def main(args=None):
args = process_args(args)
cr = countR.CountReadsPerBin(
args.bamfiles,
args.binSize,
args.numberOfSamples,
numberOfProcessors=args.numberOfProcessors,
verbose=args.verbose,
region=args.region,
extendReads=args.extendReads,
minMappingQuality=args.minMappingQuality,
ignoreDuplicates=args.ignoreDuplicates,
center_read=args.centerReads,
samFlag_include=args.samFlagInclude,
samFlag_exclude=args.samFlagExclude)
num_reads_per_bin = cr.run()
if num_reads_per_bin.sum() == 0:
import sys
sys.stderr.write(
"\nNo reads were found in {} regions sampled. Check that the\n"
"min mapping quality is not overly high and that the \n"
"chromosome names between bam files are consistant.\n"
"\n".format(num_reads_per_bin.shape[0]))
exit(1)
if args.skipZeros:
num_reads_per_bin = countR.remove_row_of_zeros(num_reads_per_bin)
total = len(num_reads_per_bin[:, 0])
x = np.arange(total).astype('float') / total # normalize from 0 to 1
i = 0
for reads in num_reads_per_bin.T:
count = np.cumsum(np.sort(reads))
count = count / count[-1] # to normalyze y from 0 to 1
plt.plot(x, count, label=args.labels[i])
plt.xlabel('rank')
plt.ylabel('fraction w.r.t. bin with highest coverage')
i += 1
plt.legend(loc='upper left')
plt.suptitle(args.plotTitle)
# set the plotFileFormat explicitly to None to trigger the
# format from the file-extension
if not args.plotFileFormat:
args.plotFileFormat = None
plt.savefig(args.plotFile.name, bbox_inches=0, format=args.plotFileFormat)
plt.close()
if args.outRawCounts:
args.outRawCounts.write("'" + "'\t'".join(args.labels) + "'\n")
fmt = "\t".join(np.repeat('%d', num_reads_per_bin.shape[1])) + "\n"
for row in num_reads_per_bin:
args.outRawCounts.write(fmt % tuple(row))
def main(args=None):
args = process_args(args)
cr = countR.CountReadsPerBin(args.bamfiles,
args.binSize,
args.numberOfSamples,
numberOfProcessors=args.numberOfProcessors,
verbose=args.verbose,
region=args.region,
extendReads=args.extendReads,
minMappingQuality=args.minMappingQuality,
ignoreDuplicates=args.ignoreDuplicates,
center_read=args.centerReads,
samFlag_include=args.samFlagInclude,
samFlag_exclude=args.samFlagExclude)
num_reads_per_bin = cr.run()
if num_reads_per_bin.sum() == 0:
import sys
sys.stderr.write(
"\nNo reads were found in {} regions sampled. Check that the\n"
"min mapping quality is not overly high and that the \n"
"chromosome names between bam files are consistant.\n"
"\n".format(num_reads_per_bin.shape[0]))
exit(1)
if args.skipZeros:
num_reads_per_bin = countR.remove_row_of_zeros(num_reads_per_bin)
total = len(num_reads_per_bin[:, 0])
x = np.arange(total).astype('float') / total # normalize from 0 to 1
i = 0
for reads in num_reads_per_bin.T:
count = np.cumsum(np.sort(reads))
count = count / count[-1] # to normalyze y from 0 to 1
plt.plot(x, count, label=args.labels[i])
plt.xlabel('rank')
plt.ylabel('fraction w.r.t. bin with highest coverage')
i += 1
plt.legend(loc='upper left')
plt.suptitle(args.plotTitle)
# set the plotFileFormat explicitly to None to trigger the
# format from the file-extension
if not args.plotFileFormat:
args.plotFileFormat = None
plt.savefig(args.plotFile.name, bbox_inches=0, format=args.plotFileFormat)
if args.outRawCounts:
args.outRawCounts.write("'" + "'\t'".join(args.labels) + "'\n")
fmt = "\t".join(np.repeat('%d', num_reads_per_bin.shape[1])) + "\n"
for row in num_reads_per_bin:
args.outRawCounts.write(fmt % tuple(row))
def main(args=None):
args = process_args(args)
if not args.outRawCounts and not args.plotFile and not args.outCoverageMetrics:
sys.exit(
"At least one of --plotFile, --outRawCounts and --outCoverageMetrics are required.\n"
)
if 'BED' in args:
bed_regions = args.BED
else:
bed_regions = None
cr = countR.CountReadsPerBin(args.bamfiles,
binLength=1,
bedFile=bed_regions,
numberOfSamples=args.numberOfSamples,
numberOfProcessors=args.numberOfProcessors,
verbose=args.verbose,
region=args.region,
blackListFileName=args.blackListFileName,
extendReads=args.extendReads,
minMappingQuality=args.minMappingQuality,
ignoreDuplicates=args.ignoreDuplicates,
center_read=args.centerReads,
samFlag_include=args.samFlagInclude,
samFlag_exclude=args.samFlagExclude,
minFragmentLength=args.minFragmentLength,
maxFragmentLength=args.maxFragmentLength,
bed_and_bin=True,
out_file_for_raw_data=args.outRawCounts)
num_reads_per_bin = cr.run()
if args.outCoverageMetrics and args.coverageThresholds:
args.coverageThresholds.sort(
) # Galaxy in particular tends to give things in a weird order
of = open(args.outCoverageMetrics, "w")
of.write("Sample\tThreshold\tPercent\n")
nbins = float(num_reads_per_bin.shape[0])
for thresh in args.coverageThresholds:
vals = np.sum(num_reads_per_bin >= thresh, axis=0)
for lab, val in zip(args.labels, vals):
of.write("{}\t{}\t{:6.3f}\n".format(lab, thresh,
100. * val / nbins))
of.close()
if args.outRawCounts:
# append to the generated file the
# labels
header = "#plotCoverage --outRawCounts\n#'chr'\t'start'\t'end'\t"
header += "'" + "'\t'".join(args.labels) + "'\n"
f = open(args.outRawCounts, 'r+')
content = f.read()
f.seek(0, 0)
f.write(header + content)
f.close()
if num_reads_per_bin.shape[0] < 2:
exit("ERROR: too few non-zero bins found.\n"
"If using --region please check that this "
"region is covered by reads.\n")
if args.skipZeros:
num_reads_per_bin = countR.remove_row_of_zeros(num_reads_per_bin)
if args.plotFile:
if args.plotFileFormat == 'plotly':
fig = go.Figure()
fig['layout']['xaxis1'] = {
'domain': [0.0, 0.48],
'anchor': 'x1',
'title': 'coverage (#reads per base)'
}
fig['layout']['xaxis2'] = {
'domain': [0.52, 1.0],
'anchor': 'x2',
'title': 'coverage (#reads per base)'
}
fig['layout']['yaxis1'] = {
'domain': [0.0, 1.0],
'anchor': 'x1',
'title': 'fraction of bases sampled'
}
fig['layout']['yaxis2'] = {
'domain': [0.0, 1.0],
'anchor': 'x2',
'title': 'fraction of bases sampled >= coverage'
}
fig['layout'].update(title=args.plotTitle)
else:
fig, axs = plt.subplots(1,
2,
figsize=(args.plotWidth, args.plotHeight))
plt.suptitle(args.plotTitle)
# plot up to two std from mean
num_reads_per_bin = num_reads_per_bin.astype(int)
sample_mean = num_reads_per_bin.mean(axis=0)
sample_std = num_reads_per_bin.std(axis=0)
sample_max = num_reads_per_bin.max(axis=0)
sample_min = num_reads_per_bin.min(axis=0)
sample_25 = np.percentile(num_reads_per_bin, 25, axis=0)
sample_50 = np.percentile(num_reads_per_bin, 50, axis=0)
sample_75 = np.percentile(num_reads_per_bin, 75, axis=0)
# use the largest 99th percentile from all samples to set the x_max value
x_max = np.max(np.percentile(num_reads_per_bin, 99, axis=0))
# plot coverage
# print headers for text output
print("sample\tmean\tstd\tmin\t25%\t50%\t75%\tmax")
