def main():
# check that everything has been installed correctly
root = os.path.dirname(os.path.abspath(__file__))
root += '/'
#Get the parameters
args, parser = get_params()
#set the required variables
debug = args.debug
# output dir
outDir = '{:s}/mmseqs2_src/'.format(os.path.realpath(
args.output_directory))
# Make some checks before extractic the package
# check that GCC is installed
gccVer, gccOk = check_gcc()
if not gccOk:
sys.stderr.write(
'\nERROR: no GCC compiler was found in your system.\n')
sys.stderr.write('Please, go to https://gcc.gnu.org\n')
sys.stderr.write(
'And follow the instructions to install the latest version of GCC in your system.\n'
)
sys.exit(-5)
# check that cmake is installed
cmake3Ver, cmake3Ok = check_cmake3()
cmakeVer, cmakeOk = check_cmake()
# if None of the versions is installed then exit with an error
if not (cmake3Ok or cmakeOk):
print(
'ERROR: you must install cmake version 3.10 or above before continuing'
)
sys.stderr.write('Please, go to https://cmake.org\n')
sys.stderr.write(
'And follow the instructions on how to install the latest version of cmake in your system.\n'
)
sys.exit(-5)
# path to the source package
tarPath = os.path.join(root, 'mmseqs2_src/mmseqs.tar.gz')
# skip the extration if the directory already exists
if os.path.isdir(outDir):
print('WARNING: the directory\n{:s}'.format(outDir))
print('already exists, if you want to extract the package,')
print('please remove the above-mentioned directory.')
print('\nEXIT: no file was extracted.')
sys.exit(-2)
# create the directory if it does not exist
systools.makedir(outDir)
#if debug:
# print('The source for MMseqs2 will be stored in\n{:s}'.format(outDir))
systools.untar(tarPath, outDir=outDir, debug=debug)
# create the build Directory
systools.makedir(os.path.join(outDir, 'build/'))
def mmseqs_createindex(dbPath, debug=False):
"""Create a index from a mmseq2 database file."""
if debug:
print('mmseqs_createindex :: START')
print('Input mmseqs2 db file:\t%s' % dbPath)
#check that the database file exist
if not os.path.isfile(dbPath):
sys.stderr.write(
'The file %s was not found, please provide the path to a mmseqs2 database file'
% dbPath)
sys.exit(-2)
#''' USE IN FUTURE VERSION OF CREATEINDEX
#print(dbPath)
tmpBname = os.path.basename(dbPath)
tmpDir = '{:s}/tmp_{:s}/'.format(
os.path.dirname(dbPath), os.path.basename(tmpBname.split('.', 1)[0]))
systools.makedir(tmpDir)
makeIdxCmd = '{:s} createindex {:s} {:s} --threads 2 -v 0'.format(
get_mmseqs_path(), dbPath, tmpDir)
#'''
# command to be executed
# EXAMPLE; mmseqs createindex in.mmseqs2_db
#makeIdxCmd = '{:s} createindex {:s} -v 0'.format(get_mmseqs_path(), dbPath)
if debug:
print('mmseqs2 createindex CMD:\t%s' % makeIdxCmd)
#execute the system call
process = subprocess.Popen(makeIdxCmd,
shell=True,
stdout=subprocess.PIPE,
stderr=subprocess.PIPE)
stdout_val, stderr_val = process.communicate() #get stdout and stderr
process.wait()
if debug:
print('STDOUT:\n%s\n' % stdout_val)
print('STDERR:\n%s\n' % stderr_val)
# make sure that the 3 idx files have been properly created
idx1 = '%s.sk6' % dbPath
if not os.path.isfile(idx1):
sys.stderr.write('The MMseqs2 index file %s could not be created.' %
idx1)
sys.exit(-2)
idx2 = '%s.sk6.index' % dbPath
if not os.path.isfile(idx2):
sys.stderr.write(
'\nWARNING: The MMseqs2 index file %s could not be created.' %
idx2)
#sys.exit(-2)
# remove the temporary directory
shutil.rmtree(path=tmpDir)
# return a output tuple
return (stdout_val, stderr_val, makeIdxCmd, idx1, idx2)
def mmseqs_createdb(inSeq, outDir=os.getcwd(), debug=False):
"""Create a database file for mmseqs2 from the input sequence file."""
if debug:
print('mmseqs_createdb :: START')
print('Input FASTA file:\t%s' % inSeq)
print('Outdir:\t%s' % outDir)
#check that the input file and the database exist
if not os.path.isfile(inSeq):
sys.stderr.write(
'The file %s was not found, please provide the path to a valid FASTA file'
% inSeq)
sys.exit(-2)
#check if the database exists
if outDir[-1] != '/':
outDir += '/'
# create dir if not already exists
systools.makedir(outDir)
# check the set db name
dbName = os.path.basename(inSeq)
dbName = dbName.split('.')[0] # take the left part of the file name
dbName = '%s.mmseqs2db' % dbName
dbPath = '%s%s' % (outDir, dbName)
# command to be executed
# EXAMPLE; mmseqs createdb in.fasta /outdir/mydb
makeDbCmd = '%s createdb %s %s -v 0' % (get_mmseqs_path(), inSeq, dbPath)
if debug:
print('mmseqs2 createdb CMD:\t%s' % makeDbCmd)
#execute the system call
process = subprocess.Popen(makeDbCmd,
shell=True,
stdout=subprocess.PIPE,
stderr=subprocess.PIPE)
stdout_val, stderr_val = process.communicate() #get stdout and stderr
process.wait()
if debug:
print('STDOUT:\n%s\n' % stdout_val)
print('STDERR:\n%s\n' % stderr_val)
#return a tuple with the results
return (stdout_val, stderr_val, makeDbCmd, dbPath)
def main():
# check that everything has been installed correctly
root = os.path.dirname(os.path.abspath(__file__))
root += '/'
#Get the parameters
args, parser = get_params()
#set the required variables
debug = args.debug
# output dir
outDir = '{:s}/sonicparanoid_test/'.format(
os.path.realpath(args.output_directory))
# path to the source package
testSrcDir = os.path.join(root, 'example/')
# skip the extration if the directory already exists
if os.path.isdir(outDir):
print('WARNING: the directory\n{:s}'.format(outDir))
print('already exists, if you want to extract the package,')
print('please remove the above-mentioned directory.')
print('\nEXIT: no file copied.')
