def filterSeq(seq_file, filter_func, filter_args={}, out_args=default_out_args,
nproc=None, queue_size=None):
"""
Filters sequences by fraction of ambiguous nucleotides
Arguments:
seq_file = the sequence file to filter
filter_func = the function to use for filtering sequences
filter_args = a dictionary of arguments to pass to filter_func
out_args = common output argument dictionary from parseCommonArgs
nproc = the number of processQueue processes;
if None defaults to the number of CPUs
queue_size = maximum size of the argument queue;
if None defaults to 2*nproc
Returns:
a list of successful output file names
"""
# Define output file label dictionary
cmd_dict = {filterLength:'length', filterMissing:'missing',
filterRepeats:'repeats', filterQuality:'quality',
maskQuality:'maskqual', trimQuality:'trimqual'}
# Print parameter info
log = OrderedDict()
log['START'] = 'FilterSeq'
log['COMMAND'] = cmd_dict.get(filter_func, filter_func.__name__)
log['FILE'] = os.path.basename(seq_file)
for k in sorted(filter_args): log[k.upper()] = filter_args[k]
log['NPROC'] = nproc
printLog(log)
# Check input type
in_type = getFileType(seq_file)
if in_type != 'fastq' and filter_func in (filterQuality, maskQuality, trimQuality):
sys.exit('ERROR: Input file must be FASTQ for %s mode' % cmd_dict[filter_func])
# Define feeder function and arguments
feed_func = feedSeqQueue
feed_args = {'seq_file': seq_file}
# Define worker function and arguments
work_func = processSeqQueue
work_args = {'process_func': filter_func,
'process_args': filter_args}
# Define collector function and arguments
collect_func = collectSeqQueue
collect_args = {'seq_file': seq_file,
'task_label': cmd_dict[filter_func],
'out_args': out_args}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func,
feed_args, work_args, collect_args,
nproc, queue_size)
# Print log
result['log']['END'] = 'FilterSeq'
printLog(result['log'])
return result['out_files']
def clusterSets(seq_file, barcode_field=default_barcode_field,
cluster_field=default_cluster_field,
ident=default_ident, seq_start=None, seq_end=None,
usearch_exec=default_usearch_exec,
out_args=default_out_args, nproc=None,
queue_size=None):
"""
Performs clustering on sets of sequences
Arguments:
seq_file = the sample sequence file name
barcode_field = the annotation containing set IDs
ident = the identity threshold for clustering sequences
seq_start = the start position to trim sequences at before clustering
seq_end = the end position to trim sequences at before clustering
usearch_exec = the path to the executable for usearch
nproc = the number of processQueue processes;
if None defaults to the number of CPUs
queue_size = maximum size of the argument queue;
if None defaults to 2*nproc
Returns:
the clustered output file name
"""
# Print parameter info
log = OrderedDict()
log['START'] = 'ClusterSets'
log['FILE'] = os.path.basename(seq_file)
log['BARCODE_FIELD'] = barcode_field
log['CLUSTER_FIELD'] = cluster_field
log['IDENTITY'] = ident
log['SEQUENCE_START'] = seq_start
log['SEQUENCE_END'] = seq_end
log['NPROC'] = nproc
printLog(log)
# Define cluster function parameters
cluster_args = {'usearch_exec':usearch_exec,
'ident':ident,
'seq_start':seq_start,
'seq_end':seq_end}
# Define feeder function and arguments
index_args = {'field': barcode_field, 'delimiter': out_args['delimiter']}
feed_func = feedSeqQueue
feed_args = {'seq_file': seq_file,
'index_func': indexSeqSets,
'index_args': index_args}
# Define worker function and arguments
work_func = processCSQueue
work_args = {'cluster_field': cluster_field,
'cluster_args': cluster_args,
'delimiter': out_args['delimiter']}
# Define collector function and arguments
collect_func = collectSeqQueue
collect_args = {'seq_file': seq_file,
'task_label': 'cluster',
'out_args': out_args,
'index_field': barcode_field}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func,
feed_args, work_args, collect_args,
nproc, queue_size)
# Print log
log = OrderedDict()
log['OUTPUT'] = result['log'].pop('OUTPUT')
for k, v in result['log'].items(): log[k] = v
log['END'] = 'ClusterSets'
printLog(log)
return result['out_files']
def filterSeq(seq_file,
filter_func,
filter_args={},
out_file=None,
out_args=default_out_args,
nproc=None,
queue_size=None):
"""
Filters sequences by fraction of ambiguous nucleotides
Arguments:
seq_file : the sequence file to filter.
filter_func : the function to use for filtering sequences.
filter_args : a dictionary of arguments to pass to filter_func.
out_file : output file name. Automatically generated from the input file if None.
out_args : common output argument dictionary from parseCommonArgs.
nproc : the number of processQueue processes;
if None defaults to the number of CPUs.
queue_size : maximum size of the argument queue;
if None defaults to 2*nproc.
Returns:
list: a list of successful output file names
"""
# Define output file label dictionary
cmd_dict = {
filterLength: 'length',
filterMissing: 'missing',
filterRepeats: 'repeats',
filterQuality: 'quality',
maskQuality: 'maskqual',
trimQuality: 'trimqual'
}
# Print parameter info
log = OrderedDict()
log['START'] = 'FilterSeq'
log['COMMAND'] = cmd_dict.get(filter_func, filter_func.__name__)
log['FILE'] = os.path.basename(seq_file)
for k in sorted(filter_args):
log[k.upper()] = filter_args[k]
log['NPROC'] = nproc
printLog(log)
# Check input type
in_type = getFileType(seq_file)
if in_type != 'fastq' and filter_func in (filterQuality, maskQuality,
trimQuality):
printError('Input file must be FASTQ for %s mode.' %
cmd_dict[filter_func])
# Define feeder function and arguments
feed_func = feedSeqQueue
feed_args = {'seq_file': seq_file}
# Define worker function and arguments
work_func = processSeqQueue
work_args = {'process_func': filter_func, 'process_args': filter_args}
# Define collector function and arguments
collect_func = collectSeqQueue
collect_args = {
'seq_file': seq_file,
'label': cmd_dict[filter_func],
'out_file': out_file,
'out_args': out_args
}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func, feed_args,
work_args, collect_args, nproc, queue_size)
# Print log
result['log']['END'] = 'FilterSeq'
printLog(result['log'])
return result['out_files']
def alignRecords(db_file,
seq_fields,
group_func,
align_func,
group_args={},
align_args={},
out_args=default_out_args,
nproc=None,
queue_size=None):
"""
Performs a multiple alignment on sets of sequences
Arguments:
db_file : filename of the input database.
seq_fields : the sequence fields to multiple align.
group_func : function to use to group records.
align_func : function to use to multiple align sequence groups.
group_args : dictionary of arguments to pass to group_func.
align_args : dictionary of arguments to pass to align_func.
out_args : common output argument dictionary from parseCommonArgs.
nproc : the number of processQueue processes.
if None defaults to the number of CPUs.
queue_size : maximum size of the argument queue.
if None defaults to 2*nproc.
Returns:
tuple : a tuple of (align-pass, align-fail) filenames.