# the determination of a sensible value for y_max of the first plot (fraction of bases sampled vs.
# coverage) is important because, depending on the data,
# it becomes very difficult to see the lines in the plot. For example, if the coverage of a sample
# is a nice gaussian curve with a large mean of 50. Then a sensible range for the y axis (fraction of
# reads having coverage=x) is (0, 0.02) which nicely shows the coverage curve. If instead the coverage is
# very por and centers close to 1 then a good y axis range is (0,1).
# the current implementation aims to find the y_value for which 50% of the reads >= x (coverage) and
# sets that as the x_axis range.
y_max = []
data = []
# We need to manually set the line colors so they're shared between the two plots.
plotly_colors = [
"#d73027", "#fc8d59", "#f33090", "#e0f3f8", "#91bfdb", "#4575b4"
]
plotly_styles = sum([
6 * ["solid"], 6 * ["dot"], 6 * ["dash"], 6 * ["longdash"],
6 * ["dashdot"], 6 * ["longdashdot"]
], [])
for idx, col in enumerate(num_reads_per_bin.T):
if args.plotFile:
frac_reads_per_coverage = np.bincount(
col.astype(int)).astype(float) / num_reads_per_bin.shape[0]
csum = np.bincount(col.astype(int))[::-1].cumsum()
csum_frac = csum.astype(float)[::-1] / csum.max()
if args.plotFileFormat == 'plotly':
color = plotly_colors[idx % len(plotly_colors)]
dash = plotly_styles[idx % len(plotly_styles)]
trace = go.Scatter(x=np.arange(0,
int(x_max) - 1),
y=frac_reads_per_coverage[:int(x_max)],
mode='lines',
xaxis='x1',
yaxis='y1',
line=dict(color=color, dash=dash),
name="{}, mean={:.1f}".format(
args.labels[idx], sample_mean[idx]),
legendgroup="{}".format(idx))
data.append(trace)
trace = go.Scatter(x=np.arange(0,
int(x_max) - 1),
y=csum_frac[:int(x_max)],
mode='lines',
xaxis='x2',
yaxis='y2',
line=dict(color=color, dash=dash),
name=args.labels[idx],
showlegend=False,
legendgroup="{}".format(idx))
data.append(trace)
else:
axs[0].plot(frac_reads_per_coverage,
label="{}, mean={:.1f}".format(
args.labels[idx], sample_mean[idx]))
axs[1].plot(csum_frac, label=args.labels[idx])
# find the indexes (i.e. the x values) for which the cumulative distribution 'fraction of bases
# sampled >= coverage' where fraction of bases sampled = 50%: `np.flatnonzero(csum_frac>0.5)`
# then find the fraction of bases sampled that that have the largest x
y_max.append(frac_reads_per_coverage[max(
np.flatnonzero(csum_frac > 0.5))])
print("{}\t{:0.2f}\t{:0.2f}\t{}\t{}\t{}\t{}\t{}\t".format(
args.labels[idx],
sample_mean[idx],
sample_std[idx],
sample_min[idx],
sample_25[idx],
sample_50[idx],
sample_75[idx],
sample_max[idx],
))
if args.plotFile:
# Don't clip plots
y_max = max(y_max)
if args.plotFileFormat == "plotly":
fig['data'] = data
fig['layout']['yaxis1'].update(
range=[0.0, min(1, y_max + (y_max * 0.10))])
fig['layout']['yaxis2'].update(range=[0.0, 1.0])
py.plot(fig, filename=args.plotFile, auto_open=False)
else:
axs[0].set_ylim(0, min(1, y_max + (y_max * 0.10)))
axs[0].set_xlim(0, x_max)
axs[0].set_xlabel('coverage (#reads per bp)')
axs[0].legend(fancybox=True, framealpha=0.5)
axs[0].set_ylabel('fraction of bases sampled')
# plot cumulative coverage
axs[1].set_xlim(0, x_max)
axs[1].set_xlabel('coverage (#reads per bp)')
axs[1].set_ylabel('fraction of bases sampled >= coverage')
axs[1].legend(fancybox=True, framealpha=0.5)
plt.savefig(args.plotFile, format=args.plotFileFormat)
plt.close()
def main(args=None):
args = process_args(args)
if not args.plotFile and not args.outRawCounts and not args.outQualityMetrics:
sys.stderr.write("\nAt least one of --plotFile, --outRawCounts or --outQualityMetrics is required.\n")
sys.exit(1)
cr = sumR.SumCoveragePerBin(
args.bamfiles,
args.binSize,
args.numberOfSamples,
blackListFileName=args.blackListFileName,
numberOfProcessors=args.numberOfProcessors,
verbose=args.verbose,
region=args.region,
extendReads=args.extendReads,
minMappingQuality=args.minMappingQuality,
ignoreDuplicates=args.ignoreDuplicates,
center_read=args.centerReads,
samFlag_include=args.samFlagInclude,
samFlag_exclude=args.samFlagExclude,
minFragmentLength=args.minFragmentLength,
maxFragmentLength=args.maxFragmentLength)
num_reads_per_bin = cr.run()
if num_reads_per_bin.sum() == 0:
import sys
sys.stderr.write(
"\nNo reads were found in {} regions sampled. Check that the\n"
"min mapping quality is not overly high and that the \n"
"chromosome names between bam files are consistant.\n"
"\n".format(num_reads_per_bin.shape[0]))
exit(1)
if args.skipZeros:
num_reads_per_bin = countR.remove_row_of_zeros(num_reads_per_bin)
total = len(num_reads_per_bin[:, 0])
x = np.arange(total).astype('float') / total # normalize from 0 to 1
if args.plotFile is not None:
i = 0
# matplotlib won't iterate through line styles by itself
pyplot_line_styles = sum([7 * ["-"], 7 * ["--"], 7 * ["-."], 7 * [":"]], [])
plotly_colors = ["#d73027", "#fc8d59", "#f33090", "#e0f3f8", "#91bfdb", "#4575b4"]
plotly_line_styles = sum([6 * ["solid"], 6 * ["dot"], 6 * ["dash"], 6 * ["longdash"], 6 * ["dashdot"], 6 * ["longdashdot"]], [])
data = []
for i, reads in enumerate(num_reads_per_bin.T):
count = np.cumsum(np.sort(reads))
count = count / count[-1] # to normalize y from 0 to 1
