def find_tree_file(wdir, name):
tmp = cmn.cmd2lines('ls -t %s/*renamed' % wdir)
if len(tmp) == 0:
tmp += cmn.cmd2lines('ls -t %s/%s*tre' % (wdir, name))
if len(tmp) == 0:
print('Error! can not find tree in %s' % wdir)
sys.exit()
return tmp[0]
def backup_finalStat(wdir):
ddir = '/project/biophysics/Nick_lab/mtang/archive/step4_postprocessing/final_stats/'
fns = cmn.cmd2lines('ls %s/*.report| grep -v all_genome' % wdir)
for fn in fns:
print('processing %s...' % fn)
fnlabel = cmn.lastName(fn)
#don't back up the ones without species
items = fnlabel.replace('_stat.report', '').split('_')
if len(items) == 1:
print('skip the fasta without sp for %s' % fn)
continue
#get the one with least NA and more data amount
dn = '%s/%s' % (ddir, fnlabel)
if os.path.exists(dn):
print('merging new and old data for %s' % fnlabel)
Nold_na, Nold_data = count_final_stat(dn)
Nnew_na, Nnew_data = count_final_stat(fn)
if Nnew_na < Nold_na: #less NA
cmn.run('cp %s %s' % (fn, dn))
else:
if Nnew_na == Nold_na: #same NA number
if Nnew_data > Nold_data:
cmn.run('cp %s %s' % (fn, dn))
else:
cmn.run('cp %s %s' % (fn, dn))
cmn.run('cd %s; cat *.report > allstat.txt' % ddir)
def old_log_newBaits_ifPossible(seqs):
fall = '/project/biophysics/Nick_lab/wli/sequencing/scripts/data/barcodes/species_barcodes_4mapping.fa'
takenNames = set(
[each.strip()[1:] for each in cmn.cmd2lines('grep ">" %s' % fall)])
fnew = '/project/biophysics/Nick_lab/wli/sequencing/scripts/data/barcodes/addedBaits_fromPipeline.fa'
seqDict = read_fa(fnew)
for name in seqs:
if name not in takenNames and (name not in seqDict):
seqDict[name] = seqs[name][20:678]
with open(fnew, 'w') as dp:
for name in seqDict:
if name not in takenNames and (name not in seqDict):
print('saving %s into database...' % name)
fasta = '>%s\n%s\n' % (name, seqDict[name])
dp.write(fasta)
fverify = '/project/biophysics/Nick_lab/wli/sequencing/scripts/data/barcodes/all_barcodes_4verify.fa'
dict2 = read_fa(fverify)
seqDict.update(dict2)
with open(fverify, 'w') as dp:
for name in seqDict:
fasta = '>%s\n%s\n' % (name.replace(
'(assembled)', '').strip('.'), seqDict[name].replace('-', 'N'))
dp.write(fasta)
cmd = 'module add blast;cd /project/biophysics/Nick_lab/wli/sequencing/scripts/data/barcodes; makeblastdb -in=all_barcodes_4verify.fa -dbtype=nucl; chmod a+w all_barcodes_4verify.*'
cmn.run(cmd)
def read_compare_file(fn, fcheck, ID):
cmd = 'grep -P \'^%s\t\' %s' % (ID, fn)
line = cmn.cmd2lines(cmd)[0]
#TODO: need to rework
if 'same' in line:
return 'mostConfident', [0]
elif 'diffGenus' in line:
return 'diffGenus', [0, 1]
elif 'takenD' in line:
return 'confident', [0]
elif 'completeDenovo' in line and ('goodCC' in line):
return 'confident', [0]
elif 'completeDenovo' in line:
return 'denovoOnly', [0]
elif 'goodCC' in line:
return 'goodRef', [1]
else:
#these sample would be somewhat problematic
if 'Error' in line:
return 'Error', [0, 1]
elif isHighRatio(line):
return 'Suspicius', [0, 1]
elif 'Gap0' not in line:
return 'PoorSample', [1]
elif 'noDenovo' in line:
return 'refOnly', [0]
else:
return 'TODO', [0, 1]
def read_baits():
fns = cmn.cmd2lines('ls baits/bait*.fa')
seqDict = {}
for fn in fns:
name, seq = cmn.file2lines(fn)
seqDict[name[1:]] = list(seq)
return seqDict
