end):
self.ax = ax
grange = GenomeRange(chrom_region, region_start, region_end)
if grange.chrom not in self.interval_tree:
grange.change_chrom_names()
bands_in_region = sorted(
self.interval_tree[grange.chrom][grange.start:grange.end])
band_height = self.properties['height']
xranges, colors = [], []
for itv in bands_in_region:
start, end = itv.begin, itv.end
band_name, band_type = itv.data[:2]
band_color = self.lookup_band_color(band_type)
xranges.append((start, end))
colors.append(band_color)
if self.properties['show_band_name'] != 'no':
if grange.length < 80_000_000:
self.plot_text(band_name, start, end, band_color)
coll = BrokenBarHCollection(xranges, (0, band_height),
facecolors=colors,
linewidths=self.properties['border_width'],
edgecolors=self.properties['border_color'])
ax.add_collection(coll)
ax.set_ylim(-0.1, band_height + 0.1)
ax.set_xlim(region_start, region_end)
self.plot_label()
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 plot_bars(self, ax):
'''
Once xranges are determined, create bars for each chr and sample.
'''
# Some fancy sorting to get the chromosomes in 1, 2. ..10, M order
keys = sorted(self.xranges,
key=lambda x:x.replace('chr','').isdigit() \
and x.replace('chr','').rjust(2,'0') \
or x.replace('chr',''))
ystart = 0
colors = self.get_colors(len(self.datasets))
yticks = []
yticklabels = []
for chrom in keys:
for i, xranges in enumerate(self.xranges[chrom]):
yrange = (ystart, self.height)
coll = BrokenBarHCollection(xranges, yrange, color=colors[i])
ax.add_collection(coll)
# save ticks and labels for plotting
center = yrange[0] + yrange[1] / 2.
yticks.append(center)
# Only label the topmost row with the chromosome.
label = i == (len(self.xranges[chrom]) - 1) and chrom or ''
yticklabels.append(label)
# Increment ystart for next iteration
ystart += self.height + self.spacing
return yticks, yticklabels
def chromosome_collections(df: pandas.DataFrame, y_positions: dict, height: float,
to_log: bool=False, **kwargs):
"""
Yields BrokenBarHCollection of features that can be added to an Axes object
:param bool to_log: whether to log info
:param DataFrame df: must at least have columns ['chrom', 'chromStart', 'chromEnd', 'colors']. If no column 'width',
it will be calculated from start/end
:param dict y_positions: keys are chromosomes, value are y-value at which to anchor the BrokenBarHCollection
:param float height: height of each BrokenBarHCollection
:param kwargs: are passed to BrokenBarHCollection
:return: BrokenBarHCollection
"""
del_width = False
if 'width' not in df.columns:
del_width = True
df['width'] = df['chromEnd'] - df['chromStart']
for chrom, group in df.groupby('chrom'):
if to_log:
print(chrom)
yrange = (y_positions[chrom], height)
xranges = group[['chromStart', 'width']].values
yield BrokenBarHCollection(
xranges, yrange, facecolors=group['colors'], **kwargs)
if del_width:
del df['width']
def plot_thresholded_envelope(self, ax_main: Axes, ax_dist: Axes):
# e_t, with segment bands, and summary stats to the right :)
logger.info("Plotting thresholded envelope..")
self.plot_signal(self.e_t,
ax=ax_main,
color=envelope_color,
lw=thicc_lw)
rm = self.reference_maker
ax_main.hlines(rm.ripple_threshold_high, *self.time_range, lw=thin_lw)
ax_main.hlines(rm.ripple_threshold_low, *self.time_range, lw=thin_lw)
add_scalebar(ax_main)
add_title(ax_main, "Thresholds $T$", threshold_color, y=0.58)
segs = self.reference_segs_test
visible_segs = segs.intersection(ax_main.get_xlim())
bars = BrokenBarHCollection(
xranges=[
tup for tup in zip(visible_segs.start, visible_segs.duration)
],
yrange=(0, rm.ripple_threshold_low),
facecolors=segment_color,
alpha=segment_alpha,
)
ax_main.add_collection(bars)
# Find and plot crossings of lower threshold
crossings_ix = nonzero(diff(self.e_t > rm.ripple_threshold_low))[0]
crossings_t = crossings_ix / self.fs
crossings_y = [rm.ripple_threshold_low] * len(crossings_t)
ax_main.plot(crossings_t, crossings_y, ".", c="black")
logger.info("Done")
logger.info("Plotting envelope density..")
self.plot_envelope_dist(ax_dist)
logger.info("Done")
ax_dist.set_ylim(ax_main.get_ylim())
def render(self, ax, chrom, pos=None):
try:
xranges = self.xranges[chrom]
colors = self.colors[chrom]
centromeres = self.centromeres[chrom]
except:
print("Error: No chromosome named: {}".format(chrom))
return
yranges = (0, 0.5)
coll = BrokenBarHCollection(xranges,
yranges,
facecolors=colors,
edgecolors='black',
linewidths=0.5)
ax.add_collection(coll)
if pos:
ax.axvline(pos, color='red', lw=4)
w = xranges[-1][0] + xranges[-1][1]
pad = w * 0.05
ax.set_xlim(0 - pad, xranges[-1][0] + xranges[-1][1] + pad)
ax.xaxis.set_visible(False)
center = yranges[0] + yranges[1] / 2.
x0, y0 = centromeres[0][0], yranges[0]
x1, y1 = centromeres[0][0], yranges[1]
x2, y2 = centromeres[0][0] + centromeres[0][1], center
cent = Polygon(np.array([[x0, y0], [x1, y1], [x2, y2]]),
closed=True,
fc=color_lookup['acen'],
ec='black',
linewidth=0.5)
ax.add_patch(cent)
x0, y0 = centromeres[1][0], center
x1, y1 = centromeres[1][0] + centromeres[1][1], yranges[1]
x2, y2 = centromeres[1][0] + centromeres[1][1], yranges[0]
cent = Polygon(np.array([[x0, y0], [x1, y1], [x2, y2]]),
closed=True,
fc=color_lookup['acen'],
ec='black',
linewidth=0.5)
ax.add_patch(cent)
ax.set_yticks([center])
ax.set_yticklabels([chrom])
ax.set_ylim(-0.2, 0.7)
[
ax.spines[loc].set_color('none')
for loc in ['top', 'left', 'right', 'bottom']
]
def plot_sample_chrom(i, sample):
"""Draw the given coordinates and colors as a horizontal series."""
