def select_pass_variants(raw_vcf, nocall_fr=0.1):
"""
Filter a vcf file. Output a vcf file with PASS positions adding a .pass to the output file
Used since it creates the neccesasary vcf index
https://software.broadinstitute.org/gatk/documentation/tooldocs/current/org_broadinstitute_hellbender_tools_walkers_variantutils_SelectVariants.php
https://gatkforums.broadinstitute.org/gatk/discussion/13127/do-gatk4-tools-ignore-vcf-sites-marked-as-filtered-or-must-they-be-removed-from-the-file
"""
#max_nocall=2,
input_vcf = os.path.abspath(raw_vcf)
check_file_exists(input_vcf)
raw_vcf_file_name = (".").join(input_vcf.split(".")[:-1])
extension = ".pass.vcf"
vcf_selected_output_file = raw_vcf_file_name + extension
cmd = [
"gatk", "SelectVariants", "--variant", input_vcf,
"--max-nocall-fraction",
str(nocall_fr), "--exclude-filtered", "--remove-unused-alternates",
"--output", vcf_selected_output_file
]
#"--max-nocall-number", str(max_nocall),
execute_subprocess(cmd)
def select_variants(raw_vcf, select_type='SNP'):
"""
https://software.broadinstitute.org/gatk/documentation/tooldocs/current/org_broadinstitute_hellbender_tools_walkers_variantutils_SelectVariants.php
gatk SelectVariants -V cohort.vcf.gz -select-type SNP -O snps.vcf.gz
"""
if select_type == "SNP":
extension = ".snp.vcf"
elif select_type == "INDEL":
extension = ".indel.vcf"
else:
print(RED + BOLD + "Choose a correct type to filter" + END_FORMATTING)
input_vcf = os.path.abspath(raw_vcf)
check_file_exists(input_vcf)
raw_vcf_file_name = (".").join(input_vcf.split(".")[:-2])
#file_name = raw_vcf_file_name.split("/")[-1] #sample_name
vcf_selected_output_file = raw_vcf_file_name + extension
#memory_param = "-Xmx" + str(args.memory) + "g"
#"--java-options", memory_param,
cmd = [
"gatk", "SelectVariants", "--variant", input_vcf,
"--select-type-to-include", select_type, "--select-type-to-include",
"MIXED", "--output", vcf_selected_output_file
]
# "--remove-unused-alternates",
execute_subprocess(cmd)
def ddtb_compare(final_database):
database_file = os.path.abspath(final_database)
check_file_exists(database_file)
presence_ddbb = import_to_pandas(database_file, header=True)
output_path = database_file.split(".")[0]
print("Output path is: " + output_path)
print(BLUE + BOLD + "Comparing all samples in " + database_file + END_FORMATTING)
prior_pairwise = datetime.datetime.now()
#Calculate pairwise snp distance for all and save file
print(CYAN + "Pairwise distance" + END_FORMATTING)
pairwise_file = output_path + ".snp.pairwise.tsv"
snp_distance_pairwise(presence_ddbb, pairwise_file)
after_pairwise = datetime.datetime.now()
print("Done with pairwise in: %s" % (after_pairwise - prior_pairwise))
#Calculate snp distance for all and save file
print(CYAN + "SNP distance" + END_FORMATTING)
snp_dist_file = output_path + ".snp.tsv"
snp_distance_matrix(presence_ddbb, snp_dist_file)
#Calculate hamming distance for all and save file
print(CYAN + "Hamming distance" + END_FORMATTING)
hmm_dist_file = output_path + ".hamming.tsv"
hamming_distance_matrix(presence_ddbb, hmm_dist_file)
"""
#Represent pairwise snp distance for all and save file
print(CYAN + "Drawing distance" + END_FORMATTING)
prior_represent = datetime.datetime.now()
png_dist_file = output_path + ".snp.distance.png"
#clustermap_dataframe(presence_ddbb, png_dist_file)
after_represent = datetime.datetime.now()
print("Done with distance drawing in: %s" % (after_represent - prior_represent))
"""
#Represent dendrogram snp distance for all and save file
print(CYAN + "Drawing dendrogram" + END_FORMATTING)
png_dend_file = output_path + ".snp.dendrogram.png"
dendogram_dataframe(presence_ddbb, png_dend_file)
#Output a Newick file distance for all and save file
print(CYAN + "Newick dendrogram" + END_FORMATTING)
newick_file = output_path + ".nwk"
linkage_to_newick(presence_ddbb, newick_file)
#Output a binary snp matrix distance in rdf format
print(CYAN + "rdf format" + END_FORMATTING)
rdf_file = output_path + ".rdf"
matrix_to_rdf(presence_ddbb, rdf_file)
#Output a list of all common snps in group compared
print(CYAN + "Common SNPs" + END_FORMATTING)
common_file = output_path + ".common.txt"
matrix_to_common(presence_ddbb, common_file)
def ddtb_compare(args):
database_file = os.path.abspath(args.final_database)
check_file_exists(database_file)
presence_ddbb = import_to_pandas(database_file, header=True)
if args.output_file:
output_file = os.path.abspath(args.output_file)
output_path = output_file.split(".")[0]
else:
output_path = database_file.split(".")[0]
print("Output path is: " + output_path)
if args.all_compare:
print(BLUE + BOLD + "Comparing all samples in " + database_file +
END_FORMATTING)
prior_pairwise = datetime.datetime.now()
#Calculate pairwise snp distance for all and save file
print(CYAN + "Pairwise distance" + END_FORMATTING)
pairwise_file = output_path + ".snp.pairwise.tsv"
snp_distance_pairwise(presence_ddbb, pairwise_file)
after_pairwise = datetime.datetime.now()
print("Done with pairwise in: %s" % (after_pairwise - prior_pairwise))
#Calculate snp distance for all and save file
print(CYAN + "SNP distance" + END_FORMATTING)
snp_dist_file = output_path + ".snp.tsv"
snp_distance_matrix(presence_ddbb, snp_dist_file)
#Calculate hamming distance for all and save file
print(CYAN + "Hamming distance" + END_FORMATTING)
hmm_dist_file = output_path + ".hamming.tsv"
hamming_distance_matrix(presence_ddbb, hmm_dist_file)
"""
#Represent pairwise snp distance for all and save file
print(CYAN + "Drawing distance" + END_FORMATTING)
prior_represent = datetime.datetime.now()
png_dist_file = output_path + ".snp.distance.png"