def search_for_old_fastq(label, wdirs):
global selfDir
alist = []
for wdir in wdirs:
cmd = 'ls %s/%s*q 2> /dev/null' % (wdir, label)
alist += [line for line in cmn.cmd2lines(cmd) if selfDir not in line]
return alist
def prune_tree(ftree, fseq):
t = ete3.Tree(ftree)
IDlist = cmn.cmd2lines('grep ">" %s|cut -d ">" -f 2' % fseq)
t.prune(IDlist)
dn = 'prune_tree.tre'
cmn.write_file(t.write(format=1), dn)
return dn
def parse_fastq_dir(wdir):
adict = {}
fns = cmn.cmd2lines('ls %s/*q' % wdir)
for line in fns:
sp = cmn.lastName(line).split('_')[0]
try:
adict[sp].append(line)
except KeyError:
adict[sp] = [line]
return adict
def do_barcode_blast(sequence):
fdb = '/project/biophysics/Nick_lab/wli/sequencing/scripts/data/barcodes/species_barcodes_4mapping.fa'
#fdb = '/project/biophysics/Nick_lab/wli/sequencing/scripts/data/barcodes/all_barcodes_NoN_0.95.fasta'
namelabel = sequence.split()[0][1:].split()[0].split('|')[0].replace('*','').split('[')[0].replace('"','').replace("'", '')
fquery = '/tmp/%s.fa' % namelabel
cmn.write_file(sequence, fquery)
cmd = 'module add blast; blastn -query %s -db %s ' % (fquery, fdb)
cmd += '-outfmt \'6 sseqid qlen slen length pident\''
lines = cmn.cmd2lines(cmd)
#cmn.run('rm %s' % fquery)
return lines
def find_annotation(CG):
if CG == 'NA':
return 'NA'
fn = '/project/biophysics/Nick_lab/wli/sequencing/scripts/data/gene_association.fb'
anno_lines = cmn.cmd2lines('grep %s %s' % (CG, fn))
annos = set([])
for line in anno_lines:
items = line.split('\t')
anno = items[9]
annos.add(anno)
return ','.join(annos)
def get_names():
adict = {}
fns = cmn.cmd2lines('ls -tr /project/biophysics/Nick_lab/wli/sequencing/scripts/data/*.sampleData')
for fn in fns:
for line in cmn.file2lines(fn):
line = line.strip()
items = line.split()
sp = items[0].split('-')[-1]
line = line.replace(items[0], sp).replace('-', '_').replace('(','').replace(')', '')
adict[sp] = '_'.join(line.split())
return adict
def do_barcode_blast(sequence, seqDict):
#fref = '/project/biophysics/Nick_lab/wli/sequencing/scripts/data/barcodes/species_barcodes_4mapping.fa'
#fadd = '/project/biophysics/Nick_lab/wli/sequencing/scripts/data/barcodes/added_from_customBaits.baitInfo'
fdb = makeBlastDatabase(seqDict)
#fdb = '/project/biophysics/Nick_lab/wli/sequencing/scripts/data/barcodes/all_barcodes_NoN_0.95.fasta'
namelabel = sequence.split()[0][1:].split()[0].split('|')[0].replace('*','').split('[')[0].replace('"','').replace("'", '')
namelabel = namelabel.replace('/', '_')
fquery = '/tmp/%s.fa' % namelabel
cmn.write_file(sequence, fquery)
cmd = 'module add blast; blastn -query %s -db %s ' % (fquery, fdb)
cmd += '-outfmt \'6 sseqid qlen slen length pident\''
lines = cmn.cmd2lines(cmd)
cmn.run('rm %s' % fquery)
return lines
def get_query_sequence(seqDict, genus, sp):
#1. anything in Eudamine file has higher priority
fEud = '/project/biophysics/Nick_lab/wli/sequencing/scripts/data/barcodes/Eudaminae-barcode-reference.txt'
cmd = 'grep %s %s' % (sp, fEud)
lines = cmn.cmd2lines(cmd)
if len(lines) == 1:
name = lines[0].split()[0]
seq = seqDict[name]
fasta = '>%s\n%s\n' % (name, seq)
qlen = len(seq.replace('N', ''))
print('pick %s for %s %s' % (name, genus, sp))
return fasta, qlen
#look it up in other files