sys.exit(-2)
# create the directory if it does not exist
systools.makedir(outDir)
# copy the test files
print(outDir)
copytree(testSrcDir, outDir, symlinks=False, ignore=None)
#copytree(testSrcDir, outDir)
if os.path.isdir(outDir):
print('INFO: all test files were succesfully copied to\n{:s}\n'.format(
outDir))
# suggest the command to run
print('Go inside the directory\n{:s}\nand type\n'.format(outDir))
print('sonicparanoid -i ./test_input -o ./test_output -m fast -t 4')
def main():
# check that everything has been installed correctly
root = os.path.dirname(os.path.abspath(__file__))
root += '/'
# get gcc version
##gccVer, gccOk = check_gcc()
# compile binaries for multi-species orthology if required
'''
check_quick_multiparanoid_installation(gccVer, gccOk)
check_quick_multiparanoid_installation(gccVer, gccOk)
'''
#### FORCE IT TO OK
check_quick_multiparanoid_installation(
'FORCED TO TRUE: Sytem specific GCC version', True)
####
# check MMseqs2 installation
# check_mmseqs_installation(root)
# start measuring the execution time
ex_start = time.perf_counter()
#Get the parameters
args, parser = get_params()
#start setting the needed variables
debug = args.debug
inDir = None
if args.input_directory is not None:
inDir = '%s/' % os.path.realpath(args.input_directory)
# output dir
outDir = '%s/' % os.path.realpath(args.output_directory)
# create input directory inside the output directory
tmpInDir = os.path.join(outDir, 'input/')
# if it already exists make sure all files in it are removed
if os.path.isdir(tmpInDir):
for el in os.listdir(tmpInDir):
os.remove(os.path.join(tmpInDir, el))
else:
systools.makedir(tmpInDir)
# move input files to the temporary input directory
inProtCnt = 0
for f in os.listdir(inDir):
if f.startswith('.'):
continue
tmpPath = os.path.join(inDir, f)
inProtCnt += 1
if os.path.isfile(tmpPath):
systools.copy(tmpPath, tmpInDir, debug=debug)
# INPUT CHECK
inDir = tmpInDir
# check integrity of input files
inputModList = check_input_files(inDir, debug=debug)
# rename the input files if where required
for tpl in inputModList:
newPath, newSymbol = tpl
print(newPath)
oldPath = newPath.replace('_no_blanks', '')
# remove the old file and rename the one with valid headers
if os.path.isfile(oldPath):
print(oldPath)
os.remove(oldPath)
systools.move(newPath, oldPath, debug=debug)
if debug:
print('Input files which FASTA header was modified:\t%d' %
len(inputModList))
# Optional directories setup
alignDir = None
if args.shared_directory is not None:
alignDir = '%s/' % os.path.realpath(args.shared_directory)
else:
alignDir = os.path.join(outDir, 'alignments/')
systools.makedir(alignDir)
dbDirectory = None
if args.mmseqs_dbs is not None:
dbDirectory = '%s/' % os.path.realpath(args.mmseqs_dbs)
else:
dbDirectory = '%smmseqs2_databases/' % outDir
cpus = args.threads
#coff = args.cutoff
coff = 40
owOrthoTbls = args.overwrite_tables
multiOnly = args.multi_species_only
skipMulti = args.skip_multi_species
runMode = args.mode
maxGenePerSp = args.max_gene_per_sp
# set the sensitivity value for MMseqs2
sensitivity = 4.0 # default
if runMode == 'sensitive':
sensitivity = 6.0
elif runMode == 'fast':
sensitivity = 2.5
elif runMode == 'most-sensitive':
sensitivity = 7.5
overwrite = args.overwrite
if overwrite:
owOrthoTbls = True
# set sensitivity using a user spcified value if needed
if args.sensitivity:
if 1. <= args.sensitivity <= 7.5:
sensitivity = round(args.sensitivity, 1)
print(
'WARNING: the run mode \'%s\' will be overwritten by the custom MMseqs sensitivity value of %s.\n'
% (runMode, str(args.sensitivity)))
else:
sys.stderr.write(
'\nERROR: the sensitivity parameter must have a value between 1.0 and 7.5\n'
)
# set the maximum length difference allowed if difference from default
if args.max_len_diff != 0.5:
if not (0. <= args.max_len_diff <= 1.0):
sys.stderr.write(
'\nERROR: the legth difference ratio must have a value between 0 and 1.\n'
)
# set the variable to control the creation of orthologous pairs
output_relations = args.output_pairs
if args.qfo_2011:
output_relations = True
updateId = None
if args.update is not None:
updateId = args.update
#check that mutually exclusive options are not selected
if multiOnly and skipMulti:
sys.stderr.write(
'\nERROR: you cannot select the options --skip-multi-species and --multi-species-only at the same time.\n'
)
sys.exit(-5)
# set the variable for MMseqs2 database indexing
idx_dbs = True
if args.no_indexing:
idx_dbs = False
# name for multispecies groups
multiSpeciesClstrNameAll = 'multispecies_clusters.tsv'
print('\nSonicParanoid will be executed with the following parameters:')
print('Input directory:\t{:s}'.format(inDir))
print('Input proteomes:\t{:d}'.format(inProtCnt))
print('Output directory:\t{:s}'.format(outDir))
print('Alignments directory:\t{:s}'.format(alignDir))
print('Create pre-filter indexes:\t{:s}'.format(str(idx_dbs)))
print('Complete overwrite:\t{:s}'.format(str(overwrite)))
print('Re-create ortholog tables:\t{:s}'.format(str(owOrthoTbls)))
print('CPUs:\t{:d}'.format(cpus))
print('Run mode:\t%s (MMseqs2 s=%s)' % (runMode, str(sensitivity)))
# check that the input directory has been provided
if (inDir is None):
sys.stderr.write('\nERROR: no input species.\n')
parser.print_help()
# Check if the run already exists
spFile = pairsFile = None
# SUGGEST THE USER TO USE THE UPDATE FEATURE
spFile = os.path.join(outDir, 'species.txt')
# check if it is an update or not
if os.path.isfile(spFile) and (not owOrthoTbls):
# fill a set with the new species names
newfSet = set()
flist = os.listdir(inDir)
for f in flist:
if f.startswith('.DS_'):
continue
newfSet.add(f)
# now create a set from old species list
oldfSet = set()
for ln in open(spFile):
oldfSet.add(ln.rstrip('\n'))
# make the union of the two sets
unionSet = oldfSet.union(newfSet)
# if the length is different than suggest the user to use
# the update or overwrite option
if len(unionSet) != oldfSet:
if updateId is None:
sys.stderr.write(
'\n\nThe file with species already exists, but the new species list is different from the existing one.'
)
sys.stderr.write(
'\nThis suggests that you have added, or removed species from the input directory.'
)
sys.stderr.write(
'\nPlease consider using the \'--update update_name\' option.'
)
sys.stderr.write(
'\nAlternatively you could completely overwrite a previous run using the \'--overwrite\' option.\n'
)
sys.exit(-6)
else:
spFile = None
# start the processing
update_run = False
if updateId is None:
if multiOnly: #skip everything and execute directly multi-species clustering
spFile = '%sspecies.txt' % outDir
pairsFile = '%sspecies_pairs.txt' % outDir
else:
spFile, pairsFile = orthodetect.run_sonicparanoid2_multiproc(
inDir,
outDir=outDir,
threads=cpus,
sharedDir=alignDir,
mmseqsDbDir=dbDirectory,
create_idx=idx_dbs,
sensitivity=sensitivity,
cutoff=coff,
confCutoff=0.05,
lenDiffThr=args.max_len_diff,
overwrite_all=overwrite,
overwrite_tbls=owOrthoTbls,
update_run=update_run,
keepAlign=args.keep_raw_alignments,
debug=debug)
#run multi-species clustering
if not skipMulti:
#copy sqltables
multiOutDir = os.path.join(outDir, 'multi_species/')
sqlPaths = orthodetect.fetch_sql_files(rootDir=outDir,
outDir=multiOutDir,
pairsFile=pairsFile,
coreOnly=False,
debug=debug)
print('Ortholog tables loaded for multi-species orthology:\t%d' %
len(sqlPaths))
sys.stdout.write('\nCreating ortholog groups...')
multisp_start = time.perf_counter()
quickparaRoot = orthodetect.get_quick_multiparanoid_src_dir()
#create the multi-species clusters
orthodetect.run_quickparanoid(sqlTblDir=multiOutDir,
outDir=multiOutDir,
srcDir=quickparaRoot,
outName=multiSpeciesClstrNameAll,
speciesFile=spFile,
maxGenePerSp=maxGenePerSp,
debug=debug)
sys.stdout.write(
'Ortholog groups creation elapsed time (seconds):\t{:s}\n'.
