def main():
def print_stacktrace_if_debug():
debug_flag = False
if 'args' in vars() and 'debug' in args:
debug_flag = args.debug
if debug_flag:
traceback.print_exc(file=sys.stdout)
error(traceback.format_exc())
try:
start_time = datetime.now()
start_time_string = start_time.strftime('%Y-%m-%d %H:%M:%S')
description = [
'~~~CRISPRessoWGS~~~',
'-Analysis of CRISPR/Cas9 outcomes from WGS data-'
]
wgs_string = r'''
____________
| __ __ |
|| |/ _ (_ |
||/\|\__)__) |
|____________|
'''
print(CRISPRessoShared.get_crispresso_header(description, wgs_string))
parser = CRISPRessoShared.getCRISPRessoArgParser(
parserTitle='CRISPRessoWGS Parameters', requiredParams={})
#tool specific optional
parser.add_argument('-b',
'--bam_file',
type=str,
help='WGS aligned bam file',
required=True,
default='bam filename')
parser.add_argument(
'-f',
'--region_file',
type=str,
help=
'Regions description file. A BED format file containing the regions to analyze, one per line. The REQUIRED\
columns are: chr_id(chromosome name), bpstart(start position), bpend(end position), the optional columns are:name (an unique indentifier for the region), guide_seq, expected_hdr_amplicon_seq,coding_seq, see CRISPResso help for more details on these last 3 parameters)',
required=True)
parser.add_argument(
'-r',
'--reference_file',
type=str,
help=
'A FASTA format reference file (for example hg19.fa for the human genome)',
default='',
required=True)
parser.add_argument(
'--min_reads_to_use_region',
type=float,
help=
'Minimum number of reads that align to a region to perform the CRISPResso analysis',
default=10)
parser.add_argument(
'--skip_failed',
help='Continue with pooled analysis even if one sample fails',
action='store_true')
parser.add_argument(
'--gene_annotations',
type=str,
help=
'Gene Annotation Table from UCSC Genome Browser Tables (http://genome.ucsc.edu/cgi-bin/hgTables?command=start), \
please select as table "knownGene", as output format "all fields from selected table" and as file returned "gzip compressed"',
default='')
parser.add_argument('--crispresso_command',
help='CRISPResso command to call',
default='CRISPResso')
args = parser.parse_args()
crispresso_options = CRISPRessoShared.get_crispresso_options()
options_to_ignore = {
'fastq_r1', 'fastq_r2', 'amplicon_seq', 'amplicon_name',
'output_folder', 'name'
}
crispresso_options_for_wgs = list(crispresso_options -
options_to_ignore)
info('Checking dependencies...')
if check_samtools() and check_bowtie2():
info('\n All the required dependencies are present!')
else:
sys.exit(1)
#check files
check_file(args.bam_file)
check_file(args.reference_file)
check_file(args.region_file)
if args.gene_annotations:
check_file(args.gene_annotations)
# for computation performed in CRISPRessoWGS (e.g. bowtie alignment, etc) use n_processes_for_wgs
n_processes_for_wgs = 1
if args.n_processes == "max":
n_processes_for_wgs = CRISPRessoMultiProcessing.get_max_processes()
else:
n_processes_for_wgs = int(args.n_processes)
# here, we set args.n_processes as 1 because this value is propagated to sub-CRISPResso runs (not for usage in CRISPRessoWGS)
args.n_processes = 1
#INIT
get_name_from_bam = lambda x: os.path.basename(x).replace('.bam', '')
if not args.name:
database_id = '%s' % get_name_from_bam(args.bam_file)
else:
clean_name = CRISPRessoShared.slugify(args.name)
if args.name != clean_name:
warn(
'The specified name {0} contained invalid characters and was changed to: {1}'
.format(
args.name,
clean_name,
), )
database_id = clean_name
OUTPUT_DIRECTORY = 'CRISPRessoWGS_on_%s' % database_id
if args.output_folder:
OUTPUT_DIRECTORY = os.path.join(
os.path.abspath(args.output_folder), OUTPUT_DIRECTORY)
_jp = lambda filename: os.path.join(
OUTPUT_DIRECTORY, filename
) #handy function to put a file in the output directory
try:
info('Creating Folder %s' % OUTPUT_DIRECTORY)
os.makedirs(OUTPUT_DIRECTORY)
info('Done!')
except:
warn('Folder %s already exists.' % OUTPUT_DIRECTORY)
log_filename = _jp('CRISPRessoWGS_RUNNING_LOG.txt')
logger.addHandler(logging.FileHandler(log_filename))
crispresso2_info_file = os.path.join(OUTPUT_DIRECTORY,
'CRISPResso2WGS_info.json')
crispresso2_info = {
'running_info': {},
'results': {
'alignment_stats': {},
'general_plots': {}
}
} #keep track of all information for this run to be pickled and saved at the end of the run
crispresso2_info['running_info'][
'version'] = CRISPRessoShared.__version__
crispresso2_info['running_info']['args'] = deepcopy(args)
crispresso2_info['running_info']['log_filename'] = os.path.basename(
log_filename)
crispresso2_info['running_info']['finished_steps'] = {}
crispresso_cmd_to_write = ' '.join(sys.argv)
if args.write_cleaned_report:
cmd_copy = sys.argv[:]
cmd_copy[0] = 'CRISPRessoWGS'
for i in range(len(cmd_copy)):
if os.sep in cmd_copy[i]:
cmd_copy[i] = os.path.basename(cmd_copy[i])
crispresso_cmd_to_write = ' '.join(
cmd_copy
) #clean command doesn't show the absolute path to the executable or other files
crispresso2_info['running_info'][
'command_used'] = crispresso_cmd_to_write
with open(log_filename, 'w+') as outfile:
outfile.write(
'CRISPResso version %s\n[Command used]:\n%s\n\n[Execution log]:\n'
% (CRISPRessoShared.__version__, crispresso_cmd_to_write))
#keep track of args to see if it is possible to skip computation steps on rerun
can_finish_incomplete_run = False
if args.no_rerun:
if os.path.exists(crispresso2_info_file):
previous_run_data = CRISPRessoShared.load_crispresso_info(
OUTPUT_DIRECTORY)
if previous_run_data['running_info'][
'version'] == CRISPRessoShared.__version__:
args_are_same = True
for arg in vars(args):
if arg == "no_rerun" or arg == "debug" or arg == "n_processes":
continue
if arg not in vars(
previous_run_data['running_info']['args']):
info(
'Comparing current run to previous run: old run had argument '
+ str(arg) + ' \nRerunning.')
args_are_same = False
elif str(
getattr(
previous_run_data['running_info']['args'],
arg)) != str(getattr(args, arg)):
info(
'Comparing current run to previous run:\n\told argument '
+ str(arg) + ' = ' + str(
getattr(
previous_run_data['running_info']
['args'], arg)) +
'\n\tnew argument: ' + str(arg) + ' = ' +
str(getattr(args, arg)) + '\nRerunning.')
args_are_same = False
if args_are_same:
if 'end_time_string' in previous_run_data:
info('Analysis already completed on %s!' %
previous_run_data['running_info']
['end_time_string'])
sys.exit(0)
else:
can_finish_incomplete_run = True
if 'finished_steps' in previous_run_data[
'running_info']:
for key in previous_run_data['running_info'][
'finished_steps'].keys():
crispresso2_info['running_info'][
'finished_steps'][
key] = previous_run_data[
'running_info'][
'finished_steps'][key]
if args.debug:
info('finished: ' + key)
else:
info(
'The no_rerun flag is set, but this analysis will be rerun because the existing run was performed using an old version of CRISPResso ('
+ str(previous_run_data['running_info']['version']) +
').')
