def main():
parser = OptionParser("usage: %prog [options]")
parser.add_option("-d",
"--dir",
dest="dataset_dir",
help="dir of dataset files")
parser.add_option("-c",
"--c",
dest="context_dir",
help="dir of context alignent files")
(options, args) = parser.parse_args()
dataset_dir = options.dataset_dir
dataset_dir = check_dirname(dataset_dir)
context_dir = options.context_dir
context_dir = check_dirname(context_dir)
aln_files = glob.glob(dataset_dir + "/*/*best.fas")
for aln_file in aln_files:
print(aln_file)
basename_dataset_dir = aln_file.split(".phy")[0].split(
"_aln")[0].split(".aln")[0]
tree = glob.glob(basename_dataset_dir + "[_.A-z]*tree*")[0]
rooted_tree = glob.glob(basename_dataset_dir + ".r.tree")[0]
basename = aln_file.split(".phy")[0].split("_aln")[0].split(
".aln")[0].split(dataset_dir)[-1]
context_alns = glob.glob(context_dir + "/%s[_.A-z]*.aln" % basename)
for context_aln in context_alns:
context_basename = context_aln.split(".aln")[0]
ctl_gtr = context_basename + "_gtr.ctl"
ctl_unr = context_basename + "_unr.ctl"
output_gtr = context_basename + "_gtr.mlb"
output_unr = context_basename + "_unr.mlb"
write_ctl_file(ctl_gtr,
context_aln,
tree,
output_gtr,
7,
fix_alpha="1",
alpha="0")
write_ctl_file(ctl_unr,
context_aln,
rooted_tree,
output_unr,
8,
fix_alpha="1",
alpha="0")
def pipeline_runner(input_dir,
output_dir,
ref_file,
NGS_or_Cirseq,
TYPE_OF_INPUT_FILE=None,
start=None,
end=None,
gaps=None,
qscore=None,
blast=None,
rep=None,
t=None,
alias="pipeline"):
input_dir = check_dirname(input_dir)
output_dir = check_dirname(output_dir)
ref_file = check_filename(ref_file)
if NGS_or_Cirseq not in [1, 2]:
raise Exception("NGS_or_Cirseq has to be 1 or 2")
cmds = "python /sternadi/home/volume1/shared/SternLab/pipeline_runner.py -i %s -o %s -r %s -NGS_or_Cirseq %i" \
% (input_dir, output_dir, ref_file, NGS_or_Cirseq)
if TYPE_OF_INPUT_FILE != None:
cmds += " -t %s" % TYPE_OF_INPUT_FILE
if start != None:
cmds += " -s %i" % start
if end != None:
cmds += " -e %i" % end
if gaps != None:
cmds += " -g %s" % gaps
if qscore != None:
cmds += " -q %i" % qscore
if blast != None:
cmds += " -b %i" % blast
if rep != None:
cmds += " -rep %i" % int(rep)
if t != None:
cmds += " -t %s" % t
print(cmds)
cmdfile = pbs_jobs.get_cmdfile_dir("pipeline.txt", alias)
tnum = 1
gmem = 2
pbs_jobs.create_pbs_cmd(cmdfile=cmdfile,
alias=alias,
jnum=tnum,
gmem=gmem,
cmds=cmds,
load_python=True)
job_id = pbs_jobs.submit(cmdfile)
return job_id
def main():
parser = OptionParser("usage: %prog [options]")
parser.add_option("-d", "--dir", dest="dir", help="directory with fastml output files")
parser.add_option("-o", "--output", dest="output", help="output file perfix")
(options, args) = parser.parse_args()
dir = options.dir
dir = check_dirname(dir)
output = options.output
if output == None:
output = "fastml_anlysis.csv"
files = glob.glob(dir + "*prob.marginal.txt")
basenames = [f.split(".prob.marginal.txt")[0] for f in files]
df = pd.DataFrame(columns=["Basename", "Mutation", "Branch", "Context", "Mutation_type",
"Codon_position", "APOBEC_context_GA","APOBEC_context_CT"])
for basename in basenames:
print(basename)
prob_marginal = basename + ".prob.marginal.txt"
seq_marginal = basename + ".seq.marginal.txt"
tree_ancestor = basename + ".tree.ancestor.txt"
basename = basename.split("/")[-1]
positions_to_remove = get_position_to_remove(prob_marginal)
ancestor_info, seqs = get_sequence_and_ancestry_data(tree_ancestor, seq_marginal)
df = go_over_positions(ancestor_info, seqs, positions_to_remove, basename, df)