if args.plotFileFormat == 'plotly':
trace = go.Scatter(x=x, y=count, mode='lines', name=args.labels[i])
trace['line'].update(dash=plotly_line_styles[i % 36], color=plotly_colors[i % 6])
data.append(trace)
else:
j = i % 35
plt.plot(x, count, label=args.labels[i], linestyle=pyplot_line_styles[j])
plt.xlabel('rank')
plt.ylabel('fraction w.r.t. bin with highest coverage')
# set the plotFileFormat explicitly to None to trigger the
# format from the file-extension
if not args.plotFileFormat:
args.plotFileFormat = None
if args.plotFileFormat == 'plotly':
fig = go.Figure()
fig['data'] = data
fig['layout'].update(title=args.plotTitle)
fig['layout']['xaxis1'].update(title="rank")
fig['layout']['yaxis1'].update(title="fraction w.r.t bin with highest coverage")
py.plot(fig, filename=args.plotFile, auto_open=False)
else:
plt.legend(loc='upper left')
plt.suptitle(args.plotTitle)
plt.savefig(args.plotFile, bbox_inches=0, format=args.plotFileFormat)
plt.close()
if args.outRawCounts is not None:
of = open(args.outRawCounts, "w")
of.write("#plotFingerprint --outRawCounts\n")
of.write("'" + "'\t'".join(args.labels) + "'\n")
fmt = "\t".join(np.repeat('%d', num_reads_per_bin.shape[1])) + "\n"
for row in num_reads_per_bin:
of.write(fmt % tuple(row))
of.close()
if args.outQualityMetrics is not None:
of = open(args.outQualityMetrics, "w")
of.write("Sample\tAUC\tSynthetic AUC\tX-intercept\tSynthetic X-intercept\tElbow Point\tSynthetic Elbow Point")
if args.JSDsample:
of.write("\tJS Distance\tSynthetic JS Distance\t% genome enriched\tdiff. enrichment\tCHANCE divergence")
else:
of.write("\tSynthetic JS Distance")
of.write("\n")
line = np.arange(num_reads_per_bin.shape[0]) / float(num_reads_per_bin.shape[0] - 1)
for idx, reads in enumerate(num_reads_per_bin.T):
counts = np.cumsum(np.sort(reads))
counts = counts / float(counts[-1])
AUC = np.sum(counts) / float(len(counts))
XInt = (np.argmax(counts > 0) + 1) / float(counts.shape[0])
elbow = (np.argmax(line - counts) + 1) / float(counts.shape[0])
expected = getExpected(np.mean(reads)) # A tuple of expected (AUC, XInt, elbow)
of.write("{0}\t{1}\t{2}\t{3}\t{4}\t{5}\t{6}".format(args.labels[idx], AUC, expected[0], XInt, expected[1], elbow, expected[2]))
if args.JSDsample:
JSD = getJSD(args, idx, num_reads_per_bin)
syntheticJSD = getSyntheticJSD(num_reads_per_bin[:, idx])
CHANCE = getCHANCE(args, idx, num_reads_per_bin)
of.write("\t{0}\t{1}\t{2}\t{3}\t{4}".format(JSD, syntheticJSD, CHANCE[0], CHANCE[1], CHANCE[2]))
else:
syntheticJSD = getSyntheticJSD(num_reads_per_bin[:, idx])
of.write("\t{0}".format(syntheticJSD))
of.write("\n")
of.close()
def main(args=None):
args = process_args(args)
if not args.outRawCounts and not args.plotFile and not args.outCoverageMetrics:
sys.exit("At least one of --plotFile, --outRawCounts and --outCoverageMetrics are required.\n")
if 'BED' in args:
bed_regions = args.BED
else:
bed_regions = None
cr = countR.CountReadsPerBin(args.bamfiles,
binLength=1,
bedFile=bed_regions,
numberOfSamples=args.numberOfSamples,
numberOfProcessors=args.numberOfProcessors,
verbose=args.verbose,
region=args.region,
blackListFileName=args.blackListFileName,
extendReads=args.extendReads,
minMappingQuality=args.minMappingQuality,
ignoreDuplicates=args.ignoreDuplicates,
center_read=args.centerReads,
samFlag_include=args.samFlagInclude,
samFlag_exclude=args.samFlagExclude,
minFragmentLength=args.minFragmentLength,
maxFragmentLength=args.maxFragmentLength,
bed_and_bin=True,
out_file_for_raw_data=args.outRawCounts)
num_reads_per_bin = cr.run()
if args.outCoverageMetrics and args.coverageThresholds:
args.coverageThresholds.sort() # Galaxy in particular tends to give things in a weird order
of = open(args.outCoverageMetrics, "w")
of.write("Sample\tThreshold\tPercent\n")
nbins = float(num_reads_per_bin.shape[0])
for thresh in args.coverageThresholds:
vals = np.sum(num_reads_per_bin >= thresh, axis=0)
for lab, val in zip(args.labels, vals):
of.write("{}\t{}\t{:6.3f}\n".format(lab, thresh, 100. * val / nbins))
of.close()
if args.outRawCounts:
# append to the generated file the
# labels
header = "#plotCoverage --outRawCounts\n#'chr'\t'start'\t'end'\t"
header += "'" + "'\t'".join(args.labels) + "'\n"
f = open(args.outRawCounts, 'r+')
content = f.read()
f.seek(0, 0)
f.write(header + content)
f.close()
if num_reads_per_bin.shape[0] < 2:
exit("ERROR: too few non-zero bins found.\n"
"If using --region please check that this "
"region is covered by reads.\n")
if args.skipZeros:
num_reads_per_bin = countR.remove_row_of_zeros(num_reads_per_bin)
if args.plotFile:
if args.plotFileFormat == 'plotly':
fig = go.Figure()
fig['layout']['xaxis1'] = {'domain': [0.0, 0.48], 'anchor': 'x1', 'title': 'coverage (#reads per base)'}
fig['layout']['xaxis2'] = {'domain': [0.52, 1.0], 'anchor': 'x2', 'title': 'coverage (#reads per base)'}
fig['layout']['yaxis1'] = {'domain': [0.0, 1.0], 'anchor': 'x1', 'title': 'fraction of bases sampled'}
fig['layout']['yaxis2'] = {'domain': [0.0, 1.0], 'anchor': 'x2', 'title': 'fraction of bases sampled >= coverage'}
fig['layout'].update(title=args.plotTitle)
else:
fig, axs = plt.subplots(1, 2, figsize=(args.plotWidth, args.plotHeight))
