Newer
Older
# -----------------------------------------------------------------------------
# Author : Katsantoni Maria, Christina Herrmann
# Company: Mihaela Zavolan, Biozentrum, Basel
# This script is part of the Zavolan lab quantification pipeline, which is used
# for analysing RNA-seq data. The table is provided by labkey as a csv file.
# If the user provides their own table the table should contain the following
# columns:
# -----------------------------------------------------------------------------
import sys
import gzip
from argparse import ArgumentParser, RawTextHelpFormatter
import os
import numpy as np
import pandas as pd
from Bio import SeqIO
from io import StringIO
from csv import writer
from pathlib import Path
# (avoids long lines in filter definitions)
from labkey.query import QueryFilter
def main():
""" Preprocess sample folder and create config file for snakemake"""
__doc__ = "Preprocess of labkey table and create " + \
"config file and sample table."
parser = ArgumentParser(description=__doc__,
formatter_class=RawTextHelpFormatter)
parser.add_argument("genomes_path",
help="Path containing the FASTA and GTF " +
" files for all organisms",
metavar="GENOMES PATH")
parser.add_argument("--input-table",
type=str,
default=None,
help="Input table in LabKey format " +
"containing the sample information;" +
"\nexactly one '--input-table' and " +
"'--remote' is required.",
metavar="FILE")
parser.add_argument("--remote",
action="store_true",
help="Fetch LabKey table via API; exactly one of " +
"'--input-table' and" +
"\n'--remote' is required.")
parser.add_argument("--project-name",
help="Name of LabKey project containing table " +
" '--table-name'; required" +
"\nif '--remote' is specified.",
metavar="STR")
parser.add_argument("--logo",
default='None',
help="zavolan lab logo path",
metavar="STR")
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
parser.add_argument("--table-name",
help="Name of LabKey table; required if '--remote'" +
" is specified.",
metavar="STR")
parser.add_argument("--input-dict",
help="Input dictionary containing the feature name " +
"conversion from LabKey to Snakemake;" +
"default: '%(default)s'",
default=os.path.join(
os.path.dirname(__file__),
'labkey_to_snakemake.dict.tsv'),
metavar="FILE")
parser.add_argument("--samples-table",
help="Output table compatible to snakemake;" +
"default: '%(default)s'",
default='samples.tsv',
metavar="FILE")
parser.add_argument("--trim_polya",
type=int,
choices=[True, False],
default=True,
help="Trim poly-As option")
parser.add_argument("--multimappers",
type=int,
default=100,
help="Number of allowed multimappers",
metavar='INT')
parser.add_argument("--soft-clip",
choices=['EndToEnd', 'Local'],
default='EndToEnd',
help="Soft-clipping option for STAR")
parser.add_argument("--pass-mode",
choices=['None', 'Basic'],
default='None',
help="2-pass mode option for STAR")
parser.add_argument("--libtype",
default='A',
help="Library type for salmon",
metavar="STR")
parser.add_argument("--config-file",
help="Configuration file to be used by Snakemake")
parser.add_argument("--abspath",
choices=[os.path.abspath, str],
default=str,
help="Absolute path")
parser.add_argument("--samples_dir",
help="Path one level within Rhea",
default='')
parser.add_argument("--output_dir",
default='',
help="Path of the results directory")
parser.add_argument("--multiqc-url",
dest="multiqc_url",
default="No url",
help="Multiqc url of the group that did the analysis")
parser.add_argument("--multiqc-intro-text",
dest="multiqc_intro_text",
default="No description provided by user",
help="Multiqc small intro text of the analysis info")
try:
options = parser.parse_args()
except(Exception):
parser.print_help()
if len(sys.argv) == 1:
parser.print_help()
sys.exit(1)
if options.remote and options.input_table:
parser.print_help()
print(
"\n[ERROR] Options '--input-table' and ",
"'--remote' are mutually exclusive.")
sys.exit(1)
if not options.remote and not options.input_table:
parser.print_help()
print("\n[ERROR] At least one of '--input-table' ",
"and '--remote' is required.")
sys.exit(1)
if options.remote and not options.project_name:
parser.print_help()
print(
"\n[ERROR] If option '--remote' is specified, ",
"option '--project-name' is required.")
sys.exit(1)
if options.remote and not options.table_name:
parser.print_help()
print(
"\n[ERROR] If option '--remote' is specified, ",
"option '--table-name' is required.")