df.to_csv(dir + output, index=False)
def main():
parser = OptionParser("usage: %prog [options]")
parser.add_option("-d",
"--dirname",
dest="dirname",
help="dirname that contains fastml result files")
parser.add_option("-o", "--output", dest="output", help="output file")
(options, args) = parser.parse_args()
dirname = options.dirname
dirname = check_dirname(dirname)
output = options.output
if output == None:
output = dirname + "/fastml_analysis_output.csv"
output = check_filename(output, Truefile=False)
files = glob.glob(dirname + "/*/*.fasta")
files = []
if files == []:
files = glob.glob(dirname + "/*seq.joint.txt")
basenames = [f.split(".")[0] for f in files]
df = pd.DataFrame(columns=[
"family", "group", "mutation", "mutation_count_in_context",
"context_count_overall", "mutation_count_overall"
])
for basename in basenames:
df = run_on_basename(basename, df)
def main():
parser = OptionParser("usage: %prog [options]")
parser.add_option("-d", "--dir", dest="dir", help="dir input fasta files")
parser.add_option("-s",
"--subtypes",
dest="subtypes",
help="subtypes to keep, seperated by comma. example A,B")
(options, args) = parser.parse_args()
dir = options.dir
dir = check_dirname(dir)
subtypes = options.subtypes.split(",")
input_files = glob.glob(dir + "/*.fasta")
for file in input_files:
fasta = open(file, "r").read()
basename = file.split(".fasta")[0]
for subtype in subtypes:
pattern = re.compile(">%s[^>]*" % subtype)
results = pattern.findall(fasta)
print("%s: %s: %s" % (file, subtype, str(len(results))))
fasta_out = "".join(results)
output_file = basename + "_%s.aln" % subtype
output = open(output_file, "w")
output.write(fasta_out)
output.close()
print("splited HIV files to subtypes")
def tophat2_runner(output_dir, bowtie_reference, fastq, alias="tophat2"):
"""
tophat2 runner
:param output_dir: output directory
:param bowtie_reference: bowtie reference path
:param fastq: fastq path
:param alias: job name (tophat2)
:return: job id
"""
output_dir = check_dirname(output_dir, Truedir=False)
bowtie_reference = check_filename(bowtie_reference, Truefile=False)
fastq = check_filename(fastq)
cmdfile = pbs_jobs.get_cmdfile_dir("tophat2", alias)
tnum = 1
gmem = 2
cmds = "/sternadi/home/volume1/taliakustin/software/tophat-2.1.1.Linux_x86_64/tophat2"\
+ " -o %s %s %s" % (output_dir, bowtie_reference, fastq)
pbs_jobs.create_pbs_cmd(cmdfile=cmdfile,
alias=alias,
jnum=tnum,
gmem=gmem,
cmds=cmds,
load_python=False)
job_id = pbs_jobs.submit(cmdfile)
return job_id
def selecton_runner(codon_aln,
output_dir=None,
tree=None,
log=None,
rate=None,
output=None,
color=None,
out_tree=None,
query_seq=None,
model="M8",
alias="selecton",
use_query_seq=False):
codon_aln = check_filename(codon_aln)
if output_dir == None:
base = codon_aln.split(".")[0] + "_selecton"
else:
base = check_dirname(output_dir)
base = base + codon_aln.split("/")[-1].split(".")[0] + "_selecton"
log = set_filenames_for_pbs_runs(log, base, "log.txt")
rate = set_filenames_for_pbs_runs(rate, base, "kaks.txt")
output = set_filenames_for_pbs_runs(output, base, "output.txt")
color = set_filenames_for_pbs_runs(color, base, "color.txt")
out_tree = set_filenames_for_pbs_runs(out_tree, base, "output_tree.txt")
if query_seq == None:
query_seq = get_longest_sequence_name_in_fasta(codon_aln)
if model == "M8":
model = ""
elif model == "M8a":
model = "-w1 -Fw"
elif model == "M7":
model = "-p1 -Fp"
if tree != None:
tree = check_filename(tree)
if use_query_seq == False:
cmds = "selecton -i %s -u %s -l %s -r %s -o %s -c %s -t %s %s" \