#clustermap_dataframe(presence_ddbb, png_dist_file)
after_represent = datetime.datetime.now()
print("Done with distance drawing in: %s" % (after_represent - prior_represent))
"""
#Represent dendrogram snp distance for all and save file
print(CYAN + "Drawing dendrogram" + END_FORMATTING)
png_dend_file = output_path + ".snp.dendrogram.png"
dendogram_dataframe(presence_ddbb, png_dend_file)
#Output a Newick file distance for all and save file
print(CYAN + "Newick dendrogram" + END_FORMATTING)
newick_file = output_path + ".nwk"
linkage_to_newick(presence_ddbb, newick_file)
else:
print("sample mode is not implemented")
"""
def hard_filter(selected_vcf, select_type='SNP'):
"""
https://software.broadinstitute.org/gatk/documentation/article.php?id=6925
https://software.broadinstitute.org/gatk/documentation/tooldocs/current/org_broadinstitute_hellbender_tools_walkers_filters_VariantFiltration.php
https://software.broadinstitute.org/gatk/documentation/article?id=23216
SNP:
gatk VariantFiltration -V snps.vcf.gz "--filter-expression", "QD < 2.0", "--filter-name", "QD2" \
"--filter-expression", "QUAL < 30.0", "--filter-name", "QUAL30" "--filter-expression", "SOR > 3.0", "--filter-name", "SOR3" "--filter-expression", "FS > 60.0", "--filter-name", "FS60" \
"--filter-expression", "MQ < 40.0", "--filter-name", "MQ40" "--filter-expression", "MQRankSum < -12.5", "--filter-name", "MQRankSum-12.5" "--filter-expression", "ReadPosRankSum < -8.0" \
, "--filter-name", "ReadPosRankSum-8" -O snps_filtered.vcf.gz
INDEL:
gatk VariantFiltration -V indels.vcf.gz "--filter-expression", "QD < 2.0", "--filter-name", "QD2" "--filter-expression", "QUAL < 30.0", "--filter-name", "QUAL30" \
-"--filter-expression", "FS > 200.0", "--filter-name", "FS200" -"--filter-expression", "ReadPosRankSum < -20.0", "--filter-name", "ReadPosRankSum-20" -O indels_filtered.vcf.gz
#--filterExpression "QD<2.0||FS>60.0||MQ<40.0||MQRankSum<-12.5||ReadPosRankSum<-8.0" --filterName "my_snp_filter"
"""
input_vcf = os.path.abspath(selected_vcf)
check_file_exists(input_vcf)
selected_vcf_file_name = (".").join(input_vcf.split(".")[:-2])
if select_type == "SNP":
extension = ".snp.hf.vcf"
vcf_hard_filtered_output_file = selected_vcf_file_name + extension
cmd = [
"gatk", "VariantFiltration", "--variant", input_vcf,
"--filter-expression", "QD < 2.0", "--filter-name", "QD2",
"--filter-expression", "QUAL < 30.0", "--filter-name", "QUAL30",
"--filter-expression", "SOR > 3.5", "--filter-name", "SOR3",
"--filter-expression", "FS > 60.0", "--filter-name", "FS60",
"--filter-expression", "MQ < 40.0", "--filter-name", "MQ40",
"--filter-expression", "DP < 10", "--filter-name", "DP10",
"--filter-expression", "MQRankSum < -12.5", "--filter-name",
"MQRankSum-12.5", "--filter-expression", "ReadPosRankSum < -8.0",
"--filter-name", "ReadPosRankSum-8", "--output",
vcf_hard_filtered_output_file
]
elif select_type == "INDEL":
extension = ".indel.hf.vcf"
vcf_hard_filtered_output_file = selected_vcf_file_name + extension
cmd = [
"gatk", "VariantFiltration", "--variant", input_vcf,
"--filter-expression", "QD < 2.0", "--filter-name", "QD2",
"--filter-expression", "QUAL < 30.0", "--filter-name", "QUAL30",
"--filter-expression", "SOR > 10.0", "--filter-name", "SOR10",
"--filter-expression", "FS > 200.0", "--filter-name", "FS200",
"--filter-expression", "ReadPosRankSum < -20.0", "--filter-name",
"ReadPosRankSum-20", "--output", vcf_hard_filtered_output_file
]
else:
print(RED + BOLD + "Choose a correct type to filter" + END_FORMATTING)
execute_subprocess(cmd)
def select_pass(raw_vcf):
"""
Homemade script
Filter a vcf file. Output a vcf file with PASS positions adding a .pass to the output file
"""
input_vcf = os.path.abspath(raw_vcf)
raw_vcf_file_name = (".").join(input_vcf.split(".")[:-1])
extension = ".pass.vcf"
vcf_selected_output_file = raw_vcf_file_name + extension
check_file_exists(input_vcf)
with open(input_vcf, "r") as f:
with open(vcf_selected_output_file, "w") as f1:
for line in f:
if line.startswith("#"):
f1.write(line)
else:
if line.split("\t")[6] == "PASS":
f1.write(line)
def ddtb_add(input_folder, output_filename, recalibrate=False, sample_filter=False, vcf_suffix=".combined.hf.SNP.final.vcf" ):
directory = os.path.abspath(input_folder)
output_filename = os.path.abspath(output_filename)
#Make sure output exist to force change name
if os.path.isfile(output_filename):
print(YELLOW + "ERROR: " + BOLD + "output database EXIST, choose a different name or manually delete" + END_FORMATTING)
sys.exit(1)
final_ddbb = blank_database()
sample_filter_list = []
#Handle sample filter
if sample_filter == False:
sample_filter_list = [x.split(".")[0] for x in os.listdir(input_folder) if x.endswith(vcf_suffix)]
else:
if os.path.isfile(sample_filter):
with open(sample_filter, 'r') as f:
for line in f:
sample_filter_list.append(line.strip())
else:
"Sample file don't exist"
sys.exit(1)
print(sample_filter_list)
if len(sample_filter_list) < 1:
print("prease provide 2 or more samples")
sys.exit(1)
#print("Previous final database contains %s rows and %s columns\n" % final_ddbb.shape)
print("The directory selected is: %s" % directory)
all_samples = 0
new_samples = 0
for filename in os.listdir(directory):
if not filename.startswith('.') and filename.endswith(vcf_suffix):
all_samples = all_samples + 1
positions_shared = []
positions_added = []
sample = filename.split(".")[0] #Manage sample name
if sample in sample_filter_list:
print("\nThe file is: %s" % filename)
file = os.path.join(directory, filename) #Whole file path
check_file_exists(file) #Manage file[s]. Check if file exist and is greater than 0
