def getPositionsToSample(chrom, start, end, stepSize):
"""
check if the region submitted to the worker
overlaps with the region to take extra effort to sample.
If that is the case, the regions to sample array is
increased to match each of the positions in the extra
effort region sampled at the same stepSize along the interval.
If a filter out tree is given, then from positions to sample
those regions are cleaned
"""
positions_to_sample = np.arange(start, end, stepSize)
if global_vars['filter_out']:
filter_out_tree = GTF(global_vars['filter_out'])
else:
filter_out_tree = None
if global_vars['extra_sampling_file']:
extra_tree = GTF(global_vars['extra_sampling_file'])
else:
extra_tree = None
if extra_tree:
orig_len = len(positions_to_sample)
try:
extra_match = extra_tree.findOverlaps(chrom, start, end)
except KeyError:
extra_match = []
if len(extra_match) > 0:
for intval in extra_match:
positions_to_sample = np.append(positions_to_sample,
list(range(intval[0], intval[1], stepSize)))
# remove duplicates
positions_to_sample = np.unique(np.sort(positions_to_sample))
if debug:
print("sampling increased to {} from {}".format(
len(positions_to_sample),
orig_len))
# skip regions that are filtered out
if filter_out_tree:
try:
out_match = filter_out_tree.findOverlaps(chrom, start, end)
except KeyError:
out_match = []
if len(out_match) > 0:
for intval in out_match:
positions_to_sample = \
positions_to_sample[
(positions_to_sample < intval[0]) |
(positions_to_sample >= intval[1])]
return positions_to_sample
def getPositionsToSample(chrom, start, end, stepSize):
"""
check if the region submitted to the worker
overlaps with the region to take extra effort to sample.
If that is the case, the regions to sample array is
increased to match each of the positions in the extra
effort region sampled at the same stepSize along the interval.
If a filter out tree is given, then from positions to sample
those regions are cleaned
"""
positions_to_sample = np.arange(start, end, stepSize)
if global_vars['filter_out']:
filter_out_tree = GTF(global_vars['filter_out'])
else:
filter_out_tree = None
if global_vars['extra_sampling_file']:
extra_tree = GTF(global_vars['extra_sampling_file'])
else:
extra_tree = None
if extra_tree:
orig_len = len(positions_to_sample)
try:
extra_match = extra_tree.findOverlaps(chrom, start, end)
except KeyError:
extra_match = []
if len(extra_match) > 0:
for intval in extra_match:
positions_to_sample = np.append(positions_to_sample,
list(range(intval[0], intval[1], stepSize)))
# remove duplicates
positions_to_sample = np.unique(np.sort(positions_to_sample))
if debug:
print("sampling increased to {} from {}".format(
len(positions_to_sample),
orig_len))
# skip regions that are filtered out
if filter_out_tree:
try:
out_match = filter_out_tree.findOverlaps(chrom, start, end)
except KeyError:
out_match = []
if len(out_match) > 0:
for intval in out_match:
positions_to_sample = \
positions_to_sample[
(positions_to_sample < intval[0]) |
(positions_to_sample >= intval[1])]
return positions_to_sample
def bam_blacklisted_reads(bam_handle, chroms_to_ignore, blackListFileName=None, numberOfProcessors=1):
blacklisted = 0
if blackListFileName is None:
return blacklisted
# Get the chromosome lengths
chromLens = {}
lines = pysam.idxstats(bam_handle.filename)
lines = toString(lines)
if type(lines) is str:
lines = lines.strip().split('\n')
for line in lines:
chrom, _len, nmapped, _nunmapped = line.split('\t')
chromLens[chrom] = int(_len)
bl = GTF(blackListFileName)
regions = []
for chrom in bl.chroms:
if (not chroms_to_ignore or chrom not in chroms_to_ignore) and chrom in chromLens:
for reg in bl.findOverlaps(chrom, 0, chromLens[chrom]):
regions.append([bam_handle.filename, chrom, reg[0], reg[1]])
if len(regions) > 0:
import multiprocessing
if len(regions) > 1 and numberOfProcessors > 1:
pool = multiprocessing.Pool(numberOfProcessors)
res = pool.map_async(bam_blacklisted_worker, regions).get(9999999)
else:
res = [bam_blacklisted_worker(x) for x in regions]
for val in res:
blacklisted += val
return blacklisted
def bam_blacklisted_reads(bam_handle, chroms_to_ignore, blackListFileName=None, numberOfProcessors=1):
blacklisted = 0
if blackListFileName is None:
return blacklisted
# Get the chromosome lengths
chromLens = {}
lines = pysam.idxstats(bam_handle.filename)
lines = toString(lines)
if type(lines) is str:
lines = lines.strip().split('\n')
for line in lines:
chrom, _len, nmapped, _nunmapped = line.split('\t')
chromLens[chrom] = int(_len)
bl = GTF(blackListFileName)
regions = []
for chrom in bl.chroms:
if (not chroms_to_ignore or chrom not in chroms_to_ignore) and chrom in chromLens:
for reg in bl.findOverlaps(chrom, 0, chromLens[chrom]):
regions.append([bam_handle.filename, chrom, reg[0], reg[1]])
if len(regions) > 0:
import multiprocessing
if len(regions) > 1 and numberOfProcessors > 1:
pool = multiprocessing.Pool(numberOfProcessors)
res = pool.map_async(bam_blacklisted_worker, regions).get(9999999)
else:
res = [bam_blacklisted_worker(x) for x in regions]
for val in res:
blacklisted += val
return blacklisted
def bam_blacklisted_reads(bam_handle, chroms_to_ignore, blackListFileName=None, numberOfProcessors=1):
blacklisted = 0
if blackListFileName is None:
return blacklisted
# Get the chromosome lengths
chromLens = {x: y for x, y in zip(bam_handle.references, bam_handle.lengths)}
bl = GTF(blackListFileName)
hasOverlaps, minOverlap = bl.hasOverlaps(returnDistance=True)
if hasOverlaps:
sys.exit("Your blacklist file(s) has (have) regions that overlap. Proceeding with such a file would result in deepTools incorrectly calculating scaling factors. As such, you MUST fix this issue before being able to proceed.\n")
if minOverlap < 1000:
sys.stderr.write("WARNING: The minimum distance between intervals in your blacklist is {}. It makes little biological sense to include small regions between two blacklisted regions. Instead, these should likely be blacklisted as well.\n".format(minOverlap))
regions = []
for chrom in bl.chroms:
if (not chroms_to_ignore or chrom not in chroms_to_ignore) and chrom in chromLens:
for reg in bl.findOverlaps(chrom, 0, chromLens[chrom]):
regions.append([bam_handle.filename, chrom, reg[0], reg[1]])
if len(regions) > 0:
import multiprocessing
if len(regions) > 1 and numberOfProcessors > 1:
pool = multiprocessing.Pool(numberOfProcessors)
res = pool.map_async(bam_blacklisted_worker, regions).get(9999999)
else:
res = [bam_blacklisted_worker(x) for x in regions]
for val in res:
blacklisted += val
return blacklisted
def makeRegions(BED, args):
"""
Given a list of BED/GTF files, make a list of regions.
These are vaguely extended as appropriate. For simplicity, the maximum of --beforeRegionStartLength
and --afterRegionStartLength are tacked on to each end and transcripts are used for GTF files.