% (codon_aln, tree, log, rate, output, color, out_tree, model)
else:
cmds = "selecton -i %s -u %s -l %s -r %s -o %s -c %s -t %s %s -q %s" \
% (codon_aln, tree, log, rate, output, color, out_tree, model, query_seq)
else:
if use_query_seq == False:
cmds = "selecton -i %s -l %s -r %s -o %s -c %s -t %s %s" \
% (codon_aln, log, rate, output, color, out_tree, model)
else:
cmds = "selecton -i %s -l %s -r %s -o %s -c %s -t %s %s -q %s" \
% (codon_aln, log, rate, output, color, out_tree, model, query_seq)
cmdfile = pbs_jobs.get_cmdfile_dir("selecton.txt", alias)
tnum = 1
gmem = 2
pbs_jobs.create_pbs_cmd(cmdfile=cmdfile,
alias=alias,
jnum=tnum,
gmem=gmem,
cmds=cmds)
job_id = pbs_jobs.submit(cmdfile)
return job_id
def main():
parser = OptionParser("usage: %prog [options]")
parser.add_option("-d", "--directory", dest="dir", help="input directory with kaks gaps files")
parser.add_option("-o", "--output", dest="output", help="output file name")
parser.add_option("-v", "--virus", dest="virus", help="virus - tells the script how to parse filenames. "
"options: influenza, tilv, influenza20, thogoto")
(options, args) = parser.parse_args()
dir = options.dir
output = options.output
virus = options.virus
dir = check_dirname(dir)
output = check_filename(output, Truefile=False)
files = glob.glob("%s/*kaks*gaps" % dir)
if len(files) == 0:
raise Exception("No files in %s" % dir)
if virus == "influenza": #add more virus name if you add anything
output_text = "POS\tAMINO\tKaKs\tconfidence_interval\tvirus\tprotein\n"
elif virus == "influenza20" or virus == "tilv" or virus == "thogoto":
output_text = "POS\tAMINO\tKaKs\tconfidence_interval\tvirus\tprotein\tsegment\n"
else:
output_text = "POS\tAMINO\tKaKs\tconfidence_interval\n"
for f in files:
print(f)
if virus == "influenza":
virus_name = "Influenza " + f.split("/")[-1].split("inf")[1].split("_")[0]
protein = f.split("/")[-1].split("_")[2]
segment = None
elif virus == "tilv":
virus_name = "TiLV"
protein = "Segment " + f.split("/")[-1].split("_")[0].split("seg")[-1]
segment = protein
elif virus == "influenza20":
virus_name = "Influenza " + f.split("/")[-1].split("Segment")[0].split("_")[1]
protein = f.split("/")[-1].split("Protein")[1].split("_")[1]
segment = "Segment " + f.split("Segment")[1].split("_")[1]
elif virus == "thogoto":
virus_name = "Thogoto"
protein = f.split("gene_")[1].split("_")[0]
segment = "Segment " + f.split("segment_")[1].split("_")[0]
#if adding more virus type this is what you have to do:
#elif virus == "XXXX":
#virus_name = XXX
#protein = XXX
else:
virus_name = None
protein = None
segment = None
output_text += kaks_file_to_txt_delimeted_results(f, virus_name, protein, segment)
output = open(output, "w")
output.write(output_text)
output.close()
def main():
parser = OptionParser("usage: %prog [options]")
parser.add_option("-d",
"--dir",
dest="dir",
help="dir of temp files of cirseq pipeline run")
parser.add_option("-o",
"--output",
dest="output",
help="output folder to save")
(options, args) = parser.parse_args()
in_dir = options.dir
out_dir = options.output
in_dir = check_dirname(in_dir)
out_dir = check_dirname(out_dir)
repeat_summmery = get_repeats_num(in_dir)
make_graph(repeat_summmery, out_dir)
def main():
parser = OptionParser("usage: %prog [options]")
parser.add_option("-d",
"--dir",
dest="freqs_dir",
help="dir with freqs file")
(options, args) = parser.parse_args()
freqs_dir = options.freqs_dir
freqs_dir = check_dirname(freqs_dir)
freqs_files = glob.glob(freqs_dir + "/*.freqs")
with_mutation_files = glob.glob(freqs_dir + "/*_with_mutations.csv")