format(str(round(time.perf_counter() - multisp_start, 3))))
# output directory for stats
relDict = '%sortholog_relations/' % outDir
# calculate stats on the generated clusters
#orthodetect.calc_ortholog_group_stats(rootDir=outDir, outDir=relDict, outName=None, pairsFile=pairsFile, debug=debug)
# ALL
orthoRelName = 'ortholog_pairs.tsv'
if args.qfo_2011:
orthoRelName = 'ortholog_pairs_benchmark.tsv'
# generate the relations
if output_relations:
orthodetect.extract_ortholog_pairs(rootDir=outDir,
outDir=relDict,
outName=orthoRelName,
pairsFile=pairsFile,
coreOnly=False,
splitMode=args.qfo_2011,
debug=debug)
else: #Update the database
update_run = True
spFile, pairsFile = orthodetect.run_sonicparanoid2_multiproc(
inDir,
outDir=outDir,
threads=cpus,
sharedDir=alignDir,
mmseqsDbDir=dbDirectory,
create_idx=idx_dbs,
sensitivity=sensitivity,
cutoff=coff,
confCutoff=0.05,
lenDiffThr=args.max_len_diff,
overwrite_all=overwrite,
overwrite_tbls=owOrthoTbls,
update_run=update_run,
keepAlign=args.keep_raw_alignments,
debug=debug)
#run multi-species clustering
if not skipMulti:
#copy sqltables
multiOutDir = os.path.join(outDir, '{:s}/'.format(updateId))
sqlPaths = orthodetect.fetch_sql_files(rootDir=outDir,
outDir=multiOutDir,
pairsFile=pairsFile,
coreOnly=False,
debug=debug)
print('Ortholog tables loaded for multi-species orthology:\t%d' %
len(sqlPaths))
sys.stdout.write('\nCreating ortholog groups...')
multisp_start = time.perf_counter()
quickparaRoot = orthodetect.get_quick_multiparanoid_src_dir()
#create the multi-species clusters
orthodetect.run_quickparanoid(sqlTblDir=multiOutDir,
outDir=multiOutDir,
srcDir=quickparaRoot,
outName=multiSpeciesClstrNameAll,
speciesFile=spFile,
maxGenePerSp=maxGenePerSp,
debug=debug)
sys.stdout.write(
'Ortholog groups creation elapsed time (seconds):\t{:s}\n'.
format(str(round(time.perf_counter() - multisp_start, 3))))
# extract ortholog pairs
relDict = '%sortholog_relations/' % outDir
orthoRelName = '{:s}_relations.tsv'.format(updateId)
if args.qfo_2011:
orthoRelName = '{:s}_relations_benchmark.tsv'.format(updateId)
if output_relations:
orthodetect.extract_ortholog_pairs(rootDir=outDir,
outDir=relDict,
outName=orthoRelName,
pairsFile=pairsFile,
coreOnly=False,
splitMode=args.qfo_2011,
debug=debug)
ex_end = round(time.perf_counter() - ex_start, 3)
sys.stdout.write(
'\nTotal elapsed time (seconds):\t{:0.3f}\n'.format(ex_end))
# remove not required files
cleanup(rootDir=outDir, debug=debug)
def process_multisp_tbl(inTbl: str, outPath: str, debug: bool = False) -> None:
"""Check consistency of table with ortholog groups and extract main stats."""
if debug:
print('process_multisp_tbl :: START')
print('Input ortholog groups table:\t{:s}'.format(inTbl))
print('Output stats file:\t{:s}'.format(outPath))
#check that the input directory is valid
if not os.path.isfile(inTbl):
sys.stderr.write(
'\nERROR (file not found): you must provide a valid path to the text file containig the ortholog groups table generated using SonicParanoid.\n'
)
sys.exit(-2)
# create the directory that will contain the output file if required
systools.makedir(os.path.dirname(outPath))
# start processing the ortholog groups
fd = open(inTbl, 'r')
# extract the head and check rthe validity of the input file
hdr_columns: List[str] = fd.readline().rstrip('\n').split('\t')
# check the hdr
if not hdr_columns[0] == 'group_id':
sys.stderr.write('\nERROR: the header is not a valid.\n')
sys.exit(
'Make sure that the ortholog groups file was generated using SonicParanoid.'
)
spCntStr: str = str(len(hdr_columns[4:-1]) / 2)
spCntStr = spCntStr.strip()
# check that the number of species is valid, for example not column was removed from the file
# in thise case the diction must give a float with ending with '.0'
if not spCntStr.endswith('.0'):
sys.stderr.write(
'\nERROR : there is a problem with the number of species found in the table.\nMake sure you did not manually remove any column from the original output.\n'
)
sys.exit(-2)
# convert the string to int
spCnt: int = int(spCntStr.split('.', 1)[0])
# variables to store the counts
totCnt: int = 0
allSpCnt: int = 0
twoSpCnt: int = 0
mostSeedsId: str
maxSeedsCnt: int = 0
# start looping through the clusters
for clstr in fd:
flds: List[str] = clstr.rstrip('\n').split('\t')
totCnt += 1
clstrId: str = flds[0]
# check if it contains all species
if int(flds[2]) == spCnt:
allSpCnt += 1
elif int(flds[2]) == 2:
twoSpCnt += 1
# find the cluster with the high amount of orthologs with confidence 1.0
seedsCnt = int(flds[3])
if seedsCnt > maxSeedsCnt:
maxSeedsCnt = seedsCnt
mostSeedsId = clstrId
fd.close()
# variables with allSp pct
allSpPct: float = round(float(allSpCnt / totCnt) * 100., 2)
twoSpPct: float = round(float(twoSpCnt / totCnt) * 100., 2)
# open the output file
ofd = open(outPath, 'w')
ofd.write('Stats for the ortholog groups file:\n{:s}\n'.format(inTbl))
ofd.write('\nClusters:\t{:d}'.format(totCnt))
ofd.write('\nSpecies:\t{:d}'.format(spCnt))
ofd.write('\nClusters with all species:\t{:d}'.format(allSpCnt))
ofd.write('\nPercentage of clusters with all species:\t{:10.2f}'.format(
allSpPct))
ofd.write('\nClusters with two species:\t{:d}'.format(twoSpCnt))
ofd.write('\nPercentage of clusters with two species:\t{:10.2f}'.format(
twoSpPct))
ofd.write('\nCluster with highest number of main orthologs:\t{:s}'.format(
mostSeedsId))
ofd.close()
def extract_fasta(clstrDict: Dict[str, Dict[str, List[str]]],
fastaDir: str,
outDir: str,
multiFasta: bool = False,
annotationDict: Dict[str, List[List[str]]] = {},
debug: bool = False) -> None:
"""Extract FASTA sequences for echa cluster."""
