def transfer_alea_files(fnlist):
transferDir = 'alea_transfer'
cmn.mkdir(transferDir)
newlist = []
for fn in fnlist:
print('transfering %s from archive server ...' % fn)
cmd = 'rsync -r [email protected]:%s %s' % (fn, transferDir)
cmn.run(cmd)
newlist.append('%s/%s' % (transferDir, cmn.lastName(fn)))
return newlist
def parse_ref(seqDict):
cmn.mkdir('baits')
newDict = {}
for i, name in enumerate(seqDict):
seq = seqDict[name]
fnlabel = 'bait%s' % i
dn = 'baits/%s.fa' % fnlabel
name = name.replace('*', '').replace('"', "'")
fasta = '>%s\n%s\n' % (name, seq)
cmn.write_file(fasta, dn)
cmd = 'module add bwa; bwa index %s -p %s' % (dn, fnlabel)
cmn.run(cmd)
newDict[name] = dn
return newDict
def attempt_to_find_genus_by_abundence(ID, fqlist):
tmpdir = 'tmp_%s' % ID
cmn.mkdir(tmpdir)
os.chdir(tmpdir)
cmn.write_lines(fqlist, 'fqlist')
cmd = '/work/archive/biophysics/Nick_lab/wli/project/sequencing/scripts/barcode_scripts/auto_rebait.py fqlist'
cmn.run(cmd)
dn = 'picked_bait.txt'
if cmn.filexist(dn):
genus = cmn.txt_read(dn).strip().split('_')[0].split()[0]
else:
genus = None
os.chdir('..')
cmn.run('cp %s/mapping_stat.info tmpStat/%s_mapping_stat.info' % (tmpdir, ID))
cmn.run('rm -r %s ' % tmpdir)
return genus
sys.exit()
try:
pre = sys.argv[4]
except:
pre = 'x'
#cores = 32 # in biohpc, it is 32
partition = 'super'
for i, arg in enumerate(sys.argv):
if arg == '-p':
partition = sys.argv[i + 1]
tmpdir = '%s_files' % pre
cmn.mkdir(tmpdir)
bundle = len(cmds) / N
for i in range(N):
cmd = cmds[i * bundle:(i + 1) * bundle]
if i == N - 1:
cmd += cmds[(i + 1) * bundle:]
dn = '%s/%s_%s' % (tmpdir, pre, i)
cmn.write_file('\n'.join(cmd), dn)
submit_job(dn, Npara, pre, i, partition)
cwd = os.getcwd()
d_stat = '%s/stat.info' % tmpdir
info = []
info.append('commands are from: %s/%s' % (cwd, sys.argv[1]))
info.append('split into %s jobs' % sys.argv[2])
'/project/biophysics/Nick_lab/wli/sequencing/mapping/SNP_calling/2_gatk/template_gatk.job'
)
template = template.replace('assembly_v0', ass_label)
fns = cmn.cmd2lines('ls ../1_bwa_align/*.sam | grep -v _v0_')
fns = [os.path.abspath(i) for i in fns]
#good_set = set('LEP18259 3318 3303'.split())
finished = cmn.cmd2lines("ls */*.vcf|cut -d '/' -f 2|cut -d '_' -f 1")
#group spiecies
group_dict = group_by_species(fns)
for slabel in group_dict:
if slabel in finished:
print('skip finished ' + slabel)
continue
cmn.mkdir(slabel)
os.chdir(slabel)
fns = group_dict[slabel]
f_sam = merge_sams(slabel, fns)
cmd = template.replace('3377', slabel)
#cmd = cmd.replace('--job-name=gatk', '--job-name=%s' % slabel)
os.chdir('..')