if with_mutation_files == []:
print("Adding mutation to freqs files")
for freqs_file in freqs_files:
print(freqs_file)
output = freqs_file.split(".freqs")[0] + "_with_mutations.csv"
add_mutation_to_freq_file(output, freqs_file=freqs_file)
with_mutation_files.append(output)
segment_files = glob.glob(freqs_dir + "/Segment_[0-9].csv") + glob.glob(
freqs_dir + "/Segment_[0-9][0-9].csv")
if segment_files == []:
print("Merging segment from different passages")
for s in range(1, 11):
specific_segment_mutation_files = glob.glob(
freqs_dir + "/P*-S%s_with_mutations.csv" % s)
segment_file, segment_freqs = merge_freqs_files(
specific_segment_mutation_files,
freqs_dir + "/Segment_%i.csv" % s)
segment_files.append(segment_file)
filtered_files = glob.glob(freqs_dir + "/Segment_[0-9]_filtered.csv") + \
glob.glob(freqs_dir + "/Segment_[0-9][0-9]_filtered.csv")
print("Filtering positions from segment csvs")
for segment_file in segment_files:
output = segment_file.split(".csv")[0] + "_filtered.csv"
filtered_file, filtered_ferqs = filter_freqs_for_regression_analysis(
output, freqs_file=segment_file)
filtered_files.append(filtered_file)
merge_dfs(filtered_files,
freqs_dir + "/All_segments_filtered_for_regression.csv")
def main():
parser = OptionParser("usage: %prog [options]")
parser.add_option("-d",
"--dir",
dest="dataset_dir",
help="dir of dataset files")
parser.add_option("-o",
"--output",
dest="output_file",
help="output file name")
(options, args) = parser.parse_args()
dataset_dir = options.dataset_dir
dataset_dir = check_dirname(dataset_dir)
output_file = options.output_file
output_file = check_filename(output_file, Truefile=False)
aln_files = glob.glob(dataset_dir + "/*/*best.fas")
df = pd.DataFrame(columns=[
"filename", "1", "0.9", "0.8", "0.7", "0.6", "0.5", "0.4", "0.3", "0.2"
])
for aln_file in aln_files:
consensus, consensus_percentage = get_consensus_percentage(aln_file)
filename = aln_file.split(dataset_dir)[-1]
print(aln_file)
df = df.append(
{
"filename": filename,
"1": consensus_percentage[1],
"0.9": consensus_percentage[0.9],
"0.8": consensus_percentage[0.8],
"0.7": consensus_percentage[0.7],
"0.6": consensus_percentage[0.6],
"0.5": consensus_percentage[0.5],
"0.4": consensus_percentage[0.4],
"0.3": consensus_percentage[0.3],
"0.2": consensus_percentage[0.2]
},
ignore_index=True)
df.to_csv(output_file, index=False)
def fastml_runner(alignment,
tree,
outdir=None,
alias="fastml",
additional_params=None):
"""
run fastml from phylogenyCode on cluster
:param alignment: alignment file path
:param tree: tree file path
:param alias: job name (default: fastml)
:param outdir: output directory for results (default: None - saves in the alignment's dir)
:return: job id
"""
alignment = check_filename(alignment)
tree = check_filename(tree)
if outdir == None:
outdir = os.path.dirname(alignment)
else:
outdir = check_dirname(outdir)
basename = os.path.basename(alignment).split(".")[0].split("_aln")[0]
newick_tree = outdir + "/" + basename + ".tree.newick.txt"
ancestor_tree = outdir + "/" + basename + ".tree.ancestor.txt"
joint_seqs = outdir + "/" + basename + ".seq.joint.txt"
marginal_seqs = outdir + "/" + basename + ".seq.marginal.txt"
joint_prob = outdir + "/" + basename + ".prob.joint.txt"
marginal_prob = outdir + "/" + basename + ".prob.marginal.txt"
cmdfile = pbs_jobs.get_cmdfile_dir("fastml.txt", alias)
tnum = 1
gmem = 1
cmds = "/sternadi/home/volume1/shared/tools/phylogenyCode/programs/fastml/fastml -s %s -t %s -mn -x %s " \