if debug:
print('\nextract_fasta :: START')
print('Cluster for which sequences will be extracted:\t{:d}'.format(
len(clstrDict)))
print('Directory with the species files: {:s}'.format(fastaDir))
print('Output directory: {:s}'.format(outDir))
print('Output multiple FASTA files: {:s}'.format(str(multiFasta)))
print('Length of annotation dictionary: {:d}'.format(
len(annotationDict)))
annotate: bool = False
if len(annotationDict) > 0:
annotate = True
# check the directory with the fasta files exist
if not os.path.isdir(fastaDir):
sys.stderr.write(
'\nERROR (file not found): you must provide a valid path to the directory containig the species files.\n'
)
sys.exit(-2)
else: # make sure it is not empty
tmpList: List[str] = os.listdir(fastaDir)
if len(tmpList) < 2:
sys.stderr.write(
'\nERROR: the directory containig the species files must contain at least two FASTA files.\n'
)
sys.exit(-5)
# will contain the species names that are actually required
requSpDict: Dict[str, str] = {}
# create the list with required species files
for clstr, sp2geneDict in clstrDict.items():
for sp, orthoList in sp2geneDict.items():
# only process if required
if sp in requSpDict:
continue
else:
# make sure there is at least one ortholog for the current species
if len(orthoList) == 1: # it could be empty
if orthoList[0][0] == '*': # then it is empty
continue
# add the specis to the dictionary
tmpPath: str = os.path.join(fastaDir, sp)
requSpDict[sp] = tmpPath
if not os.path.isfile(tmpPath):
sys.stderr.write(
'\nERROR (file not found): the species file for {:s} was not found at\n{:s}\nplease provide a valid path.\n'
.format(sp, tmpPath))
sys.exit(-2)
# load all the sequences in a dictionary
# example, tvaginalis -> geneXAB -> ATGTAGGTA
seqsDict: Dict[str, Dict[str, str]] = {}
for spFile, fastaPath in requSpDict.items():
spName: str = os.path.basename(spFile)
seqsDict[spName] = load_seqs_in_dict(fastaPath=fastaPath, debug=debug)
# queue to contain the paths of each single
tmpDq: Deque[str]
# now generate the output files
# separated in directories separated by cluster id
# and each file named clustersId-species_name
for clstr, sp2geneDict in clstrDict.items():
# create the output directory
tmpClstrDir: str = os.path.join(outDir, 'clstr{:s}/'.format(clstr))
systools.makedir(tmpClstrDir)
# now for each species extract the sequences
if multiFasta: #write one fasta file for each species
for sp, orthoList in sp2geneDict.items():
# skip the creation of files if the cluster is empty
if len(orthoList) == 1:
if orthoList[0][0] == '*':
continue
tmpFastaName = 'clstr{:s}-{:s}.fasta'.format(clstr, sp)
tmpOutPath = os.path.join(tmpClstrDir, tmpFastaName)
ofd = open(tmpOutPath, 'w')
# write the sequences
for ortho in orthoList:
if annotate:
# create the header by merging the annotations
newHdr: str
if ortho in annotationDict: # sometimes no annotation is found!
annotLists = annotationDict[ortho]
newHdr = '|'.join(
[';'.join(l) for l in annotLists])
ofd.write('>{:s}\n'.format(newHdr))
else:
ofd.write('>{:s}\n'.format(ortho))
else:
ofd.write('>{:s}\n'.format(ortho))
# write the sequence
ofd.write('{:s}\n'.format(str(seqsDict[sp][ortho])))
ofd.close()
else: #write a single FASTA file
tmpFastaName = 'clstr{:s}.fasta'.format(clstr)
tmpOutPath = os.path.join(tmpClstrDir, tmpFastaName)
ofd = open(tmpOutPath, 'w')
for sp, orthoList in sp2geneDict.items():
# skip the creation of files if the cluster is empty
if len(orthoList) == 1:
if orthoList[0][0] == '*':
continue
# write the sequences
for ortho in orthoList:
if annotate:
# create the header by merging the annotations
newHdr: str
if ortho in annotationDict: # sometimes no annotation is found!
annotLists = annotationDict[ortho]
newHdr = '|'.join(
[';'.join(l) for l in annotLists])
ofd.write('>{:s}\n'.format(newHdr))
else:
ofd.write('>{:s}\n'.format(ortho))
else:
ofd.write('>{:s}\n'.format(ortho))
# write the sequence
ofd.write('{:s}\n'.format(str(seqsDict[sp][ortho])))
ofd.close()
def extract_by_sp_cnt(inTbl: str,
min: int = 2,
max: int = 2,
outDir: str = os.getcwd(),
minConf: float = 0.1,
debug: bool = False) -> Dict[str, Dict[str, List[str]]]:
"""Extract clusters based on on the number of species of which they are composed."""
if debug:
print('\nextract_by_sp_cnt :: START')
print('Input groups table:\t{:s}'.format(inTbl))
print('Minimum number of species in cluster:\t{:d}'.format(min))
print('Maximum number of species in cluster:\t{:d}'.format(max))
print('Output directory: {:s}'.format(outDir))
print('Minimum confidence for orthologs:\t{:.2f}'.format(minConf))
#check that the input directory is valid
if not os.path.isfile(inTbl):
sys.stderr.write(
'\nERROR (file not found): you must provide a valid path to the text file containig the ortholog groups table generated using SonicParanoid.\n'
)
sys.exit(-2)
# check the minimum confidence value
if not (0.05 <= minConf <= 1.):
sys.stderr.write(
'\nWARNING: the ortholog confidence threshold must be set to a value between 0.05 and 1.0.\n'
)
sys.stderr.write('It will now be set to 0.1.\n')
min = max
# start processing the ortholog groups
fd = open(inTbl, 'r')
# extract the head and check rthe validity of the input file
hdr_columns: List[str] = fd.readline().rstrip('\n').split('\t')
# check the hdr
if not hdr_columns[0] == 'group_id':
sys.stderr.write('\nERROR: {:s}\nis not a valid header.\n')
sys.exit(
'Make sure that the ortholog groups file was generated using SonicParanoid.'
)
spCntStr: str = str(len(hdr_columns[4:-1]) / 2)
spCntStr = spCntStr.strip()
# check that the number of species is valid, for example not column was removed from the file
# in thise case the diction must give a float with ending with '.0'
if not spCntStr.endswith('.0'):
sys.stderr.write(
'\nERROR : there is a problem with the number of species found in the table.\nMake sure you did not manually remove any column from the original output.\n'
)
sys.exit(-2)
# convert the string to int
spCnt: int = int(spCntStr.split('.', 1)[0])
# More species requested than those avaliable in the input clusters
if min > spCnt:
sys.stderr.write(
'\nWARNING: {:d} species were found in the input table header, hence clusters with {:d} species cannot exist!.\n'
.format(spCnt, max))
sys.stderr.write(
'Both minimum and maximum will be set to ({:d}).\n'.format(spCnt))
