def extract_proteins_from_selected_families(
families_id_file,
fam_file,
pep_file,
output_dir="./",
pep_format="fasta",
out_prefix=None,
create_dir_for_each_family=False):
from Routines import SequenceRoutines, FileRoutines
fam_id_list = IdList()
fam_dict = SynDict()
#print(pep_file)
FileRoutines.safe_mkdir(output_dir)
out_dir = FileRoutines.check_path(output_dir)
create_directory_for_each_family = True if out_prefix else create_dir_for_each_family
if families_id_file:
fam_id_list.read(families_id_file)
fam_dict.read(fam_file, split_values=True, values_separator=",")
protein_dict = SeqIO.index_db("tmp.idx", pep_file, format=pep_format)
for fam_id in fam_id_list if families_id_file else fam_dict:
if fam_id in fam_dict:
if create_directory_for_each_family:
fam_dir = "%s%s/" % (out_dir, fam_id)
FileRoutines.safe_mkdir(fam_dir)
out_file = "%s%s.pep" % (fam_dir, out_prefix
if out_prefix else fam_id)
else:
out_file = "%s/%s.pep" % (out_dir, out_prefix
if out_prefix else fam_id)
SeqIO.write(SequenceRoutines.record_by_id_generator(
protein_dict, fam_dict[fam_id], verbose=True),
out_file,
format=pep_format)
else:
print("%s was not found" % fam_id)
os.remove("tmp.idx")
def split_proteins_per_species(dir_with_proteins,
output_dir,
input_format="fasta",
output_format="fasta"):
input_files = FileRoutines.make_list_of_path_to_files(
[dir_with_proteins] if isinstance(dir_with_proteins, str
) else dir_with_proteins)
out_dir = FileRoutines.check_path(output_dir)
FileRoutines.safe_mkdir(out_dir)
protein_dict = SeqIO.index_db("temp.idx",
input_files,
format=input_format)
syn_dict = SynDict()
for protein_id in protein_dict:
taxa_id = protein_id.split(".")[0]
# pep_id = ".".join(tmp_list[1:])
if taxa_id not in syn_dict:
syn_dict[taxa_id] = []
syn_dict[taxa_id].append(protein_id)
def renamed_records_generator(record_dict, taxa_id):
for record_id in syn_dict[taxa_id]:
record = deepcopy(record_dict[record_id])
#print(record)
record.id = ".".join(record_id.split(".")[1:])
yield record
for taxa_id in syn_dict:
out_file = "%s%s.pep" % (out_dir, taxa_id)
SeqIO.write(renamed_records_generator(protein_dict, taxa_id),
out_file,
format=output_format)
def parallel_search_tandem_repeat(self,
query_file,
output_prefix,
matching_weight=2,
mismatching_penalty=7,
indel_penalty=7,
match_probability=80,
indel_probability=10,
min_alignment_score=50,
max_period=500,
report_flanking_sequences=False,
splited_fasta_dir="splited_fasta_dir",
splited_result_dir="splited_output",
converted_output_dir="converted_output",
max_len_per_file=100000,
store_intermediate_files=False):
work_dir = os.getcwd()
splited_filename = FileRoutines.split_filename(query_file)
self.split_fasta_by_seq_len(query_file,
splited_fasta_dir,
max_len_per_file=max_len_per_file,
output_prefix=splited_filename[1])
common_options = self.parse_common_options(
matching_weight=matching_weight,
mismatching_penalty=mismatching_penalty,
indel_penalty=indel_penalty,
match_probability=match_probability,
indel_probability=indel_probability,
min_alignment_score=min_alignment_score,
max_period=max_period,
report_flanking_sequences=report_flanking_sequences,
make_dat_file=True)
common_options += " -h" # suppress html output