#write this file early on so we can check the params if we have to rerun
CRISPRessoShared.write_crispresso_info(
crispresso2_info_file,
crispresso2_info,
)
def rreplace(s, old, new):
li = s.rsplit(old)
return new.join(li)
#check if bam has the index already
if os.path.exists(rreplace(args.bam_file, ".bam", ".bai")):
info('Index file for input .bam file exists, skipping generation.')
elif os.path.exists(args.bam_file + '.bai'):
info('Index file for input .bam file exists, skipping generation.')
else:
info('Creating index file for input .bam file...')
sb.call('samtools index %s ' % (args.bam_file), shell=True)
#load gene annotation
if args.gene_annotations:
info('Loading gene coordinates from annotation file: %s...' %
args.gene_annotations)
try:
df_genes = pd.read_csv(args.gene_annotations,
compression='gzip',
sep="\t")
df_genes.txEnd = df_genes.txEnd.astype(int)
df_genes.txStart = df_genes.txStart.astype(int)
df_genes.head()
except:
raise Exception('Failed to load the gene annotations file.')
#Load and validate the REGION FILE
df_regions = pd.read_csv(args.region_file,
names=[
'chr_id', 'bpstart', 'bpend', 'Name',
'sgRNA', 'Expected_HDR', 'Coding_sequence'
],
comment='#',
sep='\t',
dtype={
'Name': str,
'chr_id': str
})
#remove empty amplicons/lines
df_regions.dropna(subset=['chr_id', 'bpstart', 'bpend'], inplace=True)
df_regions.Expected_HDR = df_regions.Expected_HDR.apply(
capitalize_sequence)
df_regions.sgRNA = df_regions.sgRNA.apply(capitalize_sequence)
df_regions.Coding_sequence = df_regions.Coding_sequence.apply(
capitalize_sequence)
#check or create names
for idx, row in df_regions.iterrows():
if pd.isnull(row.Name):
df_regions.iloc[idx, ]['Name'] = '_'.join(
map(str, [row['chr_id'], row['bpstart'], row['bpend']]))
if not len(df_regions.Name.unique()) == df_regions.shape[0]:
raise Exception('The amplicon names should be all distinct!')
df_regions.set_index('Name', inplace=True)
#df_regions.index=df_regions.index.str.replace(' ','_')
df_regions.index = df_regions.index.to_series().str.replace(' ', '_')
#extract sequence for each region
uncompressed_reference = args.reference_file
if os.path.exists(uncompressed_reference + '.fai'):
info(
'The index for the reference fasta file is already present! Skipping generation.'
)
else:
info('Indexing reference file... Please be patient!')
sb.call('samtools faidx %s >>%s 2>&1' %
(uncompressed_reference, log_filename),
shell=True)
info(
'Retrieving reference sequences for amplicons and checking for sgRNAs'
)
df_regions['sequence'] = df_regions.apply(
lambda row: get_region_from_fa(row.chr_id, row.bpstart, row.bpend,
uncompressed_reference),
axis=1)
for idx, row in df_regions.iterrows():
if not pd.isnull(row.sgRNA):
cut_points = []
guides = row.sgRNA.strip().upper().split(',')
guide_qw_centers = CRISPRessoShared.set_guide_array(
args.quantification_window_center, guides,
'guide quantification center')
for idx, current_guide_seq in enumerate(guides):
wrong_nt = find_wrong_nt(current_guide_seq)
if wrong_nt:
raise NTException(
'The sgRNA sequence %s contains wrong characters:%s'
% (current_guide_seq, ' '.join(wrong_nt)))
offset_fw = guide_qw_centers[idx] + len(
current_guide_seq) - 1
offset_rc = (-guide_qw_centers[idx]) - 1
cut_points+=[m.start() + offset_fw for \
m in re.finditer(current_guide_seq, row.sequence)]+[m.start() + offset_rc for m in re.finditer(CRISPRessoShared.reverse_complement(current_guide_seq), row.sequence)]
if not cut_points:
df_regions.iloc[idx, :]['sgRNA'] = ''
info('Cannot find guide ' + str(row.sgRNA) +
' in amplicon ' + str(idx) + ' (' + str(row) + ')')
df_regions['bpstart'] = pd.to_numeric(df_regions['bpstart'])
df_regions['bpend'] = pd.to_numeric(df_regions['bpend'])
df_regions.bpstart = df_regions.bpstart.astype(int)
df_regions.bpend = df_regions.bpend.astype(int)
if args.gene_annotations:
df_regions = df_regions.apply(
lambda row: find_overlapping_genes(row, df_genes), axis=1)
#extract reads with samtools in that region and create a bam
#create a fasta file with all the trimmed reads
info('\nProcessing each region...')
ANALYZED_REGIONS = _jp('ANALYZED_REGIONS/')
if not os.path.exists(ANALYZED_REGIONS):
os.mkdir(ANALYZED_REGIONS)
df_regions['region_number'] = np.arange(len(df_regions))
def set_filenames(row):
row_fastq_exists = False
fastq_gz_filename = os.path.join(
ANALYZED_REGIONS, '%s.fastq.gz' %
clean_filename('REGION_' + str(row.region_number)))
bam_region_filename = os.path.join(
ANALYZED_REGIONS,
'%s.bam' % clean_filename('REGION_' + str(row.region_number)))
#if bam file already exists, don't regenerate it
if os.path.isfile(fastq_gz_filename):
row_fastq_exists = True
return bam_region_filename, fastq_gz_filename, row_fastq_exists
df_regions['bam_file_with_reads_in_region'], df_regions[
'fastq_file_trimmed_reads_in_region'], df_regions[
'row_fastq_exists'] = zip(
*df_regions.apply(set_filenames, axis=1))
df_regions['n_reads'] = 0
df_regions[
'original_bam'] = args.bam_file #stick this in the df so we can parallelize the analysis and not pass params
report_reads_aligned_filename = _jp(
'REPORT_READS_ALIGNED_TO_SELECTED_REGIONS_WGS.txt')
num_rows_without_fastq = len(
df_regions[df_regions.row_fastq_exists == False])
if can_finish_incomplete_run and num_rows_without_fastq == 0 and os.path.isfile(
report_reads_aligned_filename
) and 'generation_of_fastq_files_for_each_amplicon' in crispresso2_info[
'running_info']['finished_steps']:
info('Skipping generation of fastq files for each amplicon.')