"""
# Define subcommand label dictionary
cmd_dict = {
alignAcross: 'across',
alignWithin: 'within',
alignBlocks: 'block'
}
# Print parameter info
log = OrderedDict()
log['START'] = 'AlignRecords'
log['COMMAND'] = cmd_dict.get(align_func, align_func.__name__)
log['FILE'] = os.path.basename(db_file)
log['SEQ_FIELDS'] = ','.join(seq_fields)
if 'group_fields' in group_args:
log['GROUP_FIELDS'] = ','.join(group_args['group_fields'])
if 'mode' in group_args: log['MODE'] = group_args['mode']
if 'action' in group_args: log['ACTION'] = group_args['action']
log['NPROC'] = nproc
printLog(log)
# Define feeder function and arguments
feed_func = feedDbQueue
feed_args = {
'db_file': db_file,
'group_func': group_func,
'group_args': group_args
}
# Define worker function and arguments
align_args['seq_fields'] = seq_fields
work_func = processDbQueue
work_args = {'process_func': align_func, 'process_args': align_args}
# Define collector function and arguments
collect_func = collectDbQueue
collect_args = {
'db_file': db_file,
'task_label': 'align',
'out_args': out_args,
'add_fields': ['%s_ALIGN' % f for f in seq_fields]
}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func, feed_args,
work_args, collect_args, nproc, queue_size)
# Print log
result['log']['END'] = 'AlignRecords'
printLog(result['log'])
return result['out_files']
def alignSets(seq_file, align_func, align_args, barcode_field=default_barcode_field,
calc_div=False, out_file=None, out_args=default_out_args,
nproc=None, queue_size=None):
"""
Performs a multiple alignment on sets of sequences
Arguments:
seq_file : the sample sequence file name.
align_func : the function to use to align sequence sets.
align_args : a dictionary of arguments to pass to align_func.
barcode_field : the annotation containing set IDs.
calc_div : if True calculate average pairwise error for each sequence set.
out_file : output file name. Automatically generated from the input file if None.
out_args : common output argument dictionary from parseCommonArgs
nproc : the number of processQueue processes;
if None defaults to the number of CPUs
queue_size : maximum size of the argument queue;
if None defaults to 2*nproc
Returns:
tuple: a tuple of (passing, failing) filenames.
"""
# Define subcommand label dictionary
cmd_dict = {runMuscle:'muscle', offsetSeqSet:'offset'}
# Print parameter info
log = OrderedDict()
log['START'] = 'AlignSets'
log['COMMAND'] = cmd_dict[align_func]
log['FILE'] = os.path.basename(seq_file)
if 'mode' in align_args: log['MODE'] = align_args['mode']
log['BARCODE_FIELD'] = barcode_field
if 'field' in align_args: log['OFFSET_FIELD'] = align_args['field']
log['CALC_DIV'] = calc_div
log['NPROC'] = nproc
printLog(log)
# Define feeder function and arguments
index_args = {'field': barcode_field, 'delimiter': out_args['delimiter']}
feed_func = feedSeqQueue
feed_args = {'seq_file': seq_file,
'index_func': indexSeqSets,
'index_args': index_args}
# Define worker function and arguments
work_func = processQueue
work_args = {'align_func': align_func,
'align_args': align_args,
'calc_div': calc_div,
'delimiter': out_args['delimiter']}
# Define collector function and arguments
collect_func = collectSeqQueue
collect_args = {'seq_file': seq_file,
'label': 'align',
'out_file': out_file,
'out_args': out_args,
'index_field': barcode_field}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func,
feed_args, work_args, collect_args,
nproc, queue_size)
# Print log
result['log']['END'] = 'AlignSets'
printLog(result['log'])
return result['out_files']
def buildConsensus(seq_file,
barcode_field=default_barcode_field,
min_count=default_consensus_min_count,
min_freq=default_consensus_min_freq,
min_qual=default_consensus_min_qual,
primer_field=None,
primer_freq=None,
max_gap=None,
max_error=None,
max_diversity=None,
copy_fields=None,
copy_actions=None,
dependent=False,
out_file=None,
out_args=default_out_args,
nproc=None,
queue_size=None):
"""
Generates consensus sequences
Arguments:
seq_file : the sample sequence file name
barcode_field : the annotation field containing set IDs
min_count : threshold number of sequences to define a consensus
min_freq : the frequency cutoff to assign a base
min_qual : the quality cutoff to assign a base
primer_field : the annotation field containing primer tags;
if None do not annotate with primer tags
primer_freq : the maximum primer tag frequency that must be meet to build a consensus;
if None do not filter by primer frequency
max_gap : the maximum frequency of (., -) characters allowed before
deleting a position; if None do not delete positions
max_error : a threshold defining the maximum allowed error rate to retain a read group;
if None do not calculate error rate
max_diversity : a threshold defining the average pairwise error rate required to retain a read group;
if None do not calculate diversity
dependent : if False treat barcode group sequences as independent data
copy_fields : a list of annotations to copy into consensus sequence annotations;
if None no additional annotations will be copied
copy_actions : the list of actions to take for each copy_fields;
one of ['set', 'majority', 'min', 'max', 'sum']
out_file : output file name. Automatically generated from the input file if None.
out_args : common output argument dictionary from parseCommonArgs.
nproc : the number of processQueue processes;
if None defaults to the number of CPUs
queue_size : maximum size of the argument queue;
if None defaults to 2*nproc
Returns:
list : a list of successful output file names.
"""
# Print parameter info
log = OrderedDict()
log['START'] = 'BuildConsensus'
log['FILE'] = os.path.basename(seq_file)
log['BARCODE_FIELD'] = barcode_field
log['MIN_COUNT'] = min_count
log['MIN_FREQUENCY'] = min_freq
log['MIN_QUALITY'] = min_qual
log['MAX_GAP'] = max_gap
log['PRIMER_FIELD'] = primer_field
log['PRIMER_FREQUENCY'] = primer_freq
log['MAX_ERROR'] = max_error
log['MAX_DIVERSITY'] = max_diversity
log['DEPENDENT'] = dependent
log['COPY_FIELDS'] = ','.join(
copy_fields) if copy_fields is not None else None
log['COPY_ACTIONS'] = ','.join(
copy_actions) if copy_actions is not None else None
log['NPROC'] = nproc
printLog(log)
# Set consensus building function
in_type = getFileType(seq_file)
if in_type == 'fastq':
cons_func = qualityConsensus
cons_args = {
'min_qual': min_qual,
'min_freq': min_freq,
'dependent': dependent
}
elif in_type == 'fasta':
cons_func = frequencyConsensus
cons_args = {'min_freq': min_freq}
else:
printError('Input file must be FASTA or FASTQ.')