names = list(seqDict.keys())
good_names = [name for name in names
if genus in name ]
if len(good_names) == 0:#sp is just 'sp'
print('can not find barcode for genus keyword "%s"' % genus)
good_names = names
if len(good_names) > 1:
#try to refine it
tmp = [name for name in good_names
if sp in name]
if len(tmp) != 0:
good_names = tmp
#try to see if type species is there
tmp = [name for name in good_names
if name[0] == '*']
if len(tmp) != 0:
good_names = tmp
else:
tmp = [name for name in good_names
if '*' in name]
if len(tmp) != 0:
good_names = tmp
#then randomly pick one, get the max length ones
name = max(good_names, key=lambda x: len(seqDict[x].replace('N', '-')))
seq = seqDict[name]
fasta = '>%s\n%s\n' % (name, seq)
qlen = len(seq.replace('N', ''))
print('pick %s for %s %s' % (name, genus, sp))
return fasta, qlen
def parse_info_file(wdir):
fns = cmn.cmd2lines(' ls %s/fastq*' % wdir)
adict = {}
for fn in fns:
fp = open(fn)
#with open(fn) as fp:
for line in fp:
line = line.strip()
sp = cmn.lastName(line).split('_')[0]
try:
adict[sp].append(line)
except KeyError:
adict[sp] = [line]
fp.close()
for key in list(adict.keys()):
adict[key] = set(adict[key])
return adict
def read_rep():
dn = 'rep.dict.pkl'
if cmn.filexist(dn):
print('loading repeats using precomputed data...')
return cmn.pickle_read(dn)
freps = cmn.cmd2lines('ls annotation_repeats/*.gff3')
repdict = {}
for frep in freps:
for line in cmn.file2lines(fn):
items = line.strip().split()
scaf = items[0]
if scaf not in repdict:
repdict[scaf] = set([])
i, j = list(map(int, items[3:5]))
repdict[scaf] = repdict[scaf] | set(range(i, j))
cmn.pickle_write(repdict, dn)
return repdict
def split_and_order_sp_byTree(sampleIDs):
treeDir = '/project/biophysics/Nick_lab/mtang/building_trees'
wdirs = cmn.cmd2lines('ls %s' % treeDir)
wdir_dict = get_newest_tree_dir(wdirs)
rdict = {}
for projectName in wdir_dict:
wdir = '%s/%s' % (treeDir, wdir_dict[projectName])
print('pick %s for %s' % (wdir, projectName))
IDfile = '%s/NickList' % (wdir)
IDlist = [each.replace('NVG-', '').replace('LEP-', 'LEP')
for each in cmn.file2lines(IDfile)]
overlapIDs = set(IDlist) & set(sampleIDs)
if len(overlapIDs) > 0:
ftree = find_tree_file(wdir, projectName)
ordered_IDs = order_ID_byTree(ftree, overlapIDs)
rdict[projectName] = ordered_IDs
return rdict
def backup_vcf_coverage(wdir):
ddir = '/project/biophysics/Nick_lab/mtang/archive/step4_postprocessing/check_vcf_coverage'
fns = cmn.cmd2lines('ls %s/*_vcf.cov' % wdir)
#1. only back up the new version of cov file
for fn in fns:
print('processing %s...' % fn)
lines = cmn.file2lines(fn)
items = lines[-1].strip().split()
if len(items) != 6:
print('skip old format file %s' % fn)
continue
fnlabel = cmn.lastName(fn)
dn = '%s/%s' % (ddir, fnlabel)
if os.path.exists(dn):
print('merging new and old data for %s' % fnlabel)
covOld = float(cmn.file2lines(dn)[-1].split()[-2])
cov = float(lines[-1].split()[-2])
if cov > covOld:
cmn.run('cp %s %s' % (fn, dn))
else:
cmn.run('cp %s %s' % (fn, dn))
def backup_fasta(wdir):
ddir = '/project/biophysics/Nick_lab/mtang/archive/step4_postprocessing/map2fasta'
fns = cmn.cmd2lines('ls %s/*_m2s.fa| grep -v all_genome' % wdir)
for fn in fns:
print('processing %s...' % fn)