df_regions = pd.read_csv(report_reads_aligned_filename,
comment='#',
sep='\t',
dtype={
'Name': str,
'chr_id': str
})
df_regions.set_index('Name', inplace=True)
else:
#run region extraction here
df_regions = CRISPRessoMultiProcessing.run_pandas_apply_parallel(
df_regions, extract_reads_chunk, n_processes_for_wgs)
df_regions.sort_values('region_number', inplace=True)
cols_to_print = [
"chr_id", "bpstart", "bpend", "sgRNA", "Expected_HDR",
"Coding_sequence", "sequence", "n_reads",
"bam_file_with_reads_in_region",
"fastq_file_trimmed_reads_in_region"
]
if args.gene_annotations:
cols_to_print.append('gene_overlapping')
df_regions.fillna('NA').to_csv(report_reads_aligned_filename,
sep='\t',
columns=cols_to_print,
index_label="Name")
#save progress
crispresso2_info['running_info']['finished_steps'][
'generation_of_fastq_files_for_each_amplicon'] = True
CRISPRessoShared.write_crispresso_info(
crispresso2_info_file,
crispresso2_info,
)
#Run Crispresso
info('Running CRISPResso on each region...')
crispresso_cmds = []
for idx, row in df_regions.iterrows():
if row['n_reads'] >= args.min_reads_to_use_region:
info('\nThe region [%s] has enough reads (%d) mapped to it!' %
(idx, row['n_reads']))
crispresso_cmd= args.crispresso_command + ' -r1 %s -a %s -o %s --name %s' %\
(row['fastq_file_trimmed_reads_in_region'], row['sequence'], OUTPUT_DIRECTORY, idx)
if row['sgRNA'] and not pd.isnull(row['sgRNA']):
crispresso_cmd += ' -g %s' % row['sgRNA']
if row['Expected_HDR'] and not pd.isnull(row['Expected_HDR']):
crispresso_cmd += ' -e %s' % row['Expected_HDR']
if row['Coding_sequence'] and not pd.isnull(
row['Coding_sequence']):
crispresso_cmd += ' -c %s' % row['Coding_sequence']
crispresso_cmd = CRISPRessoShared.propagate_crispresso_options(
crispresso_cmd, crispresso_options_for_wgs, args)
#logging like this causes the multiprocessing step to not block for some reason #mysteriesOfThPythonUniverse
#log_name = _jp("CRISPResso_on_"+idx) +".log"
#crispresso_cmd += " &> %s"%log_name
crispresso_cmds.append(crispresso_cmd)
# info('Running CRISPResso:%s' % crispresso_cmd)
# sb.call(crispresso_cmd,shell=True)
else:
info(
'\nThe region [%s] has too few reads mapped to it (%d)! Not running CRISPResso!'
% (idx, row['n_reads']))
CRISPRessoMultiProcessing.run_crispresso_cmds(crispresso_cmds,
n_processes_for_wgs,
'region',
args.skip_failed)
quantification_summary = []
all_region_names = []
all_region_read_counts = {}
good_region_names = []
good_region_folders = {}
header = 'Name\tUnmodified%\tModified%\tReads_total\tReads_aligned\tUnmodified\tModified\tDiscarded\tInsertions\tDeletions\tSubstitutions\tOnly Insertions\tOnly Deletions\tOnly Substitutions\tInsertions and Deletions\tInsertions and Substitutions\tDeletions and Substitutions\tInsertions Deletions and Substitutions'
header_els = header.split("\t")
header_el_count = len(header_els)
empty_line_els = [np.nan] * (header_el_count - 1)
n_reads_index = header_els.index('Reads_total') - 1
for idx, row in df_regions.iterrows():
folder_name = 'CRISPResso_on_%s' % idx
run_name = idx
all_region_names.append(run_name)
all_region_read_counts[run_name] = row.n_reads
run_file = os.path.join(_jp(folder_name), 'CRISPResso2_info.json')
if not os.path.exists(run_file):
warn(
'Skipping the folder %s: not enough reads, incomplete, or empty folder.'
% folder_name)
this_els = empty_line_els[:]
this_els[n_reads_index] = row.n_reads
to_add = [run_name]
to_add.extend(this_els)
quantification_summary.append(to_add)
else:
run_data = CRISPRessoShared.load_crispresso_info(
_jp(folder_name), )
ref_name = run_data['results']['ref_names'][
0] #only expect one amplicon sequence
n_tot = row.n_reads
n_aligned = run_data['results']['alignment_stats'][
'counts_total'][ref_name]
n_unmod = run_data['results']['alignment_stats'][
'counts_unmodified'][ref_name]
n_mod = run_data['results']['alignment_stats'][
'counts_modified'][ref_name]
n_discarded = run_data['results']['alignment_stats'][
'counts_discarded'][ref_name]
n_insertion = run_data['results']['alignment_stats'][
'counts_insertion'][ref_name]
n_deletion = run_data['results']['alignment_stats'][
'counts_deletion'][ref_name]
n_substitution = run_data['results']['alignment_stats'][
'counts_substitution'][ref_name]
n_only_insertion = run_data['results']['alignment_stats'][
'counts_only_insertion'][ref_name]
n_only_deletion = run_data['results']['alignment_stats'][
'counts_only_deletion'][ref_name]
n_only_substitution = run_data['results']['alignment_stats'][
'counts_only_substitution'][ref_name]
n_insertion_and_deletion = run_data['results'][
'alignment_stats']['counts_insertion_and_deletion'][
ref_name]
n_insertion_and_substitution = run_data['results'][
'alignment_stats']['counts_insertion_and_substitution'][
ref_name]
n_deletion_and_substitution = run_data['results'][
'alignment_stats']['counts_deletion_and_substitution'][
ref_name]
n_insertion_and_deletion_and_substitution = run_data[
'results']['alignment_stats'][
'counts_insertion_and_deletion_and_substitution'][
ref_name]
unmod_pct = "NA"
mod_pct = "NA"
if n_aligned > 0:
unmod_pct = 100 * n_unmod / float(n_aligned)
mod_pct = 100 * n_mod / float(n_aligned)
vals = [run_name]
vals.extend([
round(unmod_pct, 8),
round(mod_pct, 8), n_aligned, n_tot, n_unmod, n_mod,
n_discarded, n_insertion, n_deletion, n_substitution,
n_only_insertion, n_only_deletion, n_only_substitution,
n_insertion_and_deletion, n_insertion_and_substitution,
n_deletion_and_substitution,
n_insertion_and_deletion_and_substitution
])
quantification_summary.append(vals)
good_region_names.append(idx)
good_region_folders[idx] = folder_name
samples_quantification_summary_filename = _jp(
'SAMPLES_QUANTIFICATION_SUMMARY.txt')
df_summary_quantification = pd.DataFrame(quantification_summary,
columns=header_els)
if args.crispresso1_mode:
crispresso1_columns = [
'Name', 'Unmodified%', 'Modified%', 'Reads_aligned',
'Reads_total'
]
df_summary_quantification.fillna('NA').to_csv(
samples_quantification_summary_filename,
sep='\t',
index=None,
columns=crispresso1_columns)
else:
df_summary_quantification.fillna('NA').to_csv(
samples_quantification_summary_filename, sep='\t', index=None)
crispresso2_info['results']['alignment_stats'][
'samples_quantification_summary_filename'] = os.path.basename(
samples_quantification_summary_filename)
crispresso2_info['results']['regions'] = df_regions
crispresso2_info['results']['all_region_names'] = all_region_names
crispresso2_info['results'][
'all_region_read_counts'] = all_region_read_counts
crispresso2_info['results']['good_region_names'] = good_region_names
crispresso2_info['results'][
'good_region_folders'] = good_region_folders
crispresso2_info['results']['general_plots']['summary_plot_names'] = []
crispresso2_info['results']['general_plots'][
'summary_plot_titles'] = {}
crispresso2_info['results']['general_plots'][
'summary_plot_labels'] = {}
crispresso2_info['results']['general_plots']['summary_plot_datas'] = {}
df_summary_quantification.set_index('Name')
save_png = True
if args.suppress_report:
save_png = False
if not args.suppress_plots:
plot_root = _jp("CRISPRessoWGS_reads_summary")
CRISPRessoPlot.plot_reads_total(plot_root,
df_summary_quantification,
save_png,
args.min_reads_to_use_region)
plot_name = os.path.basename(plot_root)
crispresso2_info['results']['general_plots'][
'reads_summary_plot'] = plot_name
crispresso2_info['results']['general_plots'][
'summary_plot_names'].append(plot_name)
crispresso2_info['results']['general_plots'][
'summary_plot_titles'][
plot_name] = 'CRISPRessoWGS Read Allocation Summary'
crispresso2_info['results']['general_plots']['summary_plot_labels'][
plot_name] = 'Each bar shows the total number of reads allocated to each amplicon. The vertical line shows the cutoff for analysis, set using the --min_reads_to_use_region parameter.'