new_sample = import_VCF4_to_pandas(file) #Import files in annotated vcf format
#Check if sample exist
######################
if sample not in final_ddbb.columns.tolist():
print("Adding new sample %s to %s" % (sample, os.path.basename(output_filename)))
new_samples = new_samples + 1
new_colum_index = len(final_ddbb.columns) #extract the number of columns to insert a new one
#final_ddbb[sample] = sample #adds a new column but fills all blanks with the value sample
final_ddbb.insert(new_colum_index, sample, 0) #add a new column with defauls values = 0
#Check if position exist
########################
for position in new_sample['POS'].unique(): #extract first column in file
if position not in final_ddbb["Position"].values:
positions_added.append(int(position)) #Count new positions for stats
new_row = len(final_ddbb.index)
final_ddbb.loc[new_row,'Position'] = int(position)
final_ddbb.loc[new_row,'Samples'] = sample
final_ddbb.loc[new_row,'N'] = int(1)
final_ddbb.loc[new_row,sample] = str(1)
else:
positions_shared.append(int(position)) #Count shared positions for stats
#Check whether the column matches the value and retrieve the first position [0]
#of the object index generated
index_position = final_ddbb.index[final_ddbb["Position"] == int(position)][0]
#Add sample to corresponding cell [position, samples]
number_samples_with_position = final_ddbb.loc[index_position,'N']
names_samples_with_position = final_ddbb.loc[index_position,'Samples']
new_names_samples = names_samples_with_position + "," + sample
#Sum 1 to the numbes of samples containing the position
final_ddbb.loc[index_position,'N'] = number_samples_with_position + 1
final_ddbb.loc[index_position,'Samples'] = new_names_samples
final_ddbb.loc[index_position,sample] = str(1) #Add "1" in cell with correct position vs sample (indicate present)
print("\nSAMPLE:\t%s\nTOTAL Variants:\t%s\nShared Variants:\t%s\nNew Variants:\t%s\n"
% (sample, len(new_sample.index), len(positions_shared), len(positions_added)))
else:
print(YELLOW + "The sample " + sample + " ALREADY exist" + END_FORMATTING)
#final_ddbb = final_ddbb.fillna(0).sort_values("Position")
final_ddbb["Position"] = final_ddbb["Position"].astype(int) #TO REMOVE when nucleotides are added
final_ddbb['N'] = final_ddbb['N'].astype(int)
#final_ddbb = final_ddbb.reset_index(drop=True)
print("Final database now contains %s rows and %s columns" % final_ddbb.shape)
if recalibrate == False:
output_filename = output_filename + ".tsv"
final_ddbb.to_csv(output_filename, sep='\t', index=False)
else:
recalibrate = os.path.abspath(recalibrate)
if os.path.exists(recalibrate):
recalibrate_params = extract_recalibrate_params(recalibrate)
print("\n" + MAGENTA + "Recalibration selected" + END_FORMATTING)
print(output_filename)
output_filename = output_filename + ".revised.tsv"
final_ddbb_revised = recalibrate_ddbb_vcf(final_ddbb, recalibrate_params[0], recalibrate_params[1], recalibrate_params[2])
"""
if args.reference and args.reference != False:
final_ddbb_revised = recalibrate_ddbb_vcf(final_ddbb, recalibrate_params[0], recalibrate_params[1], args.reference)
else:
final_ddbb_revised = recalibrate_ddbb_vcf(final_ddbb, recalibrate_params[0], recalibrate_params[1], recalibrate_params[2])
"""
final_ddbb_revised.to_csv(output_filename, sep='\t', index=False)
else:
print("The directory supplied for recalculation does not exixt")
sys.exit(1)
print(output_filename)
#Create small report with basic count
#####################################
print("\n" + GREEN + "Position check Finished" + END_FORMATTING)
print(GREEN + "Added " + str(new_samples) + " samples out of " + str(all_samples) + END_FORMATTING + "\n")
def main():
"""
Create main function to capture code errors: https://stackoverflow.com/questions/6234405/logging-uncaught-exceptions-in-python
"""
# ARGUMENTS
def get_arguments():
parser = argparse.ArgumentParser(
prog='covidma.py',
description=
'Pipeline to call variants (SNVs) with any non model organism. Specialised in SARS-CoV-2'
)
input_group = parser.add_argument_group('Input', 'Input parameters')
input_group.add_argument(
'-i',
'--input',
dest="input_dir",
metavar="input_directory",
type=str,
required=True,
help='REQUIRED.Input directory containing all fast[aq] files')
input_group.add_argument('-r',
'--reference',
metavar="reference",
type=str,
required=True,
help='REQUIRED. File to map against')
input_group.add_argument(
'-a',
'--annotation',
metavar="annotation",
type=str,
required=True,
help='REQUIRED. gff3 file to annotate variants')
input_group.add_argument('-s',
'--sample',
metavar="sample",
type=str,
required=False,
help='Sample to identify further files')
input_group.add_argument(
'-L',
'--sample_list',
type=str,
required=False,
help='Sample names to analyse only in the file supplied')
input_group.add_argument(
'-p',
'--primers',
type=str,
default=
'/home/laura/DATABASES/Anotacion/COVID/primers/nCoV-2019.bed',
required=False,
help='Bed file including primers to trim')
quality_group = parser.add_argument_group(
'Quality parameters', 'parameters for diferent triming conditions')
quality_group.add_argument(
'-c',
'--coverage20',
type=int,
default=90,
required=False,
help=
'Minimum percentage of coverage at 20x to clasify as uncovered (Default 90)'
)
quality_group.add_argument('-n',
'--min_snp',
type=int,
required=False,
default=1,
help='SNP number to pass quality threshold')
output_group = parser.add_argument_group(
'Output', 'Required parameter to output results')
output_group.add_argument(
'-o',
'--output',
type=str,
required=True,
help='REQUIRED. Output directory to extract all results')
output_group.add_argument(