xranges = [(start, end - start)
for start, end in zip(sample.start, sample.end)]
bars = BrokenBarHCollection(xranges, (i, i + 1),
edgecolors="none",
facecolors=sample["color"])
axis.add_collection(bars)
def _chromosome_collections(df,
y_positions,
height,
print_names=False,
**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[chrom], height)
xranges = group[['start', 'width']].values
if print_names:
names = group[['name', 'colors']].values
names = [i for i in names if i[1] != '#ffffff']
ax = plt.gca()
t = ax.transData
canvas = ax.figure.canvas
# Plot names with different colors and spaced
for i, n in enumerate(names):
text = ax.text(0,
y_positions[chrom] - 2,
f'{n[0]}',
color=n[1],
transform=t,
fontsize=10)
text.draw(canvas.get_renderer())
ex = text.get_window_extent()
t = transforms.offset_copy(text._transform,
x=ex.width,
units='dots')
yield BrokenBarHCollection(xranges,
yrange,
facecolors=group['colors'],
**kwargs)
if del_width:
del df['width']
def contiguity_plot():
for chrom, group in chrs_contigs_regions.groupby('chrom'):
yrange = (chrom_centers[chrom], 0.5)
group['width'] = group['width'].apply(lambda x: x)
xranges = group[['chrom_start', 'width']].values
yield BrokenBarHCollection(xranges, yrange, facecolors=group['colors'])
def plot_enso_background(self, ensoindices=None, lag=0, **optinfo):
"""
Plots colored stripes in the background of plot to represent ENSO phases.
Parameters
----------
ensophases: {array-like}, optional
Array of ENSO indices (``+1`` for El Niño, ``0`` for Neutral and
``-1`` for La Niña episodes).
If None, the ENSO indices of the underlying series are used instead.
"""
if ensoindices is None:
series = self._series
if series is None or not hasattr(series, 'ensoindices') or \
series.ensoindices is None:
raise ValueError("Undefined ENSO indices!")
ensoindices = series.ensoindices
if self.xdata is None:
errmsg = "Unable to retrieve the dates of the current plot!"
raise ValueError(errmsg)
#
dates = self.xdata
clust_indices = Cluster(ensoindices.filled(0), 0)
_dates = np.empty(len(dates) + 1, int)
_dates[:-1] = dates
_dates[-1] = dates[-2]
episodes = dict([(k, zip(_dates[v[:, 0]], _dates[v[:, 1]]))
for (k, v) in clust_indices.grouped_limits().items()])
#
colors = ENSOcolors['polygons']
for (key, idx) in {'C':-1, 'N':0, 'W':+1}.iteritems():
colors[idx] = colors[key]
#
trans = blended_transform_factory(self.transData, self.transAxes)
for (k, lim) in episodes.iteritems():
_bbc = BrokenBarHCollection([(x + lag, y - x) for (x, y) in lim],
(0, 1),
facecolors=colors[k],
edgecolors=colors[k],)
_bbc.set_alpha(0.2)
_bbc.set_transform(trans)
self.add_collection(_bbc)
def bed_collections_generator(df, y_positions, height):
""" Interate dataframe
Yeilds:
Brokenbarhcollection --from BED DF to be plotted
"""
for chrom, group in df.groupby('chrom'):
yrange = (0, height)
xranges = group[['start', 'width']].values
yield BrokenBarHCollection(xranges,
yrange,
facecolors=group['colors'],
label=chrom)
def bed_collections_generator(dataframe, height):
""" Interate dataframe
Yeilds:
Brokenbarhcollection --from BED DF to be plotted
"""
for chrom, group in dataframe.groupby("chrom"):
yrange = (0, height)
xranges = group[["start", "width"]].values
yield BrokenBarHCollection(xranges,
yrange,
facecolors=group["colors"],
label=chrom)
def make_collection(self, df, chrom, ypos=0.25, height=0.5, **kwargs):
if 'width' not in df.columns:
df['width'] = df.end - df.start
df0 = df[df['chrom'] == chrom]
xranges = df0[['start', 'width']].values
colors = df0['colors'] #.values
yrange = (ypos, height)
bbhc = BrokenBarHCollection(xranges,
yrange,
facecolors=colors,
**kwargs)
xmin = df0.start.min()
xmax = df0.end.max()
return bbhc, xmin, xmax
def chromosome_collections(df, y_positions, height, **kwargs):
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[chrom], height)
xranges = group[['start', 'width']].values
yield BrokenBarHCollection(xranges,
yrange,
edgecolors=("black", ),
facecolors=group['colors'],
**kwargs)
if del_width:
del df['width']
def bed_collections_generator_combine(dataframe, y_positions, height):
""" Iterate dataframe
Args:
dataframe(pandas dataframe)
y_positions()
height
Yields:
BrokenBarHCollection
"""
for chrom, group in dataframe.groupby("chrom"):
print("chrom: {}".format(chrom))
yrange = (y_positions[chrom], height)
xranges = group[["start", "width"]].values
yield BrokenBarHCollection(xranges,
yrange,
facecolors=group["colors"],
label=chrom)
def coverage_generator_combine(dataframe, height):
"""Iterate dataframe and yeild per chromosome, like coverage_generator()
-with additional positional
Args:
dataframe --
height ---
Yeilds:
BrokenBarhcollection
"""
for chrom, group in dataframe.groupby("chrom"):
yrange = (0, height)
xranges = group[["start", "width"]].values
yield BrokenBarHCollection(xranges,
yrange,
facecolors=group["colors"],
label=chrom)
def bed_collections_generatorCombine(df, y_positions, height, **kwargs):
""" Iterate dataframe
Args:
df(pandas dataframe)
y_positions()
height
Yields:
BrokenBarHCollection
"""
for chrom, group in df.groupby('chrom'):
print("chrom: {}".format(chrom))
yrange = (y_positions[chrom], height)
xranges = group[['start', 'width']].values
yield BrokenBarHCollection(xranges,
yrange,
facecolors=group['colors'],
label=chrom)
def coverage_generatorCombine(df, y_positions, height):
"""Iterate dataframe and yeild per chromosome, like coverage_generator()
-with additional positional
Args:
df --
y_positions --
height ---
Yeilds:
BrokenBarhcollection
"""
for chrom, group in df.groupby('chrom'):
yrange = (0, height)
xranges = group[['start', 'width']].values
yield BrokenBarHCollection(xranges,
yrange,
facecolors=group['colors'],
label=chrom)
def plot(self, ax, gr: GenomeRange, **kwargs):
self.ax = ax
df = self.fetch_data(gr)
xranges, colors = [], []
band_height = self.properties['height']
for _, row in df.iterrows():
start, end = row['start'], row['end']
band_name, band_type = row['band_name'], row['band_type']
band_color = self.lookup_band_color(band_type)
xranges.append((start, end))
colors.append(band_color)
if self.properties['show_band_name'] != 'no':
if gr.length < 80_000_000:
self.plot_text(band_name, start, end, band_color)
coll = BrokenBarHCollection(xranges, (0, band_height), facecolors=colors,
linewidths=self.properties['border_width'],
edgecolors=self.properties['border_color'])
ax.add_collection(coll)
ax.set_ylim(-0.1, band_height + 0.1)
ax.set_xlim(gr.start, gr.end)
self.plot_label()
def plot_enso_background(self, ensoindices=None, lag=0, **optinfo):
"""
Plots colored stripes in the background of plot to represent ENSO phases.