crispresso2_info['results']['general_plots']['summary_plot_datas'][
plot_name] = [
('CRISPRessoWGS summary',
os.path.basename(samples_quantification_summary_filename))
]
plot_root = _jp("CRISPRessoWGS_modification_summary")
CRISPRessoPlot.plot_unmod_mod_pcts(plot_root,
df_summary_quantification,
save_png,
args.min_reads_to_use_region)
plot_name = os.path.basename(plot_root)
crispresso2_info['results']['general_plots'][
'modification_summary_plot'] = plot_name
crispresso2_info['results']['general_plots'][
'summary_plot_names'].append(plot_name)
crispresso2_info['results']['general_plots'][
'summary_plot_titles'][
plot_name] = 'CRISPRessoWGS Modification Summary'
crispresso2_info['results']['general_plots']['summary_plot_labels'][
plot_name] = 'Each bar shows the total number of reads aligned to each amplicon, divided into the reads that are modified and unmodified. The vertical line shows the cutoff for analysis, set using the --min_reads_to_use_region parameter.'
crispresso2_info['results']['general_plots']['summary_plot_datas'][
plot_name] = [
('CRISPRessoWGS summary',
os.path.basename(samples_quantification_summary_filename))
]
if not args.suppress_report and not args.suppress_plots:
if (args.place_report_in_output_folder):
report_name = _jp("CRISPResso2WGS_report.html")
else:
report_name = OUTPUT_DIRECTORY + '.html'
CRISPRessoReport.make_wgs_report_from_folder(
report_name, crispresso2_info, OUTPUT_DIRECTORY, _ROOT)
crispresso2_info['running_info']['report_location'] = report_name
crispresso2_info['running_info'][
'report_filename'] = os.path.basename(report_name)
end_time = datetime.now()
end_time_string = end_time.strftime('%Y-%m-%d %H:%M:%S')
running_time = end_time - start_time
running_time_string = str(running_time)
crispresso2_info['running_info']['end_time'] = end_time
crispresso2_info['running_info']['end_time_string'] = end_time_string
crispresso2_info['running_info']['running_time'] = running_time
crispresso2_info['running_info'][
'running_time_string'] = running_time_string
CRISPRessoShared.write_crispresso_info(
crispresso2_info_file,
crispresso2_info,
)
info('Analysis Complete!')
print(CRISPRessoShared.get_crispresso_footer())
sys.exit(0)
except Exception as e:
print_stacktrace_if_debug()
error('\n\nERROR: %s' % e)
sys.exit(-1)
def main():
def print_stacktrace_if_debug():
debug_flag = False
if 'args' in vars() and 'debug' in args:
debug_flag = args.debug
if debug_flag:
traceback.print_exc(file=sys.stdout)
error(traceback.format_exc())
try:
description = [
'~~~CRISPRessoWGS~~~',
'-Analysis of CRISPR/Cas9 outcomes from WGS data-'
]
wgs_string = r'''
____________
| __ __ |
|| |/ _ (_ |
||/\|\__)__) |
|____________|
'''
print(CRISPRessoShared.get_crispresso_header(description, wgs_string))
parser = CRISPRessoShared.getCRISPRessoArgParser(
parserTitle='CRISPRessoWGS Parameters', requiredParams={})
#tool specific optional
parser.add_argument('-b',
'--bam_file',
type=str,
help='WGS aligned bam file',
required=True,
default='bam filename')
parser.add_argument(
'-f',
'--region_file',
type=str,
help=
'Regions description file. A BED format file containing the regions to analyze, one per line. The REQUIRED\
columns are: chr_id(chromosome name), bpstart(start position), bpend(end position), the optional columns are:name (an unique indentifier for the region), guide_seq, expected_hdr_amplicon_seq,coding_seq, see CRISPResso help for more details on these last 3 parameters)',
required=True)
parser.add_argument(
'-r',
'--reference_file',
type=str,
help=
'A FASTA format reference file (for example hg19.fa for the human genome)',
default='',
required=True)
parser.add_argument(
'--min_reads_to_use_region',
type=float,
help=
'Minimum number of reads that align to a region to perform the CRISPResso analysis',
default=10)
parser.add_argument(
'--skip_failed',
help='Continue with pooled analysis even if one sample fails',
action='store_true')
parser.add_argument(
'--gene_annotations',
type=str,
help=
'Gene Annotation Table from UCSC Genome Browser Tables (http://genome.ucsc.edu/cgi-bin/hgTables?command=start), \
please select as table "knowGene", as output format "all fields from selected table" and as file returned "gzip compressed"',
default='')
parser.add_argument(
'-p',
'--n_processes',
type=int,
help='Specify the number of processes to use for the quantification.\
Please use with caution since increasing this parameter will increase the memory required to run CRISPResso.',
default=1)
parser.add_argument('--crispresso_command',
help='CRISPResso command to call',
default='CRISPResso')
args = parser.parse_args()
crispresso_options = CRISPRessoShared.get_crispresso_options()
options_to_ignore = set([
'fastq_r1', 'fastq_r2', 'amplicon_seq', 'amplicon_name',
'output_folder', 'name'
])
crispresso_options_for_wgs = list(crispresso_options -
options_to_ignore)
info('Checking dependencies...')
if check_samtools() and check_bowtie2():
info('\n All the required dependencies are present!')
else:
sys.exit(1)
#check files
check_file(args.bam_file)
check_file(args.reference_file)
check_file(args.region_file)
if args.gene_annotations:
check_file(args.gene_annotations)
#INIT
get_name_from_bam = lambda x: os.path.basename(x).replace('.bam', '')
if not args.name:
database_id = '%s' % get_name_from_bam(args.bam_file)
else:
database_id = args.name
OUTPUT_DIRECTORY = 'CRISPRessoWGS_on_%s' % database_id
if args.output_folder:
OUTPUT_DIRECTORY = os.path.join(
os.path.abspath(args.output_folder), OUTPUT_DIRECTORY)
_jp = lambda filename: os.path.join(
OUTPUT_DIRECTORY, filename
) #handy function to put a file in the output directory
try:
info('Creating Folder %s' % OUTPUT_DIRECTORY)
os.makedirs(OUTPUT_DIRECTORY)
info('Done!')