fnlabel = cmn.lastName(fn)
#don't back up the ones without species
items = fnlabel.replace('_snp_step2_MITO_m2s.fa',
'').replace('_snp_step2_m2s.fa', '').split('_')
if len(items) == 1:
print('skip the fasta without sp for %s' % fn)
continue
#get the least gapped one
dn = '%s/%s' % (ddir, fnlabel)
if os.path.exists(dn):
print('merging new and old data for %s' % fnlabel)
Nold = count_fasta_nonGap(dn)
Nnew = count_fasta_nonGap(fn)
if Nnew > Nold:
cmn.run('cp %s %s' % (fn, dn))
else:
cmn.run('cp %s %s' % (fn, dn))
#main
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
if __name__ == '__main__':
#options=parse_options()
try:
fn = sys.argv[1]
Ncores = int(sys.argv[2])
except:
print("Usage: *.py fa Ncores", file=sys.stderr)
sys.exit()
#if the nodes are less than 4 taxa, produce a random tree
cmd = "grep '>' %s" % (fn)
lines = [
each[1:].strip() for each in cmn.cmd2lines(cmd) if each.strip() != ''
]
N = len(lines)
if N < 4:
print('Warning: fastme can not make tree of less than 4 taxa')
print('Warning: so I make a fake tree...')
dn = '%s.phylip.fastme.tre' % cmn.lastName(fn)
if N == 1:
info = '(%s);\n' % lines[0]
if N == 2:
a, b = lines
info = '(%s,%s);\n' % (a, b)
elif N == 3:
a, b, c = lines
info = '((%s,%s),%s);\n' % (a, b, c)
sys.exit()
#step 1 including 1. making the pileup file, 2. correct bias, 3. sam map again 4. snp call till last step
#step 2: just the snp call using multiple CPUs
#only put 15 jobs in a node to avoid memmory problem
f_ass = '/project/biophysics/Nick_lab/wli/sequencing/Nick_request/Heli_map/SNP_calling/2_gatk/assembly_v2.fa'
#should not run for reference genome; this should just build by original snp call
ref_sp = '3935'
step1dir = 'step1_cmds'
cmn.mkdir(step1dir)
#fns = cmn.getid(fn)
fns = cmn.cmd2lines(
'ls /project/biophysics/Nick_lab/wli/sequencing/Nick_request/Heli_map/SNP_calling/2_gatk/*/realigned_reads.bam'
)
finished_pileups = cmn.cmd2lines(
'ls /project/biophysics/Nick_lab/wli/sequencing/Nick_request/Heli_map/SNP_calling/2_gatk/*/*.pileup'
)
finished = set(
[cmn.lastName(i).split('_')[0] for i in cmn.cmd2lines('ls */*.vcf')])
step1_finished = set([
cmn.lastName(i).split('/')[0]
for i in cmn.cmd2lines('ls */realigned_reads.bam')
])
template = cmn.txt_read(
'/project/biophysics/Nick_lab/wli/sequencing/myAnalysis/clean_ref_bias/1_gatk_runs/step1_job.template'
)
fn=sys.argv[1]
except:
print("Usage: *.py NickList requred_keywords", file=sys.stderr)
sys.exit()
words = sys.argv[2:]
IDs = set(cmn.file2lines(fn))
#note: cne is equal to 3574_assembly_v1
wdirs = [
'/project/biophysics/Nick_lab/mtang/archive/step4_postprocessing/map2fasta',
'/project/biophysics/Nick_lab/mtang/unbias_SNPs/*/step4_postprocessing/map2fasta'
]
alea_list = cmn.cmd2lines('ssh [email protected] "ls /archive/butterfly/unbias_pipeline_info/step4_postprocessing/map2fasta/*MITO*.fa"')
missing = []
falist = []
required = ''
if len(words) != 0:
required = '|' + '|'.join(['grep %s' % word for word in words])
faDict = {}
for ID in IDs:
taken = []
for wdir in wdirs:
cmd = 'ls %s/%s*_m2s.fa 2> /dev/null| grep MITO %s' % (wdir, ID, required)
taken += cmn.cmd2lines(cmd)
except:
print("Usage: *.py NickList requred_keywords", file=sys.stderr)
sys.exit()
words = sys.argv[2:]
IDs = set(cmn.file2lines(fn))