"-y %s -j %s -k %s -d %s -e %s -qf" % (alignment, tree, newick_tree, ancestor_tree, joint_seqs,
marginal_seqs, joint_prob, marginal_prob)
if additional_params != None:
cmds += " %s" % additional_params
pbs_jobs.create_pbs_cmd(cmdfile=cmdfile, alias=alias, gmem=gmem, cmds=cmds)
job_id = pbs_jobs.submit(cmdfile)
return job_id
def save_all_rooted_trees(tree_file, output_dir):
"""
saves all possible rooted trees for a given tree
:param tree_file: input tree path
:param output_dir: output directory for trees
:return: rooted file dictionary
"""
# save all possible rooted tree of a given tree
tree_file = check_filename(tree_file)
output_dir = check_dirname(output_dir)
basename = path.basename(path.splitext(tree_file)[0])
treefile_out = output_dir + "/" + basename
tree = Phylo.read(tree_file, "newick")
clades = list(tree.find_clades())
out_files = []
for clade in clades:
if clade.name != None:
tree.root_with_outgroup(clade)
if tree.rooted == True:
outfile = treefile_out +"_%s.txt" % clade.name
Phylo.write(tree, outfile , "newick")
out_files.append(outfile)
out_files[clade.name]["rooted_file"] = outfile
return out_files
def mlbs_to_df(output, mlbs=[], dirname=None, baltimore=True):
"""
analyzes mlb file to dataframe - extracts lnL, base frequencies and substiution matrics
:param output: output csv file path
:param mlbs: list of mlb files
:param dirname: dirname that has mlb files
:return: output file path
"""
if mlbs == [] and dirname == None:
raise Exception(
"you need to provide mlb or dirname that contains mlbs")
if mlbs != [] and dirname != None:
raise Exception("you need to provide only one - mlb or dirname")
if dirname != None:
dirname = check_dirname(dirname)
mlbs = glob.glob(dirname + "/*.mlb")
if mlbs != []:
mlbs = [check_filename(m) for m in mlbs]
output = check_filename(output, Truefile=False)
df = pd.DataFrame(columns=[
"mlb_file_name", "basename", "family", "protein", "group", "model",
"lnL", "freq_T", "freq_C", "freq_A", "freq_G", "TC", "TA", "TG", "CT",
"CA", "CG", "AT", "AC", "AG", "GT", "GC", "GA"
])
lnL_1 = re.compile("lnL.*")
lnL_2 = re.compile("\-?\d*\.\d*")
base_1 = re.compile("Base frequencies.*")
base_2 = re.compile("0.\d+")
rate_1 = re.compile("Rate matrix Q.*\n.*\n.*\n.*\n.*", re.IGNORECASE)
rate_2 = re.compile("\d+.\d+")
for mlb_file_name in mlbs:
basename = mlb_file_name.split("/")[-1].split(".mlb")[0]
print(mlb_file_name)
family = mlb_file_name.split("/")[-1].split("_")[0]
protein = mlb_file_name.split("/")[-1].split(family +
"_")[1].split(".")[0]
filename = mlb_file_name.split("/")[-1].split(family +
"_")[-1].split(".mlb")[0]
#if "_gtr" in filename or "_unrest" in filename:
# filename = filename.split("_gtr")[0]
# filename = filename.split("_unrest")[0]
model = mlb_file_name.split(".mlb")[-1]
mlb = open(mlb_file_name, "r").read()
L = lnL_1.findall(mlb)
if len(L) != 1:
L = None
elif "nan" in L[0]:
L = None
else:
L = float(lnL_2.findall(L[0])[0])
B = base_1.findall(mlb)
if len(B) != 1:
freq_T = None
freq_C = None
freq_A = None
freq_G = None
elif "nan" in B[0]:
freq_T = None
freq_C = None
freq_A = None
freq_G = None
else:
B = base_2.findall(B[0])
freq_T = float(B[0])
freq_C = float(B[1])
freq_A = float(B[2])
freq_G = float(B[3])
R = rate_1.findall(mlb)
if len(R) != 1:
TC = None
TA = None
TG = None
CT = None
CA = None
CG = None
AT = None
AC = None
AG = None
GT = None
GC = None
GA = None
elif len(R) >= 1 and "nan" in R[0]:
TC = None
TA = None
TG = None
CT = None
CA = None
CG = None
AT = None
AC = None
AG = None
GT = None
GC = None
GA = None
else:
R = R[0].split("\n")
first = R[1]