'-C',
'--noclean',
required=False,
action='store_false',
help='Clean unwanted files for standard execution')
params_group = parser.add_argument_group(
'Parameters', 'parameters for diferent stringent conditions')
params_group.add_argument('-T',
'--threads',
type=str,
dest="threads",
required=False,
default=16,
help='Threads to use')
params_group.add_argument('-M',
'--memory',
type=str,
dest="memory",
required=False,
default=32,
help='Max memory to use')
annot_group = parser.add_argument_group(
'Annotation', 'parameters for variant annotation')
annot_group.add_argument('-B',
'--annot_bed',
type=str,
default=[],
required=False,
action='append',
help='bed file to annotate')
annot_group.add_argument('-V',
'--annot_vcf',
type=str,
default=[],
required=False,
action='append',
help='vcf file to annotate')
annot_group.add_argument('-A',
'--annot_aa',
type=str,
default=[],
required=False,
action='append',
help='aminoacid file to annotate')
annot_group.add_argument('-R',
'--remove_bed',
type=str,
default=False,
required=False,
help='BED file with positions to remove')
annot_group.add_argument(
'--mash_database',
type=str,
required=False,
default=False,
help='MASH ncbi annotation containing all species database')
annot_group.add_argument('--snpeff_database',
type=str,
required=False,
default='NC_045512.2',
help='snpEFF annotation database')
compare_group = parser.add_argument_group(
'Compare', 'parameters for compare_snp')
compare_group.add_argument('-S',
'--only_snp',
required=False,
action='store_true',
help='Use INDELS while comparing')
arguments = parser.parse_args()
return arguments
args = get_arguments()
######################################################################
#####################START PIPELINE###################################
######################################################################
output = os.path.abspath(args.output)
group_name = output.split("/")[-1]
reference = os.path.abspath(args.reference)
annotation = os.path.abspath(args.annotation)
# LOGGING
# Create log file with date and time
right_now = str(datetime.datetime.now())
right_now_full = "_".join(right_now.split(" "))
log_filename = group_name + "_" + right_now_full + ".log"
log_folder = os.path.join(output, 'Logs')
check_create_dir(log_folder)
log_full_path = os.path.join(log_folder, log_filename)
logger = logging.getLogger()
logger.setLevel(logging.DEBUG)
formatter = logging.Formatter('%(asctime)s:%(message)s')
file_handler = logging.FileHandler(log_full_path)
file_handler.setLevel(logging.DEBUG)
file_handler.setFormatter(formatter)
stream_handler = logging.StreamHandler()
stream_handler.setLevel(logging.INFO)
# stream_handler.setFormatter(formatter)
logger.addHandler(stream_handler)
logger.addHandler(file_handler)
logger.info("\n\n" + BLUE + BOLD + "STARTING PIPELINE IN GROUP: " +
group_name + END_FORMATTING)
today = str(datetime.date.today())
logger.info("ARGUMENTS:")
logger.info(str(args))
# Obtain all R1 and R2 from folder
r1, r2 = extract_read_list(args.input_dir)
# Check if there are samples to filter out
sample_list_F = []
if args.sample_list == None:
logger.info("\n" + "No samples to filter")
for r1_file, r2_file in zip(r1, r2):
sample = extract_sample(r1_file, r2_file)
sample_list_F.append(sample)
else:
logger.info("samples will be filtered")
sample_list_F = file_to_list(args.sample_list)
new_samples = check_reanalysis(args.output, sample_list_F)
logger.info("\n%d samples will be analysed: %s" %
(len(new_samples), ",".join(new_samples)))
#PREPARE REFERENCE FOR MAPPING + FAI + DICT #########
#####################################################
# picard_dictionary(args)
samtools_faidx(args)
#DECLARE FOLDERS CREATED IN PIPELINE ################
#AND KEY FILES ######################################
#####################################################
# Annotation related parameters
# script_dir = os.path.dirname(os.path.realpath(__file__))
# Output related
out_qc_dir = os.path.join(output, "Quality")
out_qc_pre_dir = os.path.join(out_qc_dir, "raw") # subfolder
out_qc_post_dir = os.path.join(out_qc_dir, "processed") # subfolder
out_trim_dir = os.path.join(output, "Trimmed")
out_map_dir = os.path.join(output, "Bam")
out_variant_dir = os.path.join(output, "Variants")
out_variant_ivar_dir = os.path.join(out_variant_dir,
"ivar_raw") # subfolder
out_filtered_ivar_dir = os.path.join(out_variant_dir,
"ivar_filtered") # subfolder
out_consensus_dir = os.path.join(output, "Consensus")
out_consensus_ivar_dir = os.path.join(out_consensus_dir,
"ivar") # subfolder
out_stats_dir = os.path.join(output, "Stats")
out_stats_bamstats_dir = os.path.join(out_stats_dir,
"Bamstats") # subfolder
out_stats_coverage_dir = os.path.join(out_stats_dir,
"Coverage") # subfolder
out_compare_dir = os.path.join(output, "Compare")
out_annot_dir = os.path.join(output, "Annotation")
out_annot_snpeff_dir = os.path.join(out_annot_dir, "snpeff") # subfolder
out_annot_pangolin_dir = os.path.join(out_annot_dir,
"pangolin") # subfolder
out_annot_user_dir = os.path.join(out_annot_dir, "user") # subfolder
out_annot_user_aa_dir = os.path.join(out_annot_dir, "user_aa") # subfolder
new_sample_number = 0
for r1_file, r2_file in zip(r1, r2):
# EXtract sample name
sample = extract_sample(r1_file, r2_file)
args.sample = sample
if sample in sample_list_F:
sample_number = str(sample_list_F.index(sample) + 1)
sample_total = str(len(sample_list_F))
out_markdup_trimmed_name = sample + ".rg.markdup.trimmed.sorted.bam"
output_markdup_trimmed_file = os.path.join(
out_map_dir, out_markdup_trimmed_name)
if sample in new_samples:
new_sample_number = str(int(new_sample_number) + 1)