options_list = []
splited_files = os.listdir(splited_fasta_dir)
FileRoutines.safe_mkdir(splited_result_dir)
FileRoutines.safe_mkdir(converted_output_dir)
os.chdir(splited_result_dir)
input_dir = splited_fasta_dir if (splited_fasta_dir[0] == "/") or (splited_fasta_dir[0] == "~") \
else "../%s" % splited_fasta_dir
for filename in splited_files:
file_options = "%s/%s" % (input_dir, filename)
file_options += common_options
options_list.append(file_options)
self.parallel_execute(options_list)
os.chdir(work_dir)
trf_output_file_list = []
for filename in splited_files:
trf_output_file = "%s/%s.%i.%i.%i.%i.%i.%i.%i.dat" % (
splited_result_dir, filename, matching_weight,
mismatching_penalty, indel_penalty, match_probability,
indel_probability, min_alignment_score, max_period)
trf_output_file_list.append(trf_output_file)
trf_report = self.convert_trf_report(trf_output_file_list,
output_prefix)
"""
for suffix in (".rep", ".gff", ".simple.gff", ".short.tab", ".wide.tab", ".with_rep_seqs.gff", ".fasta"):
file_str = ""
merged_file = "%s%s" % (output_prefix, suffix)
for filename in splited_files:
file_str += " %s/%s%s" % (converted_output_dir, filename, suffix)
CGAS.cat(file_str, merged_file)
"""
if not store_intermediate_files:
shutil.rmtree(splited_fasta_dir)
shutil.rmtree(splited_result_dir)
shutil.rmtree(converted_output_dir)
return trf_report
action="store",
dest="max_memory_per_thread",
default="1G",
help="Maximum memory per thread. Default - 1G")
args = parser.parse_args()
if args.prepare_bam and ((not args.prepared_bam_prefix) or
(not args.temp_dir)):
raise ValueError(
"Options -e/--prepared_bam_prefix and -m/--temp_dir must be set if -p/--prepare_bam option is used"
)
SamtoolsV1.threads = args.threads
if args.prepare_bam or args.mix_ends:
FileRoutines.safe_mkdir(FileRoutines.check_path(args.temp_dir))
prepared_pe_bam_file = "%s.bam" % args.prepared_bam_prefix
prepared_unpaired_bam_file = (
"%s.unpaired.bam" %
args.prepared_bam_prefix) if args.mix_ends else None
"""
SamtoolsV1.prepare_bam_for_read_extraction(args.input, args.prepared_bam, temp_file_prefix=args.temp_dir,
max_memory_per_thread=args.max_memory_per_thread)
"""
SamtoolsV1.prepare_bam_for_read_extraction(
args.input,
prepared_pe_bam_file,
temp_file_prefix=args.temp_dir,
max_memory_per_thread=args.max_memory_per_thread,
bam_file_to_write_unpaired_reads=prepared_unpaired_bam_file)
if args.paired:
parser.add_argument("-i", "--input_file_list", action="store", dest="input", required=True,
type=FileRoutines.make_list_of_path_to_files_from_string,
help="Comma-separated list of input files/directories with sequences")
parser.add_argument("-o", "--output_directory", action="store", dest="output", type=FileRoutines.check_path,
help="Directory to output groups_of sequences")
parser.add_argument("-f", "--format", action="store", dest="format", default="fasta",
help="Format of input and output files. Allowed formats genbank, fasta(default)")
parser.add_argument("-e", "--extension", action="store", dest="extension",
help="Extension of output files. Default: equal to -f")
parser.add_argument("-d", "--id_file", action="store", dest="id_file",
help="File with groups of sequences to extract(.fam file).")