# Define feeder function and arguments
index_args = {'field': barcode_field, 'delimiter': out_args['delimiter']}
feed_func = feedSeqQueue
feed_args = {
'seq_file': seq_file,
'index_func': indexSeqSets,
'index_args': index_args
}
# Define worker function and arguments
work_func = processQueue
work_args = {
'cons_func': cons_func,
'cons_args': cons_args,
'min_count': min_count,
'primer_field': primer_field,
'primer_freq': primer_freq,
'max_gap': max_gap,
'max_error': max_error,
'max_diversity': max_diversity,
'copy_fields': copy_fields,
'copy_actions': copy_actions,
'delimiter': out_args['delimiter']
}
# Define collector function and arguments
collect_func = collectSeqQueue
collect_args = {
'seq_file': seq_file,
'label': 'consensus',
'out_file': out_file,
'out_args': out_args,
'index_field': barcode_field
}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func, feed_args,
work_args, collect_args, nproc, queue_size)
# Print log
result['log']['END'] = 'BuildConsensus'
printLog(result['log'])
return result['out_files']
def defineClones(db_file,
feed_func,
work_func,
collect_func,
clone_func,
cluster_func=None,
group_func=None,
group_args={},
clone_args={},
cluster_args={},
max_missing=default_max_missing,
out_args=default_out_args,
nproc=None,
queue_size=None):
"""
Define clonally related sequences
Arguments:
db_file = filename of input database
feed_func = the function that feeds the queue
work_func = the worker function that will run on each CPU
collect_func = the function that collects results from the workers
group_func = the function to use for assigning preclones
clone_func = the function to use for determining clones within preclonal groups
group_args = a dictionary of arguments to pass to group_func
clone_args = a dictionary of arguments to pass to clone_func
max_missing : maximum number of non-ACGT characters to allow in the junction sequence.
out_args = common output argument dictionary from parseCommonArgs
nproc = the number of processQueue processes;
if None defaults to the number of CPUs
queue_size = maximum size of the argument queue;
if None defaults to 2*nproc
Returns:
a list of successful output file names
"""
# Print parameter info
log = OrderedDict()
log['START'] = 'DefineClones'
log['DB_FILE'] = os.path.basename(db_file)
log['MAX_MISSING'] = max_missing
if group_func is not None:
log['GROUP_FUNC'] = group_func.__name__
log['GROUP_ARGS'] = group_args
log['CLONE_FUNC'] = clone_func.__name__
# TODO: this is yucky, but can be fixed by using a model class
clone_log = clone_args.copy()
if 'dist_mat' in clone_log: del clone_log['dist_mat']
log['CLONE_ARGS'] = clone_log
if cluster_func is not None:
log['CLUSTER_FUNC'] = cluster_func.__name__
log['CLUSTER_ARGS'] = cluster_args
log['NPROC'] = nproc
printLog(log)
# Define feeder function and arguments
feed_args = {
'db_file': db_file,
'group_func': group_func,
'group_args': group_args
}
# Define worker function and arguments
work_args = {
'max_missing': max_missing,
'clone_func': clone_func,
'clone_args': clone_args
}
# Define collector function and arguments
collect_args = {
'db_file': db_file,
'out_args': out_args,
'cluster_func': cluster_func,
'cluster_args': cluster_args
}
# Call process manager
result = manageProcesses(feed_func=feed_func,
work_func=work_func,
collect_func=collect_func,
feed_args=feed_args,
work_args=work_args,
collect_args=collect_args,
nproc=nproc,
queue_size=queue_size)
# Print log
result['log']['END'] = 'DefineClones'
printLog(result['log'])
return result['out_files']
def alignRecords(db_file,
seq_fields,
group_func,
align_func,
group_args={},
align_args={},
format='changeo',
out_file=None,
out_args=default_out_args,
nproc=None,
queue_size=None):
"""
Performs a multiple alignment on sets of sequences
Arguments:
db_file : filename of the input database.
seq_fields : the sequence fields to multiple align.
group_func : function to use to group records.
align_func : function to use to multiple align sequence groups.
group_args : dictionary of arguments to pass to group_func.
align_args : dictionary of arguments to pass to align_func.
format : output format. One of 'changeo' or 'airr'.
out_file : output file name. Automatically generated from the input file if None.
out_args : common output argument dictionary from parseCommonArgs.
nproc : the number of processQueue processes.
if None defaults to the number of CPUs.
queue_size : maximum size of the argument queue.
if None defaults to 2*nproc.
Returns:
dict : names of the 'pass' and 'fail' output files.
"""
# Define subcommand label dictionary
cmd_dict = {
alignAcross: 'across',
alignWithin: 'within',
alignBlocks: 'block'
}
# Print parameter info
log = OrderedDict()
log['START'] = 'AlignRecords'
log['COMMAND'] = cmd_dict.get(align_func, align_func.__name__)
log['FILE'] = os.path.basename(db_file)
log['SEQ_FIELDS'] = ','.join(seq_fields)
if 'group_fields' in group_args:
log['GROUP_FIELDS'] = ','.join(group_args['group_fields'])
if 'mode' in group_args: log['MODE'] = group_args['mode']
if 'action' in group_args: log['ACTION'] = group_args['action']
log['NPROC'] = nproc
printLog(log)
# Define format operators
try:
reader, writer, schema = getFormatOperators(format)
except ValueError:
printError('Invalid format %s.' % format)
# Define feeder function and arguments
if 'group_fields' in group_args and group_args['group_fields'] is not None:
group_args['group_fields'] = [
schema.toReceptor(f) for f in group_args['group_fields']
]
feed_func = feedDbQueue
feed_args = {
'db_file': db_file,
'reader': reader,
'group_func': group_func,
'group_args': group_args
}
# Define worker function and arguments
field_map = OrderedDict([(schema.toReceptor(f), '%s_align' % f)
for f in seq_fields])
align_args['field_map'] = field_map
work_func = processDbQueue
work_args = {'process_func': align_func, 'process_args': align_args}
# Define collector function and arguments
out_fields = getDbFields(db_file,
add=list(field_map.values()),
reader=reader)
out_args['out_type'] = schema.out_type
collect_func = collectDbQueue
collect_args = {
'db_file': db_file,
'label': 'align',
'fields': out_fields,
'writer': writer,
'out_file': out_file,
'out_args': out_args
}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func, feed_args,
work_args, collect_args, nproc, queue_size)
# Print log
result['log']['END'] = 'AlignRecords'
printLog(result['log'])
output = {k: v for k, v in result.items() if k in ('pass', 'fail')}
return output
def assemblePairs(head_file, tail_file, assemble_func, assemble_args={},
coord_type=default_coord_type, rc=None,
head_fields=None, tail_fields=None,
out_args=default_out_args, nproc=None, queue_size=None):
"""
Generates consensus sequences
Arguments:
head_file = the head sequence file name
tail_file = the tail sequence file name
assemble_func = the function to use to assemble paired ends
assemble_args = a dictionary of arguments to pass to the assembly function
coord_type = the sequence header format
rc = Defines which sequences ('head','tail','both') to reverse complement before assembly;
if None do not reverse complement sequences
head_fields = list of annotations in head_file records to copy to assembled record;
if None do not copy an annotation
tail_fields = list of annotations in tail_file records to copy to assembled record;
if None do not copy an annotation
out_args = common output argument dictionary from parseCommonArgs
nproc = the number of processQueue processes;
if None defaults to the number of CPUs
queue_size = maximum size of the argument queue;
if None defaults to 2*nproc
Returns:
a list of successful output file names
"""
# Define subcommand label dictionary
cmd_dict = {alignAssembly:'align', joinSeqPair:'join', referenceAssembly:'reference'}
# Print parameter info
log = OrderedDict()
log['START'] = 'AssemblePairs'
log['COMMAND'] = cmd_dict.get(assemble_func, assemble_func.__name__)
log['FILE1'] = os.path.basename(head_file)