min = spCnt
max = spCnt
# min should lower than max!
if min > max:
sys.stderr.write(
'\nWARNING: the minimum number of species ({:d}) is higher than the maximum number of species ({:d}).\n'
.format(min, max))
sys.stderr.write(
'Max will be set to the maximum number of species in the table ({:d}).\n'
.format(spCnt))
max = spCnt
# extract the species list
spList: List[str] = [] # will contain the species names
for i, el in enumerate(hdr_columns[4:-1]):
if i % 2 == 0:
spList.append(el)
# prepare the output file
if outDir[0] != '/':
outDir += '/'
outPath: str = os.path.join(
outDir,
'filtered_min{:d}_max{:d}_{:s}'.format(min, max,
os.path.basename(inTbl)))
# create the output directory if required
systools.makedir(outDir)
ofd = open(outPath, 'w')
# write the header
ofd.write('{:s}\n'.format('\t'.join(hdr_columns)))
# output dictionary
# example: clst105 -> tvaginalis -> [g1, g4, g5]
outDict: Dict[str, Dict[str, List[str]]] = {}
extractedClstrCnt: int = 0
extractedGenesCnt: int = 0
totCnt: int = 0
tmpSp: str = ''
# start looping through the clusters
for clstr in fd:
flds: List[str] = clstr.rstrip('\n').split('\t')
totCnt += 1
clstrId: str = flds[0]
spSize: int = int(flds[2])
# check if it contains all species
if min <= spSize <= max:
# write the filtered output file
ofd.write(clstr)
# keep only the usable fields
flds = flds[4:-1]
# add the id to output dictionary
outDict[clstrId] = {}
for i, el in enumerate(flds):
# extract the cluster
if i % 2 == 0:
# example of cluster
# 2336_Q9X2I8,2336_Q9X172:0.159
# create the list for the species
tmpSp = spList[int(i / 2)]
outDict[clstrId][tmpSp] = []
for ortho in el.split(','):
tmpFlds: List[str] = ortho.split(':')
tmpConf: float
# case in which multuple columns are the in the gen name
if len(tmpFlds) > 3:
if ortho[-1] == ':':
# for example, x1ab:
# it is an ortholog for sure
outDict[clstrId][tmpSp].append(ortho)
extractedGenesCnt += 1
continue
else: # the final field is the confidence
if float(tmpFlds[-1]) >= minConf:
# extract and append the gene name
outDict[clstrId][tmpSp].append(':'.join(
tmpFlds[:-1]))
extractedGenesCnt += 1
continue
else: # simpler case
if len(tmpFlds) == 2:
if float(tmpFlds[-1]) >= minConf:
outDict[clstrId][tmpSp].append(tmpFlds[0])
extractedGenesCnt += 1
else: # then the confidence must be 1.0
outDict[clstrId][tmpSp].append(tmpFlds[0])
if tmpFlds[0][0] != '*':
extractedGenesCnt += 1
# increase the count of extracted clusters
extractedClstrCnt += 1
fd.close()
# close output file
ofd.close()
# print some debug line
if debug:
print('Extracted clusters:\t{:d}'.format(len(outDict)))
print('Extracted genes:\t{:d}'.format(extractedGenesCnt))
print('Percentage of extracted clusters:\t{:.2f}'.format(
round(float(extractedClstrCnt / totCnt) * 100., 2)))
# return the main dictionary
return outDict
def extract_by_id(inTbl: str,
idList: List[str] = [],
outDir: str = os.getcwd(),
minConf: float = 0.1,
debug: bool = False) -> Dict[str, Dict[str, List[str]]]:
"""Extract clusters based on on the number of species of which they are composed."""
if debug:
print('\nextract_by_id :: START')
print('Input groups table:\t{:s}'.format(inTbl))
print('Number of clusters to be extracted:\t{:d}'.format(len(idList)))
print('IDs to be extracted:\t{:s}'.format(str(idList)))
print('Output directory: {:s}'.format(outDir))
print('Minimum confidence for orthologs:\t{:.2f}'.format(minConf))
#check that the input directory is valid
if not os.path.isfile(inTbl):
sys.stderr.write(
'\nERROR (file not found): you must provide a valid path to the text file containig the ortholog groups table generated using SonicParanoid.\n'
)
sys.exit(-2)
# Check that ar least one id is in the list
if len(idList) == 0:
sys.stderr.write(
'\nERROR: you must provide at one cluster ID to be extracted, while you have provided none.\n'
)
sys.exit(-5)
# check that there are no repeated IDs in the ID list
tmpDict: Dict[str, None] = {}
tmpList: List[str] = []
for el in idList:
if not el in tmpDict:
tmpDict[el] = None
else:
tmpList.append(el)
# remove the repeated IDs if required
if len(tmpList) > 0:
for el in tmpList:
idList.remove(el)
sys.stderr.write(
'\nWARNING: the following cluster IDs were repeated in the input ID list and were removed.'
)
sys.stderr.write('\n{:s}'.format(str(tmpList)))
sys.stderr.write(
'\nThe ID list now contains {:d} cluster IDs.\n\n'.format(
len(idList)))
# remove the tmp structure
del tmpDict
tmpList.clear()
# start processing the ortholog groups
fd = open(inTbl, 'r')
# extract the header and check the validity of the input file
hdr_columns: List[str] = fd.readline().rstrip('\n').split('\t')
# check the hdr
if not hdr_columns[0] == 'group_id':
sys.stderr.write('\nERROR: {:s}\nis not a valid header.\n')
sys.exit(
'Make sure that the ortholog groups file was generated using SonicParanoid.'
)
# extract the species count
spCntStr: str = str(len(hdr_columns[4:-1]) / 2)
spCntStr = spCntStr.strip()
# check that the number of species is valid, for example not column was removed from the file
# in thise case the dictionary must give a float with ending with '.0'
if not spCntStr.endswith('.0'):
sys.stderr.write(
'\nERROR : there is a problem with the number of species found in the table.\nMake sure you did not manually remove any column from the original output.\n'
)
sys.exit(-2)
# convert the string to int
spCnt: int = int(spCntStr.split('.', 1)[0])
# extract the species list
spList: List[str] = [] # will contain the species names
for i, el in enumerate(hdr_columns[4:-1]):
if i % 2 == 0:
spList.append(el)
# prepare the output file
outPath: str = os.path.join(
outDir, 'filtered_{:s}'.format(os.path.basename(inTbl)))
# create the output directory if required
systools.makedir(outDir)
ofd = open(outPath, 'w')
# write the header
ofd.write('{:s}\n'.format('\t'.join(hdr_columns)))
# output dictionary and other variables
# example: clst105 -> tvaginalis -> [g1, g4, g5]
outDict: Dict[str, Dict[str, List[str]]] = {}
extractedClstrCnt: int = 0
extractedGenesCnt: int = 0
totCnt: int = 0
tmpSp: str = ''
# start looping through the clusters
for clstr in fd:
flds: List[str] = clstr.rstrip('\n').split('\t')
totCnt += 1
clstrId: str = flds[0]
# extract the information from the cluster
if clstrId in idList:
# write the filtered output file
ofd.write(clstr)
# keep only the usable fields
flds = flds[4:-1]
# add the id to output dictionary
outDict[clstrId] = {}
for i, el in enumerate(flds):
# extract the cluster
if i % 2 == 0:
# example of cluster
# 2336_Q9X2I8,2336_Q9X172:0.159
# create the list for the species
tmpSp = spList[int(i / 2)]
outDict[clstrId][tmpSp] = []
for ortho in el.split(','):
tmpFlds: List[str] = ortho.split(':')
tmpConf: float
# case in which multuple columns are the in the gen name
if len(tmpFlds) > 3:
if ortho[-1] == ':':
# for example, x1ab:
# it is an ortholog for sure
outDict[clstrId][tmpSp].append(ortho)
if outDict[clstrId][tmpSp][-1][0] != '*':
extractedGenesCnt += 1
continue
else: # the final field is the confidence
if float(tmpFlds[-1]) >= minConf:
# extract and append the gene name
outDict[clstrId][tmpSp].append(':'.join(
tmpFlds[:-1]))
if outDict[clstrId][tmpSp][-1][0] != '*':
extractedGenesCnt += 1
continue
else: # simpler case
if len(tmpFlds) == 2:
if float(tmpFlds[-1]) >= minConf:
outDict[clstrId][tmpSp].append(tmpFlds[0])
extractedGenesCnt += 1
else: # then the confidence must be 1.0
outDict[clstrId][tmpSp].append(tmpFlds[0])
if tmpFlds[0][0] != '*':
extractedGenesCnt += 1
# remove the ID from the list
idList.remove(clstrId)
# increase the count of extracted clusters
extractedClstrCnt += 1
fd.close()
# close output file
ofd.close()
# print some debug line
if debug:
print('Extracted clusters:\t{:d}'.format(len(outDict)))
if len(idList) > 0:
print(
'(WARNING) The following clusters were not found: {:s}'.format(
str(idList)))
print('Extracted genes:\t{:d}'.format(extractedGenesCnt))
print('Percentage of extracted clusters:\t{:.2f}'.format(
round(float(extractedClstrCnt / totCnt) * 100., 2)))
# return the main dictionary
return outDict
def perform_parallel_orthology_inference(requiredPairsDict,
inDir,
outDir=os.getcwd(),
sharedDir=None,
cutoff=40,
confCutoff=0.05,
lenDiffThr=0.5,
threads=8,
debug=False):
"""Execute orthology inference for the required pairs."""