args = parser.parse_args()
FileRoutines.safe_mkdir(args.output)
args.extension = args.extension if args.extension else args.format
tmp_index_file = "temp.idx"
#id_list = read_ids(args.id_file)
id_list = IdSet(filename=args.id_file)
sequence_groups_id = SynDict()
sequence_groups_id.read(args.id_file, split_values=True)
#print("Parsing %s..." % args.input_file)
sequence_dict = SeqIO.index_db(tmp_index_file, args.input, format=args.format)
for group in sequence_groups_id:
SeqIO.write(SequenceRoutines.record_by_id_generator(sequence_dict, sequence_groups_id[group],
verbose=True),
"%s%s.%s" % (args.output, group, args.extension), format=args.format)
def align_samples(self,
samples_dir,
output_dir,
genome_dir,
genome_fasta=None,
samples=None,
annotation_gtf=None,
sjdboverhang=None,
genomeSAindexNbases=None,
genomeChrBinNbits=None,
genome_size=None,
feature_from_gtf_to_use_as_exon=None,
exon_tag_to_use_as_transcript_id=None,
exon_tag_to_use_as_gene_id=None,
length_of_sequences_flanking_junction=None,
junction_tab_file_list=None,
three_prime_trim=None,
five_prime_trim=None,
adapter_seq_for_three_prime_clip=None,
max_mismatch_percent_for_adapter_trimming=None,
three_prime_trim_after_adapter_clip=None,
output_type="BAM",
sort_bam=True,
max_memory_for_bam_sorting=8000000000,
include_unmapped_reads_in_bam=True,
output_unmapped_reads=True,
two_pass_mode=True,
max_intron_length=None):
#STAR.threads = threads
#STAR.path = star_dir
if genome_fasta:
STAR.index(genome_dir,
genome_fasta,
annotation_gtf=annotation_gtf,
junction_tab_file=junction_tab_file_list,
sjdboverhang=sjdboverhang,
genomeSAindexNbases=genomeSAindexNbases,
genomeChrBinNbits=genomeChrBinNbits,
genome_size=genome_size)
sample_list = samples if samples else self.get_sample_list(samples_dir)
FileRoutines.safe_mkdir(output_dir)
for sample in sample_list:
print("Handling %s" % sample)
sample_dir = "%s/%s/" % (samples_dir, sample)
alignment_sample_dir = "%s/%s/" % (output_dir, sample)
FileRoutines.safe_mkdir(alignment_sample_dir)
filetypes, forward_files, reverse_files = FileRoutines.make_lists_forward_and_reverse_files(
sample_dir)
print "\tAligning reads..."
STAR.align(
genome_dir,
forward_files,
reverse_read_list=reverse_files,
annotation_gtf=annotation_gtf if not genome_fasta else None,
feature_from_gtf_to_use_as_exon=feature_from_gtf_to_use_as_exon,
exon_tag_to_use_as_transcript_id=
exon_tag_to_use_as_transcript_id,
exon_tag_to_use_as_gene_id=exon_tag_to_use_as_gene_id,
length_of_sequences_flanking_junction=
length_of_sequences_flanking_junction,
junction_tab_file_list=junction_tab_file_list,
three_prime_trim=three_prime_trim,
five_prime_trim=five_prime_trim,
adapter_seq_for_three_prime_clip=
adapter_seq_for_three_prime_clip,
max_mismatch_percent_for_adapter_trimming=
max_mismatch_percent_for_adapter_trimming,
three_prime_trim_after_adapter_clip=
three_prime_trim_after_adapter_clip,
output_type=output_type,
sort_bam=sort_bam,
max_memory_for_bam_sorting=max_memory_for_bam_sorting,
include_unmapped_reads_in_bam=include_unmapped_reads_in_bam,
output_unmapped_reads=output_unmapped_reads,
output_dir=alignment_sample_dir,
two_pass_mode=two_pass_mode,
max_intron_length=max_intron_length)
print "\tIndexing bam file..."
resulting_bam_file = "%s/Aligned.sortedByCoord.out.bam" % alignment_sample_dir
SamtoolsV1.index(resulting_bam_file)
STAR.path = args.star_dir
if args.genome_fasta:
STAR.index(args.genome_dir,
args.genome_fasta,
annotation_gtf=args.annotation_gtf,
junction_tab_file=args.junction_tab_file,
sjdboverhang=None,
genomeSAindexNbases=None,
genomeChrBinNbits=None,
genome_size=args.genome_size)
sample_list = args.samples if args.samples else Pipeline.get_sample_list(
args.samples_dir)
FileRoutines.safe_mkdir(args.output_dir)
for sample in sample_list:
print("Handling %s" % sample)
sample_dir = "%s/%s/" % (args.samples_dir, sample)
alignment_sample_dir = "%s/%s/" % (args.output_dir, sample)
FileRoutines.safe_mkdir(alignment_sample_dir)
filetypes, forward_files, reverse_files = FileRoutines.make_lists_forward_and_reverse_files(
sample_dir)
print "\tAligning reads..."