new_sample_total = str(len(new_samples))
logger.info("\n" + WHITE_BG + "STARTING SAMPLE: " + sample +
" (" + sample_number + "/" + sample_total + ")" +
" (" + new_sample_number + "/" + new_sample_total +
")" + END_FORMATTING)
else:
logger.info("\n" + WHITE_BG + "STARTING SAMPLE: " + sample +
" (" + sample_number + "/" + sample_total + ")" +
END_FORMATTING)
if not os.path.isfile(output_markdup_trimmed_file):
args.r1_file = r1_file
args.r2_file = r2_file
##############START PIPELINE#####################
#################################################
# INPUT ARGUMENTS
################
check_file_exists(r1_file)
check_file_exists(r2_file)
args.output = os.path.abspath(args.output)
check_create_dir(args.output)
# QUALITY CHECK in RAW with fastqc
######################################################
check_create_dir(out_qc_dir)
out_qc_raw_name_r1 = (".").join(
r1_file.split('/')[-1].split('.')[0:-2]) + '_fastqc.html'
out_qc_raw_name_r2 = (".").join(
r2_file.split('/')[-1].split('.')[0:-2]) + '_fastqc.html'
output_qc_raw_file_r1 = os.path.join(out_qc_pre_dir,
out_qc_raw_name_r1)
output_qc_raw_file_r2 = os.path.join(out_qc_pre_dir,
out_qc_raw_name_r2)
if os.path.isfile(output_qc_raw_file_r1) and os.path.isfile(
output_qc_raw_file_r2):
logger.info(YELLOW + DIM + output_qc_raw_file_r1 +
" EXIST\nOmmiting QC for sample " + sample +
END_FORMATTING)
else:
logger.info(GREEN + "Checking quality in sample " +
sample + END_FORMATTING)
logger.info("R1: " + r1_file + "\nR2: " + r2_file)
fastqc_quality(r1_file, r2_file, out_qc_pre_dir,
args.threads)
"""
TODO: Human filter
"""
# QUALITY TRIMMING AND ADAPTER REMOVAL WITH fastp
###################################################
out_trim_name_r1 = sample + ".trimmed_R1.fastq.gz"
out_trim_name_r2 = sample + ".trimmed_R2.fastq.gz"
output_trimming_file_r1 = os.path.join(out_trim_dir,
out_trim_name_r1)
output_trimming_file_r2 = os.path.join(out_trim_dir,
out_trim_name_r2)
if os.path.isfile(output_trimming_file_r1) and os.path.isfile(
output_trimming_file_r2):
logger.info(YELLOW + DIM + output_trimming_file_r1 +
" EXIST\nOmmiting Trimming for sample " +
sample + END_FORMATTING)
else:
logger.info(GREEN + "Trimming sample " + sample +
END_FORMATTING)
fastp_trimming(r1_file,
r2_file,
sample,
out_trim_dir,
threads=args.threads,
min_qual=20,
window_size=10,
min_len=35)
# QUALITY CHECK in TRIMMED with fastqc
######################################################
check_create_dir(out_qc_dir)
out_qc_pos_r1 = sample + ".trimmed_R1_fastqc.html"
out_qc_pos_r2 = sample + ".trimmed_R2_fastqc.html"
output_qc_precessed_file_r1 = os.path.join(
out_qc_post_dir, out_qc_pos_r1)
output_qc_precessed_file_r2 = os.path.join(
out_qc_post_dir, out_qc_pos_r2)
if os.path.isfile(
output_qc_precessed_file_r1) and os.path.isfile(
output_qc_precessed_file_r2):
logger.info(YELLOW + DIM + output_qc_raw_file_r1 +
" EXIST\nOmmiting QC for sample " + sample +
END_FORMATTING)
else:
logger.info(GREEN +
"Checking quality in processed sample " +
sample + END_FORMATTING)
logger.info("R1: " + output_trimming_file_r1 + "\nR2: " +
output_trimming_file_r2)
fastqc_quality(output_trimming_file_r1,
output_trimming_file_r2, out_qc_post_dir,
args.threads)
# MAPPING WITH BWA - SAM TO SORTED BAM - ADD HEADER SG
#####################################################
out_map_name = sample + ".rg.sorted.bam"
output_map_file = os.path.join(out_map_dir, out_map_name)
if os.path.isfile(output_map_file):
logger.info(YELLOW + DIM + output_map_file +
" EXIST\nOmmiting Mapping for sample " +
sample + END_FORMATTING)
else:
logger.info(GREEN + "Mapping sample " + sample +
END_FORMATTING)
logger.info("R1: " + output_trimming_file_r1 + "\nR2: " +
output_trimming_file_r2 + "\nReference: " +
reference)
bwa_mapping(output_trimming_file_r1,
output_trimming_file_r2,
reference,
sample,
out_map_dir,
threads=args.threads)
sam_to_index_bam(sample,
out_map_dir,
output_trimming_file_r1,
threads=args.threads)
#MARK DUPLICATES WITH PICARDTOOLS ###################
#####################################################
out_markdup_name = sample + ".rg.markdup.sorted.bam"
output_markdup_file = os.path.join(out_map_dir,
out_markdup_name)
if os.path.isfile(output_markdup_file):
logger.info(YELLOW + DIM + output_markdup_file +
" EXIST\nOmmiting Duplucate Mark for sample " +
sample + END_FORMATTING)
else:
logger.info(GREEN + "Marking Dupes in sample " + sample +
END_FORMATTING)
logger.info("Input Bam: " + output_map_file)
picard_markdup(output_map_file)
#TRIM PRIMERS WITH ivar trim ########################
#####################################################
if os.path.isfile(output_markdup_trimmed_file):
logger.info(YELLOW + DIM + output_markdup_trimmed_file +
" EXIST\nOmmiting Duplucate Mark for sample " +
sample + END_FORMATTING)
else:
logger.info(GREEN + "Trimming primers in sample " +
sample + END_FORMATTING)
logger.info("Input Bam: " + output_markdup_file)
ivar_trim(output_markdup_file,
args.primers,
sample,
min_length=30,
min_quality=20,
sliding_window_width=4)
else:
logger.info(
YELLOW + DIM + output_markdup_trimmed_file +
" EXIST\nOmmiting BAM mapping and BAM manipulation in sample "
+ sample + END_FORMATTING)
########################END OF MAPPING AND BAM MANIPULATION#####################################################################
################################################################################################################################
#VARIANT CALLING WTIH ivar variants##################
#####################################################
check_create_dir(out_variant_dir)
out_ivar_variant_name = sample + ".tsv"
out_ivar_variant_file = os.path.join(out_variant_ivar_dir,
out_ivar_variant_name)
if os.path.isfile(out_ivar_variant_file):
logger.info(YELLOW + DIM + out_ivar_variant_file +
" EXIST\nOmmiting Variant call for sample " +
sample + END_FORMATTING)
else:
logger.info(GREEN + "Calling variants with ivar in sample " +
sample + END_FORMATTING)
ivar_variants(reference,
output_markdup_trimmed_file,
out_variant_dir,
sample,
annotation,
min_quality=15,
min_frequency_threshold=0.01,
min_depth=1)
#VARIANT FILTERING ##################################
#####################################################
check_create_dir(out_filtered_ivar_dir)
out_ivar_filtered_file = os.path.join(out_filtered_ivar_dir,
out_ivar_variant_name)
if os.path.isfile(out_ivar_filtered_file):
logger.info(YELLOW + DIM + out_ivar_filtered_file +
" EXIST\nOmmiting Variant filtering for sample " +
sample + END_FORMATTING)
else:
logger.info(GREEN + "Filtering variants in sample " + sample +
END_FORMATTING)
filter_tsv_variants(out_ivar_variant_file,
out_filtered_ivar_dir,
min_frequency=0.7,
min_total_depth=10,
min_alt_dp=4,
is_pass=True,
only_snp=False)
#CREATE CONSENSUS with ivar consensus##################
#######################################################
check_create_dir(out_consensus_dir)
check_create_dir(out_consensus_ivar_dir)
out_ivar_consensus_name = sample + ".fa"
out_ivar_consensus_file = os.path.join(out_consensus_ivar_dir,
out_ivar_consensus_name)
if os.path.isfile(out_ivar_consensus_file):
logger.info(YELLOW + DIM + out_ivar_consensus_file +
" EXIST\nOmmiting Consensus for sample " +
sample + END_FORMATTING)
else:
logger.info(GREEN + "Creating consensus with ivar in sample " +
sample + END_FORMATTING)
ivar_consensus(output_markdup_trimmed_file,
out_consensus_ivar_dir,
sample,
min_quality=20,
min_frequency_threshold=0.8,
min_depth=20,
uncovered_character='N')
logger.info(GREEN + "Replacing consensus header in " + sample +
END_FORMATTING)
replace_consensus_header(out_ivar_consensus_file)
########################CREATE STATS AND QUALITY FILTERS########################################################################
################################################################################################################################
#CREATE Bamstats#######################################
#######################################################
check_create_dir(out_stats_dir)
check_create_dir(out_stats_bamstats_dir)
out_bamstats_name = sample + ".bamstats"
out_bamstats_file = os.path.join(out_stats_bamstats_dir,
out_bamstats_name)
if os.path.isfile(out_bamstats_file):
logger.info(YELLOW + DIM + out_bamstats_file +
" EXIST\nOmmiting Bamstats for sample " + sample +
END_FORMATTING)
else:
logger.info(GREEN + "Creating bamstats in sample " + sample +
END_FORMATTING)
create_bamstat(output_markdup_trimmed_file,
out_stats_bamstats_dir,
sample,
threads=args.threads)
#CREATE Bamstats#######################################
#######################################################
check_create_dir(out_stats_coverage_dir)
out_coverage_name = sample + ".cov"
out_coverage_file = os.path.join(out_stats_coverage_dir,
out_coverage_name)
if os.path.isfile(out_coverage_file):
logger.info(YELLOW + DIM + out_coverage_file +
" EXIST\nOmmiting Bamstats for sample " + sample +
END_FORMATTING)
else:
logger.info(GREEN + "Creating coverage in sample " + sample +
END_FORMATTING)
create_coverage(output_markdup_trimmed_file,
out_stats_coverage_dir, sample)
# fastqc OUTPUT FORMAT FOR COMPARISON
######################################################
logger.info(GREEN + "Creating summary report for quality result " +
END_FORMATTING)
# format_html_image(out_qc_dir)
# coverage OUTPUT SUMMARY
######################################################
logger.info(GREEN + "Creating summary report for coverage result " +
END_FORMATTING)
obtain_group_cov_stats(out_stats_coverage_dir, group_name)
# READS and VARIANTS OUTPUT SUMMARY
######################################################
logger.info(GREEN + "Creating overal summary report " + END_FORMATTING)
obtain_overal_stats(output, group_name)
# REMOVE UNCOVERED
##############################################################################################################################
logger.info(GREEN + "Removing low quality samples" + END_FORMATTING)
# remove_low_quality(output, min_percentage_20x=args.coverage20,
# min_hq_snp=args.min_snp, type_remove='Uncovered')
#ANNOTATION WITH SNPEFF, USER INOUT AND PANGOLIN ####
#####################################################
logger.info("\n\n" + BLUE + BOLD + "STARTING ANNOTATION IN GROUP: " +
group_name + END_FORMATTING + "\n")
check_create_dir(out_annot_dir)
check_create_dir(out_annot_snpeff_dir)
check_create_dir(out_annot_pangolin_dir)
# SNPEFF
if args.snpeff_database != False:
# CHANGE FOR RAW/FILTERED ANNOTATION
for root, _, files in os.walk(out_filtered_ivar_dir):
if root == out_filtered_ivar_dir: # CHANGE FOR RAW/FILTERED ANNOTATION
for name in files:
if name.endswith('.tsv'):
sample = name.split('.')[0]
filename = os.path.join(root, name)
out_annot_file = os.path.join(out_annot_snpeff_dir,
sample + ".annot")
if os.path.isfile(out_annot_file):
logger.info(
YELLOW + DIM + out_annot_file +
" EXIST\nOmmiting snpEff Annotation for sample "
+ sample + END_FORMATTING)
else:
logger.info(GREEN +
"Annotating sample with snpEff: " +
sample + END_FORMATTING)
output_vcf = os.path.join(out_annot_snpeff_dir,
sample + '.vcf')
annotate_snpeff(filename,
output_vcf,
out_annot_file,
database=args.snpeff_database)
# USER DEFINED
if not args.annot_bed and not args.annot_vcf:
logger.info(YELLOW + BOLD +
"Ommiting User Annotation, no BED or VCF files supplied" +
END_FORMATTING)
else:
check_create_dir(out_annot_user_dir)
# CHANGE FOR RAW/FILTERED ANNOTATION
for root, _, files in os.walk(out_variant_ivar_dir):
if root == out_variant_ivar_dir: # CHANGE FOR RAW/FILTERED ANNOTATION
for name in files:
if name.endswith('.tsv'):
sample = name.split('.')[0]
logger.info(
'User bed/vcf annotation in sample {}'.format(
sample))
filename = os.path.join(root, name)
out_annot_file = os.path.join(out_annot_user_dir,
sample + ".tsv")
user_annotation(filename,
out_annot_file,
vcf_files=args.annot_vcf,
bed_files=args.annot_bed)
# USER AA DEFINED
if not args.annot_aa:
logger.info(YELLOW + BOLD +
"Ommiting User aa Annotation, no AA files supplied" +
END_FORMATTING)
else:
check_create_dir(out_annot_user_aa_dir)
for root, _, files in os.walk(out_annot_snpeff_dir):
if root == out_annot_snpeff_dir:
for name in files:
if name.endswith('.annot'):
sample = name.split('.')[0]
logger.info(
'User aa annotation in sample {}'.format(sample))
filename = os.path.join(root, name)
out_annot_aa_file = os.path.join(
out_annot_user_aa_dir, sample + ".tsv")
if os.path.isfile(out_annot_aa_file):
user_annotation_aa(out_annot_aa_file,
out_annot_aa_file,
aa_files=args.annot_aa)
else:
user_annotation_aa(filename,
out_annot_aa_file,
aa_files=args.annot_aa)
# PANGOLIN
with concurrent.futures.ThreadPoolExecutor(
max_workers=args.threads) as executor:
futures_pangolin = []
for root, _, files in os.walk(out_consensus_ivar_dir):
if root == out_consensus_ivar_dir:
for name in files:
if name.endswith('.fa'):
sample = name.split('.')[0]
filename = os.path.join(root, name)
out_pangolin_filename = sample + ".lineage.csv"
out_pangolin_file = os.path.join(
out_annot_pangolin_dir, out_pangolin_filename)
if os.path.isfile(out_pangolin_file):
logger.info(
YELLOW + DIM + out_pangolin_file +
" EXIST\nOmmiting Lineage for sample " +
sample + END_FORMATTING)
else:
logger.info(GREEN +
"Obtaining Lineage in sample " +
sample + END_FORMATTING)
future = executor.submit(annotate_pangolin,
filename,
out_annot_pangolin_dir,
out_pangolin_filename,
threads=args.threads,
max_ambig=0.6)
futures_pangolin.append(future)
for future in concurrent.futures.as_completed(
futures_pangolin):
logger.info(future.result())
# annotate_pangolin(filename, out_annot_pangolin_dir,
# out_pangolin_filename, threads=args.threads, max_ambig=0.6)
# USER AA TO HTML
annotated_samples = []
logger.info('Adapting annotation to html in {}'.format(group_name))
for root, _, files in os.walk(out_annot_user_aa_dir):
if root == out_annot_user_aa_dir:
for name in files:
if name.endswith('.tsv'):
sample = name.split('.')[0]
annotated_samples.append(sample)
filename = os.path.join(root, name)
annotation_to_html(filename, sample)
annotated_samples = [str(x) for x in annotated_samples]
report_samples_html_all = report_samples_html.replace(
'ALLSAMPLES', ('","').join(annotated_samples)) # NEW
with open(os.path.join(out_annot_user_aa_dir, '00_all_samples.html'),
'w+') as f:
f.write(report_samples_html_all)
# SNP COMPARISON using tsv variant files
######################################################
logger.info("\n\n" + BLUE + BOLD + "STARTING COMPARISON IN GROUP: " +
group_name + END_FORMATTING + "\n")
check_create_dir(out_compare_dir)
folder_compare = today + "_" + group_name
path_compare = os.path.join(out_compare_dir, folder_compare)
check_create_dir(path_compare)
full_path_compare = os.path.join(path_compare, group_name)
# ddtb_add(out_filtered_ivar_dir, full_path_compare)
compare_snp_matrix_recal = full_path_compare + ".revised.final.tsv"
compare_snp_matrix_INDEL = full_path_compare + ".revised_INDEL.final.tsv"
compare_snp_matrix_recal_intermediate = full_path_compare + ".revised_intermediate.tsv"
compare_snp_matrix_INDEL_intermediate = full_path_compare + \
".revised_INDEL_intermediate.tsv"
recalibrated_snp_matrix_intermediate = ddbb_create_intermediate(
out_variant_ivar_dir,
out_stats_coverage_dir,
min_freq_discard=0.1,
min_alt_dp=4,
only_snp=args.only_snp)
recalibrated_snp_matrix_intermediate.to_csv(
compare_snp_matrix_recal_intermediate, sep="\t", index=False)
compare_snp_matrix_INDEL_intermediate_df = remove_position_range(
recalibrated_snp_matrix_intermediate)
compare_snp_matrix_INDEL_intermediate_df.to_csv(
compare_snp_matrix_INDEL_intermediate, sep="\t", index=False)
recalibrated_revised_df = revised_df(recalibrated_snp_matrix_intermediate,
path_compare,
min_freq_include=0.7,
min_threshold_discard_sample=0.07,
min_threshold_discard_position=0.4,
remove_faulty=True,
drop_samples=True,
drop_positions=True)
recalibrated_revised_df.to_csv(compare_snp_matrix_recal,
sep="\t",
index=False)
recalibrated_revised_INDEL_df = revised_df(
compare_snp_matrix_INDEL_intermediate_df,
path_compare,
min_freq_include=0.7,
min_threshold_discard_sample=0.07,
min_threshold_discard_position=0.4,
remove_faulty=True,
drop_samples=True,
drop_positions=True)
recalibrated_revised_INDEL_df.to_csv(compare_snp_matrix_INDEL,
sep="\t",
index=False)
ddtb_compare(compare_snp_matrix_recal, distance=0)
ddtb_compare(compare_snp_matrix_INDEL, distance=0, indel=True)
logger.info("\n\n" + MAGENTA + BOLD + "COMPARING FINISHED IN GROUP: " +
group_name + END_FORMATTING + "\n")
#####################CONSENSUS WITH REFINED CALL######
######################################################
logger.info(GREEN + "Creating refined consensus" + END_FORMATTING)
create_consensus(reference, compare_snp_matrix_recal,
out_stats_coverage_dir, out_consensus_dir)
logger.info("\n\n" + MAGENTA + BOLD +