if debug:
print('\nperform_parallel_orthology_inference :: START')
print('Proteome pairs to be processed:\t{:d}'.format(
len(requiredPairsDict)))
print('Input directory:{:s}'.format(inDir))
print('Outdir:{:s}'.format(outDir))
print('Alignment directory:{:s}'.format(sharedDir))
print('Cutoff:\t{:d}'.format(cutoff))
print('Confidence cutoff for paralogs:\t{:s}'.format(str(confCutoff)))
print('Length difference filtering threshold:\t{:s}'.format(
str(lenDiffThr)))
print('CPUs (for mmseqs):\t{:d}'.format(threads))
# make sure that the directory with alignments exists
if not os.path.isdir(sharedDir):
sys.stderr.write(
'ERROR: The directory with the alignment files\n%s\nwas not found, please provide a valid path\n'
.format(sharedDir))
if not os.path.isdir(sharedDir):
sys.stderr.write(
'ERROR: The directory with the input files\n{:s}\nwas not found, please provide a valid path\n'
.format(inDir))
#create the output directory if does not exist yet
if outDir != os.getcwd():
if not os.path.isdir(outDir):
systools.makedir(outDir)
if outDir[-1] != '/':
outDir += '/'
# check if the output directory differs from the input one
if os.path.dirname(inDir) == os.path.dirname(outDir):
sys.stderr.write(
'\nERROR: the output directory {:s}\nmust be different from the one in which the input files are stored.\n'
.format(outDir))
sys.exit(-2)
# check cutoff
if cutoff < 30:
cutoff = 40
# create the queue and start adding the jobs
jobs_queue = mp.Queue()
# fill the queue with the processes
for pair in requiredPairsDict:
jobs_queue.put(pair)
# add flags for eneded jobs
for i in range(0, threads):
jobs_queue.put(None)
#sys.exit('DEBUG :: 3')
# Queue to contain the execution time
results_queue = mp.Queue(maxsize=len(requiredPairsDict))
# call the method inside workers
runningJobs = [
mp.Process(target=consume_orthology_inference_jobs,
args=(jobs_queue, results_queue, inDir, outDir, sharedDir,
cutoff, confCutoff, lenDiffThr, threads, debug))
for i_ in range(threads)
]
for proc in runningJobs:
#print('Start job\t{}'.format(proc))
proc.start()
# open the file in which the time information will be stored
execTimeOutPath = os.path.join(
sharedDir, 'orthology_ex_time_{:s}.tsv'.format(
os.path.basename(outDir.rstrip('/'))))
ofd = open(execTimeOutPath, 'w', buffering=1)
# get the results from the queue without filling the Pipe buffer
while True:
try:
p, val = results_queue.get(False, 0.01)
ofd.write('{:s}\t{:s}\n'.format(p, str(val)))
except queue.Empty:
pass
allExited = True
for t in runningJobs:
if t.exitcode is None:
allExited = False
break
if allExited & results_queue.empty():
break
ofd.close()
for proc in runningJobs:
while proc.is_alive():
proc.join()
def mmseqs_search(inSeq,
dbSeq,
dbDir=os.getcwd(),
outDir=os.getcwd(),
tmpDirName=None,
sensitivity=4.0,
evalue=1000,
threads=4,
cleanUp=False,
debug=False):
"""Align protein sequences using mmseqs2."""
if debug:
print('\nmmseqs_search :: START')
print('Input query FASTA file:\t%s' % inSeq)
print('Input target FASTA file:\t%s' % dbSeq)
print('mmseqs2 database directory:\t%s' % dbDir)
print('Output directory:\t%s' % outDir)
print('MMseqs2 tmp directory:\t{:s}'.format(tmpDirName))
print('MMseqs2 sensitivity (-s):\t%s' % str(sensitivity))
print('Threads:\t%d' % threads)
print('Remove temporary files:\t%s' % cleanUp)
#check that the input file and the database exist
if not os.path.isfile(inSeq):
sys.stderr.write(
'The query file %s was not found, please provide the path to a valid FASTA file'
% inSeq)
sys.exit(-2)
if not os.path.isfile(dbSeq):
sys.stderr.write(
'The target file %s was not found, please provide the path to a valid FASTA file'
% dbSeq)
sys.exit(-2)
# check sensitivity
if (sensitivity < 1) or sensitivity > 8.5:
sys.stderr.write(
'\nERROR: the sensitivity value for MMseqs2.0 must be a value between 1.0 and 8.5.\n'
)
sys.exit(-5)
# create directory if not previously created
systools.makedir(outDir)
systools.makedir(dbDir)
# set the tmp dir
tmpDir = None
if tmpDirName is None:
tmpDir = '%stmp_mmseqs/' % outDir
else:
tmpDir = '{:s}{:s}/'.format(outDir, tmpDirName)
systools.makedir(tmpDir)
# check the query db name
queryDBname = os.path.basename(inSeq)
queryDBname = queryDBname.split('.')[
0] # take the left part of the file name
queryDBname = '%s.mmseqs2db' % queryDBname
queryDBpath = '%s%s' % (dbDir, queryDBname)
# create the database if does not exist yet
if not os.path.isfile(queryDBpath):
mmseqs_createdb(inSeq, outDir=dbDir, debug=debug)
mmseqs_createindex(queryDBpath, debug=debug)
# check the target db name
targetDBname = os.path.basename(dbSeq)
targetDBname = targetDBname.split('.')[
0] # take the left part of the file name
targetDBname = '%s.mmseqs2db' % targetDBname
targetDBpath = '%s%s' % (dbDir, targetDBname)
# create the database if does not exist yet
if not os.path.isfile(targetDBpath):
mmseqs_createdb(dbSeq, outDir=dbDir, debug=debug)
mmseqs_createindex(targetDBpath, debug=debug)
# set output name
pairName = '%s-%s' % (os.path.basename(inSeq), os.path.basename(dbSeq))
rawOutName = 'mmseqs2raw.%s' % pairName
rawOutPath = '%s%s' % (outDir, rawOutName)
blastOutName = 'mmseqs2blast.%s' % pairName
blastOutPath = '%s%s' % (outDir, blastOutName)
# start measuring the execution time
# use perf_counter (includes time spent during sleep)
start_time = time.perf_counter()
# command to be executed
minUngappedScore = 15
# EXAMPLE; mmseqs search queryDBfile targetDBfile outputFile tmpDir -s 7.5 -e 100000 --theads threads
searchCmd = '{:s} search {:s} {:s} {:s} {:s} -s {:s} --threads {:d} -v 0 --min-ungapped-score {:d} --alignment-mode 2 --alt-ali 10'.format(
get_mmseqs_path(), queryDBpath, targetDBpath, rawOutPath, tmpDir,
str(sensitivity), threads, minUngappedScore)
if debug:
print('mmseqs2 search CMD:\t%s' % searchCmd)
# use run (or call)
subprocess.run(searchCmd, env=my_env, shell=True)
# output an error if the Alignment did not finish correctly
if not os.path.isfile(rawOutPath):