STAR.align(
args.genome_dir,
forward_files,
reverse_read_list=reverse_files,
def parallel_align(self,
list_of_files,
output_directory,
output_suffix=None,
tree_file=None,
output_format=None,
show_xml=None,
show_tree=None,
show_ancestral_sequences=None,
show_evolutionary_events=None,
showall=None,
compute_posterior_support=None,
njtree=None,
skip_insertions=False,
codon_alignment=None,
translated_alignment=None,
cmd_log_file=None,
cpus_per_task=1,
handling_mode="local",
job_name=None,
log_prefix=None,
error_log_prefix=None,
max_jobs=None,
max_running_time=None,
max_memory_per_node=None,
max_memmory_per_cpu=None,
modules_list=None,
environment_variables_dict=None):
common_options = self.parse_common_options(
tree_file=tree_file,
output_format=output_format,
show_xml=show_xml,
show_tree=show_tree,
show_ancestral_sequences=show_ancestral_sequences,
show_evolutionary_events=show_evolutionary_events,
showall=showall,
compute_posterior_support=compute_posterior_support,
njtree=njtree,
skip_insertions=skip_insertions,
codon_alignment=codon_alignment,
translated_alignment=translated_alignment)
FileRoutines.safe_mkdir(output_directory)
options_list = []
for filename in list_of_files:
basename = FileRoutines.split_filename(filename)[1]
op = common_options
op += " -d=%s" % filename
op += " -o=%s/%s.fasta" % (output_directory,
("%s_%s" % (basename, output_suffix))
if output_suffix else basename)
options_list.append(op)
if handling_mode == "local":
self.parallel_execute(options_list)
elif handling_mode == "slurm":
cmd_list = [
"%s%s %s" %
((self.path + "/") if self.path else "", self.cmd, options)
for options in options_list
]
self.slurm_run_multiple_jobs_in_wrap_mode(
cmd_list,
cmd_log_file,
max_jobs=max_jobs,
job_name=job_name,
log_prefix=log_prefix,
error_log_prefix=error_log_prefix,
cpus_per_node=None,
max_running_jobs=None,
max_running_time=max_running_time,
cpus_per_task=cpus_per_task,
max_memory_per_node=max_memory_per_node,
max_memmory_per_cpu=max_memmory_per_cpu,
modules_list=modules_list,
environment_variables_dict=environment_variables_dict)
AUGUSTUS.extract_CDS_annotations_from_output(final_gff, final_CDS_gff)
for stat_file in output_evidence_stats, output_supported_stats, \
output_swissprot_pfam_or_hints_supported_transcripts_longest_pep_evidence, \
output_swissprot_pfam_and_hints_supported_transcripts_longest_pep_evidence, \
output_swissprot_pfam_or_hints_supported_transcripts_evidence, \
output_swissprot_pfam_and_hints_supported_transcripts_evidence:
MatplotlibRoutines.percent_histogram_from_file(
stat_file,
stat_file,
data_type=None,
column_list=(2, ),
comments="#",
n_bins=20,
title="Transcript support by hints",
extensions=("png", "svg"),
legend_location="upper center",
stats_as_legend=True)
if args.pfam_db and args.swissprot_db:
db_or_hints_dir = "supported_by_db_or_hints/"
db_and_hints_dir = "supported_by_db_and_hints/"
for directory in db_and_hints_dir, db_or_hints_dir:
FileRoutines.safe_mkdir(directory)
os.system("mv %s.supported.transcripts.swissprot_or_pfam_or_hints* %s" %
(args.output, db_or_hints_dir))
os.system("mv %s.supported.transcripts.swissprot_or_pfam_and_hints* %s" %
(args.output, db_and_hints_dir))
def parallel_positive_selection_test(self,
in_dir,
tree_file,
out_dir,
results_file,
seq_type="codons",
codon_frequency="F3X4",
noisy=3,
verbose="concise",
runmode=0,
clock=0,
aminoacid_distance=None,
genetic_code=0,
fix_kappa=False,
kappa=5,
getSE=0,
RateAncestor=0,
small_difference=0.000001,
clean_data=True,
method=0):
"""
This function implements positive selection test (branch-site model)
for branch labeled in tree file using model_A vs model_A_null(omega fixed to 1) comparison
"""
FileRoutines.safe_mkdir(out_dir)
alignment_files_list = FileRoutines.make_list_of_path_to_files(in_dir)
tree_file_abs_path = os.path.abspath(tree_file)
options_list = []