first = rate_2.findall(first)
TC = first[1]
TA = first[2]
TG = first[3]
second = R[2]
second = rate_2.findall(second)
CT = second[0]
CA = second[2]
CG = second[3]
third = R[3]
third = rate_2.findall(third)
AT = third[0]
AC = third[1]
AG = third[3]
fourth = R[4]
fourth = rate_2.findall(fourth)
GT = fourth[0]
GC = fourth[1]
GA = fourth[2]
if baltimore == True:
balt = get_baltimore_classifiaction(family)
df = df.append(
{
"mlb_file_name": mlb_file_name,
"baltimore": balt,
"basename": basename,
"family": family,
"protein": protein,
"group": filename,
"model": model,
"lnL": L,
"freq_T": freq_T,
"freq_C": freq_C,
"freq_A": freq_A,
"freq_G": freq_G,
"TC": TC,
"TA": TA,
"TG": TG,
"CT": CT,
"CA": CA,
"CG": CG,
"AT": AT,
"AC": AC,
"AG": AG,
"GT": GT,
"GC": GC,
"GA": GA
},
ignore_index=True)
else:
df = df.append(
{
"mlb_file_name": mlb_file_name,
"basename": basename,
"family": family,
"protein": protein,
"group": filename,
"model": model,
"lnL": L,
"freq_T": freq_T,
"freq_C": freq_C,
"freq_A": freq_A,
"freq_G": freq_G,
"TC": TC,
"TA": TA,
"TG": TG,
"CT": CT,
"CA": CA,
"CG": CG,
"AT": AT,
"AC": AC,
"AG": AG,
"GT": GT,
"GC": GC,
"GA": GA
},
ignore_index=True)
df.to_csv(output)
return (output)
def main(args):
pipeline_path = "/sternadi/home/volume1/shared/SternLab/pipeline/runner.pl"
NGS_or_Cirseq = args.NGS_or_Cirseq
print("Pipeline to run: %s" % pipeline_path)
input_dir = args.input_dir
input_dir = check_dirname(input_dir)
output = args.output
output = check_dirname(output, Truedir=False)
reference = args.reference
reference = check_filename(reference)
start = args.start
end = args.end
if start not in [1, 2, 3]:
raise Exception("Not a valid start step - needs to be between 1:3")
if end not in [2, 3, 4]:
raise Exception("Not a valid end step - needs to be between 2:4")
type_of_input_file = args.type_of_input_file
gaps = args.gaps
if gaps not in ["Y", "N"]:
raise Exception("Not a valid gap - must be Y or N")
q_score = args.q_score
if q_score == None:
if NGS_or_Cirseq == 1:
q_score = 30
else:
q_score = 23
blast_id = args.blast_id
path_to_save_pipeline_summary = output + "/pipeline_summary.txt"
print(start, end, q_score, blast_id, NGS_or_Cirseq)
cmd = "perl {} {} {} {} {} {} {} {} {} {} {} {}".format(
pipeline_path, input_dir, output, reference, start, end,
type_of_input_file, gaps, NGS_or_Cirseq, q_score, blast_id)
print("running this pipeline command:")
print(cmd)
os.system(cmd)
# get additional statistics about this running
os.system("cd {}".format(os.path.join(input_dir, "tmp")))
# number of reads that were mapped only once
only_once_reads = subprocess.check_output(
"grep -P '^1\t' *stats -h | awk '{sum+=$2}END{print sum}'",
shell=True)
#number of reads that are "contributing to frequency counts”
freq_contr = subprocess.check_output(
"grep 'reads contributing to frequency counts' -h *stats | awk '{sum+=$1}END{print sum}'",
shell=True)
#number of bases called
num_based_called = subprocess.check_output(
"grep 'num bases called' *stats | awk -F = '{sum+=$2}END{print sum}'",
shell=True)
#number of reads that were mapped to reference
num_reads_mapped = subprocess.check_output(
"cat *blast | awk '{print $1}' | sort | uniq | wc -l", shell=True)
with open(path_to_save_pipeline_summary, "w") as o:
o.write("---- Pipeline running -----\n")
o.write("{}\n\n".format(datetime.datetime.now()))
o.write("Pipeline command used: {}\n\n".format(cmd))
o.write("Number of reads that were mapped only once: {}\n".format(
only_once_reads))
o.write(
"Number of reads that are contributing to frequency count: {}\n".