Parameters
----------
ensophases: {array-like}, optional
Array of ENSO indices (``+1`` for El Niño, ``0`` for Neutral and
``-1`` for La Niña episodes).
If None, the ENSO indices of the underlying series are used instead.
"""
if ensoindices is None:
series = self._series
if series is None or not hasattr(series, 'ensoindices') or \
series.ensoindices is None:
raise ValueError("Undefined ENSO indices!")
ensoindices = series.ensoindices
if self.xdata is None:
errmsg = "Unable to retrieve the dates of the current plot!"
raise ValueError(errmsg)
#
dates = self.xdata
clust_indices = Cluster(ensoindices.filled(0), 0)
_dates = np.empty(len(dates) + 1, int)
_dates[:-1] = dates
_dates[-1] = dates[-2]
episodes = dict([(k, zip(_dates[v[:, 0]], _dates[v[:, 1]]))
for (k, v) in clust_indices.grouped_limits().items()])
#
colors = ENSOcolors['polygons']
for (key, idx) in {'C': -1, 'N': 0, 'W': +1}.iteritems():
colors[idx] = colors[key]
#
trans = blended_transform_factory(self.transData, self.transAxes)
for (k, lim) in episodes.iteritems():
_bbc = BrokenBarHCollection(
[(x + lag, y - x) for (x, y) in lim],
(0, 1),
facecolors=colors[k],
edgecolors=colors[k],
)
_bbc.set_alpha(0.2)
_bbc.set_transform(trans)
self.add_collection(_bbc)
def get_steps(self, sigs, weights, cutoff_hz=1.0, order=2, window=4.0,
x_threshold=2.0, figname=None, min_step_window=2.0):
"""
Parameters
----------
sigs : list(ndarray(n), ndarray(n))
List of signals (1D-arrays)
"""
x = sigs[0]
y = sigs[1]
xf, xf_ds, xf_ds_dt, x_regress = self.conditioning(x, cutoff_hz=cutoff_hz,
order=order, window=window)
xf_ds_regress = x_regress[:,0]
yf, yf_ds, yf_ds_dt, y_regress = self.conditioning(y, cutoff_hz=cutoff_hz,
order=order, window=window)
yf_ds_regress = y_regress[:,0]
# select on the product of yf_ds_regress * xf_ds_regress,
# both need to be steady!
xw = weights[0]
yw = weights[1]
xy_ds = np.abs(xf_ds_regress*xw) + np.abs(yf_ds_regress*yw)
xf_sel_mask, xf_sel_arg = self.select(xy_ds, x_threshold)
step_ds_mask, steps_ds = self.steady_steps(xf_sel_mask,
step_lenght=min_step_window)
# save steps in high-res sampling of the original signal
steps = np.round(steps_ds * self.sps / self.freq_ds, 0).astype(np.int)
np.savetxt(figname.replace('.png', '_steps.txt'), steps)
# steps_ds_times = self.t_ds[steps_ds.flatten()]
# steps = np.ndarray(steps_ds.shape) * np.nan
# for k in range(steps.shape[0]):
# t0 = self.t_ds[steps[k,0]]
# t1 = self.t_ds[steps[k,1]]
# steps[k,0] = np.abs(self.time - t0).argmin()
# steps[k,0] = np.abs(self.time - t1).argmin()
if figname is not None:
print('start plotting...')
fig, axes = plotting.subplots(nrows=3, ncols=1, figsize=(8,9),
dpi=120)
ax = axes[0,0]
ax.set_title('original and filtered signals')
ax.plot(self.time, x, 'r-', alpha=0.3)
ax.plot(self.time, xf, 'r-')
ax.grid()
axr = ax.twinx()
axr.plot(self.time, y, 'g-', alpha=0.3)
axr.plot(self.time, yf, 'g-')
ax = axes[1,0]
ax.set_title('lin regr window: %1.02f sec' % window)
t_mask = self.t_ds.copy()
t_mask[~xf_sel_mask] = np.nan
x_mask = xf_ds.copy()
x_mask[~xf_sel_mask] = np.nan
ax.plot(self.t_ds, xf_ds, 'r-', alpha=1.0, label='xf ds')
ax.plot(self.t_ds, x_mask, 'k-+', alpha=0.7, label='xf select')
ax.grid()
axr = ax.twinx()
axr.plot(self.t_ds, yf_ds, 'g-', alpha=0.8, label='yx ds')
y_mask = yf_ds.copy()
y_mask[~xf_sel_mask] = np.nan
axr.plot(self.t_ds, y_mask, 'k-+', alpha=0.7, label='yf select')
xmin = axr.get_ylim()[0]
xmax = axr.get_ylim()[1]
collection = region.span_where(self.t_ds, ymin=xmin, ymax=xmax,
where=xf_sel_mask, facecolor='grey',
alpha=0.4)
axr.add_collection(collection)
leg = plotting.one_legend(ax, axr, loc='best')
leg.get_frame().set_alpha(0.5)
ax = axes[2,0]
rpl = (x_threshold, min_step_window)
ax.set_title('threshold: %1.02f, min step window: %1.2f sec' % rpl)
ax.plot(self.t_ds, np.abs(xf_ds_regress), 'r-',
label='xf lin regress', alpha=0.9)
ax.plot(self.t_ds, np.abs(yf_ds_regress), 'g-',
label='yf lin regress', alpha=0.9)
ax.plot(self.t_ds, np.abs(xy_ds), 'k-', label='xy*w', alpha=0.7)
ax.axhline(y=x_threshold, linewidth=1, color='k', linestyle='--',
aa=False)
ax.set_ylim([0,5])
xmin = ax.get_ylim()[0]
xmax = ax.get_ylim()[1]
collection = region.span_where(self.t_ds, ymin=xmin, ymax=xmax,
where=step_ds_mask, facecolor='grey',
alpha=0.4)
ax.add_collection(collection)
# axr = ax.twinx()
# axr.plot(self.t_ds, np.abs(yf_ds_regress), 'g-',
# label='yf lin regress', alpha=0.9)
# ax, axr = plotting.match_yticks(ax, axr)
# axr.set_ylim([0,5])
# leg = plotting.one_legend(ax, axr, loc='best')
# leg.get_frame().set_alpha(0.5)
ax.grid()
leg = ax.legend(loc='best')
leg.get_frame().set_alpha(0.5)
fig.tight_layout()
fig.savefig(figname)
print(figname)
return steps
def draw(self, ax):
a = self.attr
st, ed = a['st'], a['ed']
xmin = self.st #- width*self.margin
xmax = self.ed #+ width*self.margin
width = xmax - xmin #ed-st
#print 'gene,st,ed,width,margin,xmin,xmax',st,ed,width,self.margin,xmin,xmax
xmid = (xmin + xmax) / 2.
ymax = 0.8
h = 0.4
ymin = ymax - h
ymid = ymax - h / 2.
# draw genome line
ax.plot([xmin, xmax], [ymid, ymid], 'grey') # base
# draw arrows in introns
estsi = zip(a['estarts'], a['esizes'])
ists = [st + est + esi for est, esi in estsi[:-1]]
ieds = [st + est for est, esi in estsi[1:]]
if a['strand'] == '+':
dx, shape, hw = 1, 'right', 0.25
else:
dx, shape, hw = -1, 'right', 0.4
hl = 0.05 * width
arrowargs = dict(y=ymid,
dx=dx,
dy=0,
shape=shape,
fc='grey',
linewidth=0,
head_width=hw,
head_length=hl)
#print estsi
#print zip(ists,ieds)
for ist, ied in zip(ists, ieds):
iwidth = ied - ist
imid = (ist + ied) / 2.
if iwidth < 0.15 * width:
continue
#print imid
ax.arrow(imid - dx * (hl + 1) / 2., **arrowargs)
# put arrow at xmin and xmax
if st > xmin:
if dx < 0:
axmin = xmin + hl - dx
axmax = xmax - dx
else:
axmin = xmin - dx
axmax = xmax - hl - dx
ax.arrow(axmin, **arrowargs)
ax.arrow(axmax, **arrowargs)
# draw exons => BrokenBarHCollection
# draw st=>TSS & TSE=>ed
tss = a['tst'] - st # exon coords are st based
tse = a['ted'] - st
if tss == tse:
estsi1 = estsi3 = []
estsi2 = estsi
else:
estsi1 = [(x, y) for x, y in estsi if x < tss]
estsi2 = [(x, y) for x, y in estsi
if ((x + y) >= tss) & (x <= tse)]
estsi3 = [(x, y) for x, y in estsi if (x + y) > tse]
if estsi1:
x0, y0 = estsi1[-1] # last size needs fixing
if (x0 + y0) > tss:
estsi1[-1] = (x0, tss - x0)
if estsi2:
x0, y0 = estsi2[0]
if x0 < tss: # first start and size need fixing
estsi2[0] = (tss, y0 - (tss - x0))
x0, y0 = estsi2[-1]
if (x0 + y0) > tse:
estsi2[-1] = (x0, tse - x0)
if estsi3:
x0, y0 = estsi3[0]
if x0 < tse:
estsi3[0] = (tse, y0 - (tse - x0))
c = self.color
cargs = dict(facecolor=c, edgecolor=c) #, alpha=0.8)
cargs.update(self.kwargs)
#print 'estsi1',estsi1
#print 'estsi2',estsi2
#print 'estsi3',estsi3
# draw UTR
if (len(estsi1) + len(estsi3)) > 0:
yrange = (ymid - h / 4., h / 2.)
xranges = [(st + x, y) for x, y in estsi1] + [(st + x, y)
for x, y in estsi3]
bbhc = BrokenBarHCollection(xranges, yrange, **cargs)
ax.add_collection(bbhc)
#print '1,3 xranges', xranges
#print '1,3 yrange', yrange
# draw coding
yrange = (ymid - h / 2., h)
xranges = [(st + x, y) for x, y in estsi2]
#print '2 xranges', xranges
#print '2 yrange', yrange
bbhc = BrokenBarHCollection(xranges, yrange, **cargs)
ax.add_collection(bbhc)
# draw gene name
txt = '%s (%.1fkb)' % (a['name'], width / 1000)
ax.text(xmid, 0, txt, ha='center', va='bottom', fontsize=FONTSIZE)
PP.setp(ax,
xticks=[],
yticks=[],
frame_on=False,
xlim=(xmin, xmax),
ylim=(0, 1))
chrRng = ['R','7','6','5','4','3','2','1']
mydata = []
for ichr in chrRng:
os.chdir("chr%s"%ichr)
tcom = np.genfromtxt("compress.out",skip_header=1)
for itemcom in tcom:
i = itemcom[0]
c = itemcom[2]
mydata.append(["chr%s"%ichr,12500+i*50000,12500+(i+1)*50000,0,c])
os.chdir("..")