dir_list = []
basename_dir_list = []
model_list = ["Model_A", "Model_A_null"]
fix_omega_dict = {"Model_A": False, "Model_A_null": True}
for filename in alignment_files_list:
directory, basename, extension = FileRoutines.split_filename(
filename)
filename_out_dir = os.path.abspath("%s/%s/" % (out_dir, basename))
basename_dir_list.append(basename)
FileRoutines.safe_mkdir(filename_out_dir)
for model in model_list:
model_dir = "%s/%s/" % (filename_out_dir, model)
FileRoutines.safe_mkdir(model_dir)
out_file = "%s/%s/%s.out" % (filename_out_dir, model, basename)
ctl_file = "%s/%s/%s.ctl" % (filename_out_dir, model, basename)
options_list.append("%s.ctl" % basename)
dir_list.append(model_dir)
self.generate_ctl_file(os.path.abspath(filename),
tree_file_abs_path,
out_file,
ctl_file,
seq_type=seq_type,
codon_frequency=codon_frequency,
noisy=noisy,
verbose=verbose,
runmode=runmode,
clock=clock,
aminoacid_distance=aminoacid_distance,
model=2,
nssites=2,
genetic_code=genetic_code,
fix_kappa=fix_kappa,
kappa=kappa,
fix_omega=fix_omega_dict[model],
omega=1,
getSE=getSE,
RateAncestor=RateAncestor,
Mgene=0,
small_difference=small_difference,
clean_data=clean_data,
method=method)
self.parallel_execute(options_list, dir_list=dir_list)
results_dict = OrderedDict()
double_delta_dict = OrderedDict()
raw_pvalues_dict = OrderedDict()
raw_pvalues_list = []
for basename in basename_dir_list:
results_dict[basename] = OrderedDict()
for model in model_list:
output_file = "%s/%s/%s/%s.out" % (out_dir, basename, model,
basename)
codeml_report = CodeMLReport(output_file)
results_dict[basename][model] = codeml_report.LnL
skipped_genes_set = set()
for basename in basename_dir_list:
for model in model_list:
if results_dict[basename][model] is None:
print("LnL was not calculated for %s" % basename)
skipped_genes_set.add(basename)
break
else:
doubled_delta = 2 * (results_dict[basename]["Model_A"] -
results_dict[basename]["Model_A_null"])
p_value = chisqprob(doubled_delta, 1) # degrees of freedom = 1
double_delta_dict[basename] = doubled_delta
raw_pvalues_dict[basename] = p_value
raw_pvalues_list.append(p_value)
adjusted_pvalues_list = fdrcorrection0(raw_pvalues_list)[1]
#print adjusted_pvalues_list
i = 0
with open(results_file, "w") as out_fd:
out_fd.write(
"id\tmodel_a_null,LnL\tmodel_a,LnL\t2*delta\traw p-value\tadjusted p-value\n"
)
for basename in basename_dir_list:
for model in model_list:
if results_dict[basename][model] is None:
print("LnL was not calculated for %s" % basename)
break
else:
#doubled_delta = 2 * (results_dict[basename]["Model_A"] - results_dict[basename]["Model_A_null"])
#p_value = chisqprob(doubled_delta, 1) # degrees of freedom = 1
#print basename, results_dict[basename]["Model_A_null"],results_dict[basename]["Model_A"], double_delta_dict[basename], raw_pvalues_dict[basename], adjusted_pvalues_list[i]
out_fd.write(
"%s\t%f\t%f\t%f\t%f\t%f\n" %
(basename, results_dict[basename]["Model_A_null"],
results_dict[basename]["Model_A"],
double_delta_dict[basename],
raw_pvalues_dict[basename], adjusted_pvalues_list[i]))
i += 1
def parallel_codeml(self,
in_dir,
tree_file,
out_dir,
seq_type="codons",
codon_frequency="F3X4",
noisy=0,
verbose="concise",
runmode=0,
clock=0,
aminoacid_distance=None,
model=1,
nssites=0,
genetic_code=0,
fix_kappa=False,
kappa=5,
fix_omega=False,
omega=0.2,
getSE=0,
RateAncestor=0,
small_difference=0.000001,
clean_data=True,
method=0,
Mgene=None):
FileRoutines.safe_mkdir(out_dir)
alignment_files_list = FileRoutines.make_list_of_path_to_files(in_dir)
tree_file_abs_path = os.path.abspath(tree_file)
options_list = []
dir_list = []
for filename in alignment_files_list:
directory, basename, extension = FileRoutines.split_filename(
filename)
filename_out_dir = os.path.abspath("%s/%s/" % (out_dir, basename))
out_file = "%s/%s.out" % (filename_out_dir, basename)
