def transrate(submitted, trinitydir, transrate_dir, transrate_out,
trinity_fasta, sample, trimdir, sra, mmetsp):
trim_1P = trimdir + sra + ".trim_1P.fq"
trim_2P = trimdir + sra + ".trim_2P.fq"
if os.path.isfile(trim_1P) and os.path.isfile(trim_2P):
transrate_command = """
transrate --assembly={} --threads=8 \
--left={}{}.trim_1P.fq \
--right={}{}.trim_2P.fq \
--output=/tmp/transrate_out.{}
cp /tmp/transrate_out.{}/assemblies.csv {}{}.assemblies.csv
rm -rf /tmp/transrate_out.{}
""".format(trinity_fasta, trimdir, sra, trimdir, sra, sample, sample,
transrate_dir, mmetsp, sample)
print(transrate_command)
commands = [transrate_command]
process_name = "transrate"
module_name_list = ""
filename = mmetsp
submitted.append(mmetsp)
clusterfunc_py3.qsub_file(transrate_dir, process_name,
module_name_list, filename, commands)
else:
print("trimfiles not present:", trim_1P, trim_2P)
return submitted
def get_sourmash_command(mmetsp):
sourmash_command="""
sourmash compute --dna --protein /mnt/home/ljcohen/mmetsp_assemblies_trinity2.2.0/{}.trinity_out_2.2.0.Trinity.fasta -k 21 --name-from-first
""".format(mmetsp)
commands = [sourmash_command]
process_name = "sourmash"
module_name_list = [""]
filename = mmetsp
clusterfunc_py3.qsub_file("/mnt/home/ljcohen/mmetsp_sourmash/",process_name, module_name_list, filename, commands)
def consolidate(mmetsp_dir,item):
combine_orphaned_string = combine_orphaned(mmetsp_dir,item)
rename_pe_string = rename_pe(mmetsp_dir,item)
split_reads_string = split_reads(mmetsp_dir,item)
combine_string = combine(mmetsp_dir,item)
consolidate_commands=[combine_orphaned_string,rename_pe_string,split_reads_string,combine_string]
process_name="consolidate"
module_name_list = ["GNU/4.8.3", "khmer/2.0"]
clusterfunc_py3.qsub_file(mmetsp_dir,process_name,module_name_list,item,consolidate_commands)
def run_move_files(trimdir, sra):
orphan_string = make_orphans(trimdir, sra)
mv_string1, mv_string2 = move_files(trimdir, sra)
commands = [orphan_string, mv_string1, mv_string2]
process_name = "move"
module_name_list = ""
filename = sra
clusterfunc_py3.qsub_file(trimdir, process_name, module_name_list,
filename, commands)
def run_trimmomatic_TruSeq(missing, trimmed, remaining, trimdir, file1, file2,
sra):
bash_filename = trimdir + sra + ".trim.TruSeq.sh"
clusterfunc_py3.check_dir(trimdir + "qsub_files/")
listoffile = os.listdir(trimdir + "qsub_files/")
trim_file = trimdir + "qsub_files/" "trim." + sra + ".log"
matching = [s for s in listoffile if "trim." + sra + ".log" in s]
matching_string = "TrimmomaticPE: Completed successfully"
if os.path.isfile(trim_file):
with open(trim_file) as f:
content = f.readlines()
if len(matching) != 0:
trim_complete = [m for m in content if matching_string in m]
if len(trim_complete) != 0:
print("Already trimmed:", matching)
trimmed.append(sra)
else:
missing.append(trimdir)
j = """
java -jar /mnt/home/ljcohen/bin/Trimmomatic-0.33/trimmomatic-0.33.jar PE \\
-baseout {}.trim.fq \\
{} {} \\
ILLUMINACLIP:/mnt/home/ljcohen/bin/Trimmomatic-0.33/adapters/combined.fa:2:40:15 \\
SLIDINGWINDOW:4:2 \\
LEADING:2 \\
TRAILING:2 \\
MINLEN:25 &> trim.{}.log
""".format(sra, file1, file2, sra)
orphan_string = make_orphans(trimdir, sra)
commands = [j, orphan_string]
process_name = "trim"
module_name_list = ""
filename = sra
clusterfunc_py3.qsub_file(trimdir, process_name, module_name_list,
filename, commands)
else:
remaining.append(trimdir)
j = """
java -jar /mnt/home/ljcohen/bin/Trimmomatic-0.33/trimmomatic-0.33.jar PE \\
-baseout {}.trim.fq \\
{} {} \\
ILLUMINACLIP:/mnt/home/ljcohen/bin/Trimmomatic-0.33/adapters/combined.fa:2:40:15 \\