log['FILE2'] = os.path.basename(tail_file)
log['COORD_TYPE'] = coord_type
if 'ref_file' in assemble_args: log['REFFILE'] = assemble_args['ref_file']
if 'alpha' in assemble_args: log['ALPHA'] = assemble_args['alpha']
if 'max_error' in assemble_args: log['MAX_ERROR'] = assemble_args['max_error']
if 'min_len' in assemble_args: log['MIN_LEN'] = assemble_args['min_len']
if 'max_len' in assemble_args: log['MAX_LEN'] = assemble_args['max_len']
if 'scan_reverse' in assemble_args: log['SCAN_REVERSE'] = assemble_args['scan_reverse']
if 'gap' in assemble_args: log['GAP'] = assemble_args['gap']
if 'min_ident' in assemble_args: log['MIN_IDENT'] = assemble_args['min_ident']
if 'evalue' in assemble_args: log['EVALUE'] = assemble_args['evalue']
if 'max_hits' in assemble_args: log['MAX_HITS'] = assemble_args['max_hits']
if 'fill' in assemble_args: log['FILL'] = assemble_args['fill']
log['NPROC'] = nproc
printLog(log)
# Count input files
head_count = countSeqFile(head_file)
tail_count = countSeqFile(tail_file)
if head_count != tail_count:
sys.exit('Error: FILE1 (n=%i) and FILE2 (n=%i) must have the same number of records' \
% (head_count, tail_count))
# Define feeder function and arguments
feed_func = feedPairQueue
# feed_args = {'seq_file_1': head_file,
# 'seq_file_2': tail_file,
# 'index_dict': index_dict}
feed_args = {'seq_file_1': head_file,
'seq_file_2': tail_file,
'coord_type': coord_type,
'delimiter': out_args['delimiter']}
# Define worker function and arguments
process_args = {'assemble_func': assemble_func,
'assemble_args': assemble_args,
'rc': rc,
'fields_1': head_fields,
'fields_2': tail_fields,
'delimiter': out_args['delimiter']}
work_func = processSeqQueue
work_args = {'process_func': processAssembly,
'process_args': process_args}
# Define collector function and arguments
collect_func = collectPairQueue
# collect_args = {'result_count': pair_count,
# 'seq_file_1': head_file,
# 'seq_file_2': tail_file,
# 'out_args': out_args}
collect_args = {'result_count': head_count,
'seq_file_1': head_file,
'seq_file_2': tail_file,
'out_args': out_args}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func,
feed_args, work_args, collect_args,
nproc, queue_size)
# Print log
log = OrderedDict()
log['OUTPUT'] = result['log'].pop('OUTPUT')
for k, v in result['log'].items(): log[k] = v
log['END'] = 'AssemblePairs'
printLog(log)
return result['out_files']
def unifyHeaders(seq_file,
collapse_func,
set_field=default_barcode_field,
unify_field=default_unify_field,
out_file=None,
out_args=default_out_args,
nproc=None,
queue_size=None):
"""
Merges and filters annotation fields within groups
Arguments:
seq_file : the sample sequence file name.
collapse_func : the function to use for collapsing annotations.
set_field : the annotation containing set IDs.
unify_field : the field for collection criteria.
out_file : output file name. Automatically generated from the input file if None.
out_args : common output argument dictionary from parseCommonArgs.
nproc : the number of processQueue processes;
if None defaults to the number of CPUs.
queue_size : maximum size of the argument queue;
if None defaults to 2*nproc.
Returns:
str: output file name.
"""
# Print parameter info
log = OrderedDict()
log['START'] = 'UnifyHeaders'
log['FILE'] = os.path.basename(seq_file)
log['SET_FIELD'] = set_field
log['UNIFY_FIELD'] = unify_field
log['NPROC'] = nproc
printLog(log)
# Define feeder function and arguments
index_args = {'field': set_field, 'delimiter': out_args['delimiter']}
feed_func = feedSeqQueue
feed_args = {
'seq_file': seq_file,
'index_func': indexSeqSets,
'index_args': index_args
}
# Define worker function and arguments
collapse_args = {'field': unify_field, 'delimiter': out_args['delimiter']}
work_func = processSeqQueue
work_args = {'process_func': collapse_func, 'process_args': collapse_args}
# Define collector function and arguments
collect_func = collectSeqQueue
collect_args = {
'seq_file': seq_file,
'label': 'unify',
'out_file': out_file,
'out_args': out_args,
'index_field': set_field
}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func, feed_args,
work_args, collect_args, nproc, queue_size)
# Print log
log = OrderedDict()
log['OUTPUT'] = result['log'].pop('OUTPUT')
for k, v in result['log'].items():
log[k] = v
log['END'] = 'UnifyHeaders'
printLog(log)
return result['out_files']
def estimateError(seq_file, cons_func=frequencyConsensus, cons_args={},
set_field=default_barcode_field, min_count=default_min_count, max_diversity=None,
out_args=default_out_args, nproc=None, queue_size=None):
"""
Calculates error rates of sequence sets
Arguments:
seq_file = the sample sequence file name
cons_func = the function to use for consensus generation
cons_args = a dictionary of arguments for the consensus function
set_field = the annotation field containing set IDs
min_count = threshold number of sequences to consider a set
max_diversity = a threshold defining the average pairwise error rate required to retain a read group;
if None do not calculate diversity
out_args = common output argument dictionary from parseCommonArgs
nproc = the number of processQueue processes;
if None defaults to the number of CPUs
queue_size = maximum size of the argument queue;
if None defaults to 2*nproc
Returns:
a list of tuples of (position error, quality error, nucleotide pairwise error) output file names
"""
# Define subcommand label dictionary
cmd_dict = {frequencyConsensus:'freq', qualityConsensus:'qual'}
# Print parameter info
log = OrderedDict()
log['START'] = 'EstimateError'
log['FILE'] = os.path.basename(seq_file)
log['MODE'] = cmd_dict.get(cons_func, cons_func.__name__)
log['SET_FIELD'] = set_field
log['MIN_COUNT'] = min_count
log['MAX_DIVERSITY'] = max_diversity
log['NPROC'] = nproc
printLog(log)
# Check input file type
in_type = getFileType(seq_file)
if in_type != 'fastq': sys.exit('ERROR: Input file must be FASTQ')
# Define feeder function and arguments
index_args = {'field': set_field, 'delimiter': out_args['delimiter']}
feed_func = feedSeqQueue
feed_args = {'seq_file': seq_file,
'index_func': indexSeqSets,
'index_args': index_args}
# Define worker function and arguments
work_func = processEEQueue
work_args = {'cons_func': cons_func,
'cons_args': cons_args,
'min_count': min_count,
'max_diversity': max_diversity}
# Define collector function and arguments
collect_func = collectEEQueue
collect_args = {'seq_file': seq_file,
'out_args': out_args,
'set_field': set_field}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func,
feed_args, work_args, collect_args,
nproc, queue_size)
# Print log
result['log']['END'] = 'EstimateError'
printLog(result['log'])
return result['out_files']
def assemblePairs(head_file,
tail_file,
assemble_func,
assemble_args={},
coord_type=default_coord,
rc='tail',
head_fields=None,
tail_fields=None,
out_file=None,
out_args=default_out_args,
nproc=None,
queue_size=None):
"""
Generates consensus sequences
Arguments:
head_file : the head sequence file name
tail_file : the tail sequence file name
assemble_func : the function to use to assemble paired ends
assemble_args : a dictionary of arguments to pass to the assembly function
coord_type : the sequence header format
rc : Defines which sequences ('head', 'tail', 'both', 'none') to reverse complement before assembly;
if 'none' do not reverse complement sequences
head_fields : list of annotations in head_file records to copy to assembled record;
if None do not copy an annotation
tail_fields : list of annotations in tail_file records to copy to assembled record;
if None do not copy an annotation
out_file : output file name. Automatically generated from the input file if None.
out_args : common output argument dictionary from parseCommonArgs
nproc = the number of processQueue processes;
if None defaults to the number of CPUs
queue_size = maximum size of the argument queue;
if None defaults to 2*nproc
Returns:
list: a list of successful output file names.
"""
# Define subcommand label dictionary
cmd_dict = {
alignAssembly: 'align',
joinAssembly: 'join',
referenceAssembly: 'reference',
sequentialAssembly: 'sequential'
}
cmd_name = cmd_dict.get(assemble_func, assemble_func.__name__)
# Print parameter info
log = OrderedDict()
log['START'] = 'AssemblePairs'
log['COMMAND'] = cmd_name
log['FILE1'] = os.path.basename(head_file)
log['FILE2'] = os.path.basename(tail_file)
log['COORD_TYPE'] = coord_type
if 'ref_file' in assemble_args: log['REFFILE'] = assemble_args['ref_file']
if 'alpha' in assemble_args: log['ALPHA'] = assemble_args['alpha']
if 'max_error' in assemble_args:
log['MAX_ERROR'] = assemble_args['max_error']
if 'min_len' in assemble_args: log['MIN_LEN'] = assemble_args['min_len']
if 'max_len' in assemble_args: log['MAX_LEN'] = assemble_args['max_len']
if 'scan_reverse' in assemble_args:
log['SCAN_REVERSE'] = assemble_args['scan_reverse']
if 'gap' in assemble_args: log['GAP'] = assemble_args['gap']
if 'min_ident' in assemble_args:
log['MIN_IDENT'] = assemble_args['min_ident']
if 'evalue' in assemble_args: log['EVALUE'] = assemble_args['evalue']
if 'max_hits' in assemble_args: log['MAX_HITS'] = assemble_args['max_hits']
if 'fill' in assemble_args: log['FILL'] = assemble_args['fill']
if 'aligner' in assemble_args: log['ALIGNER'] = assemble_args['aligner']
log['NPROC'] = nproc
printLog(log)
# Count input files
head_count = countSeqFile(head_file)
tail_count = countSeqFile(tail_file)
if head_count != tail_count:
printError('FILE1 (n=%i) and FILE2 (n=%i) must have the same number of records.' \
% (head_count, tail_count))
# Setup for reference alignment
if cmd_name in ('reference', 'sequential'):
ref_file = assemble_args.pop('ref_file')
db_exec = assemble_args.pop('db_exec')
# Build reference sequence dictionary
assemble_args['ref_dict'] = readReferenceFile(ref_file)
# Build reference database files
try:
db_func = {
'blastn': makeBlastnDb,
'usearch': makeUBlastDb
}[assemble_args['aligner']]
ref_db, db_handle = db_func(ref_file, db_exec)
assemble_args['ref_db'] = ref_db
except:
printError('Error building reference database for aligner %s with executable %s.' \
% (assemble_args['aligner'], db_exec))
# Define feeder function and arguments
feed_func = feedPairQueue
feed_args = {
'seq_file_1': head_file,
'seq_file_2': tail_file,
'coord_type': coord_type,
'delimiter': out_args['delimiter']
}
# Define worker function and arguments
process_args = {
'assemble_func': assemble_func,
'assemble_args': assemble_args,
'rc': rc,
'fields_1': head_fields,
'fields_2': tail_fields,
'delimiter': out_args['delimiter']
}
work_func = processSeqQueue
work_args = {'process_func': assemblyWorker, 'process_args': process_args}
# Define collector function and arguments
collect_func = collectPairQueue
collect_args = {
'seq_file_1': head_file,
'seq_file_2': tail_file,
'label': 'assemble',
'out_file': out_file,
'out_args': out_args
}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func, feed_args,
work_args, collect_args, nproc, queue_size)
# Close reference database handle
if cmd_name in ('reference', 'sequential'):
try:
db_handle.close()
except AttributeError:
db_handle.cleanup()
except:
printError('Cannot close reference database file.')
# Print log
log = OrderedDict()
log['OUTPUT'] = result['log'].pop('OUTPUT')
for k, v in result['log'].items():
log[k] = v
log['END'] = 'AssemblePairs'
printLog(log)
return result['out_files']
def maskPrimers(seq_file, primer_file, mode, align_func, align_args={},
max_error=default_max_error, barcode=False,
out_args=default_out_args, nproc=None, queue_size=None):
"""
Masks or cuts primers from sample sequences using local alignment
Arguments:
seq_file = name of file containing sample sequences
primer_file = name of the file containing primer sequences
mode = defines the action taken; one of 'cut','mask','tag'
align_func = the function to call for alignment
align_arcs = a dictionary of arguments to pass to align_func
max_error = maximum acceptable error rate for a valid alignment
barcode = if True add sequence preceding primer to description
out_args = common output argument dictionary from parseCommonArgs
nproc = the number of processQueue processes;
if None defaults to the number of CPUs
queue_size = maximum size of the argument queue;
if None defaults to 2*nproc
Returns:
a list of successful output file names
"""
# Define subcommand label dictionary
cmd_dict = {alignPrimers:'align', scorePrimers:'score'}
# Print parameter info
log = OrderedDict()
log['START'] = 'MaskPrimers'
log['COMMAND'] = cmd_dict.get(align_func, align_func.__name__)
log['SEQ_FILE'] = os.path.basename(seq_file)
log['PRIMER_FILE'] = os.path.basename(primer_file)
log['MODE'] = mode
log['BARCODE'] = barcode
log['MAX_ERROR'] = max_error
if 'start' in align_args: log['START_POS'] = align_args['start']
if 'max_len' in align_args: log['MAX_LEN'] = align_args['max_len']
if 'rev_primer' in align_args: log['REV_PRIMER'] = align_args['rev_primer']
if 'skip_rc' in align_args: log['SKIP_RC'] = align_args['skip_rc']
if 'gap_penalty' in align_args:
log['GAP_PENALTY'] = ', '.join([str(x) for x in align_args['gap_penalty']])
log['NPROC'] = nproc
printLog(log)
# Create dictionary of primer sequences to pass to maskPrimers
primers = readPrimerFile(primer_file)
if 'rev_primer' in align_args and align_args['rev_primer']:
primers = {k: reverseComplement(v) for k, v in primers.items()}
# Define alignment arguments and compile primers for align mode
align_args['primers'] = primers
align_args['score_dict'] = getDNAScoreDict(mask_score=(0, 1), gap_score=(0, 0))
if align_func is alignPrimers:
align_args['max_error'] = max_error
align_args['primers_regex'] = compilePrimers(primers)
# Define sequence masking arguments
mask_args = {'mode': mode,
'barcode': barcode,
'delimiter': out_args['delimiter']}
# Define feeder function and arguments
feed_func = feedSeqQueue
feed_args = {'seq_file': seq_file}
# Define worker function and arguments
work_func = processMPQueue
work_args = {'align_func': align_func,
'align_args': align_args,
'mask_args': mask_args,
'max_error': max_error}
# Define collector function and arguments
collect_func = collectSeqQueue
collect_args = {'seq_file': seq_file,
'task_label': 'primers',
'out_args': out_args}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func,
feed_args, work_args, collect_args,
nproc, queue_size)
# Print log
result['log']['END'] = 'MaskPrimers'
printLog(result['log'])
return result['out_files']
def alignSets(seq_file, align_func, align_args, barcode_field=default_barcode_field,
calc_div=False, out_args=default_out_args, nproc=None, queue_size=None):
"""
Performs a multiple alignment on sets of sequences
Arguments:
seq_file = the sample sequence file name
align_func = the function to use to align sequence sets
align_args = a dictionary of arguments to pass to align_func
barcode_field = the annotation containing set IDs
calc_div = if True calculate average pairwise error for each sequence set
out_args = common output argument dictionary from parseCommonArgs
nproc = the number of processQueue processes;
if None defaults to the number of CPUs
queue_size = maximum size of the argument queue;
if None defaults to 2*nproc
Returns:
a tuple of (valid_file, invalid_file) names
"""
# Define subcommand label dictionary
cmd_dict = {runMuscle:'align', offsetSeqSet:'offset'}
# Print parameter info
log = OrderedDict()
log['START'] = 'AlignSets'
log['COMMAND'] = cmd_dict[align_func]
log['FILE'] = os.path.basename(seq_file)
if 'mode' in align_args: log['MODE'] = align_args['mode']
log['BARCODE_FIELD'] = barcode_field
if 'field' in align_args: log['OFFSET_FIELD'] = align_args['field']
log['CALC_DIV'] = calc_div
log['NPROC'] = nproc
printLog(log)
# Define feeder function and arguments
index_args = {'field': barcode_field, 'delimiter': out_args['delimiter']}
feed_func = feedSeqQueue
feed_args = {'seq_file': seq_file,
'index_func': indexSeqSets,
'index_args': index_args}
# Define worker function and arguments
work_func = processASQueue
work_args = {'align_func': align_func,
'align_args': align_args,
'calc_div': calc_div,
'delimiter': out_args['delimiter']}
# Define collector function and arguments
collect_func = collectSeqQueue
collect_args = {'seq_file': seq_file,
'task_label': 'align',
'out_args': out_args,
'index_field': barcode_field}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func,
feed_args, work_args, collect_args,
nproc, queue_size)
# Print log
result['log']['END'] = 'AlignSets'
printLog(result['log'])
return result['out_files']
def clusterSets(seq_file,
ident=default_cluster_ident,
length_ratio=default_length_ratio,
seq_start=0,
seq_end=None,
set_field=default_barcode_field,
cluster_field=default_cluster_field,
cluster_prefix=default_cluster_prefix,
cluster_tool=default_cluster_tool,
cluster_exec=default_cluster_exec,
out_file=None,
out_args=default_out_args,
nproc=None,
queue_size=None):
"""
Performs clustering on sets of sequences
Arguments:
seq_file : the sample sequence file name.
ident : the identity threshold for clustering sequences.
length_ratio : minimum short/long length ratio allowed within a cluster.
seq_start : the start position to trim sequences at before clustering.
seq_end : the end position to trim sequences at before clustering.
set_field : the annotation containing set IDs.
cluster_field : the name of the output cluster field.
cluster_prefix : string defining a prefix for the cluster identifier.
cluster_exec : the path to the clustering executable.
cluster_tool : the clustering tool to use; one of cd-hit or usearch.
out_file : output file name. Automatically generated from the input file if None.
out_file : output file name. Automatically generated from the input file if None.
out_args : common output argument dictionary from parseCommonArgs.
nproc : the number of processQueue processes;
if None defaults to the number of CPUs.
queue_size : maximum size of the argument queue;
if None defaults to 2*nproc.
Returns:
str: the clustered output file name.
"""
# Print parameter info
log = OrderedDict()
log['START'] = 'ClusterSets'
log['COMMAND'] = 'set'
log['FILE'] = os.path.basename(seq_file)
log['IDENTITY'] = ident
log['SEQUENCE_START'] = seq_start
log['SEQUENCE_END'] = seq_end
log['SET_FIELD'] = set_field
log['CLUSTER_FIELD'] = cluster_field
log['CLUSTER_PREFIX'] = cluster_prefix
log['CLUSTER_TOOL'] = cluster_tool
log['NPROC'] = nproc
printLog(log)
# Set cluster tool
try:
cluster_func = map_cluster_tool.get(cluster_tool)
except:
printError('Invalid clustering tool %s.' % cluster_tool)
# Check the minimum identity
if ident < min_cluster_ident[cluster_tool]:
printError('Minimum identity %s too low for clustering tool %s.' %
(str(ident), cluster_tool))
# Define cluster function parameters
cluster_args = {
'cluster_exec': cluster_exec,
'ident': ident,
'length_ratio': length_ratio,
'seq_start': seq_start,
'seq_end': seq_end
}
# Define feeder function and arguments
index_args = {'field': set_field, 'delimiter': out_args['delimiter']}
feed_func = feedSeqQueue
feed_args = {
'seq_file': seq_file,
'index_func': indexSeqSets,
'index_args': index_args
}
# Define worker function and arguments
work_func = processQueue
work_args = {
'cluster_func': cluster_func,
'cluster_args': cluster_args,
'cluster_field': cluster_field,
'cluster_prefix': cluster_prefix,
'delimiter': out_args['delimiter']
}
# Define collector function and arguments
collect_func = collectSeqQueue
collect_args = {
'seq_file': seq_file,
'label': 'cluster',
'out_file': out_file,
'out_args': out_args,
'index_field': set_field
}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func, feed_args,
work_args, collect_args, nproc, queue_size)
# Print log
log = OrderedDict()
log['OUTPUT'] = result['log'].pop('OUTPUT')
for k, v in result['log'].items():
log[k] = v
log['END'] = 'ClusterSets'
printLog(log)
return result['out_files']
def buildConsensus(seq_file, barcode_field=default_barcode_field,
min_count=default_min_count, min_freq=default_min_freq,
min_qual=default_min_qual, primer_field=None, primer_freq=None,
max_gap=None, max_error=None, max_diversity=None,
copy_fields=None, copy_actions=None, dependent=False,
out_args=default_out_args, nproc=None, queue_size=None):
"""
Generates consensus sequences
Arguments:
seq_file = the sample sequence file name
barcode_field = the annotation field containing set IDs
min_count = threshold number of sequences to define a consensus
min_freq = the frequency cutoff to assign a base
min_qual = the quality cutoff to assign a base
primer_field = the annotation field containing primer tags;
if None do not annotate with primer tags
primer_freq = the maximum primer tag frequency that must be meet to build a consensus;
if None do not filter by primer frequency
max_gap = the maximum frequency of (., -) characters allowed before
deleting a position; if None do not delete positions
max_error = a threshold defining the maximum allowed error rate to retain a read group;
if None do not calculate error rate
max_diversity = a threshold defining the average pairwise error rate required to retain a read group;
if None do not calculate diversity
dependent = if False treat barcode group sequences as independent data
copy_fields = a list of annotations to copy into consensus sequence annotations;
if None no additional annotations will be copied
copy_actions = the list of actions to take for each copy_fields;
one of ['set', 'majority', 'min', 'max', 'sum']
out_args = common output argument dictionary from parseCommonArgs
nproc = the number of processQueue processes;
if None defaults to the number of CPUs
queue_size = maximum size of the argument queue;
if None defaults to 2*nproc
Returns:
a list of successful output file names
"""
# Print parameter info
log = OrderedDict()
log['START'] = 'BuildConsensus'
log['FILE'] = os.path.basename(seq_file)
log['BARCODE_FIELD'] = barcode_field
log['MIN_COUNT'] = min_count
log['MIN_FREQUENCY'] = min_freq
log['MIN_QUALITY'] = min_qual
log['MAX_GAP'] = max_gap
log['PRIMER_FIELD'] = primer_field
log['PRIMER_FREQUENCY'] = primer_freq
log['MAX_ERROR'] = max_error
log['MAX_DIVERSITY'] = max_diversity
log['DEPENDENT'] = dependent
log['COPY_FIELDS'] = ','.join(copy_fields) if copy_fields is not None else None
log['COPY_ACTIONS'] = ','.join(copy_actions) if copy_actions is not None else None
log['NPROC'] = nproc
printLog(log)
# Set consensus building function
in_type = getFileType(seq_file)
if in_type == 'fastq':
cons_func = qualityConsensus
cons_args = {'min_qual': min_qual,
'min_freq': min_freq,
'dependent': dependent}
elif in_type == 'fasta':
cons_func = frequencyConsensus
cons_args = {'min_freq': min_freq}
else:
sys.exit('ERROR: Input file must be FASTA or FASTQ')
# Define feeder function and arguments
index_args = {'field': barcode_field, 'delimiter': out_args['delimiter']}
feed_func = feedSeqQueue
feed_args = {'seq_file': seq_file,
'index_func': indexSeqSets,
'index_args': index_args}
# Define worker function and arguments
work_func = processBCQueue
work_args = {'cons_func': cons_func,
'cons_args': cons_args,
'min_count': min_count,
'primer_field': primer_field,
'primer_freq': primer_freq,
'max_gap': max_gap,
'max_error': max_error,
'max_diversity': max_diversity,
'copy_fields': copy_fields,
'copy_actions': copy_actions,
'delimiter': out_args['delimiter']}
# Define collector function and arguments
collect_func = collectSeqQueue
collect_args = {'seq_file': seq_file,
'task_label': 'consensus',
'out_args': out_args,
'index_field': barcode_field}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func,
feed_args, work_args, collect_args,
nproc, queue_size)
# Print log
result['log']['END'] = 'BuildConsensus'
printLog(result['log'])
return result['out_files']
def maskPrimers(seq_file,
primer_file,
align_func,
align_args={},
out_file=None,
out_args=default_out_args,
nproc=None,
queue_size=None):
"""
Masks or cuts primers from sample sequences using local alignment
Arguments:
seq_file : name of file containing sample sequences.
primer_file : name of the file containing primer sequences.
align_func : the function to call for alignment.
align_arcs : a dictionary of arguments to pass to align_func.
out_file : output file name. Automatically generated from the input file if None.
out_args : common output argument dictionary from parseCommonArgs.
nproc : the number of processQueue processes;
if None defaults to the number of CPUs.
queue_size : maximum size of the argument queue;
if None defaults to 2*nproc.
Returns:
list: a list of successful output file names.
"""
# Define subcommand label dictionary
cmd_dict = {
alignPrimers: 'align',
scorePrimers: 'score',
extractPrimers: 'extract'
}
# Print parameter info
log = OrderedDict()
log['START'] = 'MaskPrimers'
log['COMMAND'] = cmd_dict.get(align_func, align_func.__name__)
log['SEQ_FILE'] = os.path.basename(seq_file)
if primer_file is not None:
log['PRIMER_FILE'] = os.path.basename(primer_file)
if 'mode' in align_args: log['MODE'] = align_args['mode']
if 'max_error' in align_args: log['MAX_ERROR'] = align_args['max_error']
if 'start' in align_args: log['START_POS'] = align_args['start']
if 'length' in align_args: log['LENGTH'] = align_args['length']
if 'max_len' in align_args: log['MAX_LEN'] = align_args['max_len']
if 'rev_primer' in align_args: log['REV_PRIMER'] = align_args['rev_primer']
if 'skip_rc' in align_args: log['SKIP_RC'] = align_args['skip_rc']
if 'gap_penalty' in align_args:
log['GAP_PENALTY'] = ', '.join(
[str(x) for x in align_args['gap_penalty']])
if 'barcode' in align_args:
log['BARCODE'] = align_args['barcode']
if 'barcode' in align_args and align_args['barcode']:
log['BARCODE_FIELD'] = align_args['barcode_field']
log['PRIMER_FIELD'] = align_args['primer_field']
log['NPROC'] = nproc
printLog(log)
# Define alignment arguments and compile primers for align mode
if primer_file is not None:
primers = readPrimerFile(primer_file)
if 'rev_primer' in align_args and align_args['rev_primer']:
primers = {k: reverseComplement(v) for k, v in primers.items()}
align_args['primers'] = primers
align_args['score_dict'] = getDNAScoreDict(mask_score=(0, 1),
gap_score=(0, 0))
if align_func is alignPrimers:
align_args['primers_regex'] = compilePrimers(primers)
align_args['delimiter'] = out_args['delimiter']
# Define feeder function and arguments
feed_func = feedSeqQueue
feed_args = {'seq_file': seq_file}
# Define worker function and arguments
work_func = processSeqQueue
work_args = {'process_func': align_func, 'process_args': align_args}
# Define collector function and arguments
collect_func = collectSeqQueue
collect_args = {
'seq_file': seq_file,
'label': 'primers',
'out_file': out_file,
'out_args': out_args
}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func, feed_args,
work_args, collect_args, nproc, queue_size)
# Print log
result['log']['END'] = 'MaskPrimers'
printLog(result['log'])
return result['out_files']
def estimateSets(seq_file,
cons_func=frequencyConsensus,
cons_args={},
set_field=default_barcode_field,
min_count=default_min_count,
max_diversity=None,
out_args=default_out_args,
nproc=None,
queue_size=None):
"""
Calculates error rates of sequence sets
Arguments:
seq_file : the sample sequence file name
cons_func : the function to use for consensus generation
cons_args : a dictionary of arguments for the consensus function
set_field : the annotation field containing set IDs
min_count : threshold number of sequences to consider a set
max_diversity : a threshold defining the average pairwise error rate required to retain a read group;
if None do not calculate diversity
out_args : common output argument dictionary from parseCommonArgs
nproc : the number of processQueue processes;
if None defaults to the number of CPUs
queue_size : maximum size of the argument queue;
if None defaults to 2*nproc
Returns:
tuple : (position error, quality error, nucleotide pairwise error) output file names
"""
# Define subcommand label dictionary
cmd_dict = {frequencyConsensus: 'freq', qualityConsensus: 'qual'}
# Print parameter info
log = OrderedDict()
log['START'] = 'EstimateError'
log['FILE'] = os.path.basename(seq_file)
log['MODE'] = cmd_dict.get(cons_func, cons_func.__name__)
log['SET_FIELD'] = set_field
log['MIN_COUNT'] = min_count
log['MAX_DIVERSITY'] = max_diversity
log['NPROC'] = nproc
printLog(log)
# Check input file type
in_type = getFileType(seq_file)
if in_type != 'fastq':
printError('Input file must be FASTQ.')
# Define feeder function and arguments
index_args = {'field': set_field, 'delimiter': out_args['delimiter']}
feed_func = feedSeqQueue
feed_args = {
'seq_file': seq_file,
'index_func': indexSeqSets,
'index_args': index_args
}
# Define worker function and arguments
work_func = processEEQueue
work_args = {
'cons_func': cons_func,
'cons_args': cons_args,
'min_count': min_count,
'max_diversity': max_diversity
}
# Define collector function and arguments
collect_func = collectEEQueue
collect_args = {
'seq_file': seq_file,
'out_args': out_args,
'set_field': set_field
}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func, feed_args,
work_args, collect_args, nproc, queue_size)
# Print log
result['log']['END'] = 'EstimateError'
printLog(result['log'])
return result['out_files']
def defineClones(db_file, feed_func, work_func, collect_func, clone_func, cluster_func=None,
group_func=None, group_args={}, clone_args={}, cluster_args={},
out_args=default_out_args, nproc=None, queue_size=None):
"""
Define clonally related sequences
Arguments:
db_file = filename of input database
feed_func = the function that feeds the queue
work_func = the worker function that will run on each CPU
collect_func = the function that collects results from the workers
group_func = the function to use for assigning preclones
clone_func = the function to use for determining clones within preclonal groups
group_args = a dictionary of arguments to pass to group_func
clone_args = a dictionary of arguments to pass to clone_func
out_args = common output argument dictionary from parseCommonArgs
nproc = the number of processQueue processes;
if None defaults to the number of CPUs
queue_size = maximum size of the argument queue;
if None defaults to 2*nproc
Returns:
a list of successful output file names
"""
# Print parameter info
log = OrderedDict()
log['START'] = 'DefineClones'
log['DB_FILE'] = os.path.basename(db_file)
if group_func is not None:
log['GROUP_FUNC'] = group_func.__name__
log['GROUP_ARGS'] = group_args
log['CLONE_FUNC'] = clone_func.__name__
# TODO: this is yucky, but can be fixed by using a model class
clone_log = clone_args.copy()
if 'dist_mat' in clone_log: del clone_log['dist_mat']
log['CLONE_ARGS'] = clone_log
if cluster_func is not None:
log['CLUSTER_FUNC'] = cluster_func.__name__
log['CLUSTER_ARGS'] = cluster_args
log['NPROC'] = nproc
printLog(log)
# Define feeder function and arguments
feed_args = {'db_file': db_file,
'group_func': group_func,
'group_args': group_args}
# Define worker function and arguments
work_args = {'clone_func': clone_func,
'clone_args': clone_args}
# Define collector function and arguments
collect_args = {'db_file': db_file,
'out_args': out_args,
'cluster_func': cluster_func,
'cluster_args': cluster_args}
# Call process manager
result = manageProcesses(feed_func, work_func, collect_func,
feed_args, work_args, collect_args,
nproc, queue_size)
# Print log
result['log']['END'] = 'DefineClones'
printLog(result['log'])
return result['out_files']
def defineClones(db_file,
seq_field=default_junction_field,
v_field=default_v_field,
j_field=default_j_field,
max_missing=default_max_missing,
group_fields=None,
group_func=groupByGene,
group_args={},
clone_func=distanceClones,
clone_args={},
format=default_format,
out_file=None,
out_args=default_out_args,
nproc=None,
queue_size=None):
"""
Define clonally related sequences
Arguments:
db_file : filename of input database.
seq_field : sequence field used to determine clones.
v_field : field containing the V call.
j_field : field containing the J call.
max_missing : maximum number of non-ACGT characters to allow in the junction sequence.
group_fields : additional annotation fields to use to group preclones;
if None use only V and J.
group_func : the function to use for assigning preclones.
group_args : a dictionary of arguments to pass to group_func.
clone_func : the function to use for determining clones within preclonal groups.
clone_args : a dictionary of arguments to pass to clone_func.
format : input and output format.
out_file : output file name. Automatically generated from the input file if None.
out_args : common output argument dictionary from parseCommonArgs.
nproc : the number of processQueue processes;
if None defaults to the number of CPUs.
queue_size : maximum size of the argument queue;
if None defaults to 2*nproc.
Returns:
dict: dictionary of output pass and fail files.
"""
# Print parameter info
log = OrderedDict()
log['START'] = 'DefineClones'
log['FILE'] = os.path.basename(db_file)
log['SEQ_FIELD'] = seq_field
log['V_FIELD'] = v_field
log['J_FIELD'] = j_field
log['MAX_MISSING'] = max_missing
log['GROUP_FIELDS'] = ','.join(
group_fields) if group_fields is not None else None
for k in sorted(group_args):
log[k.upper()] = group_args[k]
for k in sorted(clone_args):
if k != 'dist_mat': log[k.upper()] = clone_args[k]
log['NPROC'] = nproc
printLog(log)
# Define format operators
try:
reader, writer, schema = getFormatOperators(format)
except ValueError:
printError('Invalid format %s.' % format)
# Translate to Receptor attribute names
seq_field = schema.toReceptor(seq_field)
v_field = schema.toReceptor(v_field)
j_field = schema.toReceptor(j_field)
if group_fields is not None:
group_fields = [schema.toReceptor(f) for f in group_fields]
# Define feeder function and arguments
group_args['group_fields'] = group_fields
group_args['v_field'] = v_field
group_args['j_field'] = j_field
feed_args = {
'db_file': db_file,
'reader': reader,
'group_func': group_func,
'group_args': group_args
}
# Define worker function and arguments
filter_args = {
'seq_field': seq_field,
'v_field': v_field,
'j_field': j_field,
'max_missing': max_missing
}
clone_args['seq_field'] = seq_field
work_args = {
'process_func': clone_func,
'process_args': clone_args,
'filter_func': filterMissing,
'filter_args': filter_args
}
# Define collector function and arguments
out_fields = getDbFields(db_file,
add=schema.fromReceptor('clone'),
reader=reader)
out_args['out_type'] = schema.out_type
collect_args = {
'db_file': db_file,
'fields': out_fields,
'writer': writer,
'out_file': out_file,
'out_args': out_args
}
# Check for required columns
try:
required = ['junction']
checkFields(required, out_fields, schema=schema)
except LookupError as e:
printError(e)
# Call process manager
result = manageProcesses(feed_func=feedDbQueue,
work_func=processDbQueue,
collect_func=collectQueue,
feed_args=feed_args,
work_args=work_args,
collect_args=collect_args,
nproc=nproc,
queue_size=queue_size)
# Print log
result['log']['END'] = 'DefineClones'
printLog(result['log'])
output = {k: v for k, v in result.items() if k in ('pass', 'fail')}
return output