cmn.write_file(cmd, 'gatk%s.job' % slabel)
cmn.run('sbatch gatk%s.job' % slabel)
try:
odir, f_ass = sys.argv[1:3]
except:
print("Usage: *.py filelist assembly_v0.fa", file=sys.stderr)
print("you should index assembly_v0.fa first with -p assembly_v0", file=sys.stderr)
print("using command /home2/wli/local/bwa-0.7.12/bwa index ", file=sys.stderr)
sys.exit()
#fns = cmn.cmd2lines('ls %s/*.fq' % odir)
fns = cmn.getid(odir)
group_dict = separate_by_label(fns)
ass_label = cmn.find_between(cmn.lastName(f_ass), 'assembly_', '.fa')
cmn.mkdir('job_files')
cmn.mkdir('cmd_files')
for plabel in group_dict:
print('processing lib %s' % plabel)
each = group_dict[plabel]
#also parse the files inside this function
#return the file name after parsing
paired, unpaired = separate_by_pair(plabel, each)
if paired == None:
continue
label = '%s_%s' % (plabel, ass_label)
#index_label = cmn.lastName(f_ass).replace('.fa', '')
index_label = f_ass.replace('.fa', '')
cmd = ''
cmd += '/home2/wli/local/bwa-0.7.12/bwa mem -t 32 -M %s %s %s > %s_paired.sam;\n' % (index_label, paired[0], paired[1], label)
kept_spdir_files = 'realigned_reads_step2.bam snp_step2.vcf$'.split()
for each in spdirs:
print(each)
wdir_label = cmn.lastName(each)
dwdir = '%s/%s' % (ddir, wdir_label)
if os.path.exists(dwdir):
print(
'the destination directory has already exists! please check manually to choose which one to keep:'
)
print('distination dir: %s' % dwdir)
print('current dir: %s' % each)
print('\n')
continue
cmn.mkdir(dwdir)
fbam = '%s/realigned_reads_step2.bam' % (each)
if os.path.exists(fbam):
cmd = 'cp %s/realigned_reads_step2.bam %s' % (each, dwdir)
else:
fbam = '%s/realigned_reads.bam' % each
if os.path.exists(fbam):
cmd = 'cp %s/realigned_reads.bam %s' % (each, dwdir)
else:
print('Error, can not find bam file!')
cmn.run(cmd)
#print cmd
fvcf = spdirs[each]
cmd = 'cp %s %s' % (fvcf, dwdir)
cmn.run(cmd)
defline = lines[0]
seq = ''.join(lines[1:])
adict[defline] = seq
return adict
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
#main
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
if __name__ == '__main__':
#fn = 'all_genomes_noGap.fa'
#fn = 'all_genomes_charGap.fa'
try:
fn = sys.argv[1]
except:
print('*.py all_genomes_charGap.fa ')
sys.exit()
adict = read_fa(fn)
fnlabel = cmn.lastName(fn).replace('.fa', '')
outdir = 'splitS_%s' % fnlabel
cmn.mkdir(outdir)
for i, key in enumerate(adict):
seq = adict[key]
fasta = '>%s\n%s\n' % (key, seq)
dn = '%s/%s_%s.fa' % (outdir, fnlabel, i)
cmn.write_file(fasta, dn)
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
#main
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
if __name__ == '__main__':
#options=parse_options()
try:
read, fn, direction = sys.argv[1:4]
except:
print("Usage: *.py", file=sys.stderr)
sys.exit()
fished_reads = []
cmn.mkdir('grep_out')
if True:
with open(fn) as fp:
for lineN, line in enumerate(fp):
if lineN % 4 != 1: #only take the sequence
continue
line = line.strip()
if direction == 'backward':
line = line[::-1]
#find match forward and + strand
i1 = line.find(read)
if i1 != -1:
fished_reads.append(line[i1:])
#in the reverse strand
import sys
python_lib = '/work/00412/mtang/sequencing/scripts'
if python_lib not in sys.path:
sys.path.append(python_lib)
import cmn
import os
fromDir = os.path.abspath(sys.argv[1])
toDir = os.path.abspath(sys.argv[2])
wdirs = cmn.cmd2lines('ls %s | grep ^sampleRun_' % fromDir)
#toKeep = ['*.txt', '*.report', 'barcode_count', '*_contig.fa', 'denovo_barcode.fa', 'bait0_denovo.br']
toKeep = [
'*.txt', '*.report', '*_contig.fa', 'denovo_barcode.fa', 'bait0_denovo.br'
]
for wdir in wdirs:
eachToDir = '%s/%s' % (toDir, wdir)
cmn.mkdir(eachToDir)
eachFromDir = '%s/%s' % (fromDir, wdir)
for fn in toKeep:
cmd = 'cp %s/%s %s' % (eachFromDir, fn, eachToDir)
print(cmd)
cmn.run(cmd)
pairDict = {}
for fn in fns:
key = '_'.join(cmn.lastName(fn).split('_')[:-1])
#if '250' in key or '500' in key:
# print 'skip short lib: %s' % fn
# cmn.run('ln -s %s' % fn)
# continue
try:
pairDict[key].append(fn)
except KeyError:
pairDict[key] = [fn]
cmn.mkdir('logs')
cmds = []
for key in pairDict:
each = pairDict[key]
if len(each) == 2:
each.sort()
cmd = '/project/biophysics/Nick_lab/wli/sequencing/scripts/re-pair-reads_wenlin %s %s %s >& logs/%s_run.log &' % (
each[0], each[1], key, key)
cmds.append(cmd)
else:
print('cannot find pair for %s' % str(each))
for iii in each:
cmn.run('ln -s %s' % iii)
cmds.append('wait')
import sys
python_lib = '/work/biophysics/mtang/SNP_calling/scripts'
if python_lib not in sys.path:
sys.path.append(python_lib)
import cmn
import os
jobs = [line.strip().split()[-1] for line in cmn.getid(sys.argv[1])]
fromDir = sys.argv[2].rstrip('/') #the dir ends with step3
cwd = os.getcwd()
cmn.mkdir('job_files')
cmn.mkdir('step3_gatk')
fromPdir = '/'.join(fromDir.split('/')[:-1])
cmn.run('ln -s %s/step2_bwa_mapping' % fromPdir)
fjobs = []
#1. copy the directory to current
for job in jobs:
wdir = job[4:-4]
current = '%s/%s' % (fromDir, wdir)
cmd = 'cp -r %s step3_gatk' % current
print('forking data for %s' % current)
cmn.run(cmd)
new = '%s/step3_gatk/%s' % (cwd, wdir)
user = cmn.cmd2info('echo $USER').strip()
user_label = user[0]
#check if all the files has contains
falist = cmn.file2lines(fn)
bad_falist = [
fa for fa in falist
if not cmn.filexist(fa) and '/archive/butterfly/' not in fa
]
if len(bad_falist) != 0:
print('Error!')