#mydata = [["chr1",0,50000,0,1],
#["chr1",50000,100000,0,2],
#["chr1",100000,150000,0,1],["chr2",150000,200000,0,3],["chr2",200000,250000,0,4]]
for xranges, yrange, colors, label in ideograms(mydata):
coll = BrokenBarHCollection(xranges, yrange, facecolors=colors)
ax.add_collection(coll)
center = yrange[0] + yrange[1]/2.
yticks.append(center)
yticklabels.append(label)
d[label] = xranges
ax.axis('tight')
ax.set_yticks(yticks)
ax.set_yticklabels(yticklabels)
ax.set_xticks([])
plt.savefig("compress.pdf")
plt.show()
### plot compressibilities out as curve
if False:
def details(file):
height = 0.9
spacing = 0.9
def ideograms(fn):
last_chrom = None
last_specie = None
last_population = None
fin = open(fn)
fin.readline()
xranges, color = [], []
ymin = 0
for line in fin:
chrom, start, stop, specie, population, stain = line.strip().split(
)
start = int(start)
stop = int(stop)
width = stop - start
if chrom == last_chrom or (last_chrom is None):
xranges.append((start, width))
color.append(colors[stain])
last_chrom = chrom
last_specie = specie
last_population = population
continue
ymin += height + spacing
yrange = (ymin, height)
yield xranges, yrange, color, last_chrom, last_specie, last_population
xranges, color = [], []
xranges.append((start, width))
color.append(colors[stain])
last_chrom = chrom
last_specie = specie
last_population = population
# last one
ymin += height + spacing
yrange = (ymin, height)
yield xranges, yrange, color, last_chrom, last_specie, last_population
fig = plt.figure(figsize=(15, 15))
ax = fig.add_subplot(111)
d = {}
yticks = []
yticklabels = []
for xranges, yrange, color, chms, species, populations in ideograms(file):
coll = BrokenBarHCollection(xranges, yrange, facecolors=color)
ax.add_collection(coll)
center = yrange[0] + yrange[1] / 2.
yticks.append(center)
label = '%s %s' % (species, populations)
yticklabels.append(label)
d[chms] = xranges
values = []
bp = []
for inter in xranges:
values.append(inter[0])
bp.append(inter[1])
values.append(bp[-1] + values[-1])
for i in range(0, len(values) - 1):
xlabel = '%d bp' % (bp[i])
ax.annotate(xlabel,
xy=(values[i + 1] / 2 + values[i] / 2,
yrange[0] + yrange[1]),
xytext=(values[i + 1] / 2 + values[i] / 2,
yrange[0] + yrange[1]))
ax.set_title('Chromosomes')
ax.axis('tight')
ax.set_yticks(yticks)
ax.set_yticklabels(yticklabels)
ax.set_xticks([])
plt.show(block=False)
def main(args, parser):
# Get the contig length list
ctglens = dict()
with open(args.fai, 'r') as fai:
for l in fai:
s = l.rstrip().split()
ctglens[s[0]] = s[1]
# Create windows
winlist = defaultdict(list)
# offset bp to add for stitching contigs together in one line
ctgoffset = dict()
lastbp = 0
for c in ctglens:
ctgoffset[c] = lastbp + 100
for i in range(0, ctglens[c], args.binsize):
winlist[c].append(window(c, i, i + args.binsize))
lastbp += ctglens[c]
# read each sam region and count the reads
with pysam.AlignmentFile(args.bam, 'rb') as bamfile:
for c, w in winlist.items():
for i, win in enumerate(w):
count = 0
for s in bamfile.fetch(c, win.start, win.end):
if s.is_secondary:
continue
count += 1
winlist = updateWin(winlist, c, i, count)
# Now, read in the human readable text file and process that
hapset = set()
with open(args.human, 'r') as human:
human.readline()
for l in human:
s = l.rstrip().split()
# determine where the contig start falls
for i, win in enumerate(winlist[s[2]]):
if int(s[3]) < win.end and int(s[3]) >= win.start:
winlist = updateWin(winlist, s[2], i, int(s[6]), s[4])
print(f'Updating window: {s[2]} {win.start} {win.end} to {s[6]} for Hap {s[4]}')
hapset.add(s[4])
# OK, data is in! Let's try plotting
raw = defaultdict(list)
bars = list()
for c, w in winlist.items():
bars.append([ctgoffset[c], ctglens[c]])
for win in winlist:
for h in hapset:
raw["contig"].append(c)
raw["start"].append(win.start + ctgoffset[c])
raw["end"].append(win.end + ctgoffset[c])
raw["hap"].append(h)
raw["count"].append(win.getCount(h))
df = pandas.DataFrame(raw)
df.to_csv(args.output + '.wins', sep='\t', header=True)
fig = plt.figure(figsize=(6,8))
ax = df[['start', 'hap', 'count']].plot.area(x='start', y='count', colormap='viridis')
ax.add_collection(BrokenBarHCollection(bars, [-1, 1], facecolors=plt.get_cmap('tab20')))
ax.axis('tight')
plt.savefig(args.output + '.pdf')
def labeled_intervals(intervals,
labels,
label_set=None,
base=None,
height=None,
extend_labels=True,
ax=None,
tick=True,
**kwargs):
'''Plot labeled intervals with each label on its own row.
Parameters
----------
intervals : np.ndarray, shape=(n, 2)
segment intervals, in the format returned by
:func:`mir_eval.io.load_intervals` or
:func:`mir_eval.io.load_labeled_intervals`.
labels : list, shape=(n,)
reference segment labels, in the format returned by
:func:`mir_eval.io.load_labeled_intervals`.
label_set : list
An (ordered) list of labels to determine the plotting order.
If not provided, the labels will be inferred from
``ax.get_yticklabels()``.
If no ``yticklabels`` exist, then the sorted set of unique values
in ``labels`` is taken as the label set.
base : np.ndarray, shape=(n,), optional
Vertical positions of each label.
By default, labels are positioned at integers
``np.arange(len(labels))``.
height : scalar or np.ndarray, shape=(n,), optional
Height for each label.
If scalar, the same value is applied to all labels.
By default, each label has ``height=1``.
extend_labels : bool
If ``False``, only values of ``labels`` that also exist in
``label_set`` will be shown.
If ``True``, all labels are shown, with those in `labels` but
not in `label_set` appended to the top of the plot.
A horizontal line is drawn to indicate the separation between
values in or out of ``label_set``.
ax : matplotlib.pyplot.axes
An axis handle on which to draw the intervals.
If none is provided, a new set of axes is created.
tick : bool
If ``True``, sets tick positions and labels on the y-axis.
kwargs
Additional keyword arguments to pass to
`matplotlib.collection.BrokenBarHCollection`.