format(freq_contr))
o.write("Number of bases called: {}\n".format(num_based_called))
o.write("Number of reads mapped to reference: {}\n".format(
num_reads_mapped))
# create a simple coverage plot
freq_file_path = os.path.join(
input_dir, [f for f in os.listdir(input_dir) if f.endswith("freq")][0])
freq_file_path = check_filename(freq_file_path)
label = os.path.basename(freq_file_path).split('.')[0]
df = pd.read_csv(freq_file_path)
df = df.drop_duplicates("Pos")
plt.plot(df['Pos'].values,
df['Read_count'].values,
label=label,
color='darkorange')
plt.title("Coverage {}".format(label), fontsize=16)
plt.xlabel("Position in the genome (bp)")
plt.ylabel("Read count")
plt.savefig(os.path.join(input_dir, 'coverage.png'), format='png')
print("Ran pipeline")
def main(args):
pipeline_path = "/sternadi/home/volume1/shared/SternLab/pipeline/runner.pl"
NGS_or_Cirseq = args.NGS_or_Cirseq
print("Pipeline to run: %s" % pipeline_path)
input_dir = args.input_dir
input_dir = check_dirname(input_dir)
output = args.output
output = check_dirname(output, Truedir=False)
reference = args.ref
reference = check_filename(reference)
start = args.start
end = args.end
if start not in [1, 2, 3]:
raise Exception("Not a valid start step - needs to be between 1:3")
if end not in [2, 3, 4]:
raise Exception("Not a valid end step - needs to be between 2:4")
type_of_input_file = args.type_of_input_file
gaps = args.gaps
if gaps not in ["Y", "N"]:
raise Exception("Not a valid gap - must be Y or N")
q_score = args.q_score
if q_score == None:
if NGS_or_Cirseq == 1:
q_score = 30
else:
q_score = 23
blast_id = args.blast
evalue = args.evalue
repeats = args.repeats
if repeats <= 0:
raise Exception(
"Number of repeats sholud be a positive integer, entered a non-positive value"
)
if repeats > 1 and NGS_or_Cirseq == 1:
print("WARNING:: running NGS mapping with more then 1 repeat")
if repeats == 1 and NGS_or_Cirseq == 2:
print("WARNING:: running CirSeq mapping with 1 repeat")
#prefix = args.prefix
path_to_save_pipeline_summary = output + "/pipeline_summary.txt"
print(start, end, q_score, blast_id, NGS_or_Cirseq)
cmd = "perl {} {} {} {} {} {} {} {} {} {} {} {} {}".format(
pipeline_path, input_dir, output, reference, start, end,
type_of_input_file, gaps, NGS_or_Cirseq, q_score, blast_id, evalue,
repeats)
print("running this pipeline command:")
print(cmd)
os.system(cmd)
# get additional statistics about this running
os.chdir(os.path.join(output, "tmp"))
os.system("pwd")
# number of reads that were mapped only once
only_once_reads = subprocess.getoutput(
"grep -P '^1\t' *stats -h | awk '{sum+=$2}END{print sum}'")
# number of reads that were mapped exactly twice
twice_mapped_reads = subprocess.getoutput(
"grep -P '^2\t' *stats -h | awk '{sum+=$2}END{print sum}'")
#number of reads that are "contributing to frequency counts”
freq_contr = subprocess.getoutput(
"grep 'reads contributing to frequency counts' -h *stats | awk '{sum+=$1}END{print sum}'"
)
#number of bases called
num_based_called = subprocess.getoutput(
"grep 'num bases called' *stats | awk -F = '{sum+=$2}END{print sum}'")
#number of reads that were mapped to reference
num_reads_mapped = subprocess.getoutput(
"cat *blast | awk '{print $1}' | sort | uniq | wc -l")
#total number of reads
num_reads = subprocess.getoutput("cat *fasta | grep '^>' | wc -l")
with open(path_to_save_pipeline_summary, "w") as o:
o.write("---- Pipeline running -----\n")
o.write("{}\n\n".format(datetime.datetime.now()))
o.write("Pipeline command used:\n{}\n\n".format(cmd))
o.write("Blast parameters: %id for blast = {}, E value = {}\n".format(
blast_id, evalue))
o.write("Number of repeats used: {}\n".format(repeats))
o.write("Number of reads: {}\n".format(num_reads))
o.write("Number of reads mapped to reference: {}\n".format(
num_reads_mapped))
o.write("Number of reads that were mapped only once: {}\n".format(
only_once_reads))
o.write("Number of reads that were mapped exactly twice: {}\n".format(
twice_mapped_reads))
o.write(
"Number of reads that are contributing to frequency count: {}\n".