print('the following files are errorous:')
print('\n'.join(bad_falist))
sys.exit()
transferDir = 'archiveTransfer'
cmn.mkdir(transferDir)
alea_list = [fa for fa in falist if '/archive/butterfly' in fa]
biohpc_list = set(falist) - set(alea_list)
newlist = transfer_alea_files(alea_list)
newlist += list(biohpc_list)
dn = 'new.falist'
cmn.write_lines(newlist, dn)
#backup this newlist
cmn.mkdir('../falist_info')
dirlabel = os.getcwd().rstrip('/').split('/')[-1]
backFn = '../falist_info/%s.falist' % dirlabel
if __name__ == '__main__':
#options=parse_options()
try:
fns = [os.path.abspath(each) for each in sys.argv[3:]]
#KmerCut = int(sys.argv[1])
KmerSize = int(sys.argv[1])
Ncpu = int(sys.argv[2])
except:
print("Usage: *.py KmerCut KmerSize(19) Ncpu R1.fq R2.fq",
file=sys.stderr)
sys.exit()
outlabel = cmn.lastName(fns[0]).split('_')[0]
tmpDir = '%s_jf' % outlabel
cmn.mkdir(tmpDir)
#step1, run Jellyfish
print('running Jellyfish to get Kmer count...')
os.chdir(tmpDir)
cmd = 'jellyfish count -m %s -t %s -s 10000000000 -c 8 --timing=jf.err --canonical ' % (
KmerSize, Ncpu)
cmd += ' '.join(fns)
cmn.run(cmd)
cmd = 'jellyfish histo mer_counts.jf > %smer_histo.txt' % KmerSize
cmn.run(cmd)
cmd = 'jellyfish dump -c mer_counts.jf > %smer_counts' % KmerSize
cmn.run(cmd)
#step2, filter out reads with high Kmers
except:
print('usage: *.py fsam fass', file=sys.stderr)
sys.exit()
cmd = 'module add samtools; samtools faidx %s' % fass
cmn.run(cmd)
cmd = 'module add picard/1.117; java -jar $PICARD/CreateSequenceDictionary.jar R=%s O=%s.dict' % (
fass, fass[:-3])
cmn.run(cmd)
template = cmn.txt_read(
'/project/biophysics/Nick_lab/wli/sequencing/scripts/templates/template_gatk_bias_fromSam.job'
)
template = template.replace('[WL_ref]', fass)
template = template.replace('[INPUT.sam]', fsam)
sampleId = cmn.lastName(fsam).replace('highQ_', '').split('_')[0]
dnlabel = '%s_%s' % (cmn.lastName(fsam).replace(
'.sam', ''), cmn.lastName(fass).replace('.fa', ''))
cmn.mkdir(dnlabel)
os.chdir(dnlabel)
cwd = os.getcwd()
pre_cmds = 'cd %s\n' % cwd
template = template.replace('5642', sampleId)
template = template.replace('[WL_preprossing]', pre_cmds)
cmn.write_file(template, 'gatk%s.job' % sampleId)
#cmn.run('sbatch gatk%s.job' % sampleId)
isIndexed = True
print('###############################################')
if not isIndexed:
print('**********************************************')
print('\nimportant!!!')
