def generate_backbone(self):
_LOG.info("Reading input sequences: %s" %(self.options.sequence_file))
sequences = MutableAlignment()
sequences.read_file_object(self.options.sequence_file)
if (options().backbone_size is None):
options().backbone_size = min(100,int(.20*sequences.get_num_taxa()))
_LOG.info("Backbone size set to: %d" %(options().backbone_size))
backbone_sequences = sequences.get_hard_sub_alignment(random.sample(sequences.keys(), options().backbone_size))
[sequences.pop(i) for i in backbone_sequences.keys()]
_LOG.info("Writing query and backbone set. ")
query = get_temp_file("query", "backbone", ".fas")
backbone = get_temp_file("backbone", "backbone", ".fas")
_write_fasta(sequences, query)
_write_fasta(backbone_sequences, backbone)
_LOG.info("Generating sate backbone alignment and tree. ")
satealignJob = SateAlignJob()
moleculeType = options().molecule
if (options().molecule == 'amino'):
moleculeType = 'protein'
satealignJob.setup(backbone,options().backbone_size,self.options.outdir,moleculeType,options().cpu)
satealignJob.run()
satealignJob.read_results()
options().placement_size = self.options.backbone_size
options().alignment_file = open(self.options.outdir + "/sate.fasta")
options().tree_file = open(self.options.outdir + "/sate.fasttree")
_LOG.info("Backbone alignment written to %s.\nBackbone tree written to %s" % (options().alignment_file, options().tree_file))
options().fragment_file = query
def generate_backbone(self):
_LOG.info("Reading input sequences: %s" %(self.options.sequence_file))
sequences = MutableAlignment()
sequences.read_file_object(self.options.sequence_file)
fragments = MutableAlignment()
if (options().median_full_length is not None):
if (options().median_full_length == -1):
seq_lengths = sorted([len(seq) for seq in sequences.values()])
lengths = len(seq_lengths)
if lengths % 2:
options().median_full_length = (seq_lengths[lengths / 2] + seq_lengths[lengths / 2 - 1]) / 2.0
else:
options().median_full_length = seq_lengths[lengths / 2]
(min_length,max_length) = (int(options().median_full_length*(1-options().backbone_threshold)),int(options().median_full_length*(1+options().backbone_threshold)))
frag_names = [name for name in sequences if len(sequences[name]) > max_length or len(sequences[name]) < min_length]
if (len(frag_names) > 0):
fragments = sequences.get_hard_sub_alignment(frag_names)
[sequences.pop(i) for i in fragments.keys()]
if (options().backbone_size is None):
options().backbone_size = min(1000,int(sequences.get_num_taxa()))
_LOG.info("Backbone size set to: %d" %(options().backbone_size))
if (options().backbone_size > len(sequences.keys())):
options().backbone_size = len(sequences.keys())
backbone_sequences = sequences.get_hard_sub_alignment(random.sample(sequences.keys(), options().backbone_size))
[sequences.pop(i) for i in backbone_sequences.keys()]
_LOG.info("Writing backbone set. ")
backbone = get_temp_file("backbone", "backbone", ".fas")
_write_fasta(backbone_sequences, backbone)
_LOG.info("Generating pasta backbone alignment and tree. ")
pastaalignJob = PastaAlignJob()
moleculeType = options().molecule
if (options().molecule == 'amino'):
moleculeType = 'protein'
pastaalignJob.setup(backbone,options().backbone_size,self.options.outdir,moleculeType,options().cpu)
pastaalignJob.run()
pastaalignJob.read_results()
options().placement_size = self.options.backbone_size
options().alignment_file = open(self.options.outdir + "/pasta.fasta")
options().tree_file = open(self.options.outdir + "/pasta.fasttree")
_LOG.info("Backbone alignment written to %s.\nBackbone tree written to %s" % (options().alignment_file, options().tree_file))
sequences.set_alignment(fragments)
if (len(sequences) == 0):
_LOG.info("No query sequences to align. Final alignment saved as %s" % self.get_output_filename("alignment.fasta"))
shutil.copyfile(self.options.outdir + "/pasta.fasta", self.get_output_filename("alignment.fasta"))
sys.exit(0)
else:
query = get_temp_file("query", "backbone", ".fas")
options().fragment_file = query
_write_fasta(sequences, query)
def read_and_divide_fragments(self, chunks, extra_frags={}):
max_chunk_size = self.options.max_chunk_size
_LOG.debug(
"start reading fragment files and breaking to at least %s chunks but at most %s sequences "
% (str(chunks), str(max_chunk_size)))
self.root_problem.fragments = MutableAlignment()
self.root_problem.fragments.read_file_object(
self.options.fragment_file)
# test if input fragment names might collide with reference names.
# code contribution by Stefan Janssen (June 13th, 2018)
ids_reference = set(self.root_problem.subalignment.keys())
ids_inputfragments = set(self.root_problem.fragments.keys())
ids_overlap = ids_reference & ids_inputfragments
if len(ids_overlap) > 0:
raise ValueError(
("Your input fragment file contains %i sequences, whose names "
"overlap with names in your reference. Please rename your inp"
"ut fragments and re-start. Duplicate names are:\n '%s'") %
(len(ids_overlap), "'\n '".join(ids_overlap)))
for (k, v) in extra_frags.items():
self.root_problem.fragments[k] = v.replace("-", "")
alg_chunks = self.root_problem.fragments.divide_to_equal_chunks(
chunks, max_chunk_size)
ret = []
for i in range(0, len(alg_chunks)):
temp_file = None
if alg_chunks[i]:
temp_file = get_temp_file("fragment_chunk_%d" % i,
"fragment_chunks", ".fasta")
alg_chunks[i].write_to_path(temp_file)
ret.append(temp_file)
_LOG.debug("fragment files read and divided.")
return ret
def read_and_divide_fragments(self, chunks, extra_frags={}):
max_chunk_size = self.options.max_chunk_size
_LOG.debug(
("start reading fragment files and breaking to at least %s chunks"
" but at most %s sequences ") %
(str(chunks), str(max_chunk_size)))
self.root_problem.fragments = MutableAlignment()
self.root_problem.fragments.read_file_object(
self.options.fragment_file)
# test if input fragment names might collide with reference names.
# code contribution by Stefan Janssen (June 13th, 2018)
ids_reference = set(self.root_problem.subalignment.keys())
ids_inputfragments = set(self.root_problem.fragments.keys())
ids_overlap = ids_reference & ids_inputfragments
if len(ids_overlap) > 0 and not self.options.ignore_overlap:
raise ValueError(
("Your input fragment file contains %i sequences, whose names "
"overlap with names in your reference. Please rename your inp"
"ut fragments and re-start. Duplicate names are:\n '%s'") %
(len(ids_overlap), "'\n '".join(ids_overlap)))
elif len(ids_overlap) > 0:
_LOG.debug("Ignoring following %i query sequences present "
"in the backbone: \n '%s'" %
(len(ids_overlap), "' , '".join(ids_overlap)))
self.root_problem.fragments = self.root_problem.fragments.\
get_soft_sub_alignment(ids_inputfragments - ids_reference)
# test if input fragment names contain whitespaces / tabs which would
# cause hmmsearch to fail.
# code contribution by Stefan Janssen (June 22nd, 2018)
ids_inputfragments_spaces = [
id_ for id_ in ids_inputfragments if (' ' in id_) or ('\t' in id_)
]
if len(ids_inputfragments_spaces) > 0:
raise ValueError(
("Your input fragment file contains %i sequences, whose names "
"contain either whitespaces: ' ' or tabulator '\\t' symbols. "
"Please rename your input fragments and re-start. Affected "
"names are:\n '%s'") %
(len(ids_inputfragments_spaces),
"'\n '".join(ids_inputfragments_spaces)))
for (k, v) in extra_frags.items():
self.root_problem.fragments[k] = v.replace("-", "")
alg_chunks = self.root_problem.fragments.divide_to_equal_chunks(
chunks, max_chunk_size)
ret = []
for i in range(0, len(alg_chunks)):
temp_file = None
if alg_chunks[i]:
temp_file = get_temp_file("fragment_chunk_%d" % i,
"fragment_chunks", ".fasta")
alg_chunks[i].write_to_path(temp_file)
ret.append(temp_file)
_LOG.debug("fragment files read and divided.")
return ret
def read_and_divide_fragments(self, chunks, extra_frags={}):
max_chunk_size = self.options.max_chunk_size
_LOG.debug(
("start reading fragment files and breaking to at least %s chunks"
" but at most %s sequences ") % (
str(chunks), str(max_chunk_size)))
self.root_problem.fragments = MutableAlignment()
self.root_problem.fragments.read_file_object(
self.options.fragment_file)
# test if input fragment names might collide with reference names.
# code contribution by Stefan Janssen (June 13th, 2018)
ids_reference = set(self.root_problem.subalignment.keys())
ids_inputfragments = set(self.root_problem.fragments.keys())
ids_overlap = ids_reference & ids_inputfragments
if len(ids_overlap) > 0:
raise ValueError((
"Your input fragment file contains %i sequences, whose names "
"overlap with names in your reference. Please rename your inp"
"ut fragments and re-start. Duplicate names are:\n '%s'") %
(len(ids_overlap), "'\n '".join(ids_overlap)))
# test if input fragment names contain whitespaces / tabs which would
# cause hmmsearch to fail.
# code contribution by Stefan Janssen (June 22nd, 2018)
ids_inputfragments_spaces = [
id_
for id_ in ids_inputfragments
if (' ' in id_) or ('\t' in id_)]
if len(ids_inputfragments_spaces) > 0:
raise ValueError((
"Your input fragment file contains %i sequences, whose names "
"contain either whitespaces: ' ' or tabulator '\\t' symbols. "
"Please rename your input fragments and re-start. Affected "
"names are:\n '%s'") %
(len(ids_inputfragments_spaces),
"'\n '".join(ids_inputfragments_spaces)))
for (k, v) in extra_frags.items():
self.root_problem.fragments[k] = v.replace("-", "")
alg_chunks = self.root_problem.fragments.divide_to_equal_chunks(
chunks, max_chunk_size)
ret = []
for i in range(0, len(alg_chunks)):
temp_file = None
if alg_chunks[i]:
temp_file = get_temp_file(
"fragment_chunk_%d" % i, "fragment_chunks", ".fasta")
alg_chunks[i].write_to_path(temp_file)
ret.append(temp_file)
_LOG.debug("fragment files read and divided.")
return ret
def generate_backbone(self):
_LOG.info("Reading input sequences: %s" % (self.options.sequence_file))
sequences = MutableAlignment()
sequences.read_file_object(self.options.sequence_file)
if (options().backbone_size is None):
options().backbone_size = min(100,
int(.20 * sequences.get_num_taxa()))
_LOG.info("Backbone size set to: %d" % (options().backbone_size))
backbone_sequences = sequences.get_hard_sub_alignment(
random.sample(sequences.keys(),
options().backbone_size))
[sequences.pop(i) for i in backbone_sequences.keys()]
_LOG.info("Writing query and backbone set. ")
query = get_temp_file("query", "backbone", ".fas")
backbone = get_temp_file("backbone", "backbone", ".fas")
_write_fasta(sequences, query)
_write_fasta(backbone_sequences, backbone)
_LOG.info("Generating sate backbone alignment and tree. ")
satealignJob = SateAlignJob()
moleculeType = options().molecule
if (options().molecule == 'amino'):
moleculeType = 'protein'
satealignJob.setup(backbone,
options().backbone_size, self.options.outdir,
moleculeType,
options().cpu)
satealignJob.run()
satealignJob.read_results()
options().placement_size = self.options.backbone_size
options().alignment_file = open(self.options.outdir + "/sate.fasta")
options().tree_file = open(self.options.outdir + "/sate.fasttree")
_LOG.info(
"Backbone alignment written to %s.\nBackbone tree written to %s" %
(options().alignment_file, options().tree_file))
options().fragment_file = query
def read_and_divide_fragments(self, chunks, extra_frags = {}):
_LOG.debug("start reading fragment files and breaking to chunks: %d" %chunks)
self.root_problem.fragments = MutableAlignment()
self.root_problem.fragments.read_file_object(self.options.fragment_file)
for (k,v) in extra_frags.iteritems():
self.root_problem.fragments[k] = v.replace("-","")
alg_chunks = self.root_problem.fragments.divide_to_equal_chunks(chunks)
ret = []
for i in xrange(0,chunks):
temp_file = get_temp_file("fragment_chunk_%d" %i, "fragment_chunks", ".fasta")
alg_chunks[i].write_to_path(temp_file)
ret.append(temp_file)
_LOG.debug("fragment files read and divided.")
return ret
def read_and_divide_fragments(self, chunks, extra_frags={}):
_LOG.debug("start reading fragment files and breaking to chunks: %d" %
chunks)
self.root_problem.fragments = MutableAlignment()
self.root_problem.fragments.read_file_object(
self.options.fragment_file)
for (k, v) in extra_frags.iteritems():
self.root_problem.fragments[k] = v.replace("-", "")
alg_chunks = self.root_problem.fragments.divide_to_equal_chunks(chunks)
ret = []
for i in xrange(0, chunks):
temp_file = get_temp_file("fragment_chunk_%d" % i,
"fragment_chunks", ".fasta")
alg_chunks[i].write_to_path(temp_file)
ret.append(temp_file)
_LOG.debug("fragment files read and divided.")
return ret
def save_checkpoint(checkpoint_manager):
'''
This is the callback function that is called periodically to save the
current state of the system.
'''
# Note: this module is not bullet proof in terms of race conditions.
# Most importantly, it is possible (though extremely unlikely) that
# while the new temp path is being written (f.write...)
if checkpoint_manager.is_checkpointing:
# checkpoint_manager.lock.acquire()
checkpoint_manager.saving = True
newTmpDest = get_temp_file("dump", "checkpoints")
_LOG.info("Checkpoint is being updated: %s" % newTmpDest)
oldTmpFile = open(checkpoint_manager.checkpoint_path).readlines()
oldTmpFile = None if len(oldTmpFile) == 0 else oldTmpFile[-1].split(
",")[0]
checkpoint_manager.update_time()
currenlimit = sys.getrecursionlimit()
sys.setrecursionlimit(100000)
picklefile = gzip.GzipFile(newTmpDest, 'wb')
pickle.dump(checkpoint_manager.checkpoint_state, picklefile, 2)
picklefile.close()
sys.setrecursionlimit(currenlimit)
f = open(checkpoint_manager.checkpoint_path, "a")
f.write("%s, %s\n" % (newTmpDest, datetime.datetime.now()))
f.close()
if oldTmpFile is not None:
os.remove(oldTmpFile)
_LOG.info("Checkpoint Saved to: %s and linked in %s." %
(newTmpDest, checkpoint_manager.checkpoint_path))
checkpoint_manager.saving = False
# checkpoint_manager.lock.release()
checkpoint_manager.timer = threading.Timer(
options().checkpoint_interval,
save_checkpoint,
args=[checkpoint_manager])
checkpoint_manager.timer.setDaemon(True)
checkpoint_manager.timer.start()
def save_checkpoint(checkpoint_manager):
'''
This is the callback function that is called periodically to save the
current state of the system.
'''
# Note: this module is not bullet proof in terms of race conditions.
# Most importantly, it is possible (though extremely unlikely) that
# while the new temp path is being written (f.write...)
if checkpoint_manager.is_checkpointing:
# checkpoint_manager.lock.acquire()
checkpoint_manager.saving = True
newTmpDest = get_temp_file("dump", "checkpoints")
_LOG.info("Checkpoint is being updated: %s" % newTmpDest)
oldTmpFile = open(checkpoint_manager.checkpoint_path).readlines()
oldTmpFile = None if len(oldTmpFile) == 0 else oldTmpFile[-1].split(
",")[0]
checkpoint_manager.update_time()
currenlimit = sys.getrecursionlimit()
sys.setrecursionlimit(100000)
picklefile = gzip.GzipFile(newTmpDest, 'wb')
pickle.dump(checkpoint_manager.checkpoint_state, picklefile, 2)
picklefile.close()
sys.setrecursionlimit(currenlimit)
f = open(checkpoint_manager.checkpoint_path, "a")
f.write("%s, %s\n" % (newTmpDest, datetime.datetime.now()))
f.close()
if oldTmpFile is not None:
os.remove(oldTmpFile)
_LOG.info("Checkpoint Saved to: %s and linked in %s." % (
newTmpDest, checkpoint_manager.checkpoint_path))
checkpoint_manager.saving = False
# checkpoint_manager.lock.release()
checkpoint_manager.timer = threading.Timer(
options().checkpoint_interval, save_checkpoint,
args=[checkpoint_manager])
checkpoint_manager.timer.setDaemon(True)
checkpoint_manager.timer.start()
def generate_backbone(self):
_LOG.info("Reading input sequences: %s" % (self.options.sequence_file))
sequences = MutableAlignment()
sequences.read_file_object(self.options.sequence_file)
sequences.degap()
fragments = MutableAlignment()
if (options().median_full_length is not None
or options().full_length_range is not None):
if (options().median_full_length == -1):
seq_lengths = sorted(
[len(seq) for seq in list(sequences.values())])
lengths = len(seq_lengths)
l2 = int(lengths / 2)
if lengths % 2:
options().median_full_length = (seq_lengths[l2] +
seq_lengths[l2 + 1]) / 2.0
else:
options().median_full_length = seq_lengths[l2]
if options().full_length_range is not None:
L = sorted(int(x) for x in options().full_length_range.split())
min_length = L[0]
max_length = L[1]
else:
(min_length,
max_length) = (int(options().median_full_length *
(1 - options().backbone_threshold)),
int(options().median_full_length *
(1 + options().backbone_threshold)))
_LOG.info(
"Full length sequences are set to be from %d to %d character long"
% (min_length, max_length))
frag_names = [
name for name in sequences if len(sequences[name]) > max_length
or len(sequences[name]) < min_length
]
if (len(frag_names) > 0):
_LOG.info("Detected %d fragmentary sequences" %
len(frag_names))
fragments = sequences.get_hard_sub_alignment(frag_names)
[sequences.pop(i) for i in list(fragments.keys())]
if (options().backbone_size is None):
options().backbone_size = min(1000, int(sequences.get_num_taxa()))
_LOG.info("Backbone size set to: %d" % (options().backbone_size))
if (options().backbone_size > len(list(sequences.keys()))):
options().backbone_size = len(list(sequences.keys()))
sample = sorted(
random.sample(sorted(list(sequences.keys())),
options().backbone_size))
backbone_sequences = sequences.get_hard_sub_alignment(sample)
_LOG.debug("Backbone: %s" % (sorted(list(backbone_sequences.keys()))))
[sequences.pop(i) for i in list(backbone_sequences.keys())]
_LOG.info("Writing backbone set. ")
backbone = get_temp_file("backbone", "backbone", ".fas")
_write_fasta(backbone_sequences, backbone)
_LOG.info("Generating pasta backbone alignment and tree. ")
pastaalignJob = PastaAlignJob()
moleculeType = options().molecule
if (options().molecule == 'amino'):
moleculeType = 'protein'
pastaalignJob.setup(backbone,
options().backbone_size, moleculeType,
options().cpu, **vars(options().pasta))
pastaalignJob.run()
(a_file, t_file) = pastaalignJob.read_results()
shutil.copyfile(t_file, self.get_output_filename("pasta.fasttree"))
shutil.copyfile(a_file, self.get_output_filename("pasta.fasta"))
options().placement_size = self.options.backbone_size
options().alignment_file = open(
self.get_output_filename("pasta.fasta"))
options().tree_file = open(self.get_output_filename("pasta.fasttree"))
_LOG.info(
"Backbone alignment written to %s.\nBackbone tree written to %s" %
(options().alignment_file, options().tree_file))
sequences.set_alignment(fragments)
if (len(sequences) == 0):
sequences = MutableAlignment()
sequences.read_file_object(open(self.options.alignment_file.name))
self.results = ExtendedAlignment(fragment_names=[])
self.results.set_alignment(sequences)
_LOG.info(
"No query sequences to align. Final alignment saved as %s" %
self.get_output_filename("alignment.fasta"))
self.output_results()
sys.exit(0)
else:
query = get_temp_file("query", "backbone", ".fas")
options().fragment_file = query
_write_fasta(sequences, query)