sys.stderr.write(
'\nERROR: the MMseqs2 raw alignment file was not generated.\n')
sys.exit(-2)
# stop counter
# use perf_counter (includes time spent during sleep)
end_search = time.perf_counter()
# use process_time (user + system CPU time, no sleep time)
#end_search = time.process_time()
search_time = round(end_search - start_time, 2)
# convert the output to tab-separated BLAST output
# EXAMPLE: mmseqs convertalis query.db target.db query_target_rawout query_target_blastout
convertCmd = '%s convertalis %s %s %s %s -v 0 --format-mode 0' % (
get_mmseqs_path(), queryDBpath, targetDBpath, rawOutPath, blastOutPath)
# perform the file conversion
subprocess.run(convertCmd, env=my_env, shell=True)
if debug:
print('mmseqs2 convertalis CMD:\t%s' % convertCmd)
# exec time conversion
#convert_time = round(time.time() - end_search, 2)
# use perf_counter (includes time spent during sleep)
convert_time = round(time.perf_counter() - end_search, 2)
# use process_time (user + system CPU time, no sleep time)
#convert_time = round(time.process_time() - end_search, 2)
# cleanup output directory
if cleanUp:
mmseqs_cleanup(inDir=outDir, debug=debug)
# output an error if the Alignment could not be converted
if not os.path.isfile(blastOutPath):
sys.stderr.write(
'\nERROR: the MMseqs2 raw alignment could not be converted inot the BLAST alignment format.\n'
)
sys.exit(-2)
return (blastOutPath, search_time, convert_time)
def consume_orthology_inference_jobs(jobs_queue,
results_queue,
inDir,
outDir=os.getcwd(),
sharedDir=None,
cutoff=40,
confCutoff=0.05,
lenDiffThr=0.5,
threads=8,
debug=False):
"""Perform orthology inference in parallel."""
while True:
current_pair = jobs_queue.get(True, 1)
if current_pair is None:
break
# create the output directory iof needed
# prepare the run
sp1, sp2 = current_pair.split('-', 1)
runDir = os.path.join(outDir, current_pair)
systools.makedir(runDir)
inSp1 = os.path.join(inDir, sp1)
inSp2 = os.path.join(inDir, sp2)
# check that the input files do exist
if not os.path.isfile(inSp1):
sys.stderr.write(
'ERROR: The input file for {:s} was not found, please provide a valid path\n.'
.format(sp1))
if not os.path.isfile(inSp2):
sys.stderr.write(
'ERROR: The input file for {:s} was not found, please provide a valid path\n.'
.format(sp2))
# prepare the names of the required alignments
# copy AA
AA = '{:s}-{:s}'.format(sp1, sp1)
shPathAA = os.path.join(sharedDir, AA)
if not os.path.isfile(shPathAA):
sys.stderr.write(
'ERROR: The alignment file for {:s} was not found, please generate alignments first\n.'
.format(AA))
# copy BB
BB = '{:s}-{:s}'.format(sp2, sp2)
shPathBB = os.path.join(sharedDir, BB)
if not os.path.isfile(shPathBB):
sys.stderr.write(
'ERROR: The alignment file for {:s} was not found, please generate alignments first\n.'
.format(BB))
# copy AB
AB = '{:s}-{:s}'.format(sp1, sp2)
shPathAB = os.path.join(sharedDir, AB)
if not os.path.isfile(shPathAB):
sys.stderr.write(
'ERROR: The alignment file for {:s} was not found, please generate alignments first\n.'
.format(AB))
# copy BA
BA = '{:s}-{:s}'.format(sp2, sp1)
shPathBA = os.path.join(sharedDir, BA)
if not os.path.isfile(shPathBA):
sys.stderr.write(
'ERROR: The alignment file for {:s} was not found, please generate alignments first\n.'
.format(BA))
#sys.exit('DEBUG :: workers :: consume_orthology_inference_jobs :: after files copy')
# prepare paths for output tables
outTable = os.path.join(runDir, 'table.{:s}'.format(current_pair))
outSql = os.path.join(runDir, 'sqltable.{:s}'.format(current_pair))
# infer orthologs
# use perf_counter (includes time spent during sleep)
orthology_prediction_start = time.perf_counter()
inpyranoid.infer_orthologs(inSp1,
inSp2,
alignDir=sharedDir,
outDir=runDir,
confCutoff=confCutoff,
lenDiffThr=lenDiffThr,
debug=False)
#sys.exit('DEBUG :: workers :: consume_orthology_inference_jobs :: after orthology')
#check that all the files have been created
if not os.path.isfile(outTable):
sys.stderr.write(
'WARNING: the ortholog table file %s was not generated.' %
outTable)
outTable = None
if not os.path.isfile(outSql):
sys.stderr.write('WARNING: the SQL table %s was not generated.' %
outSql)
outSql = None
#everything went ok!
# use perf_counter (includes time spent during sleep)
end_time = time.perf_counter()
orthology_prediction_tot = round(end_time - orthology_prediction_start,
2)
#sys.exit('DEBUG :: workers :: consume_orthology_inference_jobs :: orthology done!')
# add the execution time to the results queue
results_queue.put((current_pair, str(orthology_prediction_tot)))
if debug:
sys.stdout.write(
'\nOrthology prediction {:s} (seconds):\t{:s}\n'.format(
current_pair, str(orthology_prediction_tot)))
def filter_ortholog_table(abTbl,
a,
b,
outDir=os.getcwd(),
lenThr=0.25,
debug=False):
'''Filter ortholog table based on sequence legths.'''
if debug:
print('filter_ortholog_table :: START')
print('Ortholog table: %s' % abTbl)
print('Proteome A: %s' % a)
print('Proteome B: %s' % b)
print('Output directory: %s' % outDir)
print('Length difference threshold: %s' % str(lenThr))
# load sequence lengths for A and B
lenDictA = load_seq_lengths(a, debug)
lenDictB = load_seq_lengths(b, debug)
# load the information from a clusters
# EXAMPLE
#OrtoId Score OrtoA OrtoB
#1 1163 1423_Q9KWU4 1.0 9606_P11498 1.0
#2 963 1423_P09339 1.0 9606_P21399 1.0 9606_P48200 0.201
# these will contain info for paralogs for each of the 2 species
if outDir[-1] != '/':
outDir = '%s/' % outDir
# check that the output directory is different from the one of the input file
inDir = '%s/' % os.path.dirname(abTbl)
if inDir == outDir:
sys.exit(
'The output directory must be different from that of the input table.'
)
# create output directory if needed
systools.makedir(outDir)
# new table path
abTblNew = '%s%s' % (outDir, os.path.basename(abTbl))
# rejected list file path
rjctTbl = '%s%s' % (outDir,
os.path.basename(abTbl.replace('table.', 'rejected.')))