Returns
-------
ax : matplotlib.pyplot.axes._subplots.AxesSubplot
A handle to the (possibly constructed) plot axes
'''
# Get the axes handle
ax, _ = __get_axes(ax=ax)
# Make sure we have a numpy array
intervals = np.atleast_2d(intervals)
if label_set is None:
# If we have non-empty pre-existing tick labels, use them
label_set = [_.get_text() for _ in ax.get_yticklabels()]
# If none of the label strings have content, treat it as empty
if not any(label_set):
label_set = []
else:
label_set = list(label_set)
# Put additional labels at the end, in order
if extend_labels:
ticks = label_set + sorted(set(labels) - set(label_set))
elif label_set:
ticks = label_set
else:
ticks = sorted(set(labels))
style = dict(linewidth=1)
style.update(next(ax._get_patches_for_fill.prop_cycler))
# Swap color -> facecolor here so we preserve edgecolor on rects
style['facecolor'] = style.pop('color')
style.update(kwargs)
if base is None:
base = np.arange(len(ticks))
if height is None:
height = 1
if np.isscalar(height):
height = height * np.ones_like(base)
seg_y = dict()
for ybase, yheight, lab in zip(base, height, ticks):
seg_y[lab] = (ybase, yheight)
xvals = defaultdict(list)
for ival, lab in zip(intervals, labels):
if lab not in seg_y:
continue
xvals[lab].append((ival[0], ival[1] - ival[0]))
for lab in seg_y:
ax.add_collection(BrokenBarHCollection(xvals[lab], seg_y[lab],
**style))
# Pop the label after the first time we see it, so we only get
# one legend entry
style.pop('label', None)
# Draw a line separating the new labels from pre-existing labels
if label_set != ticks:
ax.axhline(len(label_set), color='k', alpha=0.5)
if tick:
ax.grid(True, axis='y')
ax.set_yticks([])
ax.set_yticks(base)
ax.set_yticklabels(ticks, va='bottom')
ax.yaxis.set_major_formatter(IntervalFormatter(base, ticks))
if base.size:
__expand_limits(ax, [base.min(), (base + height).max()], which='y')
if intervals.size:
__expand_limits(ax, [intervals.min(), intervals.max()], which='x')
return ax
def main(argv):
file_metadata = ""
dir_post = ""
output_mark = ""
genome = ""
method = -1
file_input_extension = ""
file_output_extension = ""
title_label = ""
libraries = 'all'
type_junction = 'all'
good_directory_list = []
check_result_tlx = False
check_result_filter_stats_txt = False
total_junction = 0
#pd.options.mode.chained_assignment = None
try:
opts, args = getopt.getopt(sys.argv[1:], 'm:g:p:o:e:i:w:t:', [
'file_metadata=', 'genome=', 'dir_post=', 'output_mark=',
'method=', 'input_mark=', 'libraries=', 'type_junction=', 'help'
])
except getopt.GetoptError:
usage()
sys.exit(2)
##############################OPTIONS##############################
print("\n")
for opt, arg in opts:
if opt in ('-h', '--help'):
usage()
sys.exit(2)
elif opt in ('-m', '--file_metadata'):
file_metadata = arg
elif opt in ('-g', '--genome'):
genome = arg
elif opt in ('-p', '--dir_post'):
dir_post = arg
elif opt in ('-o', '--output_mark'):
output_mark = arg
elif opt in ('-e', '--method'):
method = arg
elif opt in ('-i', '--input_mark'):
input_mark = arg
elif opt in ('-w', '--libraries'):
libraries = arg
elif opt in ('-t', '--type_junction'):
type_junction = arg
else:
print("Error : Bad option -> " + opt)
usage()
sys.exit(2)
##############################CHECK UP/SET UP##############################
# CHECK METADATA FILE
if file_metadata == "" or not os.path.exists(file_metadata):
print("Error : You have to set a metadata file !\n")
usage()
sys.exit(2)
else:
# READ METADATA FILE
metadata = pd.read_table(file_metadata, sep='\t')
# FILTER METADATA FILE IF GENOME INPUT
if genome != "":
metadata = metadata.loc[metadata['Assembly'] == genome]
if metadata.empty:
print(
"Error : This assembly does not exist in the metadata file !\n"
)
usage()
sys.exit(2)
else:
print("Error : You have to set a genome name !\n")
usage()
sys.exit(2)
# CHECK POSTPROCESS DIRECTORY
if not os.path.exists(dir_post):
print("Error : You have to set a postprocess directory !\n")
usage()
sys.exit(2)
else:
if dir_post[-1] != "/":
dir_post += "/"
# CHECK METHOD
try:
method = int(method)
if method == 0:
title_label = "Number of double stranded breaks after the primer at each position divided by the maximum of breaks by library"
elif method == 1:
title_label = "Log2 of number of double stranded breaks after the primer at each position divided by log2 of the maximum of breaks by library"
else:
print("Error : Method option needs to be 0 or 1 !\n")
usage()
sys.exit(2)
except:
print(
"Error : You have to set an integer (0 or 1) to method option !\n")
usage()
sys.exit(2)
# CHECK INPUT MARKS HISTORY
if input_mark == "":
print("Warning : You will process the raw file !\n")
# CHECK OUTPUT MARK
if output_mark == "":
print("Error : You have to set an output mark !\n")
usage()
sys.exit(2)
# SELECT INPUT FILES
if input_mark == "":
file_input_extension = ".tlx"
else:
file_input_extension = "_" + "_".join(input_mark.split(",")) + ".tlx"
# TEST IF INPUT EXIST IN AT LEAST ON LIBRARY
check_input_mark = False
for library in metadata['Library'].tolist():
if os.path.exists(dir_post + library + "/" + library + "_Legitimate" +
file_input_extension) or os.path.exists(
dir_post + library + "/" + library +
"_Illegitimate" + file_input_extension):
check_input_mark = True
if not check_input_mark:
print(
"Error : Your input marks can not localize a good legitimate or illegitimate file !\n"
)
usage()
sys.exit(2)
# CHECK LIBRARIES
array_libraries = []
if libraries == 'all':
array_libraries = metadata['Library'].tolist()
else:
for library in libraries.split(","):
if library in metadata['Library'].tolist():
array_libraries.append(library)
else:
print("Warning : {" + library +
"} does not exist in metadata file with this genome !")