#note: cne is equal to 3574_assembly_v1
wdirs = [
'/project/biophysics/Nick_lab/mtang/archive/step4_postprocessing/vcf2map',
'/project/biophysics/Nick_lab/mtang/unbias_SNPs/*/step4_postprocessing/vcf2map'
]
alea_list = cmn.cmd2lines(
'ssh [email protected] "ls /archive/butterfly/unbias_pipeline_info/step4_postprocessing/vcf2map/*.map| grep -v mitogenome"'
)
missing = []
falist = []
required = ''
if len(words) != 0:
for word in words:
word = word.strip()
if word == '3574_assembly_v1' or word == 'cne':
word = '"3574_assembly_v1\|cne"'
required += '| grep %s' % word
words = set(words)
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
#main
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
if __name__ == '__main__':
#options=parse_options()
try:
wdir = sys.argv[1]
except:
print("Usage: *.py wdir", file=sys.stderr)
sys.exit()
total = 0
unaligned = 0
bestDir = cmn.txt_read('%s/best_mapping.txt' % wdir)
fns = cmn.cmd2lines('ls %s/%s/*.sam' % (wdir, bestDir))
sp = fns[0].split('/')[-3]
for fn in fns:
fp = open(fn)
#with open(fn) as fp:
for line in fp:
if line[0] == '@':
continue
else:
total += 1
if line.strip().split()[2] == '*':
unaligned += 1
fp.close()
print(sp, bestDir, (total - unaligned), total)
import sys
import os
python_lib = '/work/biophysics/mtang/SNP_calling/scripts'
if python_lib not in sys.path:
sys.path.append(python_lib)
import cmn
#1. read in data
fns = cmn.getid(sys.argv[1])
falist = cmn.cmd2lines('ls *m2s.fa')
finished_maps = set([fn.replace('_m2s.fa', '.map') for fn in falist])
isGood = True
cmds = []
for fn in fns:
label = cmn.lastName(fn)
if label in finished_maps:
continue
isGood = False
if 'MITO' in label:
cmd = '/work/biophysics/mtang/SNP_calling/scripts/map2fasta_mito.py %s' % fn
else:
cmd = '/work/biophysics/mtang/SNP_calling/scripts/map2fasta.py %s' % fn
cmds.append(cmd)
if python_lib not in sys.path:
sys.path.append(python_lib)
import cmn
import os
from fullname_lib import get_names_4barcode
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
#main
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
if __name__ == '__main__':
#infoLines = cmn.cmd2lines('head -n 1 sampleRun*/rescued_read_assembled_mis1*.txt')
IDlist = cmn.cmd2lines("ls -d sampleRun_* |grep -v fake|cut -d '_' -f 2")
nameDict = get_names_4barcode()
for ID in IDlist:
items = nameDict[ID].replace('?', '').split()
ID, genus, sp = items[:3]
print('sampleInfo', ID, genus, sp)
fn = 'sampleRun_%s/good_read_assembled.txt' % ID
#label = '%s_%s' % (genus, sp)
cmd = 'head %s -n 2| grep %s' % (fn, genus)
print(cmd)
info = cmn.cmd2info(cmd).strip()
if info == '':
print('please re-run', ID, genus, sp)
def group_fastq(fns):
adict = {}
for fn in fns:
key = cmn.lastName(fn).split('_')[0]
try:
adict[key].append(fn)
except KeyError:
adict[key] = [fn]
return adict
#~~~~~~~~main~~~~~~~~~~~~~~#
wdir = sys.argv[1].rstrip('/')
selfDir = os.path.abspath(wdir)
fastqs = cmn.cmd2lines('ls %s/*q' % wdir)
print(fastqs)
log_info = []
outdir = '%s/fastq_thisBatch' % wdir
cmn.mkdir(outdir)
hasCombined = False
for fastq in fastqs:
label = '.'.join(cmn.lastName(fastq).split('.')[:-1])
print('processing %s' % label)
old_fastqs = search_for_old_fastq(label, search_dirs)