# new table path
abTblNew = '%s%s' % (outDir, os.path.basename(abTbl))
# rejected list file path
rjctTbl = '%s%s' % (outDir,
os.path.basename(abTbl.replace('table.', 'rejected.')))
# open output files
ofdNewTbl = open(abTblNew, 'w')
ofdRjct = open(rjctTbl, 'w')
# count read and wrote genes
orthoRdCntA = inparaRdCntA = orthoRdCntB = inparaRdCntB = 0
orthoWrtCntA = inparaWrtCntA = orthoWrtCntB = inparaWrtCntB = 0
for ln in open(abTbl):
if ln[0] == 'O':
ofdNewTbl.write(ln)
continue
ln = ln.rstrip('\n')
clstrId, score, paraA, paraB = ln.split('\t')
# extract orthologs and inparalogs from A
orthoListA, inparaDictRawA = extract_paralogs(paraA, debug=debug)
orthoRdCntA += len(orthoListA)
inparaRdCntA += len(inparaDictRawA)
# If there are InParalogs then check if they should be kept or not
keptInpaListA = []
droppedInpaDictA = OrderedDict()
if len(inparaDictRawA):
#print('ClstrID:\t%s'%clstrId)
# set ortholog length for A
lenListOrthoA = []
if len(orthoListA) > 1:
lenListOrthoA = calc_ortholog_leghths(orthoListA,
lenDictA,
debug=debug)
elif len(orthoListA) == 0:
sys.exit('ERROR: at least one ortholog must be found!')
else:
# add the only available length
lenListOrthoA.append(lenDictA[orthoListA[0]])
# filter Inparalogs from A
droppedInpaDictA, keptInpaListA = filter_inparalogs(
inparaDictRawA,
lenDictA,
orthoLenList=lenListOrthoA,
lenRatioThr=lenThr,
debug=debug)
'''
if clstrId == '777':
print(orthoListA)
print(inparaDictRawA)
print(lenListOrthoA)
print(droppedInpaDictA)
print(keptInpaListA)
sys.exit('Test single cluster')
#'''
# extract orthologs and inparalogs from B
orthoListB, inparaDictRawB = extract_paralogs(paraB, debug=debug)
orthoRdCntB += len(orthoListB)
inparaRdCntB += len(inparaDictRawB)
# If there are InParalogs then check if they should be kept or not
keptInpaListB = []
droppedInpaDictB = OrderedDict()
if len(inparaDictRawB):
# set ortholog length for B
lenListOrthoB = []
if len(orthoListB) > 1:
lenListOrthoB = calc_ortholog_leghths(orthoListB,
lenDictB,
debug=debug)
elif len(orthoListB) == 0:
sys.exit('ERROR: at least one ortholog must be found!')
else:
# add the only available length
lenListOrthoB.append(lenDictB[orthoListB[0]])
# filter Inparalogs from B
droppedInpaDictB, keptInpaListB = filter_inparalogs(
inparaDictRawB,
lenDictB,
orthoLenList=lenListOrthoB,
lenRatioThr=lenThr,
debug=debug)
# START WRITING THE NEW TABLE
ofdNewTbl.write('%s\t%s\t' % (clstrId, score))
# Write the output cluster for A
# Write cores orthologs for A
tmpLnList = []
for orthoTmpGene in orthoListA:
tmpLnList.append('%s 1.0' % (orthoTmpGene))
ofdNewTbl.write(' '.join(tmpLnList))
orthoWrtCntA += len(tmpLnList)
# Write rejected inparalogs
for k in droppedInpaDictA:
tmpLenDiff, tmpConf, inparaVsOrthoRatio = droppedInpaDictA[k]
ofdRjct.write(
'%s\t%s\t%s\t%s\t%s\t%s\n' %
(clstrId, score, k, tmpConf, tmpLenDiff, inparaVsOrthoRatio))
# reset tmp list
tmpLnList.clear()
# write valid inparalogs to cluster
for tmpInparaA in keptInpaListA:
tmpLnList.append('%s %s' %
(tmpInparaA, inparaDictRawA[tmpInparaA]))
if len(tmpLnList) > 0:
ofdNewTbl.write(' %s' % (' '.join(tmpLnList)))
inparaWrtCntA += len(tmpLnList)
tmpLnList.clear()
# now start writing the right part of the cluster
ofdNewTbl.write('\t')
# Write core orthologs for B
tmpLnList.clear()
for orthoTmpGene in orthoListB:
tmpLnList.append('%s 1.0' % (orthoTmpGene))
ofdNewTbl.write(' '.join(tmpLnList))
orthoWrtCntB += len(tmpLnList)
# Write rejected inparalogs
for k in droppedInpaDictB:
tmpLenDiff, tmpConf, inparaVsOrthoRatio = droppedInpaDictB[k]
ofdRjct.write(
'%s\t%s\t%s\t%s\t%s\t%s\n' %
(clstrId, score, k, tmpConf, tmpLenDiff, inparaVsOrthoRatio))
# reset tmp list
tmpLnList.clear()
# write valid inparalogs to cluster
for tmpInparaB in keptInpaListB:
tmpLnList.append('%s %s' %
(tmpInparaB, inparaDictRawB[tmpInparaB]))
if len(tmpLnList) > 0:
ofdNewTbl.write(' %s' % (' '.join(tmpLnList)))
inparaWrtCntB += len(tmpLnList)
tmpLnList.clear()
# close the cluster line
ofdNewTbl.write('\n')
###### TEST #########
'''
# Try to rewrite the table as it was originally
ofdNewTbl.write('%s\t%s\t'%(clstrId, score))
tmpLnList = []
# write cores orthologs for A
for orthoTmpGene in orthoListA:
tmpLnList.append('%s 1.0'%(orthoTmpGene))
ofdNewTbl.write(' '.join(tmpLnList))
orthoWrtCntA += len(tmpLnList)
# reset tmp list
tmpLnList.clear()
for k in inparaDictRawA:
tmpLnList.append('%s %s'%(k, inparaDictRawA[k]))
if len(tmpLnList) > 0:
ofdNewTbl.write(' %s'%(' '.join(tmpLnList)))
inparaWrtCntA += len(tmpLnList)
tmpLnList.clear()
#'''
'''
# now start with the right part of the cluster
ofdNewTbl.write('\t')
# write the orthologs for B
for orthoTmpGene in orthoListB:
tmpLnList.append('%s 1.0'%(orthoTmpGene))
ofdNewTbl.write(' '.join(tmpLnList))
orthoWrtCntB += len(tmpLnList)
# reset tmp list
tmpLnList.clear()
# write InParalogs
for k in inparaDictRawB:
tmpLnList.append('%s %s'%(k, inparaDictRawB[k]))
if len(tmpLnList) > 0:
ofdNewTbl.write(' %s'%(' '.join(tmpLnList)))
inparaWrtCntB += len(tmpLnList)
ofdNewTbl.write('\n')
######################
#'''
# close output files
ofdNewTbl.close()
ofdRjct.close()
if debug:
print('\nRead orthologs A/B; inparalogs A/B:')
print('%d\t%d\t%d\t%d' %
(orthoRdCntA, orthoRdCntB, inparaRdCntA, inparaRdCntB))
print('\nWritten orthologs A/B; inparalogs A/B:')
print('%d\t%d\t%d\t%d' %
(orthoWrtCntA, orthoWrtCntB, inparaWrtCntA, inparaWrtCntB))