"#####END OF PIPELINE COVID MULTI ANALYSIS#####" +
END_FORMATTING + "\n")
def ddtb_add(args):
directory = os.path.abspath(args.folder)
output_file = os.path.abspath(args.output_file)
#Select NEW vs UPDATE
if args.subtask == 'new' :
final_ddbb = blank_database()
elif args.subtask == 'update':
update_database = os.path.abspath(args.update_database)
if update_database == output_file:
print(RED + "ERROR: " + END_FORMATTING + BOLD + "Pick a diferent name for the output database" + END_FORMATTING)
sys.exit(1)
else:
final_ddbb = import_to_pandas(update_database, header=True)
#Make sure output exist to force change name
if os.path.isfile(output_file):
print(YELLOW + "ERROR: " + BOLD + "output database EXIST, choose a different name or manually delete" + END_FORMATTING)
sys.exit(1)
print("Previous final database contains %s rows and %s columns\n" % final_ddbb.shape)
print("The directory selected is: %s" % directory)
all_samples = 0
new_samples = 0
for filename in os.listdir(directory):
if not filename.startswith('.') and filename.endswith(args.suffix):
print("\nThe file is: %s" % filename)
all_samples = all_samples + 1
positions_shared = []
positions_added = []
sample = filename.split(".")[0] #Manage sample name
file = os.path.join(directory, filename) #Whole file path
check_file_exists(file) #Manage file[s]. Check if file exist and is greater than 0
new_sample = import_VCF4_to_pandas(file) #Import files in annotated vcf format
#Handle each new_sample
#print("This file contains %s SNPs" % len(new_sample.index))
#Check if sample exist
######################
if sample not in final_ddbb.columns.tolist():
print("Adding new sample %s to %s" % (sample, os.path.basename(args.output_file)))
new_samples = new_samples + 1
new_colum_index = len(final_ddbb.columns) #extract the number of columns to insert a new one
#final_ddbb[sample] = sample #adds a new column but fills all blanks with the value sample
final_ddbb.insert(new_colum_index, sample, 0) #add a new column with defauls values = 0
#Check if position exist
########################
for position in new_sample['POS'].unique(): #extract first column in file
if position not in final_ddbb["Position"].values:
positions_added.append(position) #Count new positions for stats
new_row = len(final_ddbb.index)
final_ddbb.loc[new_row,'Position'] = position
final_ddbb.loc[new_row,'Samples'] = sample
final_ddbb.loc[new_row,'N'] = int(1)
final_ddbb.loc[new_row,sample] = str(1)
else:
positions_shared.append(position) #Count shared positions for stats
#Check whether the column matches the value and retrieve the first position [0]
#of the object index generated
index_position = final_ddbb.index[final_ddbb["Position"] == position][0]
#Add sample to corresponding cell [position, samples]
number_samples_with_position = final_ddbb.loc[index_position,'N']
names_samples_with_position = final_ddbb.loc[index_position,'Samples']
new_names_samples = names_samples_with_position + "," + sample
#Sum 1 to the numbes of samples containing the position
final_ddbb.loc[index_position,'N'] = number_samples_with_position + 1
final_ddbb.loc[index_position,'Samples'] = new_names_samples
final_ddbb.loc[index_position,sample] = str(1) #Add "1" in cell with correct position vs sample (indicate present)
print("\nSAMPLE:\t%s\nTOTAL Variants:\t%s\nShared Variants:\t%s\nNew Variants:\t%s\n"
% (sample, len(new_sample.index), len(positions_shared), len(positions_added)))
else:
print(YELLOW + "The sample " + sample + " ALREADY exist" + END_FORMATTING)
final_ddbb = final_ddbb.fillna(0).sort_values("Position") #final_ddbb = final_ddbb["Position"].astype(int)
final_ddbb['N'] = final_ddbb['N'].astype(int)
final_ddbb = final_ddbb.reset_index(drop=True)
print("Final database now contains %s rows and %s columns" % final_ddbb.shape)
if args.recalibrate == False:
final_ddbb.to_csv(output_file, sep='\t', index=False)
else:
args.recalibrate = os.path.abspath(args.recalibrate)
if os.path.exists(args.recalibrate):
recalibrate_params = extract_recalibrate_params(args.recalibrate)
print("\n" + MAGENTA + "Recalibration selected" + END_FORMATTING)
output_file = (".").join(output_file.split(".")[:-1]) + ".revised.tsv"
final_ddbb_revised = recalibrate_ddbb_vcf(final_ddbb, recalibrate_params[0], recalibrate_params[1], recalibrate_params[2])
final_ddbb_revised.to_csv(output_file, sep='\t', index=False)
else:
print("The directory supplied for recalculation does not exixt")
sys.exit(1)
#Create small report with basic count
#####################################
print("\n" + GREEN + "Position check Finished" + END_FORMATTING)
print(GREEN + "Added " + str(new_samples) + " samples out of " + str(all_samples) + END_FORMATTING + "\n")
#pd.set_option('display.precision', 0)
#pd.reset_option('^display.', silent=True) #Reset options in case I mess up
output_bqsr_file = os.path.join(out_map_dir, out_bqsr_name)
if not os.path.isfile(output_bqsr_file):
args.r1_file = r1_file
args.r2_file = r2_file
print("\n" + WHITE_BG + "STARTING SAMPLE: " + sample + " (" +
sample_number + "/" + sample_total + ")" + END_FORMATTING)
##############START PIPELINE#####################
#################################################
#INPUT ARGUMENTS
################
check_file_exists(args.r1_file)
check_file_exists(args.r2_file)
args.output = os.path.abspath(args.output)
check_create_dir(args.output)
#QUALITY CHECK
##############
"""
TODO: Quality check
TODO: Human filter
"""
#QUALITY TRIMMING AND ADAPTER REMOVAL WITH bbduk.sh
###################################################
out_trim_name_r1 = sample + "_R1.clean.fastq.gz"
out_trim_name_r2 = sample + "_R2.clean.fastq.gz"