SLIDINGWINDOW:4:2 \\
LEADING:2 \\
TRAILING:2 \\
MINLEN:25 &> trim.{}.log
""".format(sra, file1, file2, sra)
orphan_string = make_orphans(trimdir, sra)
commands = [j, orphan_string]
process_name = "trim"
module_name_list = ""
filename = sra
clusterfunc_py3.qsub_file(trimdir, process_name, module_name_list,
filename, commands)
return missing, trimmed, remaining
def run_filter_abund(diginormdir, sra):
keep_dir = diginormdir + "qsub_files/"
filter_string = """
filter-abund.py -V -Z 18 {}norm.C20k20.ct {}*.keep
""".format(diginormdir, keep_dir)
extract_paired_string = extract_paired(diginormdir)
commands = [filter_string, extract_paired_string]
process_name = "filtabund"
module_name_list = ["GNU/4.8.3", "khmer/2.0"]
filename = sra
clusterfunc_py3.qsub_file(diginormdir, process_name, module_name_list,
filename, commands)
def run_diginorm(diginormdir, interleavedir, trimdir, sra):
normalize_median_string = """
normalize-by-median.py -p -k 20 -C 20 -M 4e9 \\
--savegraph {}norm.C20k20.ct \\
-u {}orphans.fq.gz \\
{}*.fq
""".format(diginormdir, trimdir, interleavedir)
normalize_median_command = [normalize_median_string]
process_name = "diginorm"
module_name_list = ["GNU/4.8.3", "khmer/2.0"]
filename = sra
clusterfunc_py3.qsub_file(diginormdir, process_name, module_name_list,
filename, normalize_median_command)
def run_diginorm(mmetsp_dir, mmetsp):
normalize_median_string = """
normalize-by-median.py -p -k 20 -C 20 -M 4e9 \\
--savegraph {}norm.C20k20.ct \\
-u {}orphans.fq.gz \\
{}*.interleaved.fq
""".format(mmetsp_dir, mmetsp_dir, mmetsp_dir)
#s=subprocess.Popen("cat diginorm.sh",shell=True)
# s.wait()
normalize_median_command = [normalize_median_string]
process_name = "diginorm"
module_name_list = ["GNU/4.8.3", "khmer/2.0"]
filename = mmetsp
clusterfunc_py3.qsub_file(mmetsp_dir, process_name, module_name_list,
filename, normalize_median_command)
def transrate(transrate_dir, sample, trinity_fasta, mmetsp_assemblies_dir, filename):
transrate_command = """
transrate -o /tmp/{} \\
--assembly {} \\
--reference {} \\
--threads 8
cp /tmp/{}/assemblies.csv {}{}.assemblies.csv
rm -rf /tmp/{}*
""".format(sample, trinity_fasta, filename,sample,transrate_dir,sample,sample)
commands = [transrate_command]
process_name = "trans_ref"
module_name_list = ""
filename = sample
#print(transrate_command)
clusterfunc_py3.qsub_file(mmetsp_assemblies_dir,process_name,module_name_list,filename,commands)
def transrate(transrate_dir, sample, trinity_fasta, mmetsp_assemblies_dir, filename):
transrate_command = """
transrate -o /tmp/{}_forw \\
--assembly {} \\
--reference {} \\
--threads 8
cp /tmp/{}_forw/{}*/contigs.csv {}{}.contigs.csv
rm -rf /tmp/{}_forw*
""".format(sample, trinity_fasta, filename,sample,sample,transrate_dir,sample,sample)
commands = [transrate_command]
process_name = "trans_ref"
module_name_list = ""
filename = sample
#print(transrate_command)
clusterfunc_py3.qsub_file(mmetsp_assemblies_dir,process_name,module_name_list,filename,commands)
def interleave_reads(trimdir, sra, interleavedir):
interleavefile = interleavedir + sra + ".trimmed.interleaved.fq"
if os.path.isfile(interleavefile):
print("already interleaved")
else:
interleave_string = "interleave-reads.py " + trimdir + sra + \
".trim_1P.fq " + trimdir + sra + ".trim_2P.fq > " + interleavefile
print(interleave_string)
interleave_command = [interleave_string]
process_name = "interleave"
module_name_list = ["GNU/4.8.3", "khmer/2.0"]
filename = sra
clusterfunc_py3.qsub_file(interleavedir, process_name,
module_name_list, filename,
interleave_command)
def transrate_reverse(transrate_dir, sample, trinity_fasta, mmetsp_assemblies_dir, filename):
transrate_command = """
transrate -o /tmp/{}_rev \\
--assembly {} \\
--reference {} \\
--threads 8
cp /tmp/{}_rev/assemblies.csv {}{}.assemblies.csv
rm -rf /tmp/{}_rev*
""".format(sample, filename,trinity_fasta,sample,transrate_dir,sample,sample)
#print("This is the reverse transrate command:")
commands = [transrate_command]
process_name = "trans_ref_reverse"
module_name_list = ""
filename = sample
print(transrate_command)
clusterfunc_py3.qsub_file(mmetsp_assemblies_dir,process_name,module_name_list,filename,commands)
def run_trinity(trinitydir, left, right, mmetsp):
trinity_command = """
set -x
# stops execution if there is an error
set -e
if [ -f {}trinity_out_2.2.0.Trinity.fasta ]; then exit 0 ; fi
Trinity --left {} \\
--right {} --output /tmp/{}.trinity_out_2.2.0 --full_cleanup --seqType fq --max_memory 50G --CPU 16
cp /tmp/{}.trinity_out_2.2.0.Trinity.fasta /mnt/home/ljcohen/oysterriver_assemblies/
rm -rf /tmp/{}.trinity_out_2.2.0*
""".format(trinitydir, left, right, mmetsp, mmetsp, mmetsp)
commands = [trinity_command]
process_name = "trinity_2.2.0"
module_name_list = ["trinity/2.2.0"]
filename = mmetsp
clusterfunc_py3.qsub_file(trinitydir, process_name, module_name_list,
filename, commands)
def rename_files(trinitydir, diginormdir, diginormfile, SRA):
# takes diginormfile in,splits reads and put into newdir
rename_orphans = combine_orphans(diginormdir)
split_paired = "split-paired-reads.py -d " + diginormdir + " " + diginormfile
rename_string1 = "cat " + diginormdir + "*.1 > " + trinitydir + SRA + ".left.fq"
rename_string2 = "cat " + diginormdir + \
"*.2 > " + trinitydir + SRA + ".right.fq"
rename_string3 = "gunzip -c " + diginormdir + \
"orphans.keep.abundfilt.fq.gz >> " + trinitydir + SRA + ".left.fq"
commands = [
rename_orphans, split_paired, rename_string1, rename_string2,
rename_string3
]
process_name = "rename"
module_name_list = ["GNU/4.8.3", "khmer/2.0"]
filename = SRA
clusterfunc_py3.qsub_file(diginormdir, process_name, module_name_list,
filename, commands)
def fastqc_report(fastq_file_list, newdir, fastqcdir, filename):
# imports list of files in each directory
print(fastq_file_list)
print(fastqcdir + filename)
if glob.glob(fastqcdir + filename + "_*_fastqc.zip"):
print("fastqc already complete:", filename)
else:
# creates command to generate fastqc reports from all files in list
file_string = str(fastq_file_list)
# print fastq_file_list
file_string = " ".join(fastq_file_list)
# print file_string
fastqc_string = "fastqc -o " + fastqcdir + " " + file_string
print("fastqc reports being generated for: " + str(fastq_file_list))
fastqc_command = [fastqc_string]
process_name = "fastqc"
module_name_list = ""
filename = filename
clusterfunc_py3.qsub_file(fastqcdir, process_name,
module_name_list, filename, fastqc_command)
def run_busco(busco_dir,sample,basedir,filename):
#protists_ensembl
#eukaryota_odb9
busco_command = """
source ~/.bashrc
module load GNU/4.8.3
module unload python
module load parallel
source activate busco_v3
python /mnt/home/ljcohen/bin/busco/scripts/run_BUSCO.py \
-i {}{} \
-o {} -l /mnt/home/ljcohen/bin/busco/eukaryota_odb9 \
-m tran --cpu 8
""".format(basedir,filename,sample)
print(busco_command)
commands = [busco_command]
process_name = "busco_euk"
module_name_list = ""
filename = sample
clusterfunc_py3.qsub_file(busco_dir, process_name,module_name_list, filename, commands)
def run_streaming_diginorm(trimdir, SRA, diginormdir):
# from Jessica's streaming protocol:
diginormfile = diginormdir + SRA + ".stream.diginorm.sh"
# os.chdir(diginormdir)
stream_string = """#!/bin/bash
(interleave-reads.py {}{}.trim_1P.fq {}{}.trim_2P.fq && zcat {}orphans.fq.gz)| \\
(trim-low-abund.py -V -k 20 -Z 18 -C 2 - -o - -M 4e9 --diginorm --diginorm-coverage=20) | \\
(extract-paired-reads.py --gzip -p {}{}.paired.gz -s {}{}.single.gz) > /dev/null
""".format(trimdir, SRA, trimdir, SRA, trimdir, diginormdir, SRA, diginormdir, SRA)
print(stream_string)
# with open(diginormfile,"w") as diginorm_script:
# diginorm_script.write(stream_string)
#s=subprocess.Popen("sudo bash "+diginormfile,shell=True)
# s.wait()
# print "file written:",diginormfile
# os.chdir("/home/ubuntu/MMETSP/")
streaming_diginorm_command = [stream_string]
module_load_list = []
process_name = "diginorm_stream"
clusterfunc_py3.qsub_file(diginormdir, process_name,
module_load_list, SRA, streaming_diginorm_command)
def interleave_reads(mmetsp_dir, mmetsp):
interleave_string = """
cd {}
for filename in *.trim_1P.fq
do
base=$(basename $filename .fq)
echo $base
base2=${{base/_1P/_2P}}
echo $base2
output=${{base/_1P/}}.interleaved.fq
#echo $output
(interleave-reads.py ${{base}}.fq ${{base2}}.fq | gzip > $output)
done
""".format(mmetsp_dir)
print(interleave_string)
interleave_command = [interleave_string]
process_name = "interleave"
module_name_list = ["GNU/4.8.3", "khmer/2.0"]
filename = mmetsp
clusterfunc_py3.qsub_file(mmetsp_dir, process_name, module_name_list,
filename, interleave_command)
def quant_salmon(salmon_indexdir, salmondir, sra, mmetsp, newdir,
trinity_fasta):
file1 = newdir + "trim/" + sra + ".trim_1P.fq"
file2 = newdir + "trim/" + sra + ".trim_2P.fq"
if os.path.isfile(file1):
print("file exists:", file1)
else:
print("missing:", file1)
if os.path.isfile(file2):
print("file exists:", file2)
index, salmon_index_string = salmon_index(salmondir, salmon_indexdir, sra,
trinity_fasta)
salmon_string = "salmon quant -i " + index + " --libType IU -1 " + file1 + \
" -2 " + file2 + " -o " + salmondir + mmetsp + "_" + sra + ".quant --dumpEq --auxDir aux"
commands = [salmon_index_string, salmon_string]
print(salmon_index_string)
print(salmon_string)
process_name = "salmon"
module_name_list = ""
filename = sra
clusterfunc_py3.qsub_file(salmondir, process_name, module_name_list,
filename, commands)
def run_dammit(dammit_string,dammitdir,mmetsp):
dammit_command = [dammit_string]
process_name = "dammit"
module_name_list = []
filename = mmetsp
clusterfunc_py3.qsub_file(dammit_dir, process_name, module_name_list, filename, dammit_command)
def run_dammit(dammit_string,dammitdir,mmetsp):
dammit_command = [dammit_string]
process_name = "dammit"
module_name_list = []
filename = mmetsp
clusterfunc_py3.qsub_file(dammit_dir, process_name, module_name_list, filename, dammit_command)
import os
import os.path
from os.path import basename
import subprocess
from subprocess import Popen, PIPE
import glob
# custom Lisa module
import clusterfunc_py3
def fastqc_report(fastq_file_list, newdir, fastqcdir, filename):
print fastq_file_list
print fastqcdir + filename
file_string = str(fastq_file_list)
# print fastq_file_list
file_string = " ".join(fastq_file_list)
# print file_string
fastqc_string = "fastqc -o " + fastqcdir + " " + file_string
print "fastqc reports being generated for: " + str(fastq_file_list)
fastqc_command = [fastqc_string]
process_name = "fastqc"
module_name_list = ""
filename = filename
clusterfunc_py3.qsub_file(fastqcdir, process_name,
module_name_list, filename, fastqc_command)
with open("~/trimmed_files.txt") as