except:
warn('Folder %s already exists.' % OUTPUT_DIRECTORY)
log_filename = _jp('CRISPRessoWGS_RUNNING_LOG.txt')
logging.getLogger().addHandler(logging.FileHandler(log_filename))
with open(log_filename, 'w+') as outfile:
outfile.write('[Command used]:\n%s\n\n[Execution log]:\n' %
' '.join(sys.argv))
crispresso2WGS_info_file = os.path.join(OUTPUT_DIRECTORY,
'CRISPResso2WGS_info.pickle')
crispresso2_info = {
} #keep track of all information for this run to be pickled and saved at the end of the run
crispresso2_info['version'] = CRISPRessoShared.__version__
crispresso2_info['args'] = deepcopy(args)
crispresso2_info['log_filename'] = os.path.basename(log_filename)
def rreplace(s, old, new):
li = s.rsplit(old)
return new.join(li)
bam_index = ''
#check if bam has the index already
if os.path.exists(rreplace(args.bam_file, ".bam", ".bai")):
info('Index file for input .bam file exists, skipping generation.')
bam_index = args.bam_file.rreplace(".bam", ".bai")
elif os.path.exists(args.bam_file + '.bai'):
info('Index file for input .bam file exists, skipping generation.')
bam_index = args.bam_file + '.bai'
else:
info('Creating index file for input .bam file...')
sb.call('samtools index %s ' % (args.bam_file), shell=True)
bam_index = args.bam_file + '.bai'
#load gene annotation
if args.gene_annotations:
info('Loading gene coordinates from annotation file: %s...' %
args.gene_annotations)
try:
df_genes = pd.read_table(args.gene_annotations,
compression='gzip')
df_genes.txEnd = df_genes.txEnd.astype(int)
df_genes.txStart = df_genes.txStart.astype(int)
df_genes.head()
except:
info('Failed to load the gene annotations file.')
#Load and validate the REGION FILE
df_regions = pd.read_csv(args.region_file,
names=[
'chr_id', 'bpstart', 'bpend', 'Name',
'sgRNA', 'Expected_HDR', 'Coding_sequence'
],
comment='#',
sep='\t',
dtype={'Name': str})
#remove empty amplicons/lines
df_regions.dropna(subset=['chr_id', 'bpstart', 'bpend'], inplace=True)
df_regions.Expected_HDR = df_regions.Expected_HDR.apply(
capitalize_sequence)
df_regions.sgRNA = df_regions.sgRNA.apply(capitalize_sequence)
df_regions.Coding_sequence = df_regions.Coding_sequence.apply(
capitalize_sequence)
#check or create names
for idx, row in df_regions.iterrows():
if pd.isnull(row.Name):
df_regions.ix[idx, 'Name'] = '_'.join(
map(str, [row['chr_id'], row['bpstart'], row['bpend']]))
if not len(df_regions.Name.unique()) == df_regions.shape[0]:
raise Exception('The amplicon names should be all distinct!')
df_regions = df_regions.set_index('Name')
#df_regions.index=df_regions.index.str.replace(' ','_')
df_regions.index = df_regions.index.to_series().str.replace(' ', '_')
#extract sequence for each region
uncompressed_reference = args.reference_file
if os.path.exists(uncompressed_reference + '.fai'):
info(
'The index for the reference fasta file is already present! Skipping generation.'
)
else:
info('Indexing reference file... Please be patient!')
sb.call('samtools faidx %s >>%s 2>&1' %
(uncompressed_reference, log_filename),
shell=True)
df_regions['sequence'] = df_regions.apply(
lambda row: get_region_from_fa(row.chr_id, row.bpstart, row.bpend,
uncompressed_reference),
axis=1)
for idx, row in df_regions.iterrows():
if not pd.isnull(row.sgRNA):
cut_points = []
for current_guide_seq in row.sgRNA.strip().upper().split(','):
wrong_nt = find_wrong_nt(current_guide_seq)
if wrong_nt:
raise NTException(
'The sgRNA sequence %s contains wrong characters:%s'
% (current_guide_seq, ' '.join(wrong_nt)))
offset_fw = args.quantification_window_center + len(
current_guide_seq) - 1
offset_rc = (-args.quantification_window_center) - 1
cut_points+=[m.start() + offset_fw for \
m in re.finditer(current_guide_seq, row.sequence)]+[m.start() + offset_rc for m in re.finditer(CRISPRessoShared.reverse_complement(current_guide_seq), row.sequence)]
if not cut_points:
df_regions.ix[idx, 'sgRNA'] = ''
df_regions['bpstart'] = pd.to_numeric(df_regions['bpstart'])
df_regions['bpend'] = pd.to_numeric(df_regions['bpend'])
df_regions.bpstart = df_regions.bpstart.astype(int)
df_regions.bpend = df_regions.bpend.astype(int)
if args.gene_annotations:
df_regions = df_regions.apply(
lambda row: find_overlapping_genes(row, df_genes), axis=1)
#extract reads with samtools in that region and create a bam
#create a fasta file with all the trimmed reads
info('\nProcessing each region...')
ANALYZED_REGIONS = _jp('ANALYZED_REGIONS/')
if not os.path.exists(ANALYZED_REGIONS):
os.mkdir(ANALYZED_REGIONS)
df_regions['n_reads'] = 0
df_regions['bam_file_with_reads_in_region'] = ''
df_regions['fastq.gz_file_trimmed_reads_in_region'] = ''
for idx, row in df_regions.iterrows():
if row['sequence']:
fastq_gz_filename = os.path.join(
ANALYZED_REGIONS,
'%s.fastq.gz' % clean_filename('REGION_' + str(idx)))
bam_region_filename = os.path.join(
ANALYZED_REGIONS,
'%s.bam' % clean_filename('REGION_' + str(idx)))
#create place-holder fastq files
open(fastq_gz_filename, 'w+').close()
region = '%s:%d-%d' % (row.chr_id, row.bpstart, row.bpend - 1)
info('\nExtracting reads in:%s and create the .bam file: %s' %
(region, bam_region_filename))
#extract reads in region
cmd = r'''samtools view -b -F 4 %s %s > %s ''' % (
args.bam_file, region, bam_region_filename)
#print cmd
sb.call(cmd, shell=True)
#index bam file
cmd = r'''samtools index %s ''' % (bam_region_filename)
#print cmd
sb.call(cmd, shell=True)
info('Trim reads and create a fastq.gz file in: %s' %
fastq_gz_filename)
#trim reads in bam and convert in fastq
n_reads = write_trimmed_fastq(bam_region_filename,
row['bpstart'], row['bpend'],
fastq_gz_filename)
df_regions.ix[idx, 'n_reads'] = n_reads
df_regions.ix[
idx, 'bam_file_with_reads_in_region'] = bam_region_filename
df_regions.ix[
idx,
'fastq.gz_file_trimmed_reads_in_region'] = fastq_gz_filename
df_regions.fillna('NA').to_csv(
_jp('REPORT_READS_ALIGNED_TO_SELECTED_REGIONS_WGS.txt'), sep='\t')
#Run Crispresso
info('\nRunning CRISPResso on each region...')