plt.suptitle(args.plotTitle)
# plot up to two std from mean
num_reads_per_bin = num_reads_per_bin.astype(int)
sample_mean = num_reads_per_bin.mean(axis=0)
sample_std = num_reads_per_bin.std(axis=0)
sample_max = num_reads_per_bin.max(axis=0)
sample_min = num_reads_per_bin.min(axis=0)
sample_25 = np.percentile(num_reads_per_bin, 25, axis=0)
sample_50 = np.percentile(num_reads_per_bin, 50, axis=0)
sample_75 = np.percentile(num_reads_per_bin, 75, axis=0)
# use the largest 99th percentile from all samples to set the x_max value
x_max = np.max(np.percentile(num_reads_per_bin, 99, axis=0))
# plot coverage
# print headers for text output
print("sample\tmean\tstd\tmin\t25%\t50%\t75%\tmax")
# the determination of a sensible value for y_max of the first plot (fraction of bases sampled vs.
# coverage) is important because, depending on the data,
# it becomes very difficult to see the lines in the plot. For example, if the coverage of a sample
# is a nice gaussian curve with a large mean of 50. Then a sensible range for the y axis (fraction of
# reads having coverage=x) is (0, 0.02) which nicely shows the coverage curve. If instead the coverage is
# very por and centers close to 1 then a good y axis range is (0,1).
# the current implementation aims to find the y_value for which 50% of the reads >= x (coverage) and
# sets that as the x_axis range.
y_max = []
data = []
# We need to manually set the line colors so they're shared between the two plots.
plotly_colors = ["#d73027", "#fc8d59", "#f33090", "#e0f3f8", "#91bfdb", "#4575b4"]
plotly_styles = sum([6 * ["solid"], 6 * ["dot"], 6 * ["dash"], 6 * ["longdash"], 6 * ["dashdot"], 6 * ["longdashdot"]], [])
for idx, col in enumerate(num_reads_per_bin.T):
if args.plotFile:
frac_reads_per_coverage = np.bincount(col.astype(int)).astype(float) / num_reads_per_bin.shape[0]
csum = np.bincount(col.astype(int))[::-1].cumsum()
csum_frac = csum.astype(float)[::-1] / csum.max()
if args.plotFileFormat == 'plotly':
color = plotly_colors[idx % len(plotly_colors)]
dash = plotly_styles[idx % len(plotly_styles)]
trace = go.Scatter(x=np.arange(0, int(x_max) - 1),
y=frac_reads_per_coverage[:int(x_max)],
mode='lines',
xaxis='x1',
yaxis='y1',
line=dict(color=color, dash=dash),
name="{}, mean={:.1f}".format(args.labels[idx], sample_mean[idx]),
legendgroup="{}".format(idx))
data.append(trace)
trace = go.Scatter(x=np.arange(0, int(x_max) - 1),
y=csum_frac[:int(x_max)],
mode='lines',
xaxis='x2',
yaxis='y2',
line=dict(color=color, dash=dash),
name=args.labels[idx],
showlegend=False,
legendgroup="{}".format(idx))
data.append(trace)
else:
axs[0].plot(frac_reads_per_coverage, label="{}, mean={:.1f}".format(args.labels[idx], sample_mean[idx]))
axs[1].plot(csum_frac, label=args.labels[idx])
# find the indexes (i.e. the x values) for which the cumulative distribution 'fraction of bases
# sampled >= coverage' where fraction of bases sampled = 50%: `np.flatnonzero(csum_frac>0.5)`
# then find the fraction of bases sampled that that have the largest x
y_max.append(frac_reads_per_coverage[max(np.flatnonzero(csum_frac > 0.5))])
print("{}\t{:0.2f}\t{:0.2f}\t{}\t{}\t{}\t{}\t{}\t".format(args.labels[idx],
sample_mean[idx],
sample_std[idx],
sample_min[idx],
sample_25[idx],
sample_50[idx],
sample_75[idx],
sample_max[idx],
))
if args.plotFile:
# Don't clip plots
y_max = max(y_max)
if args.plotFileFormat == "plotly":
fig['data'] = data
fig['layout']['yaxis1'].update(range=[0.0, min(1, y_max + (y_max * 0.10))])
fig['layout']['yaxis2'].update(range=[0.0, 1.0])
py.plot(fig, filename=args.plotFile, auto_open=False)
else:
axs[0].set_ylim(0, min(1, y_max + (y_max * 0.10)))
axs[0].set_xlim(0, x_max)
axs[0].set_xlabel('coverage (#reads per bp)')
axs[0].legend(fancybox=True, framealpha=0.5)
axs[0].set_ylabel('fraction of bases sampled')
# plot cumulative coverage
axs[1].set_xlim(0, x_max)
axs[1].set_xlabel('coverage (#reads per bp)')
axs[1].set_ylabel('fraction of bases sampled >= coverage')
axs[1].legend(fancybox=True, framealpha=0.5)
plt.savefig(args.plotFile, format=args.plotFileFormat)
plt.close()
def main(args=None):
args = process_args(args)
cr = countR.CountReadsPerBin(args.bamfiles,
binLength=1,
numberOfSamples=args.numberOfSamples,
numberOfProcessors=args.numberOfProcessors,
verbose=args.verbose,
region=args.region,
blackListFileName=args.blackListFileName,
extendReads=args.extendReads,
minMappingQuality=args.minMappingQuality,
ignoreDuplicates=args.ignoreDuplicates,
center_read=args.centerReads,
samFlag_include=args.samFlagInclude,
samFlag_exclude=args.samFlagExclude,
minFragmentLength=args.minFragmentLength,
maxFragmentLength=args.maxFragmentLength,
out_file_for_raw_data=args.outRawCounts)
num_reads_per_bin = cr.run()
sys.stderr.write("Number of non zero bins "
"used: {}\n".format(num_reads_per_bin.shape[0]))
if args.outRawCounts:
# append to the generated file the
# labels
header = "#'chr'\t'start'\t'end'\t"
header += "'" + "'\t'".join(args.labels) + "'\n"
f = open(args.outRawCounts, 'r+')
content = f.read()
f.seek(0, 0)
f.write(header + content)
f.close()
if num_reads_per_bin.shape[0] < 2:
exit("ERROR: too few non-zero bins found.\n"
"If using --region please check that this "
"region is covered by reads.\n")
if args.skipZeros:
num_reads_per_bin = countR.remove_row_of_zeros(num_reads_per_bin)
fig, axs = plt.subplots(1, 2, figsize=(15, 5))
plt.suptitle(args.plotTitle)
# plot up to two std from mean
num_reads_per_bin = num_reads_per_bin.astype(int)
sample_mean = num_reads_per_bin.mean(axis=0)
sample_std = num_reads_per_bin.std(axis=0)
sample_max = num_reads_per_bin.max(axis=0)
sample_min = num_reads_per_bin.min(axis=0)
sample_25 = np.percentile(num_reads_per_bin, 25, axis=0)
sample_50 = np.percentile(num_reads_per_bin, 50, axis=0)
sample_75 = np.percentile(num_reads_per_bin, 75, axis=0)
# use the largest 99th percentile from all samples to set the x_max value
x_max = np.max(np.percentile(num_reads_per_bin, 99, axis=0))
# plot coverage
# print headers for text output
print("sample\tmean\tstd\tmin\t25%\t50%\t75%\tmax")
# the determination of a sensible value for y_max of the first plot (fraction of bases sampled vs.
# coverage) is important because, depending on the data,
# it becomes very difficult to see the lines in the plot. For example, if the coverage of a sample
# is a nice gaussian curve with a large mean of 50. Then a sensible range for the y axis (fraction of
# reads having coverage=x) is (0, 0.02) which nicely shows the coverage curve. If instead the coverage is
# very por and centers close to 1 then a good y axis range is (0,1).
# the current implementation aims to find the y_value for which 50% of the reads >= x (coverage) and
# sets that as the x_axis range.
y_max = []
for idx, col in enumerate(num_reads_per_bin.T):
frac_reads_per_coverage = np.bincount(col.astype(int)).astype(float) / num_reads_per_bin.shape[0]
axs[0].plot(frac_reads_per_coverage, label="{}, mean={:.1f}".format(args.labels[idx], sample_mean[idx]))
csum = np.bincount(col.astype(int))[::-1].cumsum()
csum_frac = csum.astype(float)[::-1] / csum.max()
axs[1].plot(csum_frac, label=args.labels[idx])
# find the indexes (i.e. the x values) for which the cumulative distribution 'fraction of bases
# sampled >= coverage' where fraction of bases sampled = 50%: `np.flatnonzero(csum_frac>0.5)`
# then find the fraction of bases sampled that that have the largest x
y_max.append(frac_reads_per_coverage[max(np.flatnonzero(csum_frac > 0.5))])
print("{}\t{:0.2f}\t{:0.2f}\t{}\t{}\t{}\t{}\t{}\t".format(args.labels[idx],
sample_mean[idx],
sample_std[idx],
sample_min[idx],
sample_25[idx],
sample_50[idx],
sample_75[idx],
sample_max[idx],
))
# The 'good' x-axis is computed for each sample. The lower value is favored in which
# distributions with a wider x-range can better be seen.
y_max = min(y_max)
axs[0].set_ylim(0, min(1, y_max + (y_max * 0.10)))
axs[0].set_xlim(0, x_max)
axs[0].set_xlabel('coverage (#reads per bp)')
axs[0].legend(fancybox=True, framealpha=0.5)
axs[0].set_ylabel('fraction of bases sampled')
# plot cumulative coverage
axs[1].set_xlim(0, x_max)
axs[1].set_xlabel('coverage (#reads per bp)')
axs[1].set_ylabel('fraction of bases sampled >= coverage')
axs[1].legend(fancybox=True, framealpha=0.5)
plt.savefig(args.plotFile, format=args.plotFileFormat)
plt.close()
def main(args=None):
args = process_args(args)
if not args.plotFile and not args.outRawCounts and not args.outQualityMetrics:
sys.stderr.write(
"\nAt least one of --plotFile, --outRawCounts or --outQualityMetrics is required.\n"
)
sys.exit(1)
cr = sumR.SumCoveragePerBin(args.bamfiles,
args.binSize,
args.numberOfSamples,
blackListFileName=args.blackListFileName,
numberOfProcessors=args.numberOfProcessors,
verbose=args.verbose,
region=args.region,
extendReads=args.extendReads,
minMappingQuality=args.minMappingQuality,
ignoreDuplicates=args.ignoreDuplicates,
center_read=args.centerReads,
samFlag_include=args.samFlagInclude,
samFlag_exclude=args.samFlagExclude,
minFragmentLength=args.minFragmentLength,
maxFragmentLength=args.maxFragmentLength)
num_reads_per_bin = cr.run()
if num_reads_per_bin.sum() == 0:
import sys
sys.stderr.write(
"\nNo reads were found in {} regions sampled. Check that the\n"
"min mapping quality is not overly high and that the \n"
"chromosome names between bam files are consistant.\n"
"\n".format(num_reads_per_bin.shape[0]))
exit(1)
if args.skipZeros:
num_reads_per_bin = countR.remove_row_of_zeros(num_reads_per_bin)
total = len(num_reads_per_bin[:, 0])
x = np.arange(total).astype('float') / total # normalize from 0 to 1
if args.plotFile:
i = 0
# matplotlib won't iterate through line styles by itself
pyplot_line_styles = sum(
[7 * ["-"], 7 * ["--"], 7 * ["-."], 7 * [":"]], [])
for i, reads in enumerate(num_reads_per_bin.T):
count = np.cumsum(np.sort(reads))
count = count / count[-1] # to normalize y from 0 to 1
j = i % 35
plt.plot(x,
count,
label=args.labels[i],
linestyle=pyplot_line_styles[j])
plt.xlabel('rank')
plt.ylabel('fraction w.r.t. bin with highest coverage')
plt.legend(loc='upper left')
plt.suptitle(args.plotTitle)
# set the plotFileFormat explicitly to None to trigger the
# format from the file-extension
if not args.plotFileFormat:
args.plotFileFormat = None
plt.savefig(args.plotFile.name,
bbox_inches=0,
format=args.plotFileFormat)