ctl_file = "%s/%s.ctl" % (filename_out_dir, basename)
options_list.append(ctl_file)
dir_list.append(filename_out_dir)
FileRoutines.safe_mkdir(filename_out_dir)
self.generate_ctl_file(os.path.abspath(filename),
tree_file_abs_path,
out_file,
ctl_file,
seq_type=seq_type,
codon_frequency=codon_frequency,
noisy=noisy,
verbose=verbose,
runmode=runmode,
clock=clock,
aminoacid_distance=aminoacid_distance,
model=model,
nssites=nssites,
genetic_code=genetic_code,
fix_kappa=fix_kappa,
kappa=kappa,
fix_omega=fix_omega,
omega=omega,
getSE=getSE,
RateAncestor=RateAncestor,
Mgene=Mgene,
small_difference=small_difference,
clean_data=clean_data,
method=method)
self.parallel_execute(options_list, dir_list=dir_list)
dest="output",
type=FileRoutines.check_path,
help="Output directory")
#parser.add_argument("-p", "--convert_options", action="store", dest="convert_options",
# help="Options for convert")
parser.add_argument("-d",
"--dont_make_negative",
action="store_true",
dest="dont_negative",
help="Dont make negative")
args = parser.parse_args()
temp_dir = "temp/"
FileRoutines.safe_mkdir(temp_dir)
BioConvert.threads = args.threads
Convert.threads = args.threads
BioConvert.parallel_convert(args.input, temp_dir)
if args.dont_negative:
os.rename(temp_dir, args.output)
else:
converted_files = os.listdir(temp_dir)
converted_files = list(
map(lambda s: "%s%s" % (temp_dir, s), converted_files))
Convert.parallel_convert(
converted_files, args.output,
type=FileRoutines.check_path,
help="Directory to write fam files named by species names")
parser.add_argument("-d", "--syn_file", action="store", dest="syn_file", required=True,
help="File with taxa ids and species names")
parser.add_argument("-k", "--key_index", action="store", dest="key_index", type=int, default=0,
help="Key column in file with synonyms(0-based)")
parser.add_argument("-v", "--value_index", action="store", dest="value_index", type=int, default=1,
help="Value column in file with synonyms(0-based)")
parser.add_argument("-c", "--comments_prefix", action="store", dest="comments_prefix", default="#",
help="Prefix of comments in synonyms file")
parser.add_argument("-m", "--columns_separator", action="store", dest="separator", default="\t",
help="Column separator in file with synonyms")
parser.add_argument("-e", "--header", action="store_true", dest="header", default=False,
help="Header is present in synonyms file. Default - False")
args = parser.parse_args()
syn_dict = SynDict()
syn_dict.read(args.syn_file, header=args.header, separator=args.separator, key_index=args.key_index,
value_index=args.value_index, comments_prefix=args.comments_prefix)
FileRoutines.safe_mkdir(args.output_files_dir)
input_files = os.listdir(args.input_files_dir)
for filename in input_files:
directory, taxon_id, extension = FileRoutines.split_filename(filename)
if taxon_id not in syn_dict:
print("Species name was not found for taxon %s" % taxon_id)
continue
shutil.copy("%s%s" % (args.input_files_dir, filename),
"%s%s%s" % (args.output_files_dir, syn_dict[taxon_id], extension))
parser.add_argument("-n",
"--check_file_contains_gene_counts",
action="store_true",
dest="check_with_counts",
default=False,
help="File to check contains gene counts")
parser.add_argument("-o",
"--out_dir",
action="store",
dest="out_dir",
default="compare_dir",
help="Output directory")
args = parser.parse_args()
FileRoutines.safe_mkdir(args.out_dir)
ref_clusters_dict = read_cluster_file(args.ref_file,
with_counts=args.ref_with_counts)
check_clusters_dict = read_cluster_file(args.file_to_check,
with_counts=args.check_with_counts)
totally_in_ref = len(ref_clusters_dict)
totally = len(check_clusters_dict)
synonym_file = "synonym.t"
contained_fully_in_file = "contained_fully_in.t"
contained_in_file = "contained_in.t"
include_file = "include.t"
all_file = "all.t"
synonym_dict = OrderedDict()