crispresso_cmds = []
for idx, row in df_regions.iterrows():
if row['n_reads'] >= args.min_reads_to_use_region:
info('\nThe region [%s] has enough reads (%d) mapped to it!' %
(idx, row['n_reads']))
crispresso_cmd= args.crispresso_command + ' -r1 %s -a %s -o %s --name %s' %\
(row['fastq.gz_file_trimmed_reads_in_region'],row['sequence'],OUTPUT_DIRECTORY,idx)
if row['sgRNA'] and not pd.isnull(row['sgRNA']):
crispresso_cmd += ' -g %s' % row['sgRNA']
if row['Expected_HDR'] and not pd.isnull(row['Expected_HDR']):
crispresso_cmd += ' -e %s' % row['Expected_HDR']
if row['Coding_sequence'] and not pd.isnull(
row['Coding_sequence']):
crispresso_cmd += ' -c %s' % row['Coding_sequence']
crispresso_cmd = CRISPRessoShared.propagate_crispresso_options(
crispresso_cmd, crispresso_options_for_wgs, args)
crispresso_cmds.append(crispresso_cmd)
# info('Running CRISPResso:%s' % crispresso_cmd)
# sb.call(crispresso_cmd,shell=True)
else:
info(
'\nThe region [%s] has too few reads mapped to it (%d)! Not running CRISPResso!'
% (idx, row['n_reads']))
CRISPRessoMultiProcessing.run_crispresso_cmds(crispresso_cmds,
args.n_processes,
'region',
args.skip_failed)
quantification_summary = []
all_region_names = []
all_region_read_counts = {}
good_region_names = []
good_region_folders = {}
header = 'Name\tUnmodified%\tModified%\tReads_aligned\tReads_total\tUnmodified\tModified\tDiscarded\tInsertions\tDeletions\tSubstitutions\tOnly Insertions\tOnly Deletions\tOnly Substitutions\tInsertions and Deletions\tInsertions and Substitutions\tDeletions and Substitutions\tInsertions Deletions and Substitutions'
header_els = header.split("\t")
header_el_count = len(header_els)
empty_line_els = [np.nan] * (header_el_count - 1)
n_reads_index = header_els.index('Reads_total') - 1
for idx, row in df_regions.iterrows():
folder_name = 'CRISPResso_on_%s' % idx
run_name = idx
all_region_names.append(run_name)
all_region_read_counts[run_name] = row.n_reads
run_file = os.path.join(_jp(folder_name),
'CRISPResso2_info.pickle')
if not os.path.exists(run_file):
warn(
'Skipping the folder %s: not enough reads, incomplete, or empty folder.'
% folder_name)
this_els = empty_line_els[:]
this_els[n_reads_index] = row.n_reads
to_add = [run_name]
to_add.extend(this_els)
quantification_summary.append(to_add)
else:
run_data = cp.load(open(run_file, 'rb'))
ref_name = run_data['ref_names'][
0] #only expect one amplicon sequence
n_tot = row.n_reads
n_aligned = run_data['counts_total'][ref_name]
n_unmod = run_data['counts_unmodified'][ref_name]
n_mod = run_data['counts_modified'][ref_name]
n_discarded = run_data['counts_discarded'][ref_name]
n_insertion = run_data['counts_insertion'][ref_name]
n_deletion = run_data['counts_deletion'][ref_name]
n_substitution = run_data['counts_substitution'][ref_name]
n_only_insertion = run_data['counts_only_insertion'][ref_name]
n_only_deletion = run_data['counts_only_deletion'][ref_name]
n_only_substitution = run_data['counts_only_substitution'][
ref_name]
n_insertion_and_deletion = run_data[
'counts_insertion_and_deletion'][ref_name]
n_insertion_and_substitution = run_data[
'counts_insertion_and_substitution'][ref_name]
n_deletion_and_substitution = run_data[
'counts_deletion_and_substitution'][ref_name]
n_insertion_and_deletion_and_substitution = run_data[
'counts_insertion_and_deletion_and_substitution'][ref_name]
unmod_pct = "NA"
mod_pct = "NA"
if n_aligned > 0:
unmod_pct = 100 * n_unmod / float(n_aligned)
mod_pct = 100 * n_mod / float(n_aligned)
vals = [run_name]
vals.extend([
round(unmod_pct, 8),
round(mod_pct, 8), n_aligned, n_tot, n_unmod, n_mod,
n_discarded, n_insertion, n_deletion, n_substitution,
n_only_insertion, n_only_deletion, n_only_substitution,
n_insertion_and_deletion, n_insertion_and_substitution,
n_deletion_and_substitution,
n_insertion_and_deletion_and_substitution
])
quantification_summary.append(vals)
good_region_names.append(idx)
good_region_folders[idx] = folder_name
samples_quantification_summary_filename = _jp(
'SAMPLES_QUANTIFICATION_SUMMARY.txt')
df_summary_quantification = pd.DataFrame(quantification_summary,
columns=header_els)
if args.crispresso1_mode:
crispresso1_columns = [
'Name', 'Unmodified%', 'Modified%', 'Reads_aligned',
'Reads_total'
]
df_summary_quantification.fillna('NA').to_csv(
samples_quantification_summary_filename,
sep='\t',
index=None,
columns=crispresso1_columns)
else:
df_summary_quantification.fillna('NA').to_csv(
samples_quantification_summary_filename, sep='\t', index=None)
crispresso2_info[
'samples_quantification_summary_filename'] = os.path.basename(
samples_quantification_summary_filename)
crispresso2_info['regions'] = df_regions
crispresso2_info['all_region_names'] = all_region_names
crispresso2_info['all_region_read_counts'] = all_region_read_counts
crispresso2_info['good_region_names'] = good_region_names
crispresso2_info['good_region_folders'] = good_region_folders
crispresso2_info['summary_plot_names'] = []
crispresso2_info['summary_plot_titles'] = {}
crispresso2_info['summary_plot_labels'] = {}
crispresso2_info['summary_plot_datas'] = {}
df_summary_quantification.set_index('Name')
save_png = True
if args.suppress_report:
save_png = False
plot_root = _jp("CRISPRessoWGS_modification_summary")
CRISPRessoPlot.plot_unmod_mod_pcts(plot_root,
df_summary_quantification, save_png,
args.min_reads_to_use_region)
plot_name = os.path.basename(plot_root)
crispresso2_info['summary_plot_root'] = plot_name
crispresso2_info['summary_plot_names'].append(plot_name)
crispresso2_info['summary_plot_titles'][
plot_name] = 'CRISPRessoWGS Modification Summary'
crispresso2_info['summary_plot_labels'][
plot_name] = 'Each bar shows the total number of reads aligned to each amplicon, divided into the reads that are modified and unmodified. The vertical line shows the cutoff for analysis, set using the --min_reads_to_use_region parameter.'