plt.close()
if args.outRawCounts:
args.outRawCounts.write("'" + "'\t'".join(args.labels) + "'\n")
fmt = "\t".join(np.repeat('%d', num_reads_per_bin.shape[1])) + "\n"
for row in num_reads_per_bin:
args.outRawCounts.write(fmt % tuple(row))
args.outRawCounts.close()
if args.outQualityMetrics:
args.outQualityMetrics.write(
"Sample\tAUC\tSynthetic AUC\tX-intercept\tSynthetic X-intercept\tElbow Point\tSynthetic Elbow Point"
)
if args.JSDsample:
args.outQualityMetrics.write(
"\tJS Distance\tSynthetic JS Distance\t% genome enriched\tdiff. enrichment\tCHANCE divergence"
)
args.outQualityMetrics.write("\n")
line = np.arange(
num_reads_per_bin.shape[0]) / float(num_reads_per_bin.shape[0] - 1)
for idx, reads in enumerate(num_reads_per_bin.T):
counts = np.cumsum(np.sort(reads))
counts = counts / float(counts[-1])
AUC = np.sum(counts) / float(len(counts))
XInt = (np.argmax(counts > 0) + 1) / float(counts.shape[0])
elbow = (np.argmax(line - counts) + 1) / float(counts.shape[0])
expected = getExpected(
np.mean(reads)) # A tuple of expected (AUC, XInt, elbow)
args.outQualityMetrics.write(
"{0}\t{1}\t{2}\t{3}\t{4}\t{5}\t{6}".format(
args.labels[idx], AUC, expected[0], XInt, expected[1],
elbow, expected[2]))
if args.JSDsample:
JSD = getJSD(args, idx, num_reads_per_bin)
syntheticJSD = getSyntheticJSD(num_reads_per_bin[:, idx])
CHANCE = getCHANCE(args, idx, num_reads_per_bin)
args.outQualityMetrics.write(
"\t{0}\t{1}\t{2}\t{3}\t{4}".format(JSD, syntheticJSD,
CHANCE[0], CHANCE[1],
CHANCE[2]))
args.outQualityMetrics.write("\n")
args.outQualityMetrics.close()
def main(args=None):
args = process_args(args)
cr = countR.CountReadsPerBin(args.bamfiles,
binLength=1,
numberOfSamples=args.numberOfSamples,
numberOfProcessors=args.numberOfProcessors,
verbose=args.verbose,
region=args.region,
blackListFileName=args.blackListFileName,
extendReads=args.extendReads,
minMappingQuality=args.minMappingQuality,
ignoreDuplicates=args.ignoreDuplicates,
center_read=args.centerReads,
samFlag_include=args.samFlagInclude,
samFlag_exclude=args.samFlagExclude,
minFragmentLength=args.minFragmentLength,
maxFragmentLength=args.maxFragmentLength,
out_file_for_raw_data=args.outRawCounts)
num_reads_per_bin = cr.run()
sys.stderr.write("Number of non zero bins "
"used: {}\n".format(num_reads_per_bin.shape[0]))
if args.outRawCounts:
# append to the generated file the
# labels
header = "#'chr'\t'start'\t'end'\t"
header += "'" + "'\t'".join(args.labels) + "'\n"
f = open(args.outRawCounts, 'r+')
content = f.read()
f.seek(0, 0)
f.write(header + content)
f.close()
if num_reads_per_bin.shape[0] < 2:
exit("ERROR: too few non-zero bins found.\n"
"If using --region please check that this "
"region is covered by reads.\n")
if args.skipZeros:
num_reads_per_bin = countR.remove_row_of_zeros(num_reads_per_bin)
fig, axs = plt.subplots(1, 2, figsize=(15, 5))
plt.suptitle(args.plotTitle)
# plot up to two std from mean
num_reads_per_bin = num_reads_per_bin.astype(int)
sample_mean = num_reads_per_bin.mean(axis=0)
sample_std = num_reads_per_bin.std(axis=0)
sample_max = num_reads_per_bin.max(axis=0)
sample_min = num_reads_per_bin.min(axis=0)
sample_25 = np.percentile(num_reads_per_bin, 25, axis=0)
sample_50 = np.percentile(num_reads_per_bin, 50, axis=0)
sample_75 = np.percentile(num_reads_per_bin, 75, axis=0)
# use the largest 99th percentile from all samples to set the x_max value
x_max = np.max(np.percentile(num_reads_per_bin, 99, axis=0))
# plot coverage
# print headers for text output
print("sample\tmean\tstd\tmin\t25%\t50%\t75%\tmax")
# the determination of a sensible value for y_max of the first plot (fraction of bases sampled vs.
# coverage) is important because, depending on the data,
# it becomes very difficult to see the lines in the plot. For example, if the coverage of a sample
# is a nice gaussian curve with a large mean of 50. Then a sensible range for the y axis (fraction of
# reads having coverage=x) is (0, 0.02) which nicely shows the coverage curve. If instead the coverage is
# very por and centers close to 1 then a good y axis range is (0,1).
# the current implementation aims to find the y_value for which 50% of the reads >= x (coverage) and
# sets that as the x_axis range.
y_max = []
for idx, col in enumerate(num_reads_per_bin.T):
frac_reads_per_coverage = np.bincount(
col.astype(int)).astype(float) / num_reads_per_bin.shape[0]
axs[0].plot(frac_reads_per_coverage,
label="{}, mean={:.1f}".format(args.labels[idx],
sample_mean[idx]))
csum = np.bincount(col.astype(int))[::-1].cumsum()
csum_frac = csum.astype(float)[::-1] / csum.max()
axs[1].plot(csum_frac, label=args.labels[idx])
# find the indexes (i.e. the x values) for which the cumulative distribution 'fraction of bases
# sampled >= coverage' where fraction of bases sampled = 50%: `np.flatnonzero(csum_frac>0.5)`
# then find the fraction of bases sampled that that have the largest x
y_max.append(frac_reads_per_coverage[max(
np.flatnonzero(csum_frac > 0.5))])
print("{}\t{:0.2f}\t{:0.2f}\t{}\t{}\t{}\t{}\t{}\t".format(
args.labels[idx],
sample_mean[idx],
sample_std[idx],
sample_min[idx],
sample_25[idx],
sample_50[idx],
sample_75[idx],
sample_max[idx],
))
# The 'good' x-axis is computed for each sample. The lower value is favored in which
# distributions with a wider x-range can better be seen.
y_max = min(y_max)
axs[0].set_ylim(0, min(1, y_max + (y_max * 0.10)))
axs[0].set_xlim(0, x_max)
axs[0].set_xlabel('coverage (#reads per bp)')
axs[0].legend(fancybox=True, framealpha=0.5)
axs[0].set_ylabel('fraction of bases sampled')
# plot cumulative coverage
axs[1].set_xlim(0, x_max)
axs[1].set_xlabel('coverage (#reads per bp)')
axs[1].set_ylabel('fraction of bases sampled >= coverage')
axs[1].legend(fancybox=True, framealpha=0.5)
plt.savefig(args.plotFile, format=args.plotFileFormat)
plt.close()
def main(args=None):
args = process_args(args)
cr = sumR.SumCoveragePerBin(
args.bamfiles,
args.binSize,
args.numberOfSamples,
blackListFileName=args.blackListFileName,
numberOfProcessors=args.numberOfProcessors,
verbose=args.verbose,
region=args.region,
extendReads=args.extendReads,
minMappingQuality=args.minMappingQuality,
ignoreDuplicates=args.ignoreDuplicates,
center_read=args.centerReads,
samFlag_include=args.samFlagInclude,
samFlag_exclude=args.samFlagExclude,
minFragmentLength=args.minFragmentLength,
maxFragmentLength=args.maxFragmentLength)
num_reads_per_bin = cr.run()
if num_reads_per_bin.sum() == 0:
import sys
sys.stderr.write(
"\nNo reads were found in {} regions sampled. Check that the\n"
"min mapping quality is not overly high and that the \n"
"chromosome names between bam files are consistant.\n"
"\n".format(num_reads_per_bin.shape[0]))
exit(1)
if args.skipZeros:
num_reads_per_bin = countR.remove_row_of_zeros(num_reads_per_bin)
total = len(num_reads_per_bin[:, 0])
x = np.arange(total).astype('float') / total # normalize from 0 to 1
i = 0
# matplotlib won't iterate through line styles by itself
pyplot_line_styles = sum([7 * ["-"], 7 * ["--"], 7 * ["-."], 7 * [":"], 7 * ["."]], [])
for i, reads in enumerate(num_reads_per_bin.T):
count = np.cumsum(np.sort(reads))
count = count / count[-1] # to normalize y from 0 to 1
j = i % 35
plt.plot(x, count, label=args.labels[i], linestyle=pyplot_line_styles[j])
plt.xlabel('rank')
plt.ylabel('fraction w.r.t. bin with highest coverage')
plt.legend(loc='upper left')
plt.suptitle(args.plotTitle)
# set the plotFileFormat explicitly to None to trigger the
# format from the file-extension
if not args.plotFileFormat:
args.plotFileFormat = None
plt.savefig(args.plotFile.name, bbox_inches=0, format=args.plotFileFormat)
plt.close()
if args.outRawCounts:
args.outRawCounts.write("'" + "'\t'".join(args.labels) + "'\n")
fmt = "\t".join(np.repeat('%d', num_reads_per_bin.shape[1])) + "\n"
for row in num_reads_per_bin:
args.outRawCounts.write(fmt % tuple(row))
args.outRawCounts.close()
if args.outQualityMetrics:
args.outQualityMetrics.write("Sample\tAUC\tSynthetic AUC\tX-intercept\tSynthetic X-intercept\tElbow Point\tSynthetic Elbow Point")
if args.JSDsample:
args.outQualityMetrics.write("\tJS Distance\tSynthetic JS Distance\t% genome enriched\tdiff. enrichment\tCHANCE divergence")
args.outQualityMetrics.write("\n")
line = np.arange(num_reads_per_bin.shape[0]) / float(num_reads_per_bin.shape[0] - 1)
for idx, reads in enumerate(num_reads_per_bin.T):
counts = np.cumsum(np.sort(reads))
counts = counts / float(counts[-1])
AUC = np.sum(counts) / float(len(counts))
XInt = (np.argmax(counts > 0) + 1) / float(counts.shape[0])
elbow = (np.argmax(line - counts) + 1) / float(counts.shape[0])
expected = getExpected(np.mean(reads)) # A tuple of expected (AUC, XInt, elbow)
args.outQualityMetrics.write("{0}\t{1}\t{2}\t{3}\t{4}\t{5}\t{6}".format(args.labels[idx], AUC, expected[0], XInt, expected[1], elbow, expected[2]))
if args.JSDsample:
JSD = getJSD(args, idx, num_reads_per_bin)
syntheticJSD = getSyntheticJSD(num_reads_per_bin[:, idx])
CHANCE = getCHANCE(args, idx, num_reads_per_bin)
args.outQualityMetrics.write("\t{0}\t{1}\t{2}\t{3}\t{4}".format(JSD, syntheticJSD, CHANCE[0], CHANCE[1], CHANCE[2]))
args.outQualityMetrics.write("\n")
args.outQualityMetrics.close()
def main(args=None):
args = process_args(args)
if not args.plotFile and not args.outRawCounts and not args.outQualityMetrics:
sys.stderr.write("\nAt least one of --plotFile, --outRawCounts or --outQualityMetrics is required.\n")
sys.exit(1)
cr = sumR.SumCoveragePerBin(
args.bamfiles,
args.binSize,
args.numberOfSamples,
blackListFileName=args.blackListFileName,
numberOfProcessors=args.numberOfProcessors,
verbose=args.verbose,
region=args.region,
extendReads=args.extendReads,
minMappingQuality=args.minMappingQuality,
ignoreDuplicates=args.ignoreDuplicates,
center_read=args.centerReads,
samFlag_include=args.samFlagInclude,
samFlag_exclude=args.samFlagExclude,
minFragmentLength=args.minFragmentLength,
maxFragmentLength=args.maxFragmentLength)
num_reads_per_bin = cr.run()
if num_reads_per_bin.sum() == 0:
import sys
sys.stderr.write(
"\nNo reads were found in {} regions sampled. Check that the\n"
"min mapping quality is not overly high and that the \n"
"chromosome names between bam files are consistant.\n"
"For small genomes, decrease the --numberOfSamples.\n"
"\n".format(num_reads_per_bin.shape[0]))
exit(1)
if args.skipZeros:
num_reads_per_bin = countR.remove_row_of_zeros(num_reads_per_bin)