format(freq_contr))
o.write("Number of bases called: {}\n".format(num_based_called))
#get back to the freq file directory
os.chdir(output)
# create a simple coverage plot
freq_file_path = os.path.join(
output, [f for f in os.listdir(output) if ".freq" in f][0])
freq_file_path = check_filename(freq_file_path)
label = os.path.basename(freq_file_path).split('.')[0]
df = pd.read_csv(freq_file_path, sep='\t')
df = df[(df.Ref != '-') & (df.Ref == df.Base)].drop_duplicates("Pos")
plt.plot(df['Pos'].values,
df['Read_count'].values,
label=label,
color='darkorange')
plt.title("Coverage {}".format(label), fontsize=16)
plt.xlabel("Position in the genome (bp)")
plt.ylabel("Read count")
plt.savefig(os.path.join(output, 'coverage.png'), format='png')
print("Ran pipeline")
def r4s_runner(tree_file, seq_file, outfile, dirname, tree_outfile=None, unormelized_outfile=None, log_outfile=None, \
ref_seq = None, n_categories = 4, alias = "r4s"):
"""
run r4site on cluster
:param tree_file: input tree file path
:param seq_file: input sequence file path
:param outfile: outfile path
:param dirname: dirname for ouput files
:param tree_outfile: output tree file path (default: None)
:param unormelized_outfile: unormelized rated output file (default: None)
:param log_outfile: output log file (default: None)
:param alias: job name (default: r4s)
:return: job id
"""
tree_file = check_filename(tree_file)
seq_file = check_filename(seq_file)
dirname = check_dirname(dirname)
if tree_outfile != None:
tree_outfile = check_filename(tree_outfile, Truefile=False)
else:
tree_outfile = dirname + "/" + "out-tree"
if unormelized_outfile != None:
unormelized_outfile = check_filename(unormelized_outfile,
Truefile=False)
else:
unormelized_outfile = dirname + "/out-unormelized"
if log_outfile != None:
log_outfile = check_filename(log_outfile, Truefile=False)
else:
log_outfile = dirname + "/out-log"
cmdfile = pbs_jobs.get_cmdfile_dir("r4s_cmd.txt", alias)
tnum = 1
gmem = 2
ref_seq_parameter = " -a " + ref_seq if ref_seq is not None else ""
if tree_file != None:
cmds = "/sternadi/home/volume1/shared/tools/rate4site"\
+ " -t " + tree_file\
+ " -s " + seq_file\
+ " -o " + outfile\
+ ref_seq_parameter \
+ " -x " + tree_outfile\
+ " -y " + unormelized_outfile\
+ " -V 10"\
+ " -l " + log_outfile\
+ " -Mh -k " + n_categories
else:
cmds = "/sternadi/home/volume1/shared/tools/rate4site"\
+ " -s " + seq_file\
+ " -o " + outfile \
+ ref_seq_parameter\
+ " -x " + tree_outfile\
+ " -y " + unormelized_outfile\
+ " -V 10"\
+ " -l " + log_outfile\
+ " -Mh -k " + n_categories
pbs_jobs.create_pbs_cmd(cmdfile=cmdfile,
alias=alias,
jnum=tnum,
gmem=gmem,
cmds=cmds)
job_id = pbs_jobs.submit(cmdfile)
return job_id