crispresso2_info['summary_plot_datas'][plot_name] = [
('CRISPRessoWGS summary',
os.path.basename(samples_quantification_summary_filename))
]
plot_root = _jp("CRISPRessoWGS_reads_summary")
CRISPRessoPlot.plot_reads_total(plot_root, df_summary_quantification,
save_png, args.min_reads_to_use_region)
plot_name = os.path.basename(plot_root)
crispresso2_info['summary_plot_root'] = plot_name
crispresso2_info['summary_plot_names'].append(plot_name)
crispresso2_info['summary_plot_titles'][
plot_name] = 'CRISPRessoWGS Read Allocation Summary'
crispresso2_info['summary_plot_labels'][
plot_name] = 'Each bar shows the total number of reads allocated to each amplicon. The vertical line shows the cutoff for analysis, set using the --min_reads_to_use_region parameter.'
crispresso2_info['summary_plot_datas'][plot_name] = [
('CRISPRessoWGS summary',
os.path.basename(samples_quantification_summary_filename))
]
if not args.suppress_report:
report_name = _jp('CRISPResso2WGS_report.html')
CRISPRessoReport.make_wgs_report_from_folder(
report_name, crispresso2_info, OUTPUT_DIRECTORY, _ROOT)
cp.dump(crispresso2_info, open(crispresso2WGS_info_file, 'wb'))
info('Analysis Complete!')
print(CRISPRessoShared.get_crispresso_footer())
sys.exit(0)
except Exception as e:
print_stacktrace_if_debug()
error('\n\nERROR: %s' % e)
sys.exit(-1)
def main():
def print_stacktrace_if_debug():
debug_flag = False
if 'args' in vars() and 'debug' in args:
debug_flag = args.debug
if debug_flag:
traceback.print_exc(file=sys.stdout)
error(traceback.format_exc())
try:
description = [
'~~~CRISPRessoWGS~~~',
'-Analysis of CRISPR/Cas9 outcomes from WGS data-'
]
wgs_string = r'''
____________
| __ __ |
|| |/ _ (_ |
||/\|\__)__) |
|____________|
'''
print(CRISPRessoShared.get_crispresso_header(description, wgs_string))
parser = CRISPRessoShared.getCRISPRessoArgParser(
parserTitle='CRISPRessoWGS Parameters', requiredParams={})
#tool specific optional
parser.add_argument('-b',
'--bam_file',
type=str,
help='WGS aligned bam file',
required=True,
default='bam filename')
parser.add_argument(
'-f',
'--region_file',
type=str,
help=
'Regions description file. A BED format file containing the regions to analyze, one per line. The REQUIRED\
columns are: chr_id(chromosome name), bpstart(start position), bpend(end position), the optional columns are:name (an unique indentifier for the region), guide_seq, expected_hdr_amplicon_seq,coding_seq, see CRISPResso help for more details on these last 3 parameters)',
required=True)
parser.add_argument(
'-r',
'--reference_file',
type=str,
help=
'A FASTA format reference file (for example hg19.fa for the human genome)',
default='',
required=True)
parser.add_argument(
'--min_reads_to_use_region',
type=float,
help=
'Minimum number of reads that align to a region to perform the CRISPResso analysis',
default=10)
parser.add_argument(
'--skip_failed',
help='Continue with pooled analysis even if one sample fails',
action='store_true')
parser.add_argument(
'--gene_annotations',
type=str,
help=
'Gene Annotation Table from UCSC Genome Browser Tables (http://genome.ucsc.edu/cgi-bin/hgTables?command=start), \
please select as table "knowGene", as output format "all fields from selected table" and as file returned "gzip compressed"',
default='')
parser.add_argument(
'-p',
'--n_processes',
type=int,
help='Specify the number of processes to use for the quantification.\
Please use with caution since increasing this parameter will increase the memory required to run CRISPResso.',
default=1)
parser.add_argument('--crispresso_command',
help='CRISPResso command to call',
default='CRISPResso')
args = parser.parse_args()
crispresso_options = CRISPRessoShared.get_crispresso_options()
options_to_ignore = set([
'fastq_r1', 'fastq_r2', 'amplicon_seq', 'amplicon_name',
'output_folder', 'name'
])
crispresso_options_for_wgs = list(crispresso_options -
options_to_ignore)
info('Checking dependencies...')
if check_samtools() and check_bowtie2():
info('\n All the required dependencies are present!')
else:
sys.exit(1)
#check files
check_file(args.bam_file)
check_file(args.reference_file)
check_file(args.region_file)
if args.gene_annotations:
check_file(args.gene_annotations)
#INIT
get_name_from_bam = lambda x: os.path.basename(x).replace('.bam', '')
if not args.name:
database_id = '%s' % get_name_from_bam(args.bam_file)
else:
database_id = args.name
OUTPUT_DIRECTORY = 'CRISPRessoWGS_on_%s' % database_id
if args.output_folder:
OUTPUT_DIRECTORY = os.path.join(
os.path.abspath(args.output_folder), OUTPUT_DIRECTORY)
_jp = lambda filename: os.path.join(
OUTPUT_DIRECTORY, filename
) #handy function to put a file in the output directory
try:
info('Creating Folder %s' % OUTPUT_DIRECTORY)
os.makedirs(OUTPUT_DIRECTORY)
info('Done!')
except:
warn('Folder %s already exists.' % OUTPUT_DIRECTORY)
log_filename = _jp('CRISPRessoWGS_RUNNING_LOG.txt')
logging.getLogger().addHandler(logging.FileHandler(log_filename))
with open(log_filename, 'w+') as outfile:
outfile.write(
'[Command used]:\nCRISPRessoWGS %s\n\n[Execution log]:\n' %
' '.join(sys.argv))
#check if bam has the index already
if os.path.exists(args.bam_file + '.bai'):
info('Index file for input .bam file exists, skipping generation.')
else:
info('Creating index file for input .bam file...')
sb.call('samtools index %s ' % (args.bam_file), shell=True)
#load gene annotation
if args.gene_annotations:
info('Loading gene coordinates from annotation file: %s...' %
args.gene_annotations)
try:
df_genes = pd.read_table(args.gene_annotations,
compression='gzip')
df_genes.txEnd = df_genes.txEnd.astype(int)
df_genes.txStart = df_genes.txStart.astype(int)
df_genes.head()
except:
info('Failed to load the gene annotations file.')
#Load and validate the REGION FILE
df_regions = pd.read_csv(args.region_file,
names=[
'chr_id', 'bpstart', 'bpend', 'Name',
'sgRNA', 'Expected_HDR', 'Coding_sequence'
],
comment='#',
sep='\t',
dtype={'Name': str})
#remove empty amplicons/lines
df_regions.dropna(subset=['chr_id', 'bpstart', 'bpend'], inplace=True)
df_regions.Expected_HDR = df_regions.Expected_HDR.apply(
capitalize_sequence)
df_regions.sgRNA = df_regions.sgRNA.apply(capitalize_sequence)
df_regions.Coding_sequence = df_regions.Coding_sequence.apply(
capitalize_sequence)
#check or create names
for idx, row in df_regions.iterrows():
if pd.isnull(row.Name):
df_regions.ix[idx, 'Name'] = '_'.join(
map(str, [row['chr_id'], row['bpstart'], row['bpend']]))
if not len(df_regions.Name.unique()) == df_regions.shape[0]:
raise Exception('The amplicon names should be all distinct!')
df_regions = df_regions.set_index('Name')
#df_regions.index=df_regions.index.str.replace(' ','_')
df_regions.index = df_regions.index.to_series().str.replace(' ', '_')
#extract sequence for each region
uncompressed_reference = args.reference_file
if os.path.exists(uncompressed_reference + '.fai'):
info(
'The index for the reference fasta file is already present! Skipping generation.'