dn = '%s/%s' % (outdir, cmn.lastName(fastq))
if not os.path.exists(dn):
cmn.run('mv %s %s' % (fastq, dn))
else:
except:
print(
"Usage: *.py ../step1_gather_data/mapping_info.txt ../step2_bwa_mapping ../step1_gather_data/require_SNPs.dict.pkl TACC_IDs",
file=sys.stderr)
sys.exit()
cwd = os.getcwd()
#subsetIDs = set(cmn.getid(fsubset))
subsetJobs = set([
cmn.lastName(line.replace('sbatch', '').strip())[4:-4]
for line in cmn.file2lines(fsubset)
])
#1. read in info
fsams = cmn.cmd2lines('ls %s/*/*/*.sam' % mapdir)
#print fsams
samdirs = set(['/'.join(fsam.split('/')[:-2]) for fsam in fsams])
#print samdirs
require_refs = cmn.pickle_read(freq)
fq_dict = {}
refdict = {}
#1. tell by reftable
#make the requirement by the reftable
for line in cmn.file2lines(freftable):
items = line.strip().split()
sp = items[0]
fastqs = items[1].split(',')
fq_dict[sp] = fastqs
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
#main
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
if __name__ == '__main__':
#options=parse_options()
try:
indir, label = sys.argv[1:3]
except:
print("Usage: *.py ../1_process_alignment/noGap_splits noGap",
file=sys.stderr)
sys.exit()
fns = [os.path.abspath(i) for i in cmn.cmd2lines('ls %s/*' % indir)]
wdir = 'split_run_%s' % label
cmn.mkdir(wdir)
os.chdir(wdir)
cmn.mkdir('job_files')
for count, fn in enumerate(fns):
cmn.run('ln -s %s' % fn)
fn_new = cmn.lastName(fn)
cmd = 'rm *%s_%s; /home2/wli/local/RAxML/raxmlHPC-PTHREADS-SSE3 -m GTRGAMMA -s %s -n %s_%s -p 7112 -T 48 ' % (
label, count, fn_new, label, count)
dn = 'job_files/sg%s.job' % count
cmn.run('/home2/wli/my_programs/make_job.py "%s" -p 256GB -t 33 > %s' %
(cmd, dn))
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
#main
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
if __name__ == '__main__':
#options=parse_options()
try:
fn = sys.argv[1]
except:
print("Usage: *.py *.report", file=sys.stderr)
sys.exit()
fcomp = 'compare.check'
cmd = 'grep -v same compare.check'
lines = cmn.cmd2lines(cmd)
#exclude those with gap0 and nothing in report file
badSp = set([])
for line in cmn.file2lines(fn):
if line[0] == '#':
continue
sp = line.split()[0].split('_')[0]
badSp.add(sp)
for line in lines:
items = line.strip().split()
sp = items[0]
if sp not in badSp and items[2] == 'Gap0':
if 'no' in items[-1]:
line = 'goodReport:' + line
stackSeq = parse_del_p(stackSeq, del_p)
cleanSeq = parse_del_p(cleanSeq, del_p)
threadSeq = parse_del_p(threadSeq, del_p)
return threadSeq, stackSeq, cleanSeq
def parse_del_p(seq, del_p):
new = [char for i, char in enumerate(seq) if i not in del_p]
return ''.join(new)
if __name__ == '__main__':
#olines = cmn.cmd2lines('grep "thread\|stack" sampleRun_*/good_read_assembled.txt')
#lines = cmn.cmd2lines('grep -H "threaded_\|stack_\|clean_" sampleRun_*/rescued_read_assembled_mis1*.txt')
wdirs = cmn.cmd2lines('ls -d sampleRun_*')
#cmn.mkdir('sampleRun_fake')
#cmn.run('touch sampleRun_fake/good_read_assembled.txt')
#cmn.run('touch sampleRun_fake/rescued_read_assembled_mis1.txt')
#time.sleep(2)
cmn.run('rm cannot_fixed_indel.txt 2> /dev/null')
#frecords = cmn.cmd2lines('ls sampleRun_*/pickingLog.txt')
stack_lines = {}
thread_lines = {}
clean_lines = {}
leftN = 20
barcodeLength = 658
for wdir in wdirs:
