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Second fix in results restructuring

Merged BIOPZ-Bak Maciej requested to merge fix_results_restructuring into master
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+ 46
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@@ -897,7 +897,7 @@ rule alfa_concat_results:
"alfa_qc_all_samples.concat.log"))
singularity:
"docker://zavolab/imagemagick:6.9.10-slim"
"docker://zavolab/imagemagick:7.0.8"
shell:
"""
@@ -969,15 +969,15 @@ rule prepare_files_for_report:
"ALFA_plots.concat.png")
output:
samples_dir = directory(os.path.join(
samples_dir_result = directory(os.path.join(
config["output_dir"],
"samples")),
samples_dir_log = directory(os.path.join(
config["log_dir"],
"samples"))
params:
results_dir = config["output_dir"],
log_dir = config["log_dir"],
log_samples_dir = os.path.join(
config["log_dir"],
"samples")
log:
stderr = os.path.join(
config["log_dir"],
@@ -988,8 +988,8 @@ rule prepare_files_for_report:
run:
# remove "single/paired end" from the results directories
os.mkdir(output.samples_dir)
# move paired end results
os.mkdir(output.samples_dir_result)
# copy paired end results
paired_end_dir = glob.glob(
os.path.join(
params.results_dir,
@@ -1003,13 +1003,7 @@ rule prepare_files_for_report:
params.results_dir,
"samples",
sample_name))
shutil.rmtree(
os.path.join(
params.results_dir,
"paired_end"),
ignore_errors=False,
onerror=None)
# move single end results
# copy single end results
single_end_dir = glob.glob(
os.path.join(
params.results_dir,
@@ -1023,16 +1017,10 @@ rule prepare_files_for_report:
params.results_dir,
"samples",
sample_name))
shutil.rmtree(
os.path.join(
params.results_dir,
"single_end"),
ignore_errors=False,
onerror=None)
# remove "single/paired end" from the logs directories
os.mkdir(params.log_samples_dir)
# move paired end results
os.mkdir(output.samples_dir_log)
# copy paired end results
paired_end_dir = glob.glob(
os.path.join(
params.log_dir,
@@ -1046,13 +1034,7 @@ rule prepare_files_for_report:
params.log_dir,
"samples",
sample_name))
shutil.rmtree(
os.path.join(
params.log_dir,
"paired_end"),
ignore_errors=False,
onerror=None)
# move single end results
# copy single end results
single_end_dir = glob.glob(
os.path.join(
params.log_dir,
@@ -1066,12 +1048,6 @@ rule prepare_files_for_report:
params.log_dir,
"samples",
sample_name))
shutil.rmtree(
os.path.join(
params.log_dir,
"single_end"),
ignore_errors=False,
onerror=None)
# encapsulate salmon quantification results
all_samples_dirs = glob.glob(
@@ -1112,12 +1088,12 @@ rule prepare_files_for_report:
"*_fastqc.zip"))
for zipfile in fastq_zip_list:
sample_name = zipfile.split("/")[-3]
zipfile_path_chunks = zipfile.split("/")
new_path = os.path.abspath(
os.path.join(
*(zipfile_path_chunks[:-1])))
absolute_path_zipfile = os.path.abspath(zipfile)
zipfile_path_chunks = absolute_path_zipfile.split(os.path.sep)
dir_path_to_zipfile = os.path.sep + os.path.join(
(*zipfile_path_chunks[:-1]))
with ZipFile(zipfile, 'r') as zip_f:
zip_f.extractall(new_path)
zip_f.extractall(dir_path_to_zipfile)
fastqc_data_f = os.path.join(
zipfile[:-4],
"fastqc_data.txt")
@@ -1178,14 +1154,43 @@ rule prepare_files_for_report:
"ALFA",
"ALFA_plots.concat_mqc.png"))
# remove old result directories
shutil.rmtree(
os.path.join(
params.results_dir,
"paired_end"),
ignore_errors=False,
onerror=None)
shutil.rmtree(
os.path.join(
params.results_dir,
"single_end"),
ignore_errors=False,
onerror=None)
shutil.rmtree(
os.path.join(
params.log_dir,
"paired_end"),
ignore_errors=False,
onerror=None)
shutil.rmtree(
os.path.join(
params.log_dir,
"single_end"),
ignore_errors=False,
onerror=None)
rule prepare_MultiQC_config:
'''
Prepare config for the MultiQC
'''
input:
multiqc_input_dir = os.path.join(
samples_dir_result = os.path.join(
config["output_dir"],
"samples"),
samples_dir_log = os.path.join(
config["log_dir"],
"samples")
output:
multiqc_config = os.path.join(
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