)
else:
info('Indexing reference file... Please be patient!')
sb.call('samtools faidx %s >>%s 2>&1' %
(uncompressed_reference, log_filename),
shell=True)
df_regions['sequence'] = df_regions.apply(
lambda row: get_region_from_fa(row.chr_id, row.bpstart, row.bpend,
uncompressed_reference),
axis=1)
for idx, row in df_regions.iterrows():
if not pd.isnull(row.sgRNA):
cut_points = []
for current_guide_seq in row.sgRNA.strip().upper().split(','):
wrong_nt = find_wrong_nt(current_guide_seq)
if wrong_nt:
raise NTException(
'The sgRNA sequence %s contains wrong characters:%s'
% (current_guide_seq, ' '.join(wrong_nt)))
offset_fw = args.quantification_window_center + len(
current_guide_seq) - 1
offset_rc = (-args.quantification_window_center) - 1
cut_points+=[m.start() + offset_fw for \
m in re.finditer(current_guide_seq, row.sequence)]+[m.start() + offset_rc for m in re.finditer(CRISPRessoShared.reverse_complement(current_guide_seq), row.sequence)]
if not cut_points:
df_regions.ix[idx, 'sgRNA'] = ''
df_regions = df_regions.convert_objects(convert_numeric=True)
df_regions.bpstart = df_regions.bpstart.astype(int)
df_regions.bpend = df_regions.bpend.astype(int)
if args.gene_annotations:
df_regions = df_regions.apply(
lambda row: find_overlapping_genes(row, df_genes), axis=1)
#extract reads with samtools in that region and create a bam
#create a fasta file with all the trimmed reads
info('\nProcessing each regions...')
ANALYZED_REGIONS = _jp('ANALYZED_REGIONS/')
if not os.path.exists(ANALYZED_REGIONS):
os.mkdir(ANALYZED_REGIONS)
df_regions['n_reads'] = 0
df_regions['bam_file_with_reads_in_region'] = ''
df_regions['fastq.gz_file_trimmed_reads_in_region'] = ''
for idx, row in df_regions.iterrows():
if row['sequence']:
fastq_gz_filename = os.path.join(
ANALYZED_REGIONS,
'%s.fastq.gz' % clean_filename('REGION_' + str(idx)))
bam_region_filename = os.path.join(
ANALYZED_REGIONS,
'%s.bam' % clean_filename('REGION_' + str(idx)))
#create place-holder fastq files
open(fastq_gz_filename, 'w+').close()
region = '%s:%d-%d' % (row.chr_id, row.bpstart, row.bpend - 1)
info('\nExtracting reads in:%s and create the .bam file: %s' %
(region, bam_region_filename))
#extract reads in region
cmd = r'''samtools view -b -F 4 %s %s > %s ''' % (
args.bam_file, region, bam_region_filename)
#print cmd
sb.call(cmd, shell=True)
#index bam file
cmd = r'''samtools index %s ''' % (bam_region_filename)
#print cmd
sb.call(cmd, shell=True)
info('Trim reads and create a fastq.gz file in: %s' %
fastq_gz_filename)
#trim reads in bam and convert in fastq
n_reads = write_trimmed_fastq(bam_region_filename,
row['bpstart'], row['bpend'],
fastq_gz_filename)
df_regions.ix[idx, 'n_reads'] = n_reads
df_regions.ix[
idx, 'bam_file_with_reads_in_region'] = bam_region_filename
df_regions.ix[
idx,
'fastq.gz_file_trimmed_reads_in_region'] = fastq_gz_filename
df_regions.fillna('NA').to_csv(
_jp('REPORT_READS_ALIGNED_TO_SELECTED_REGIONS_WGS.txt'), sep='\t')
#Run Crispresso
info('\nRunning CRISPResso on each regions...')
crispresso_cmds = []
for idx, row in df_regions.iterrows():
if row['n_reads'] >= args.min_reads_to_use_region:
info('\nThe region [%s] has enough reads (%d) mapped to it!' %
(idx, row['n_reads']))
crispresso_cmd= args.crispresso_command + ' -r1 %s -a %s -o %s --name %s' %\
(row['fastq.gz_file_trimmed_reads_in_region'],row['sequence'],OUTPUT_DIRECTORY,idx)
if row['sgRNA'] and not pd.isnull(row['sgRNA']):
crispresso_cmd += ' -g %s' % row['sgRNA']
if row['Expected_HDR'] and not pd.isnull(row['Expected_HDR']):
crispresso_cmd += ' -e %s' % row['Expected_HDR']
if row['Coding_sequence'] and not pd.isnull(
row['Coding_sequence']):
crispresso_cmd += ' -c %s' % row['Coding_sequence']
crispresso_cmd = CRISPRessoShared.propagate_crispresso_options(
crispresso_cmd, crispresso_options_for_wgs, args)
crispresso_cmds.append(crispresso_cmd)
# info('Running CRISPResso:%s' % crispresso_cmd)
# sb.call(crispresso_cmd,shell=True)
else:
info(
'\nThe region [%s] has too few reads mapped to it (%d)! Skipping the running of CRISPResso!'
% (idx, row['n_reads']))
CRISPRessoMultiProcessing.run_crispresso_cmds(crispresso_cmds,
args.n_processes,
'region',
args.skip_failed)
quantification_summary = []
for idx, row in df_regions.iterrows():
folder_name = 'CRISPResso_on_%s' % idx
try:
quantification_file, amplicon_names, amplicon_info = CRISPRessoShared.check_output_folder(
_jp(folder_name))
for amplicon_name in amplicon_names:
N_TOTAL = float(amplicon_info[amplicon_name]['Total'])
N_UNMODIFIED = float(
amplicon_info[amplicon_name]['Unmodified'])
N_MODIFIED = float(
amplicon_info[amplicon_name]['Modified'])
quantification_summary.append([
idx, amplicon_name, N_UNMODIFIED / N_TOTAL * 100,
N_MODIFIED / N_TOTAL * 100, N_TOTAL, row.n_reads
])
except CRISPRessoShared.OutputFolderIncompleteException as e:
quantification_summary.append(
[idx, "", np.nan, np.nan, np.nan, row.n_reads])
warn(
'Skipping the folder %s: not enough reads, incomplete, or empty folder.'
% folder_name)
df_summary_quantification = pd.DataFrame(quantification_summary,
columns=[
'Name', 'Amplicon',
'Unmodified%',
'Modified%',
'Reads_aligned',
'Reads_total'
])
df_summary_quantification.fillna('NA').to_csv(
_jp('SAMPLES_QUANTIFICATION_SUMMARY.txt'), sep='\t', index=None)
info('All Done!')
print(CRISPRessoShared.get_crispresso_footer())
sys.exit(0)
except Exception as e:
print_stacktrace_if_debug()
error('\n\nERROR: %s' % e)
sys.exit(-1)