sys.stdout.write('Reading input file...\n')
if options.remote is True:
input_table = api_fetch_labkey_table(
project_name=options.project_name,
query_name=options.table_name)
input_table.to_csv(options.input_table, sep='\t', index=False)
else:
input_table = pd.read_csv(
options.input_table,
header=0,
sep='\t',
index_col=None,
comment='#',
engine='python')
input_dict = pd.read_csv(
options.input_dict,
header=0,
sep='\t',
index_col=None,
comment='#',
engine='python')
input_dict.set_index('snakemake', inplace=True, drop=True)
sys.stdout.write('Create snakemake table...\n')
snakemake_table = pd.DataFrame()
for index, row in input_table.iterrows():
snakemake_table.loc[index, 'sample'] = row[
input_dict.loc['replicate_name', 'labkey']] + "_" + row[
input_dict.loc['condition', 'labkey']]
if row[input_dict.loc['seqmode', 'labkey']] == 'PAIRED':
elif row[input_dict.loc['seqmode', 'labkey']] == 'SINGLE':
fq1 = options.abspath(
os.path.join(
options.samples_dir,
row[input_dict.loc['fastq_path', 'labkey']],
row[input_dict.loc['fq1', 'labkey']]))
snakemake_table.loc[index, 'fq1'] = fq1
read_length = get_read_length(fq1)
snakemake_table.loc[index, 'index_size'] = read_length
snakemake_table.loc[index, 'kmer'] = infer_kmer_length(read_length)
snakemake_table.loc[index, 'fq1_3p'] = row[
input_dict.loc['fq1_3p', 'labkey']]
snakemake_table.loc[index, 'fq1_5p'] = row[
input_dict.loc['fq1_5p', 'labkey']]
organism = row[input_dict.loc['organism', 'labkey']].replace(
' ', '_').lower()
snakemake_table.loc[index, 'organism'] = organism
snakemake_table.loc[index, 'gtf'] = options.abspath(
os.path.join(
options.genomes_path,
organism,
'annotation.gtf'))
snakemake_table.loc[index, 'gtf_filtered'] = options.abspath(
os.path.join(
options.genomes_path,
organism,
'annotation.gtf'))
snakemake_table.loc[index, 'genome'] = options.abspath(
os.path.join(
options.genomes_path,
organism,
'genome.fa'))
snakemake_table.loc[index, 'tr_fasta_filtered'] = options.abspath(
os.path.join(
options.genomes_path,
organism,
'transcriptome.fa'))
snakemake_table.loc[index, 'sd'] = row[
input_dict.loc['sd', 'labkey']]
snakemake_table.loc[index, 'mean'] = row[
input_dict.loc['mean', 'labkey']]
snakemake_table.loc[index, 'multimappers'] = options.multimappers
snakemake_table.loc[index, 'soft_clip'] = options.soft_clip
snakemake_table.loc[index, 'pass_mode'] = options.pass_mode
snakemake_table.loc[index, 'libtype'] = options.libtype
if options.trim_polya is True:
fq1_polya_3p, fq1_polya_5p = trim_polya(
row[input_dict.loc['mate1_direction', 'labkey']])
snakemake_table.loc[index, 'fq1_polya_3p'] = fq1_polya_3p
snakemake_table.loc[index, 'fq1_polya_5p'] = fq1_polya_5p
snakemake_table.loc[index, 'kallisto_directionality'] = \
get_kallisto_directionality(
row[input_dict.loc['mate1_direction', 'labkey']])
snakemake_table.loc[index, 'alfa_directionality'] = \
get_alfa_directionality(
row[input_dict.loc['mate1_direction', 'labkey']])
plus, minus = get_alfa_plus_minus(
row[input_dict.loc['mate1_direction', 'labkey']])
snakemake_table.loc[index, 'alfa_plus'] = plus
snakemake_table.loc[index, 'alfa_minus'] = minus
if row[input_dict.loc['seqmode', 'labkey']] == 'PAIRED':
fq2 = options.abspath(
os.path.join(
options.samples_dir,
row[input_dict.loc['fastq_path', 'labkey']],
row[input_dict.loc['fq2', 'labkey']]))
snakemake_table.loc[index, 'fq2'] = fq2
snakemake_table.loc[index, 'fq2_3p'] = row[
input_dict.loc['fq2_3p', 'labkey']]
snakemake_table.loc[index, 'fq2_5p'] = row[
input_dict.loc['fq2_5p', 'labkey']]
if options.trim_polya is True:
fq2_polya_3p, fq2_polya_5p = trim_polya(
row[input_dict.loc['mate2_direction', 'labkey']])