print('please re-run this script after all references are indexed!\n')
print('**********************************************')
###############################
#all the steps below would put into the job files
template = cmn.txt_read(
'/work/biophysics/mtang/SNP_calling/scripts/templates/template_gatk_unbias4TACC.job'
)
cmn.mkdir('job_files')
fjobs = []
for sp in refdict:
#if sp.split('_')[0] not in subsetIDs:
# continue
snp_list = refdict[sp]
for samdir, ref in snp_list:
label = '%s_%s' % (sp, ref)
if label not in subsetJobs:
continue
print('processing %s' % label)
#a. make directory
olabel = '%s_%s' % (sp, ref)
wdir = '%s/%s' % (cwd, olabel)
wdir4TACC = '../%s' % olabel
cmn.run('cp %s/mapping_stat.info tmpStat/%s_mapping_stat.info' % (tmpdir, ID))
cmn.run('rm -r %s ' % tmpdir)
return genus
if __name__=='__main__':
#options=parse_options()
try:
#fn, f_table = sys.argv[1:3]
fn = sys.argv[1]
except:
print("Usage: *.py fqlist", file=sys.stderr)
sys.exit()
cmn.mkdir('tmpStat')
IDlist = set([])
fq_groups = {}
for line in cmn.file2lines(fn):
Id = cmn.lastName(line).split('_')[0]
Id = Id.replace('NVG-', '').replace('11-BOA-','').replace('LEP-', 'LEP')
IDlist.add(Id)
fq = os.path.abspath(line)
try:
fq_groups[Id].append(fq)
except KeyError:
fq_groups[Id] = [fq]
nameDict = get_names_4barcode()
fqlist = cmn.file2lines(fn)
groupDict = {}
for fq in fqlist:
ID = cmn.lastName(fq).split('_')[0]
try:
groupDict[ID].append(fq)
except KeyError:
groupDict[ID] = [fq]
for sample in groupDict:
fqlist = groupDict[sample]
#fqlist = cmn.cmd2lines('ls /project/biophysics/Nick_lab/wli/sequencing/Eudamine/BEAST_timing/tmp_link_fastq/%s*.fastq' % sample)
#fqlist = cmn.cmd2lines('ls /work/biophysics/wli/workspace/filtered_6313*q')
wdir = 'mitoD_%s' % sample
cmn.mkdir(wdir)
os.chdir(wdir)
cwd = os.getcwd()
info = template.replace('[cwd]', cwd)
info = info.replace('[fq_files]', ' '.join(fqlist))
info = info.replace('[sample]', sample)
#prepare quake infiles
fqlist_local = []
for fq in fqlist:
cmn.run('ln -s ' + fq)
fqlist_local.append(cmn.lastName(fq))
cmn.write_lines(fqlist_local, 'fqlist')
cmn.run('ln -s fqlist infiles')
#make fq2fa comand
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
#main
#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
if __name__ == '__main__':
#options=parse_options()
try:
fn = sys.argv[1]
except:
print("Usage: *.py", file=sys.stderr)
sys.exit()
adict = {}
with open(fn) as fp:
for line in fp:
if line[0] == '>':
label = line.strip()
else:
seq = line.strip()
adict[label] = '%s\n%s\n' % (label, seq)
times = 10
keys = list(adict.keys())
cmn.mkdir('shuffle_genome')
for each in range(times):
random.shuffle(keys)
new = [adict[key] for key in keys]
dn = 'shuffle_genome/%s_shuffle%s' % (cmn.lastName(fn), each)
cmn.write_file(''.join(new), dn)
try:
fn = sys.argv[1]
except:
print("Usage: *.py filelist", file=sys.stderr)
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')
])
cwd = os.getcwd()
#1. read in info
refs = set([])
rdict = {}
for line in cmn.file2lines(finfo):
sp, fastq, ref = line.strip().split()
try:
rdict[sp].append((fastq, ref))
except KeyError:
rdict[sp] = [(fastq, ref)]
refs.add(ref)
#2. prepare reference jobs
refdir = '/work/biophysics/mtang/SNP_calling/indexed_references'
cmn.mkdir(refdir)
os.chdir(refdir)
index_cmds = ['cd %s' % refdir]
for ref in refs:
if not os.path.exists(cmn.lastName(ref)):
#cmn.run('ln -s %s' % ref)
cmn.run('cp %s %s/' % (ref, refdir))
ref = cmn.lastName(ref)
reflabel = ref.replace('.fa', '')
checkFn = reflabel + '.pac'
if cmn.filexist(checkFn):
print('found finished ref for %s, skip it' % ref)
continue
cmd = '/home2/wli/local/bwa-0.7.12/bwa index %s -p %s &' % (ref,
reflabel)
index_cmds.append(cmd)