"""
itree = GTF(BED, transcriptID=args.transcriptID, transcript_id_designator=args.transcript_id_designator)
o = []
extend = 0
# The before/after stuff is specific to computeMatrix
if "beforeRegionsStartLength" in args:
extend = max(args.beforeRegionsStartLength, args.afterRegionsStartLength)
for chrom in itree.chroms:
regs = itree.findOverlaps(chrom, 0, 4294967295) # bigWig files use 32 bit coordinates
for reg in regs:
o.append([chrom, max(0, reg[0] - extend), reg[1] + extend])
del itree
return o
def bam_blacklisted_reads(bam_handle,
chroms_to_ignore,
blackListFileName=None,
numberOfProcessors=1):
blacklisted = 0
if blackListFileName is None:
return blacklisted
# Get the chromosome lengths
chromLens = {
x: y
for x, y in zip(bam_handle.references, bam_handle.lengths)
}
bl = GTF(blackListFileName)
hasOverlaps, minOverlap = bl.hasOverlaps(returnDistance=True)
if hasOverlaps:
sys.exit(
"Your blacklist file(s) has (have) regions that overlap. Proceeding with such a file would result in deepTools incorrectly calculating scaling factors. As such, you MUST fix this issue before being able to proceed.\n"
)
if minOverlap < 1000:
sys.stderr.write(
"WARNING: The minimum distance between intervals in your blacklist is {}. It makes little biological sense to include small regions between two blacklisted regions. Instead, these should likely be blacklisted as well.\n"
.format(minOverlap))
regions = []
for chrom in bl.chroms:
if (not chroms_to_ignore
or chrom not in chroms_to_ignore) and chrom in chromLens:
for reg in bl.findOverlaps(chrom, 0, chromLens[chrom]):
regions.append([bam_handle.filename, chrom, reg[0], reg[1]])
if len(regions) > 0:
import multiprocessing
if len(regions) > 1 and numberOfProcessors > 1:
pool = multiprocessing.Pool(numberOfProcessors)
res = pool.map_async(bam_blacklisted_worker, regions).get(9999999)
else:
res = [bam_blacklisted_worker(x) for x in regions]
for val in res:
blacklisted += val
return blacklisted
def makeRegions(BED, args):
"""
Given a list of BED/GTF files, make a list of regions.
These are vaguely extended as appropriate. For simplicity, the maximum of --beforeRegionStartLength
and --afterRegionStartLength are tacked on to each end and transcripts are used for GTF files.
"""
itree = GTF(BED,
transcriptID=args.transcriptID,
transcript_id_designator=args.transcript_id_designator)
o = []
extend = 0
# The before/after stuff is specific to computeMatrix
if "beforeRegionStartLength" in args:
extend = max(args.beforeRegionStartLength, args.afterRegionStartLength)
for chrom in itree.chroms:
regs = itree.findOverlaps(
chrom, 0, 4294967295) # bigWig files use 32 bit coordinates
for reg in regs:
o.append([chrom, max(0, reg[0] - extend), reg[1] + extend])
del itree
return o
def count_reads_in_region(self, chrom, start, end, bed_regions_list=None):
"""Counts the reads in each bam file at each 'stepSize' position
within the interval (start, end) for a window or bin of size binLength.
The stepSize controls the distance between bins. For example,
a step size of 20 and a bin size of 20 will create bins next to
each other. If the step size is smaller than the bin size the
bins will overlap.
If a list of bedRegions is given, then the number of reads
that overlaps with each region is counted.
Parameters
----------
chrom : str
Chrom name
start : int
start coordinate
end : int
end coordinate
bed_regions_list: list
List of list of tuples of the form (start, end)
corresponding to bed regions to be processed.
If not bed file was passed to the object constructor
then this list is empty.
Returns
-------
numpy array
The result is a numpy array that as rows each bin
and as columns each bam file.
Examples
--------
Initialize some useful values
>>> test = Tester()
>>> c = CountReadsPerBin([test.bamFile1, test.bamFile2], 25, 0, stepSize=50)
The transpose is used to get better looking numbers. The first line
corresponds to the number of reads per bin in the first bamfile.
>>> _array, __ = c.count_reads_in_region(test.chrom, 0, 200)
>>> _array
array([[0., 0.],
[0., 1.],
[1., 1.],
[1., 2.]])
"""
if start > end:
raise NameError("start %d bigger that end %d" % (start, end))
if self.stepSize is None and bed_regions_list is None:
raise ValueError("stepSize is not set!")
# array to keep the read counts for the regions
subnum_reads_per_bin = []
start_time = time.time()
bam_handles = []
for fname in self.bamFilesList:
try:
bam_handles.append(bamHandler.openBam(fname))
except SystemExit:
sys.exit(sys.exc_info()[1])
except:
bam_handles.append(pyBigWig.open(fname))
blackList = None
if self.blackListFileName is not None:
blackList = GTF(self.blackListFileName)
# A list of lists of tuples
transcriptsToConsider = []
if bed_regions_list is not None:
transcriptsToConsider = [x[1] for x in bed_regions_list]
else:
if self.stepSize == self.binLength:
transcriptsToConsider.append([(start, end, self.binLength)])
else:
for i in range(start, end, self.stepSize):
if i + self.binLength > end:
break
if blackList is not None and blackList.findOverlaps(
chrom, i, i + self.binLength):
continue
transcriptsToConsider.append([(i, i + self.binLength)])
if self.save_data:
_file = open(deeptools.utilities.getTempFileName(suffix='.bed'),
'w+t')
_file_name = _file.name
else:
_file_name = ''
for bam in bam_handles:
for trans in transcriptsToConsider:
tcov = self.get_coverage_of_region(bam, chrom, trans)
if bed_regions_list is not None:
subnum_reads_per_bin.append(np.sum(tcov))
else:
subnum_reads_per_bin.extend(tcov)
subnum_reads_per_bin = np.concatenate([subnum_reads_per_bin]).reshape(
-1, len(self.bamFilesList), order='F')
if self.save_data:
idx = 0
for i, trans in enumerate(transcriptsToConsider):
if len(trans[0]) != 3:
starts = ",".join([str(x[0]) for x in trans])
ends = ",".join([str(x[1]) for x in trans])
_file.write("\t".join([chrom, starts, ends]) + "\t")
_file.write("\t".join(
["{}".format(x)
for x in subnum_reads_per_bin[i, :]]) + "\n")
else:
for exon in trans:
for startPos in range(exon[0], exon[1], exon[2]):
if idx >= subnum_reads_per_bin.shape[0]:
# At the end of chromosomes (or due to blacklisted regions), there are bins smaller than the bin size
# Counts there are added to the bin before them, but range() will still try to include them.
break
_file.write("{0}\t{1}\t{2}\t".format(
chrom, startPos, startPos + exon[2]))
_file.write("\t".join([
"{}".format(x)
for x in subnum_reads_per_bin[idx, :]
]) + "\n")
idx += 1
_file.close()
if self.verbose:
endTime = time.time()
rows = subnum_reads_per_bin.shape[0]
print("%s countReadsInRegions_worker: processing %d "
"(%.1f per sec) @ %s:%s-%s" %
(multiprocessing.current_process().name, rows, rows /
(endTime - start_time), chrom, start, end))
return subnum_reads_per_bin, _file_name
def get_coverage_of_region(self, bamHandle, chrom, regions,
fragmentFromRead_func=None):
"""
Returns a numpy array that corresponds to the number of reads
that overlap with each tile.
>>> test = Tester()
>>> import pysam
>>> c = SumCoveragePerBin([], stepSize=1, extendReads=300)
For this case the reads are length 36. The number of overlapping
read fragments is 4 and 5 for the positions tested. Note that reads are
NOT extended, due to there being a 0 length input list of BAM files!
>>> c.get_coverage_of_region(pysam.AlignmentFile(test.bamFile_PE), 'chr2',
... [(5000833, 5000834), (5000834, 5000835)])
array([4., 5.])
In the following case the reads length is 50. Reads are not extended.
>>> c.extendReads=False
>>> c.get_coverage_of_region(pysam.AlignmentFile(test.bamFile2), '3R', [(148, 150), (150, 152), (152, 154)])
array([2., 4., 4.])
"""
if not fragmentFromRead_func:
fragmentFromRead_func = self.get_fragment_from_read
nbins = len(regions)
if len(regions[0]) == 3:
nbins = 0
for reg in regions:
nbins += (reg[1] - reg[0]) // reg[2]
coverages = np.zeros(nbins, dtype='float64')
if self.defaultFragmentLength == 'read length':
extension = 0
else:
extension = self.maxPairedFragmentLength
blackList = None
if self.blackListFileName is not None:
blackList = GTF(self.blackListFileName)
vector_start = 0
for idx, reg in enumerate(regions):
if len(reg) == 3:
tileSize = int(reg[2])
nRegBins = (reg[1] - reg[0]) // tileSize
else:
nRegBins = 1
tileSize = int(reg[1] - reg[0])
# Blacklisted regions have a coverage of 0
if blackList and blackList.findOverlaps(chrom, reg[0], reg[1]):
continue
regStart = int(max(0, reg[0] - extension))
regEnd = reg[1] + int(extension)
# If alignments are extended and there's a blacklist, ensure that no
# reads originating in a blacklist are fetched
if blackList and reg[0] > 0 and extension > 0:
o = blackList.findOverlaps(chrom, regStart, reg[0])
if o is not None and len(o) > 0:
regStart = o[-1][1]
o = blackList.findOverlaps(chrom, reg[1], regEnd)
if o is not None and len(o) > 0:
regEnd = o[0][0]
start_time = time.time()
# caching seems faster. TODO: profile the function
c = 0
try:
# BAM input
if chrom not in bamHandle.references:
raise NameError("chromosome {} not found in bam file".format(chrom))
except:
# bigWig input, as used by plotFingerprint
if bamHandle.chroms(chrom):
_ = np.array(bamHandle.stats(chrom, regStart, regEnd, type="mean", nBins=nRegBins), dtype=np.float)
_[np.isnan(_)] = 0.0
_ = _ * tileSize
coverages += _
continue
else:
raise NameError("chromosome {} not found in bigWig file with chroms {}".format(chrom, bamHandle.chroms()))
prev_pos = set()
lpos = None
# of previous processed read pair
for read in bamHandle.fetch(chrom, regStart, regEnd):
if read.is_unmapped:
continue
if self.minMappingQuality and read.mapq < self.minMappingQuality:
continue
# filter reads based on SAM flag
if self.samFlag_include and read.flag & self.samFlag_include != self.samFlag_include:
continue
if self.samFlag_exclude and read.flag & self.samFlag_exclude != 0:
continue
# Fragment lengths
tLen = getTLen(read)
if self.minFragmentLength > 0 and tLen < self.minFragmentLength:
continue
if self.maxFragmentLength > 0 and tLen > self.maxFragmentLength:
continue
# get rid of duplicate reads that have same position on each of the
# pairs
if self.ignoreDuplicates:
# Assuming more or less concordant reads, use the fragment bounds, otherwise the start positions
if tLen >= 0:
s = read.pos
e = s + tLen
else:
s = read.pnext
e = s - tLen
if read.reference_id != read.next_reference_id:
e = read.pnext
if lpos is not None and lpos == read.reference_start \
and (s, e, read.next_reference_id, read.is_reverse) in prev_pos:
continue
if lpos != read.reference_start:
prev_pos.clear()
lpos = read.reference_start
prev_pos.add((s, e, read.next_reference_id, read.is_reverse))
# since reads can be split (e.g. RNA-seq reads) each part of the
# read that maps is called a position block.
try:
position_blocks = fragmentFromRead_func(read)
except TypeError:
# the get_fragment_from_read functions returns None in some cases.
# Those cases are to be skipped, hence the continue line.
continue
last_eIdx = None
for fragmentStart, fragmentEnd in position_blocks:
if fragmentEnd is None or fragmentStart is None:
continue
fragmentLength = fragmentEnd - fragmentStart
if fragmentLength == 0:
continue
# skip reads that are not in the region being
# evaluated.
if fragmentEnd <= reg[0] or fragmentStart >= reg[1]:
continue
if fragmentStart < reg[0]:
fragmentStart = reg[0]
if fragmentEnd > reg[0] + len(coverages) * tileSize:
fragmentEnd = reg[0] + len(coverages) * tileSize
sIdx = vector_start + max((fragmentStart - reg[0]) // tileSize, 0)
eIdx = vector_start + min(np.ceil(float(fragmentEnd - reg[0]) / tileSize).astype('int'), nRegBins)
if eIdx >= len(coverages):
eIdx = len(coverages) - 1
if last_eIdx is not None:
sIdx = max(last_eIdx, sIdx)
if sIdx >= eIdx:
continue
# First bin
if fragmentEnd < reg[0] + (sIdx + 1) * tileSize:
_ = fragmentEnd - fragmentStart
else:
_ = reg[0] + (sIdx + 1) * tileSize - fragmentStart
if _ > tileSize:
_ = tileSize
coverages[sIdx] += _
_ = sIdx + 1
while _ < eIdx:
coverages[_] += tileSize
_ += 1
while eIdx - sIdx >= nRegBins:
eIdx -= 1
if eIdx > sIdx:
_ = fragmentEnd - (reg[0] + eIdx * tileSize)
if _ > tileSize:
_ = tileSize
elif _ < 0:
_ = 0
coverages[eIdx] += _
last_eIdx = eIdx
c += 1
if self.verbose:
endTime = time.time()
print("%s, processing %s (%.1f per sec) reads @ %s:%s-%s" % (
multiprocessing.current_process().name, c, c / (endTime - start_time), chrom, reg[0], reg[1]))
vector_start += nRegBins
# change zeros to NAN
if self.zerosToNans:
coverages[coverages == 0] = np.nan
return coverages
def get_coverage_of_region(self, bamHandle, chrom, regions,
fragmentFromRead_func=None):
"""
Returns a numpy array that corresponds to the number of reads
that overlap with each tile.
>>> test = Tester()
>>> import pysam
>>> c = CountReadsPerBin([], stepSize=1, extendReads=300)
For this case the reads are length 36. The number of overlapping
read fragments is 4 and 5 for the positions tested.
>>> c.get_coverage_of_region(pysam.AlignmentFile(test.bamFile_PE), 'chr2',
... [(5000833, 5000834), (5000834, 5000835)])
array([ 4., 5.])
In the following example a paired read is extended to the fragment length which is 100
The first mate starts at 5000000 and the second at 5000064. Each mate is
extended to the fragment length *independently*
At position 500090-500100 one fragment of length 100 overlap, and after position 5000101
there should be zero reads.
>>> c.zerosToNans = True
>>> c.get_coverage_of_region(pysam.AlignmentFile(test.bamFile_PE), 'chr2',
... [(5000090, 5000100), (5000100, 5000110)])
array([ 1., nan])
In the following case the reads length is 50. Reads are not extended.
>>> c.extendReads=False
>>> c.get_coverage_of_region(pysam.AlignmentFile(test.bamFile2), '3R', [(148, 150), (150, 152), (152, 154)])
array([ 1., 2., 2.])
"""
if not fragmentFromRead_func:
fragmentFromRead_func = self.get_fragment_from_read
nbins = len(regions)
if len(regions[0]) == 3:
nbins = 0
for reg in regions:
nbins += (reg[1] - reg[0]) // reg[2]
coverages = np.zeros(nbins, dtype='float64')
if self.defaultFragmentLength == 'read length':
extension = 0
else:
extension = self.maxPairedFragmentLength
blackList = None
if self.blackListFileName is not None:
blackList = GTF(self.blackListFileName)
vector_start = 0
for idx, reg in enumerate(regions):
if len(reg) == 3:
tileSize = int(reg[2])
nRegBins = (reg[1] - reg[0]) // tileSize
else:
nRegBins = 1
tileSize = int(reg[1] - reg[0])
# Blacklisted regions have a coverage of 0
if blackList and blackList.findOverlaps(chrom, reg[0], reg[1]):
continue
regStart = int(max(0, reg[0] - extension))
regEnd = reg[1] + int(extension)
# If alignments are extended and there's a blacklist, ensure that no
# reads originating in a blacklist are fetched
if blackList and reg[0] > 0 and extension > 0:
o = blackList.findOverlaps(chrom, regStart, reg[0])
if o is not None and len(o) > 0:
regStart = o[-1][1]
o = blackList.findOverlaps(chrom, reg[1], regEnd)
if o is not None and len(o) > 0:
regEnd = o[0][0]
start_time = time.time()
# caching seems faster. TODO: profile the function
c = 0
if chrom in bamHandle.references:
reads = [r for r in bamHandle.fetch(chrom, regStart, regEnd)
if r.flag & 4 == 0]
else:
raise NameError("chromosome {} not found in bam file".format(chrom))
prev_start_pos = None # to store the start positions
# of previous processed read pair
for read in reads:
if self.minMappingQuality and read.mapq < self.minMappingQuality:
continue
# filter reads based on SAM flag
if self.samFlag_include and read.flag & self.samFlag_include != self.samFlag_include:
continue
if self.samFlag_exclude and read.flag & self.samFlag_exclude != 0:
continue
# Fragment lengths
tLen = deeptools.utilities.getTLen(read)
if self.minFragmentLength > 0 and tLen < self.minFragmentLength:
continue
if self.maxFragmentLength > 0 and tLen > self.maxFragmentLength:
continue
# get rid of duplicate reads that have same position on each of the
# pairs
if self.ignoreDuplicates and prev_start_pos \
and prev_start_pos == (read.reference_start, read.pnext, read.is_reverse):
continue
# since reads can be split (e.g. RNA-seq reads) each part of the
# read that maps is called a position block.
try:
position_blocks = fragmentFromRead_func(read)
except TypeError:
# the get_fragment_from_read functions returns None in some cases.
# Those cases are to be skipped, hence the continue line.
continue
last_eIdx = None
for fragmentStart, fragmentEnd in position_blocks:
if fragmentEnd is None or fragmentStart is None:
continue
fragmentLength = fragmentEnd - fragmentStart
if fragmentLength == 0:
continue
# skip reads that are not in the region being
# evaluated.
if fragmentEnd <= reg[0] or fragmentStart >= reg[1]:
continue
if fragmentStart < reg[0]:
fragmentStart = reg[0]
if fragmentEnd > reg[0] + len(coverages) * tileSize:
fragmentEnd = reg[0] + len(coverages) * tileSize
sIdx = vector_start + max((fragmentStart - reg[0]) // tileSize, 0)
eIdx = vector_start + min(np.ceil(float(fragmentEnd - reg[0]) / tileSize).astype('int'), nRegBins)
if last_eIdx is not None:
sIdx = max(last_eIdx, sIdx)
if sIdx >= eIdx:
continue
coverages[sIdx:eIdx] += 1
last_eIdx = eIdx
prev_start_pos = (read.reference_start, read.pnext, read.is_reverse)
c += 1
if self.verbose:
endTime = time.time()
print("%s, processing %s (%.1f per sec) reads @ %s:%s-%s" % (
multiprocessing.current_process().name, c, c / (endTime - start_time), chrom, reg[0], reg[1]))
vector_start += nRegBins
# change zeros to NAN
if self.zerosToNans:
coverages[coverages == 0] = np.nan
return coverages
def get_coverage_of_region(self,
bamHandle,
chrom,
regions,
fragmentFromRead_func=None):
"""
Returns a numpy array that corresponds to the number of reads
that overlap with each tile.
>>> test = Tester()
>>> import pysam
>>> c = SumCoveragePerBin([], stepSize=1, extendReads=300)
For this case the reads are length 36. The number of overlapping
read fragments is 4 and 5 for the positions tested. Note that reads are
NOT extended, due to there being a 0 length input list of BAM files!
>>> c.get_coverage_of_region(pysam.AlignmentFile(test.bamFile_PE), 'chr2',
... [(5000833, 5000834), (5000834, 5000835)])
array([ 4., 5.])
In the following case the reads length is 50. Reads are not extended.
>>> c.extendReads=False
>>> c.get_coverage_of_region(pysam.AlignmentFile(test.bamFile2), '3R', [(148, 150), (150, 152), (152, 154)])
array([ 2., 4., 4.])
"""
if not fragmentFromRead_func:
fragmentFromRead_func = self.get_fragment_from_read
nbins = len(regions)
if len(regions[0]) == 3:
nbins = 0
for reg in regions:
nbins += (reg[1] - reg[0]) // reg[2]
coverages = np.zeros(nbins, dtype='float64')
if self.defaultFragmentLength == 'read length':
extension = 0
else:
extension = self.maxPairedFragmentLength
blackList = None
if self.blackListFileName is not None:
blackList = GTF(self.blackListFileName)
vector_start = 0
for idx, reg in enumerate(regions):
if len(reg) == 3:
tileSize = int(reg[2])
nRegBins = (reg[1] - reg[0]) // tileSize
else:
nRegBins = 1
tileSize = int(reg[1] - reg[0])
# Blacklisted regions have a coverage of 0
if blackList and blackList.findOverlaps(chrom, reg[0], reg[1]):
continue
regStart = int(max(0, reg[0] - extension))
regEnd = reg[1] + int(extension)
# If alignments are extended and there's a blacklist, ensure that no
# reads originating in a blacklist are fetched
if blackList and reg[0] > 0 and extension > 0:
o = blackList.findOverlaps(chrom, regStart, reg[0])
if o is not None and len(o) > 0:
regStart = o[-1][1]
o = blackList.findOverlaps(chrom, reg[1], regEnd)
if o is not None and len(o) > 0:
regEnd = o[0][0]
start_time = time.time()
# caching seems faster. TODO: profile the function
c = 0
try:
# BAM input
if chrom in bamHandle.references:
reads = [
r for r in bamHandle.fetch(chrom, regStart, regEnd)
if r.flag & 4 == 0
]
else:
raise NameError(
"chromosome {} not found in bam file".format(chrom))
except:
# bigWig input, as used by plotFingerprint
if bamHandle.chroms(chrom):
_ = np.array(bamHandle.stats(chrom,
regStart,
regEnd,
type="mean",
nBins=nRegBins),
dtype=np.float)
_[np.isnan(_)] = 0.0
_ = _ * tileSize
coverages += _
continue
else:
raise NameError(
"chromosome {} not found in bigWig file with chroms {}"
.format(chrom, bamHandle.chroms()))
prev_start_pos = None # to store the start positions
# of previous processed read pair
for read in reads:
if self.minMappingQuality and read.mapq < self.minMappingQuality:
continue
# filter reads based on SAM flag
if self.samFlag_include and read.flag & self.samFlag_include != self.samFlag_include:
continue
if self.samFlag_exclude and read.flag & self.samFlag_exclude != 0:
continue
# Fragment lengths
if self.minFragmentLength > 0 and abs(
read.template_length) < self.minFragmentLength:
continue
if self.maxFragmentLength > 0 and abs(
read.template_length) > self.maxFragmentLength:
continue
# get rid of duplicate reads that have same position on each of the
# pairs
if self.ignoreDuplicates and prev_start_pos \
and prev_start_pos == (read.reference_start, read.pnext, read.is_reverse):
continue
# since reads can be split (e.g. RNA-seq reads) each part of the
# read that maps is called a position block.
try:
position_blocks = fragmentFromRead_func(read)
except TypeError:
# the get_fragment_from_read functions returns None in some cases.
# Those cases are to be skipped, hence the continue line.
continue
last_eIdx = None
for fragmentStart, fragmentEnd in position_blocks:
if fragmentEnd is None or fragmentStart is None:
continue
fragmentLength = fragmentEnd - fragmentStart
if fragmentLength == 0:
continue
# skip reads that are not in the region being
# evaluated.
if fragmentEnd <= reg[0] or fragmentStart >= reg[1]:
continue
if fragmentStart < reg[0]:
fragmentStart = reg[0]
if fragmentEnd > reg[0] + len(coverages) * tileSize:
fragmentEnd = reg[0] + len(coverages) * tileSize
sIdx = vector_start + max(
(fragmentStart - reg[0]) // tileSize, 0)
eIdx = vector_start + min(
np.ceil(float(fragmentEnd - reg[0]) /
tileSize).astype('int'), nRegBins)
if eIdx >= len(coverages):
eIdx = len(coverages) - 1
if last_eIdx is not None:
sIdx = max(last_eIdx, sIdx)
if sIdx >= eIdx:
continue
# First bin
if fragmentEnd < reg[0] + (sIdx + 1) * tileSize:
_ = fragmentEnd - fragmentStart
else:
_ = reg[0] + (sIdx + 1) * tileSize - fragmentStart
if _ > tileSize:
_ = tileSize
coverages[sIdx] += _
_ = sIdx + 1
while _ < eIdx:
coverages[_] += tileSize
_ += 1
while eIdx - sIdx >= nRegBins:
eIdx -= 1
if eIdx > sIdx:
_ = fragmentEnd - (reg[0] + eIdx * tileSize)
if _ > tileSize:
_ = tileSize
elif _ < 0:
_ = 0
coverages[eIdx] += _
last_eIdx = eIdx
prev_start_pos = (read.reference_start, read.pnext,
read.is_reverse)
c += 1
if self.verbose:
endTime = time.time()
print("%s, processing %s (%.1f per sec) reads @ %s:%s-%s" %
(multiprocessing.current_process().name, c, c /
(endTime - start_time), chrom, reg[0], reg[1]))
vector_start += nRegBins
# change zeros to NAN
if self.zerosToNans:
coverages[coverages == 0] = np.nan
return coverages
def mapReduce(staticArgs, func, chromSize,
genomeChunkLength=None,
region=None,
bedFile=None,
blackListFileName=None,
numberOfProcessors=4,
verbose=False,
includeLabels=False,
keepExons=False,
transcriptID="transcriptID",
exonID="exonID",
transcript_id_designator="transcript_id",
self_=None):
"""
Split the genome into parts that are sent to workers using a defined
number of procesors. Results are collected and returned.
For each genomic region the given 'func' is called using
the following parameters:
chrom, start, end, staticArgs
The *arg* are static, *pickable* variables that need to be sent
to workers.
The genome chunk length corresponds to a fraction of the genome, in bp,
that is send to each of the workers for processing.
Depending on the type of process a larger or shorter regions may be
preferred
:param chromSize: A list of duples containing the chromosome
name and its length
:param region: The format is chr:start:end:tileSize (see function
getUserRegion)
:param staticArgs: tuple of arguments that are sent to the given 'func'
:param func: function to call. The function is called using the
following parameters (chrom, start, end, staticArgs)
:param bedFile: Is a bed file is given, the args to the func to be
called are extended to include a list of bed
defined regions.
:param blackListFileName: A list of regions to exclude from all computations.
Note that this has genomeChunkLength resolution...
:param self_: In case mapreduce should make a call to an object
the self variable has to be passed.
:param includeLabels: Pass group and transcript labels into the calling
function. These are added to the static args
(groupLabel and transcriptName).
If "includeLabels" is true, a tuple of (results, labels) is returned
"""
if not genomeChunkLength:
genomeChunkLength = 1e5
genomeChunkLength = int(genomeChunkLength)
if verbose:
print("genome partition size for multiprocessing: {0}".format(
genomeChunkLength))
region_start = 0
region_end = None
# if a region is set, that means that the task should only cover
# the given genomic position
if region:
chromSize, region_start, region_end, genomeChunkLength = getUserRegion(chromSize, region)
if verbose:
print("chrom size: {0}, region start: {1}, region end: {2}, "
"genome chunk length sent to each procesor: {3}".format(chromSize, region_start, region_end, genomeChunkLength))
if bedFile:
defaultGroup = None
if len(bedFile) == 1:
defaultGroup = "genes"
bed_interval_tree = GTF(bedFile, defaultGroup=defaultGroup, transcriptID=transcriptID, exonID=exonID, transcript_id_designator=transcript_id_designator, keepExons=keepExons)
if blackListFileName:
blackList = GTF(blackListFileName)
TASKS = []
# iterate over all chromosomes
for chrom, size in chromSize:
# the start is zero unless a specific region is defined
start = 0 if region_start == 0 else region_start
for startPos in range(start, size, genomeChunkLength):
endPos = min(size, startPos + genomeChunkLength)
# Reject a chunk if it overlaps
if blackListFileName:
regions = blSubtract(blackList, chrom, [startPos, endPos])
else:
regions = [[startPos, endPos]]
for reg in regions:
if self_ is not None:
argsList = [self_]
else:
argsList = []
argsList.extend([chrom, reg[0], reg[1]])
# add to argument list the static list received the the function
argsList.extend(staticArgs)
# if a bed file is given, append to the TASK list,
# a list of bed regions that overlap with the
# current genomeChunk.
if bedFile:
# This effectively creates batches of intervals, which is
# generally more performant due to the added overhead of
# initializing additional workers.
# TODO, there's no point in including the chromosome
if includeLabels:
bed_regions_list = [[chrom, x[4], x[2], x[3], x[5], x[6]] for x in bed_interval_tree.findOverlaps(chrom, reg[0], reg[1], trimOverlap=True, numericGroups=True, includeStrand=True)]
else:
bed_regions_list = [[chrom, x[4], x[5], x[6]] for x in bed_interval_tree.findOverlaps(chrom, reg[0], reg[1], trimOverlap=True, includeStrand=True)]
if len(bed_regions_list) == 0:
continue
# add to argument list, the position of the bed regions to use
argsList.append(bed_regions_list)
TASKS.append(tuple(argsList))
if len(TASKS) > 1 and numberOfProcessors > 1:
if verbose:
print(("using {} processors for {} "
"number of tasks".format(numberOfProcessors,
len(TASKS))))
random.shuffle(TASKS)
pool = multiprocessing.Pool(numberOfProcessors)
res = pool.map_async(func, TASKS).get(9999999)
else:
res = list(map(func, TASKS))
if includeLabels:
if bedFile:
return res, bed_interval_tree.labels
else:
return res, None
return res
def get_coverage_of_region_with_intron(self,
bamHandle,
chrom,
regions,
fragmentFromRead_func=None):
"""
Rewrite deeptools.CountReadsPerBin.get_coverage_of_region
Args:
bamHandle (AlignmentFile): Bam object
chrom (str): Chrom
regions (list): List of block
fragmentFromRead_func (function): Function to get fragment from read
Returns:
float: coverages
"""
if not fragmentFromRead_func:
fragmentFromRead_func = self.get_fragment_from_read
nbins = len(regions)
if len(regions[0]) == 3:
nbins = 0
for reg in regions:
nbins += (reg[1] - reg[0]) // reg[2]
coverages = np.zeros(nbins, dtype='float64')
if self.defaultFragmentLength == 'read length':
extension = 0
else:
extension = self.maxPairedFragmentLength
blackList = None
if self.blackListFileName is not None:
blackList = GTF(self.blackListFileName)
vector_start = 0
for idx, reg in enumerate(regions):
if len(reg) == 3:
tileSize = int(reg[2])
nRegBins = (reg[1] - reg[0]) // tileSize
else:
nRegBins = 1
tileSize = int(reg[1] - reg[0])
# Blacklisted regions have a coverage of 0
if blackList and blackList.findOverlaps(chrom, reg[0], reg[1]):
continue
regStart = int(max(0, reg[0] - extension))
regEnd = reg[1] + int(extension)
# If alignments are extended and there's a blacklist, ensure that no
# reads originating in a blacklist are fetched
if blackList and reg[0] > 0 and extension > 0:
o = blackList.findOverlaps(chrom, regStart, reg[0])
if o is not None and len(o) > 0:
regStart = o[-1][1]
o = blackList.findOverlaps(chrom, reg[1], regEnd)
if o is not None and len(o) > 0:
regEnd = o[0][0]
start_time = time.time()
# caching seems faster.
c = 0
if chrom in bamHandle.references:
reads = [
r for r in bamHandle.fetch(chrom, regStart, regEnd)
if r.flag & 4 == 0
]
else:
raise NameError(
"chromosome {} not found in bam file".format(chrom))
prev_start_pos = None # to store the start positions
# of previous processed read pair
for read in reads:
if self.minMappingQuality and read.mapq < self.minMappingQuality:
continue
# filter reads based on SAM flag
if self.samFlag_include and read.flag & self.samFlag_include != self.samFlag_include:
continue
if self.samFlag_exclude and read.flag & self.samFlag_exclude != 0:
continue
# Fragment lengths
tLen = deeptools.utilities.getTLen(read)
if self.minFragmentLength > 0 and tLen < self.minFragmentLength:
continue
if self.maxFragmentLength > 0 and tLen > self.maxFragmentLength:
continue
# get rid of duplicate reads that have same position on each of the
# pairs
if self.ignoreDuplicates and prev_start_pos \
and prev_start_pos == (read.reference_start, read.pnext, read.is_reverse):
continue
# since reads can be split (e.g. RNA-seq reads) each part of the
# read that maps is called a position block.
try:
position_blocks = fragmentFromRead_func(read)
except TypeError:
# the get_fragment_from_read functions returns None in some cases.
# Those cases are to be skipped, hence the continue line.
continue
# Rewrite !!!
sIdx = vector_start + max(
(read.reference_start - reg[0]) // tileSize, 0)
eIdx = vector_start + min(
np.ceil(float(read.reference_end - reg[0]) /
tileSize).astype('int'), nRegBins)
coverages[sIdx:eIdx] += 1
prev_start_pos = (read.reference_start, read.pnext,
read.is_reverse)
c += 1
if self.verbose:
endTime = time.time()
print("%s, processing %s (%.1f per sec) reads @ %s:%s-%s" %
(multiprocessing.current_process().name, c, c /
(endTime - start_time), chrom, reg[0], reg[1]))
vector_start += nRegBins
# change zeros to NAN
if self.zerosToNans:
coverages[coverages == 0] = np.nan
return coverages
def count_reads_in_region_with_intron(self,
chrom,
start,
end,
bed_regions_list=None):
"""
Rewrite deeptools.CountReadsPerBin.count_reads_in_region
Args:
chrom (str): Chrom
start (int): Start position
end (int): End position
bed_regions_list (list): List of bed region
Returns:
tuple: subnum_reads_per_bin, file_name
"""
if start > end:
raise NameError("start %d bigger that end %d" % (start, end))
if self.stepSize is None:
raise ValueError("stepSize is not set!")
# array to keep the read counts for the regions
subnum_reads_per_bin = []
start_time = time.time()
bam_handlers = []
for fname in self.bamFilesList:
try:
bam_handlers.append(bamHandler.openBam(fname))
except:
bam_handlers.append(pyBigWig.open(fname))
blackList = None
if self.blackListFileName is not None:
blackList = GTF(self.blackListFileName)
# A list of lists of tuples
transcriptsToConsider = []
if bed_regions_list is not None:
transcriptsToConsider = [x[1] for x in bed_regions_list]
else:
if self.stepSize == self.binLength:
transcriptsToConsider.append([(start, end, self.binLength)])
else:
for i in range(start, end, self.stepSize):
if i + self.binLength > end:
break
if blackList is not None and blackList.findOverlaps(
chrom, i, i + self.binLength):
continue
transcriptsToConsider.append([(i, i + self.binLength)])
if self.save_data:
_file = open(deeptools.utilities.getTempFileName(suffix='.bed'),
'w+t')
_file_name = _file.name
else:
_file_name = ''
for bam in bam_handlers:
for trans in transcriptsToConsider:
tcov = self.get_coverage_of_region_with_intron(
bam, chrom, trans)
if bed_regions_list is not None:
subnum_reads_per_bin.append(np.sum(tcov))
else:
subnum_reads_per_bin.extend(tcov)
subnum_reads_per_bin = np.concatenate([subnum_reads_per_bin]).reshape(
-1, len(self.bamFilesList), order='F')
if self.save_data:
idx = 0
for i, trans in enumerate(transcriptsToConsider):
if len(trans[0]) != 3:
starts = ",".join([str(x[0]) for x in trans])
ends = ",".join([str(x[1]) for x in trans])
_file.write("\t".join([chrom, starts, ends]) + "\t")
_file.write("\t".join(
["{}".format(x)
for x in subnum_reads_per_bin[i, :]]) + "\n")
else:
for exon in trans:
for startPos in range(exon[0], exon[1], exon[2]):
if idx >= subnum_reads_per_bin.shape[0]:
# At the end of chromosomes (or due to blacklisted regions), there are bins smaller than the bin size
# Counts there are added to the bin before them, but range() will still try to include them.
break
_file.write("{0}\t{1}\t{2}\t".format(
chrom, startPos, startPos + exon[2]))
_file.write("\t".join([
"{}".format(x)
for x in subnum_reads_per_bin[idx, :]
]) + "\n")
idx += 1
_file.close()
if self.verbose:
endTime = time.time()
rows = subnum_reads_per_bin.shape[0]
print("%s countReadsInRegions_worker: processing %d "
"(%.1f per sec) @ %s:%s-%s" %
(multiprocessing.current_process().name, rows, rows /
(endTime - start_time), chrom, start, end))
return subnum_reads_per_bin, _file_name
def get_coverage_of_region(self,
bamHandle,
chrom,
regions,
fragmentFromRead_func=None):
"""
Returns a numpy array that corresponds to the number of reads
that overlap with each tile.
>>> test = Tester()
>>> import pysam
>>> c = CountReadsPerBin([], stepSize=1, extendReads=300)
For this case the reads are length 36. The number of overlapping
read fragments is 4 and 5 for the positions tested.
>>> c.get_coverage_of_region(pysam.AlignmentFile(test.bamFile_PE), 'chr2',
... [(5000833, 5000834), (5000834, 5000835)])
array([4., 5.])
In the following example a paired read is extended to the fragment length which is 100
The first mate starts at 5000000 and the second at 5000064. Each mate is
extended to the fragment length *independently*
At position 500090-500100 one fragment of length 100 overlap, and after position 5000101
there should be zero reads.
>>> c.zerosToNans = True
>>> c.get_coverage_of_region(pysam.AlignmentFile(test.bamFile_PE), 'chr2',
... [(5000090, 5000100), (5000100, 5000110)])
array([ 1., nan])
In the following case the reads length is 50. Reads are not extended.
>>> c.extendReads=False
>>> c.get_coverage_of_region(pysam.AlignmentFile(test.bamFile2), '3R', [(148, 150), (150, 152), (152, 154)])
array([1., 2., 2.])
"""
if not fragmentFromRead_func:
fragmentFromRead_func = self.get_fragment_from_read
nbins = len(regions)
if len(regions[0]) == 3:
nbins = 0
for reg in regions:
nbins += (reg[1] - reg[0]) // reg[2]
coverages = np.zeros(nbins, dtype='float64')
if self.defaultFragmentLength == 'read length':
extension = 0
else:
extension = self.maxPairedFragmentLength
blackList = None
if self.blackListFileName is not None:
blackList = GTF(self.blackListFileName)
vector_start = 0
for idx, reg in enumerate(regions):
if len(reg) == 3:
tileSize = int(reg[2])
nRegBins = (reg[1] - reg[0]) // tileSize
else:
nRegBins = 1
tileSize = int(reg[1] - reg[0])
# Blacklisted regions have a coverage of 0
if blackList and blackList.findOverlaps(chrom, reg[0], reg[1]):
continue
regStart = int(max(0, reg[0] - extension))
regEnd = reg[1] + int(extension)
# If alignments are extended and there's a blacklist, ensure that no
# reads originating in a blacklist are fetched
if blackList and reg[0] > 0 and extension > 0:
o = blackList.findOverlaps(chrom, regStart, reg[0])
if o is not None and len(o) > 0:
regStart = o[-1][1]
o = blackList.findOverlaps(chrom, reg[1], regEnd)
if o is not None and len(o) > 0:
regEnd = o[0][0]
start_time = time.time()
# caching seems faster. TODO: profile the function
c = 0
if chrom not in bamHandle.references:
raise NameError(
"chromosome {} not found in bam file".format(chrom))
prev_pos = set()
lpos = None
# of previous processed read pair
for read in bamHandle.fetch(chrom, regStart, regEnd):
if read.is_unmapped:
continue
if self.minMappingQuality and read.mapq < self.minMappingQuality:
continue
# filter reads based on SAM flag
if self.samFlag_include and read.flag & self.samFlag_include != self.samFlag_include:
continue
if self.samFlag_exclude and read.flag & self.samFlag_exclude != 0:
continue
# Fragment lengths
tLen = deeptools.utilities.getTLen(read)
if self.minFragmentLength > 0 and tLen < self.minFragmentLength:
continue
if self.maxFragmentLength > 0 and tLen > self.maxFragmentLength:
continue
# get rid of duplicate reads that have same position on each of the
# pairs
if self.ignoreDuplicates:
# Assuming more or less concordant reads, use the fragment bounds, otherwise the start positions
if tLen >= 0:
s = read.pos
e = s + tLen
else:
s = read.pnext
e = s - tLen
if read.reference_id != read.next_reference_id:
e = read.pnext
if lpos is not None and lpos == read.reference_start \
and (s, e, read.next_reference_id, read.is_reverse) in prev_pos:
continue
if lpos != read.reference_start:
prev_pos.clear()
lpos = read.reference_start
prev_pos.add(
(s, e, read.next_reference_id, read.is_reverse))
# since reads can be split (e.g. RNA-seq reads) each part of the
# read that maps is called a position block.
try:
position_blocks = fragmentFromRead_func(read)
except TypeError:
# the get_fragment_from_read functions returns None in some cases.
# Those cases are to be skipped, hence the continue line.
continue
last_eIdx = None
for fragmentStart, fragmentEnd in position_blocks:
if fragmentEnd is None or fragmentStart is None:
continue
fragmentLength = fragmentEnd - fragmentStart
if fragmentLength == 0:
continue
# skip reads that are not in the region being
# evaluated.
if fragmentEnd <= reg[0] or fragmentStart >= reg[1]:
continue
if fragmentStart < reg[0]:
fragmentStart = reg[0]
if fragmentEnd > reg[0] + len(coverages) * tileSize:
fragmentEnd = reg[0] + len(coverages) * tileSize
sIdx = vector_start + max(
(fragmentStart - reg[0]) // tileSize, 0)
eIdx = vector_start + min(
np.ceil(float(fragmentEnd - reg[0]) /
tileSize).astype('int'), nRegBins)
if last_eIdx is not None:
sIdx = max(last_eIdx, sIdx)
if sIdx >= eIdx:
continue
sIdx = int(sIdx)
eIdx = int(eIdx)
coverages[sIdx:eIdx] += 1
last_eIdx = eIdx
c += 1
if self.verbose:
endTime = time.time()
print("%s, processing %s (%.1f per sec) reads @ %s:%s-%s" %
(multiprocessing.current_process().name, c, c /
(endTime - start_time), chrom, reg[0], reg[1]))
vector_start += nRegBins
# change zeros to NAN
if self.zerosToNans:
coverages[coverages == 0] = np.nan
return coverages
def count_reads_in_region(self, chrom, start, end, bed_regions_list=None):
"""Counts the reads in each bam file at each 'stepSize' position
within the interval (start, end) for a window or bin of size binLength.
The stepSize controls the distance between bins. For example,
a step size of 20 and a bin size of 20 will create bins next to
each other. If the step size is smaller than the bin size the
bins will overlap.
If a list of bedRegions is given, then the number of reads
that overlaps with each region is counted.
Parameters
----------
chrom : str
Chrom name
start : int
start coordinate
end : int
end coordinate
bed_regions_list: list
List of list of tuples of the form (start, end)
corresponding to bed regions to be processed.
If not bed file was passed to the object constructor
then this list is empty.
Returns
-------
numpy array
The result is a numpy array that as rows each bin
and as columns each bam file.
Examples
--------
Initialize some useful values
>>> test = Tester()
>>> c = CountReadsPerBin([test.bamFile1, test.bamFile2], 25, 0, stepSize=50)
The transpose is used to get better looking numbers. The first line
corresponds to the number of reads per bin in the first bamfile.
>>> _array, __ = c.count_reads_in_region(test.chrom, 0, 200)
>>> _array
array([[ 0., 0.],
[ 0., 1.],
[ 1., 1.],
[ 1., 2.]])
"""
if start > end:
raise NameError("start %d bigger that end %d" % (start, end))
if self.stepSize is None:
raise ValueError("stepSize is not set!")
# array to keep the read counts for the regions
subnum_reads_per_bin = []
start_time = time.time()
bam_handlers = []
for fname in self.bamFilesList:
try:
bam_handlers.append(bamHandler.openBam(fname))
except:
bam_handlers.append(pyBigWig.open(fname))
blackList = None
if self.blackListFileName is not None:
blackList = GTF(self.blackListFileName)
# A list of lists of tuples
transcriptsToConsider = []
if bed_regions_list is not None:
transcriptsToConsider = [x[1] for x in bed_regions_list]
else:
if self.stepSize == self.binLength:
transcriptsToConsider.append([(start, end, self.binLength)])
else:
for i in range(start, end, self.stepSize):
if i + self.binLength > end:
break
if blackList is not None and blackList.findOverlaps(chrom, i, i + self.binLength):
continue
transcriptsToConsider.append([(i, i + self.binLength)])
if self.save_data:
_file = open(deeptools.utilities.getTempFileName(suffix='.bed'), 'w+t')
_file_name = _file.name
else:
_file_name = ''
for bam in bam_handlers:
for trans in transcriptsToConsider:
tcov = self.get_coverage_of_region(bam, chrom, trans)
if bed_regions_list is not None:
subnum_reads_per_bin.append(np.sum(tcov))
else:
subnum_reads_per_bin.extend(tcov)
subnum_reads_per_bin = np.concatenate([subnum_reads_per_bin]).reshape(-1, len(self.bamFilesList), order='F')
if self.save_data:
idx = 0
for i, trans in enumerate(transcriptsToConsider):
if len(trans[0]) != 3:
starts = ",".join([str(x[0]) for x in trans])
ends = ",".join([str(x[1]) for x in trans])
_file.write("\t".join([chrom, starts, ends]) + "\t")
_file.write("\t".join(["{}".format(x) for x in subnum_reads_per_bin[i, :]]) + "\n")
else:
for exon in trans:
for startPos in range(exon[0], exon[1], exon[2]):
if idx >= subnum_reads_per_bin.shape[0]:
# At the end of chromosomes (or due to blacklisted regions), there are bins smaller than the bin size
# Counts there are added to the bin before them, but range() will still try to include them.
break
_file.write("{0}\t{1}\t{2}\t".format(chrom, startPos, startPos + exon[2]))
_file.write("\t".join(["{}".format(x) for x in subnum_reads_per_bin[idx, :]]) + "\n")
idx += 1
_file.close()
if self.verbose:
endTime = time.time()
rows = subnum_reads_per_bin.shape[0]
print("%s countReadsInRegions_worker: processing %d "
"(%.1f per sec) @ %s:%s-%s" %
(multiprocessing.current_process().name,
rows, rows / (endTime - start_time), chrom, start, end))
return subnum_reads_per_bin, _file_name
def mapReduce(staticArgs,
func,
chromSize,
genomeChunkLength=None,
region=None,
bedFile=None,
blackListFileName=None,
numberOfProcessors=4,
verbose=False,
includeLabels=False,
keepExons=False,
transcriptID="transcriptID",
exonID="exonID",
transcript_id_designator="transcript_id",
self_=None):
"""
Split the genome into parts that are sent to workers using a defined
number of procesors. Results are collected and returned.
For each genomic region the given 'func' is called using
the following parameters:
chrom, start, end, staticArgs
The *arg* are static, *pickable* variables that need to be sent
to workers.
The genome chunk length corresponds to a fraction of the genome, in bp,
that is send to each of the workers for processing.
Depending on the type of process a larger or shorter regions may be
preferred
:param chromSize: A list of duples containing the chromosome
name and its length
:param region: The format is chr:start:end:tileSize (see function
getUserRegion)
:param staticArgs: tuple of arguments that are sent to the given 'func'
:param func: function to call. The function is called using the
following parameters (chrom, start, end, staticArgs)
:param bedFile: Is a bed file is given, the args to the func to be
called are extended to include a list of bed
defined regions.
:param blackListFileName: A list of regions to exclude from all computations.
Note that this has genomeChunkLength resolution...
:param self_: In case mapreduce should make a call to an object
the self variable has to be passed.
:param includeLabels: Pass group and transcript labels into the calling
function. These are added to the static args
(groupLabel and transcriptName).
If "includeLabels" is true, a tuple of (results, labels) is returned
"""
if not genomeChunkLength:
genomeChunkLength = 1e5
genomeChunkLength = int(genomeChunkLength)
if verbose:
print("genome partition size for multiprocessing: {0}".format(
genomeChunkLength))
region_start = 0
region_end = None
# if a region is set, that means that the task should be only cover
# the given genomic position
if region:
chromSize, region_start, region_end, genomeChunkLength = getUserRegion(
chromSize, region)
if verbose:
print("chrom size: {0}, region start: {1}, region end: {2}, "
"genome chunk length sent to each procesor: {3}".format(
chromSize, region_start, region_end, genomeChunkLength))
if bedFile:
defaultGroup = None
if len(bedFile) == 1:
defaultGroup = "genes"
bed_interval_tree = GTF(
bedFile,
defaultGroup=defaultGroup,
transcriptID=transcriptID,
exonID=exonID,
transcript_id_designator=transcript_id_designator,
keepExons=keepExons)
if blackListFileName:
blackList = GTF(blackListFileName)
TASKS = []
# iterate over all chromosomes
for chrom, size in chromSize:
# the start is zero unless a specific region is defined
start = 0 if region_start == 0 else region_start
for startPos in range(start, size, genomeChunkLength):
endPos = min(size, startPos + genomeChunkLength)
# Reject a chunk if it overlaps
if blackListFileName:
regions = blSubtract(blackList, chrom, [startPos, endPos])
else:
regions = [[startPos, endPos]]
for reg in regions:
if self_ is not None:
argsList = [self_]
else:
argsList = []
argsList.extend([chrom, reg[0], reg[1]])
# add to argument list the static list received the the function
argsList.extend(staticArgs)
# if a bed file is given, append to the TASK list,
# a list of bed regions that overlap with the
# current genomeChunk.
if bedFile:
# This effectively creates batches of intervals, which is
# generally more performant due to the added overhead of
# initializing additional workers.
# TODO, there's no point in including the chromosome
if includeLabels:
bed_regions_list = [[
chrom, x[4], x[2], x[3], x[5], x[6]
] for x in bed_interval_tree.findOverlaps(
chrom,
reg[0],
reg[1],
trimOverlap=True,
numericGroups=True,
includeStrand=True)]
else:
bed_regions_list = [[
chrom, x[4], x[5], x[6]
] for x in bed_interval_tree.findOverlaps(
chrom,
reg[0],
reg[1],
trimOverlap=True,
includeStrand=True)]
if len(bed_regions_list) == 0:
continue
# add to argument list, the position of the bed regions to use
argsList.append(bed_regions_list)
TASKS.append(tuple(argsList))
if len(TASKS) > 1 and numberOfProcessors > 1:
if verbose:
print(("using {} processors for {} "
"number of tasks".format(numberOfProcessors, len(TASKS))))
random.shuffle(TASKS)
pool = multiprocessing.Pool(numberOfProcessors)
res = pool.map_async(func, TASKS).get(9999999)
else:
res = list(map(func, TASKS))
if includeLabels:
if bedFile:
return res, bed_interval_tree.labels
else:
return res, None
return res