total = len(num_reads_per_bin[:, 0])
x = np.arange(total).astype('float') / total # normalize from 0 to 1
if args.plotFile is not None:
i = 0
# matplotlib won't iterate through line styles by itself
pyplot_line_styles = sum([7 * ["-"], 7 * ["--"], 7 * ["-."], 7 * [":"]], [])
plotly_colors = ["#d73027", "#fc8d59", "#f33090", "#e0f3f8", "#91bfdb", "#4575b4"]
plotly_line_styles = sum([6 * ["solid"], 6 * ["dot"], 6 * ["dash"], 6 * ["longdash"], 6 * ["dashdot"], 6 * ["longdashdot"]], [])
data = []
for i, reads in enumerate(num_reads_per_bin.T):
count = np.cumsum(np.sort(reads))
count = count / count[-1] # to normalize y from 0 to 1
if args.plotFileFormat == 'plotly':
trace = go.Scatter(x=x, y=count, mode='lines', name=args.labels[i])
trace['line'].update(dash=plotly_line_styles[i % 36], color=plotly_colors[i % 6])
data.append(trace)
else:
j = i % len(pyplot_line_styles)
plt.plot(x, count, label=args.labels[i], linestyle=pyplot_line_styles[j])
plt.xlabel('rank')
plt.ylabel('fraction w.r.t. bin with highest coverage')
# set the plotFileFormat explicitly to None to trigger the
# format from the file-extension
if not args.plotFileFormat:
args.plotFileFormat = None
if args.plotFileFormat == 'plotly':
fig = go.Figure()
fig['data'] = data
fig['layout'].update(title=args.plotTitle)
fig['layout']['xaxis1'].update(title="rank")
fig['layout']['yaxis1'].update(title="fraction w.r.t bin with highest coverage")
py.plot(fig, filename=args.plotFile, auto_open=False)
else:
plt.legend(loc='upper left')
plt.suptitle(args.plotTitle)
plt.savefig(args.plotFile, bbox_inches=0, format=args.plotFileFormat)
plt.close()
if args.outRawCounts is not None:
of = open(args.outRawCounts, "w")
of.write("#plotFingerprint --outRawCounts\n")
of.write("'" + "'\t'".join(args.labels) + "'\n")
fmt = "\t".join(np.repeat('%d', num_reads_per_bin.shape[1])) + "\n"
for row in num_reads_per_bin:
of.write(fmt % tuple(row))
of.close()
if args.outQualityMetrics is not None:
of = open(args.outQualityMetrics, "w")
of.write("Sample\tAUC\tSynthetic AUC\tX-intercept\tSynthetic X-intercept\tElbow Point\tSynthetic Elbow Point")
if args.JSDsample:
of.write("\tJS Distance\tSynthetic JS Distance\t% genome enriched\tdiff. enrichment\tCHANCE divergence")
else:
of.write("\tSynthetic JS Distance")
of.write("\n")
line = np.arange(num_reads_per_bin.shape[0]) / float(num_reads_per_bin.shape[0] - 1)
for idx, reads in enumerate(num_reads_per_bin.T):
counts = np.cumsum(np.sort(reads))
counts = counts / float(counts[-1])
AUC = np.sum(counts) / float(len(counts))
XInt = (np.argmax(counts > 0) + 1) / float(counts.shape[0])
elbow = (np.argmax(line - counts) + 1) / float(counts.shape[0])
expected = getExpected(np.mean(reads)) # A tuple of expected (AUC, XInt, elbow)
of.write("{0}\t{1}\t{2}\t{3}\t{4}\t{5}\t{6}".format(args.labels[idx], AUC, expected[0], XInt, expected[1], elbow, expected[2]))
if args.JSDsample:
JSD = getJSD(args, idx, num_reads_per_bin)
syntheticJSD = getSyntheticJSD(num_reads_per_bin[:, idx])
CHANCE = getCHANCE(args, idx, num_reads_per_bin)
of.write("\t{0}\t{1}\t{2}\t{3}\t{4}".format(JSD, syntheticJSD, CHANCE[0], CHANCE[1], CHANCE[2]))
else:
syntheticJSD = getSyntheticJSD(num_reads_per_bin[:, idx])
of.write("\t{0}".format(syntheticJSD))
of.write("\n")
of.close()
def main(args=None):
args = process_args(args)
cr = countR.CountReadsPerBin(args.bamfiles,
binLength=1,
numberOfSamples=args.numberOfSamples,
numberOfProcessors=args.numberOfProcessors,
verbose=args.verbose,
region=args.region,
extendReads=args.extendReads,
minMappingQuality=args.minMappingQuality,
ignoreDuplicates=args.ignoreDuplicates,
center_read=args.centerReads,
samFlag_include=args.samFlagInclude,
samFlag_exclude=args.samFlagExclude)
num_reads_per_bin = cr.run()
sys.stderr.write("Number of non zero bins "
"used: {}\n".format(num_reads_per_bin.shape[0]))
if num_reads_per_bin.shape[0] < 2:
exit("ERROR: too few non zero bins found.\n"
"If using --region please check that this "
"region is covered by reads.\n")
if args.skipZeros:
num_reads_per_bin = countR.remove_row_of_zeros(num_reads_per_bin)
if args.outRawCounts:
args.outRawCounts.write("'" + "'\t'".join(args.labels) + "'\n")
fmt = "\t".join(np.repeat('%d', num_reads_per_bin.shape[1])) + "\n"
for row in num_reads_per_bin:
args.outRawCounts.write(fmt % tuple(row))
fig, axs = plt.subplots(1, 2, figsize=(15, 5))
plt.suptitle(args.plotTitle)
# plot up to two std from mean
sample_mean = num_reads_per_bin.mean(axis=0)
std = max(num_reads_per_bin.std(axis=0))
y_max = max(sample_mean) + 3 * std
# plot coverage
for idx, col in enumerate(num_reads_per_bin.T):
axs[0].plot(np.bincount(col.astype(int)).astype(float) /
num_reads_per_bin.shape[0],
label="{}, mean={:.1f}".format(args.labels[idx],
sample_mean[idx]))
csum = np.bincount(col.astype(int))[::-1].cumsum()
axs[1].plot(csum.astype(float)[::-1] / csum.max(),
label=args.labels[idx])
axs[0].set_xlim(0, y_max)
axs[0].set_xlabel('coverage')
axs[0].legend()
axs[0].set_ylabel('fraction of bases sampled')
# plot cumulative coverage
axs[1].set_xlim(0, y_max)
axs[1].set_xlabel('coverage')
axs[1].set_ylabel('fraction of bases sampled >= coverage')
axs[1].legend()
plt.savefig(args.plotFile.name, format=args.plotFileFormat)