snakemake_table.loc[index, 'fq2_polya_3p'] = fq2_polya_3p
snakemake_table.loc[index, 'fq2_polya_5p'] = fq2_polya_5p
snakemake_table.fillna('XXXXXXXXXXXXX', inplace=True)
snakemake_table = snakemake_table.astype(
{
"sd": int,
"mean": int,
"multimappers": int,
"kmer": int,
"index_size": int,
}
)
snakemake_table.to_csv(
options.samples_table,
sep='\t',
header=True,
index=False)
321
322
323
324
325
326
327
328
329
330
331
332
333
334
335
336
337
338
339
340
341
342
343
344
345
346
347
348
349
350
351
352
353
354
355
356
357
358
359
360
361
362
363
364
365
366
samples = options.abspath(
os.path.join(
options.samples_dir,
options.samples_table))
output_dir = options.abspath(
os.path.join(
options.output_dir,
"results"))
logdir = options.abspath(
os.path.join(
options.output_dir,
"logs"))
kallisto_indexes = options.abspath(
os.path.join(
options.output_dir,
"results",
"kallisto_indexes"))
salmon_indexes = options.abspath(
os.path.join(
options.output_dir,
"results",
"salmon_indexes"))
star_indexes = options.abspath(
os.path.join(
options.output_dir,
"results",
"star_indexes"))
alfa_indexes = options.abspath(
os.path.join(
options.output_dir,
"results",
"alfa_indexes"))
logo = options.abspath(
os.path.join(
options.logo))
multiqc_url = options.multiqc_url
multiqc_intro_text = options.multiqc_intro_text
# Read file and infer read size for sjdbovwerhang
with open(options.config_file, 'w') as config_file:
config_file.write(f'''---
samples: "{samples}"
output_dir: "{output_dir}"
log_dir: "{logdir}"
kallisto_indexes: "{kallisto_indexes}"
salmon_indexes: "{salmon_indexes}"
star_indexes: "{star_indexes}"
alfa_indexes: "{alfa_indexes}"
logo: "{logo}"
multiqc_url: "{multiqc_url}"
multiqc_intro_text: "{multiqc_intro_text}"
...''')
sys.stdout.write('Create snakemake table finished successfully...\n')
sys.stdout.write('Create config file...\n')
sys.stdout.write('Create config file finished successfully...\n')
return
def api_fetch_labkey_table(project_name=None, query_name=None):
group_path = os.path.join('/Zavolan Group', project_name)
server_context = labkey.utils.create_server_context(
'labkey.scicore.unibas.ch', group_path, 'labkey', use_ssl=True)
schema_name = "lists"
results = labkey.query.select_rows(server_context, schema_name, query_name)
input_table = pd.DataFrame(results["rows"])
return input_table
def get_read_length(filename):
with gzip.open(filename, "rt") as handle:
for record in SeqIO.parse(handle, "fastq"):
read_length = len(record.seq)
break
return read_length
def infer_kmer_length(read_length):
if read_length <= 50:
elif read_length > 50:
kmer = 31
return kmer
def get_kallisto_directionality(directionality):
if directionality == 'SENSE':
final_direction = '--fr'
elif directionality == 'ANTISENSE':
final_direction = '--rf'
else:
final_direction = ''
return final_direction
def get_alfa_directionality(directionality):
if directionality == 'SENSE':
final_direction = 'fr-firststrand'
elif directionality == 'ANTISENSE':
final_direction = 'fr-secondstrand'
else:
final_direction = ''
return final_direction
def get_alfa_plus_minus(directionality):
if directionality == 'SENSE':
plus = 'str1'
minus = 'str2'
elif directionality == 'ANTISENSE':
minus = 'str1'
plus = 'str2'
else:
plus = ''
minus = ''
return plus, minus
def trim_polya(sense):
if sense == 'SENSE':
polya_3p = 'AAAAAAAAAAAAAAAAA'
polya_5p = 'XXXXXXXXXXXXXXXXX'
elif sense == 'ANTISENSE':
polya_3p = 'XXXXXXXXXXXXXXXXX'
polya_5p = 'TTTTTTTTTTTTTTTTT'
polya_3p = 'XXXXXXXXXXXXXXXXX'
polya_5p = 'XXXXXXXXXXXXXXXXX'
return polya_3p, polya_5p
if __name__ == '__main__':
try:
main()
except KeyboardInterrupt:
sys.stderr.write("User interrupt!" + os.linesep)
sys.exit(0)