print("Warning : {" + library + "} will not be used !")
if type_junction != 'all' and type_junction != 'legitimate' and type_junction != 'illegitimate':
print(
"Error : Type junction only stand for all, legitimate or illegitimate value !\n"
)
usage()
sys.exit(2)
# SELECT OUTPUT FILES
if file_input_extension != "":
file_output_extension = file_input_extension[:-4] + "_" + output_mark + ".png"
else:
file_output_extension = "_" + output_mark + ".png"
##############################PRINTS##############################
print('\n-----------------------------------------')
print('Metadata file : ' + file_metadata)
print('Genome : ' + genome)
print('Postprocess directory : ' + dir_post)
print('Method : ' + str(method))
print('Libraries : ' + libraries)
print('Type junction : ' + type_junction)
print('Input file extension: ' + file_input_extension)
print('Output file extension : ' + file_output_extension)
print('-----------------------------------------\n')
##############################PROGRAMS##############################
fig = plt.figure()
ax = fig.add_subplot(111)
d = {}
yticks = []
yticklabels = []
track_number = 0
yrange = []
coff_leg_ille_graph = 0
# LOOP OVER EACH LIBRARIES
for library in array_libraries:
# print(library)
# CHECK DIRECTORY EXISTS
if not os.path.exists(dir_post + library):
print("Warning : " + dir_post + " does not contains {" + library +
"}")
print("Warning : {" + library + "} will not be filtered")
else:
# CHECK INPUT FILE EXISTS
if os.path.exists(dir_post + library + "/" + library +
"_Legitimate" + file_input_extension):
df_legitimate = pd.read_csv(dir_post + library + "/" +
library + "_Legitimate" +
file_input_extension,
sep='\t',
header=0,
index_col=None)
df_legitimate = df_legitimate.drop(
columns=df_legitimate.columns[11:])
else:
print("Error : The Legitimate file for " + library +
" is missing !\n")
usage()
sys.exit(2)
if os.path.exists(dir_post + library + "/" + library +
"_Illegitimate" + file_input_extension):
df_illegitimate = pd.read_csv(dir_post + library + "/" +
library + "_Illegitimate" +
file_input_extension,
sep='\t',
header=0,
index_col=None)
df_illegitimate = df_illegitimate.drop(
columns=df_illegitimate.columns[11:])
else:
print("Error : The Illegitimate file for " + library +
" is missing !\n")
usage()
sys.exit(2)
metadata = metadata[(metadata['Library'].isin(array_libraries))]
metadata_sort = pd.DataFrame(columns=list(metadata.columns.values))
for i in array_libraries:
for index, row in metadata.iterrows():
if i == row['Library']:
metadata_sort = metadata_sort.append(row)
metadata = metadata_sort
#metadata = metadata.sort_values(['Library'], ascending=[True])
global_list = dir_post + metadata['Library']
# for i in global_list:
# print(i)
nb_files = len(global_list)
# DICTIONNARY WITH ILLEGITIMATES AND LEGITIMATES JUNCTIONS
distance_dict = {"illegitimates": {}, "legitimates": {}}
# OPEN TLX FILES ONE BY ONE
for result_file in global_list:
label = result_file.split("/")[-1]
# YRANGE USED AT THE END TO HORIZONTAL SPACE BAR
yrange.append(((track_number * 1.8) + (track_number * 1.8) + 1.8 +
coff_leg_ille_graph, 1))
if type_junction == 'all':
yrange.append(((track_number * 1.8) + (track_number * 1.8) + 3.6 +
coff_leg_ille_graph, 1))
coff_leg_ille_graph += 1
# DICTIONNARY LABEL INSIDE ILLEGITIMATES AND LEGITIMATES DICTIONNARIES
distance_dict["illegitimates"][label] = {}
distance_dict["legitimates"][label] = {}
# with open(result_file+"/"+label+"_result.tlx", 'r') as f_tlx:
with open(
result_file + "/" + label + "_Legitimate" +
file_input_extension, 'r') as f_tlx:
f_tlx.readline()
for line in f_tlx:
if pd.isnull(metadata.loc[metadata['Library'] == label]
['MID'].values[0]):
len_mid = 0
else:
len_mid = len(metadata.loc[metadata['Library'] == label]
['MID'].values[0])
if pd.isnull(metadata.loc[metadata['Library'] == label]
['Primer'].values[0]):
len_primer = 0
else:
len_primer = len(metadata.loc[metadata['Library'] == label]
['Primer'].values[0])
distance = int(
int(line.split("\t")[9]) -
int(line.split("\t")[8])) - (len_mid + len_primer)
if distance not in distance_dict["legitimates"][label]:
distance_dict["legitimates"][label][distance] = 1
else:
distance_dict["legitimates"][label][distance] += 1
total_junction += 1
with open(
result_file + "/" + label + "_Illegitimate" +
file_input_extension, 'r') as f_tlx:
f_tlx.readline()
for line in f_tlx:
if pd.isnull(metadata.loc[metadata['Library'] == label]
['MID'].values[0]):
len_mid = 0
else:
len_mid = len(metadata.loc[metadata['Library'] == label]
['MID'].values[0])
if pd.isnull(metadata.loc[metadata['Library'] == label]
['Primer'].values[0]):
len_primer = 0
else:
len_primer = len(metadata.loc[metadata['Library'] == label]
['Primer'].values[0])
distance = int(
int(line.split("\t")[9]) -
int(line.split("\t")[8])) - (len_mid + len_primer)
if distance not in distance_dict["illegitimates"][label]:
distance_dict["illegitimates"][label][distance] = 1
else:
distance_dict["illegitimates"][label][distance] += 1
total_junction += 1
# ADD MAX_DISTANCE AND MAX_DISTANCE_COUNT TO ILLEGITIMATES
max_distance = 0
max_distance_count = 0
if len(distance_dict["illegitimates"][label]) > 0:
# max_distance
max_distance = max(
distance_dict["illegitimates"][label].iteritems(),
key=operator.itemgetter(0))[0]
# max_distance_count
max_distance_count = max(
distance_dict["illegitimates"][label].iteritems(),
key=operator.itemgetter(1))[1]
distance_dict["illegitimates"][label]["max_distance"] = max_distance
distance_dict["illegitimates"][label][
"max_distance_count"] = max_distance_count
# ADD MAX_DISTANCE AND MAX_DISTANCE_COUNT TO LEGITIMATES
max_distance = 0
max_distance_count = 0
if len(distance_dict["legitimates"][label]) > 0:
# max_distance
max_distance = max(distance_dict["legitimates"][label].iteritems(),
key=operator.itemgetter(0))[0]
# max_distance_count
max_distance_count = max(
distance_dict["legitimates"][label].iteritems(),
key=operator.itemgetter(1))[1]
distance_dict["legitimates"][label]["max_distance"] = max_distance
distance_dict["legitimates"][label][
"max_distance_count"] = max_distance_count
track_number += 1
# print(distance_dict)
max_distance_all = 0
max_distance_count_all = 0
# Define max_distance_all and max_distance_count_all
for legitimate, label_dict in distance_dict.items():
for key, value in label_dict.items():
if max_distance_all < int(label_dict[key]['max_distance']):
max_distance_all = int(label_dict[key]['max_distance'])
if max_distance_count_all < int(
label_dict[key]['max_distance_count']):
max_distance_count_all = int(
label_dict[key]['max_distance_count'])
# print(max_distance_all)
# print(max_distance_count_all)
yrange_count = 0
for bad_label in global_list:
label = bad_label.split("/")[-1]
# MANAGE ARRAYS
#distance_dict["illegitimates"][label] = manageArray(
# distance_dict["illegitimates"][label], max_distance_count_all, method)
#distance_dict["legitimates"][label] = manageArray(
# distance_dict["legitimates"][label], max_distance_count_all, method)
max_label_leg_ille = max(
distance_dict["legitimates"][label]["max_distance_count"],
distance_dict["illegitimates"][label]["max_distance_count"])
distance_dict["illegitimates"][label] = manageArray(
distance_dict["illegitimates"][label], max_label_leg_ille, method)
distance_dict["legitimates"][label] = manageArray(
distance_dict["legitimates"][label], max_label_leg_ille, method)
#distance_dict["illegitimates"][label] = manageArray(distance_dict["illegitimates"][label], total_junction, method)
#distance_dict["legitimates"][label] = manageArray(distance_dict["legitimates"][label], total_junction, method)
distance_dict["illegitimates"][label] = collections.OrderedDict(
sorted(distance_dict["illegitimates"][label].items()))
distance_dict["legitimates"][label] = collections.OrderedDict(
sorted(distance_dict["legitimates"][label].items()))
# CONCATENATE LEGITIMATE AND ILLEGITIMATE DISTANCE AND COUNTS (USE FOR
# COLORS)
xranges_leg = []
colors_leg = []
xranges_illeg = []
colors_illeg = []
# print(distance_dict["illegitimates"][label])
for key, value in distance_dict["legitimates"][label].items():
xranges_leg.append((key, 1))
colors_leg.append((0.0, 0.0, 0.0, value))
for key, value in distance_dict["illegitimates"][label].items():
xranges_illeg.append((key, 1))
colors_illeg.append((1.0, 0.0, 0.0, value))
##############################WORKS##############################
#xranges=[(29, 1),(30, 1),(31, 1)]
#yrange=(1.8, 1)
#colors=[(0.0, 0.0, 0.0, 0.012),(0.0, 0.0, 0.0, 0.008),(0.0, 0.0, 0.0, 0.012)]
#################################################################
# print("xranges")
# print(xranges)
# print(type(xranges))
# print("yrange")
# print(yrange[yrange_count])
# print(type(yrange[yrange_count]))
# print("colors")
# print(colors)
# print(type(colors))
if type_junction == 'all':
# LEGITIMATE DISPLAY
coll = BrokenBarHCollection(xranges_leg,
yrange[yrange_count],
facecolors=colors_leg,
edgecolors=colors_leg)
ax.add_collection(coll)
center = yrange[yrange_count][0] + yrange[yrange_count][1] / 2.0
yticks.append(center)
yticklabels.append(label + "_legi")
d[label + "legi"] = xranges_leg
yrange_count += 1
# ILLEGITIMATE DISPLAY
coll = BrokenBarHCollection(xranges_illeg,
yrange[yrange_count],
facecolors=colors_illeg,
edgecolors=colors_illeg)
ax.add_collection(coll)
center = yrange[yrange_count][0] + yrange[yrange_count][1] / 2.0
yticks.append(center)
yticklabels.append(label + "_illegi")
d[label + "illegi"] = xranges_illeg
yrange_count += 1
elif type_junction == 'legitimate':
# LEGITIMATE DISPLAY
coll = BrokenBarHCollection(xranges_leg,
yrange[yrange_count],
facecolors=colors_leg,
edgecolors=colors_leg)
ax.add_collection(coll)
center = yrange[yrange_count][0] + yrange[yrange_count][1] / 2.0
yticks.append(center)
yticklabels.append(label + "_legi")
d[label + "legi"] = xranges_leg
yrange_count += 1
elif type_junction == 'illegitimate':
# ILLEGITIMATE DISPLAY
coll = BrokenBarHCollection(xranges_illeg,
yrange[yrange_count],
facecolors=colors_illeg,
edgecolors=colors_illeg)
ax.add_collection(coll)
center = yrange[yrange_count][0] + yrange[yrange_count][1] / 2.0
yticks.append(center)
yticklabels.append(label + "_illegi")
d[label + "illegi"] = xranges_illeg
yrange_count += 1
else:
print(
"Error in Type junction attribute : all, legitimate or illegitimate value !\n"
)
usage()
sys.exit(2)
# SET UP DISPLAY BACKGROUND
ax.axis('tight')
ax.set_xlim([0, max_distance_all + 10])
ax.set_yticks(yticks)
ax.set_yticklabels(yticklabels)
step_length = (int(max_distance_all / 100) * 100) / 20
if step_length == 0:
step_length = 5
ax.set_xticks(range(0, max_distance_all + 10, step_length))
ax.get_xaxis().get_major_formatter().set_scientific(False)
plt.xlabel("Position from bait primer")
plt.axes().xaxis.set_minor_locator(MultipleLocator(1))
# SET UP TITLE
plt.title(title_label, fontdict=None, loc='center')
fig = plt.gcf()
fig.set_size_inches(22, 10)
# SAVE DISPLAY
fig.savefig(dir_post + genome + file_output_extension,
format='png',
bbox_inches='tight')