def run_anim_jobs(joblist: List[ComparisonJob], args: Namespace) -> None:
"""Pass ANIm nucmer jobs to the scheduler.
:param joblist: list of ComparisonJob namedtuples
:param args: command-line arguments for the run
"""
logger = logging.getLogger(__name__)
if args.scheduler == "multiprocessing":
logger.info("Running jobs with multiprocessing")
if not args.workers:
logger.debug("(using maximum number of worker threads)")
else:
logger.debug("(using %d worker threads, if available)", args.workers)
cumval = run_mp.run_dependency_graph(
[_.job for _ in joblist], workers=args.workers
)
if cumval > 0:
logger.error(
"At least one NUCmer comparison failed. Please investigate (exiting)"
)
raise PyaniException("Multiprocessing run failed in ANIm")
logger.info("Multiprocessing run completed without error")
else:
logger.info("Running jobs with SGE")
logger.debug("Setting jobarray group size to %d", args.sgegroupsize)
run_sge.run_dependency_graph(
[_.job for _ in joblist],
jgprefix=args.jobprefix,
sgegroupsize=args.sgegroupsize,
sgeargs=args.sgeargs,
)
def calculate_anim(infiles, org_lengths):
"""Returns ANIm result dataframes for files in input directory.
- infiles - paths to each input file
- org_lengths - dictionary of input sequence lengths, keyed by sequence
Finds ANI by the ANIm method, as described in Richter et al (2009)
Proc Natl Acad Sci USA 106: 19126-19131 doi:10.1073/pnas.0906412106.
All FASTA format files (selected by suffix) in the input directory
are compared against each other, pairwise, using NUCmer (which must
be in the path). NUCmer output is stored in the output directory.
The NUCmer .delta file output is parsed to obtain an alignment length
and similarity error count for every unique region alignment between
the two organisms, as represented by the sequences in the FASTA files.
These are processed to give matrices of aligned sequence lengths,
average nucleotide identity (ANI) percentages, coverage (aligned
percentage of whole genome), and similarity error cound for each pairwise
comparison.
"""
logger.info("Running ANIm")
logger.info("Generating NUCmer command-lines")
# Schedule NUCmer runs
if not args.skip_nucmer:
joblist = anim.generate_nucmer_jobs(
infiles, args.outdirname, nucmer_exe=args.nucmer_exe, maxmatch=args.maxmatch
)
if args.scheduler == "multiprocessing":
logger.info("Running jobs with multiprocessing")
cumval = run_mp.run_dependency_graph(joblist, verbose=args.verbose, logger=logger)
logger.info("Cumulative return value: %d" % cumval)
if 0 < cumval:
logger.warning("At least one NUCmer comparison failed. " + "ANIm may fail.")
else:
logger.info("All multiprocessing jobs complete.")
else:
logger.info("Running jobs with SGE")
run_sge.run_dependency_graph(joblist, verbose=args.verbose, logger=logger)
else:
logger.warning("Skipping NUCmer run (as instructed)!")
# Process resulting .delta files
logger.info("Processing NUCmer .delta files.")
try:
data = anim.process_deltadir(args.outdirname, org_lengths)
except ZeroDivisionError:
logger.error("One or more NUCmer output files has a problem.")
if not args.skip_nucmer:
if 0 < cumval:
logger.error("This is possibly due to NUCmer run failure, " + "please investigate")
else:
logger.error(
"This is possibly due to a NUCmer comparison "
+ "being too distant for use. Please consider "
+ "using the --maxmatch option."
)
logger.error(last_exception())
return data
def run_blast(args: Namespace, logger: Logger, infiles: List[Path],
blastdir: Path) -> Tuple:
"""Run BLAST commands for ANIb methods.
:param args: Namespace of command-line options
:param logger: logging object
:param infiles: iterable of sequence files to compare
:param blastdir: path of directory to fragment BLASTN databases
Runs BLAST database creation and comparisons, returning the cumulative
return values of the BLAST tool subprocesses, and the fragment sizes for
each input file
"""
if not args.skip_blastn:
logger.info("Fragmenting input files, and writing to %s",
args.outdirname)
fragfiles, fraglengths = make_sequence_fragments(
args, logger, infiles, blastdir)
# Run BLAST database-building and executables from a jobgraph
logger.info("Creating job dependency graph")
jobgraph = anib.make_job_graph(
infiles, fragfiles,
anib.make_blastcmd_builder(args.method, blastdir))
if args.scheduler == "multiprocessing":
logger.info("Running dependency graph with multiprocessing")
cumval = run_mp.run_dependency_graph(jobgraph, logger=logger)
if cumval > 0:
logger.warning(
f"At least one BLAST run failed. {args.method} may fail. Please investigate."
)
else:
logger.info("All multiprocessing jobs complete.")
elif args.scheduler == "SGE":
logger.info("Running dependency graph with SGE")
run_sge.run_dependency_graph(jobgraph)
else:
logger.error(
f"Scheduler {args.scheduler} not recognised (exiting)")
raise SystemError(1)
else:
logger.warning("Skipping BLASTN runs (as instructed)!")
# Import fragment lengths from JSON
if args.method == "ANIblastall":
fragpath = blastdir / "fraglengths.json"
logger.info(f"Loading sequence fragments from {fragpath}")
with open(fragpath, "rU") as ifh:
fraglengths = json.load(ifh)
else:
fraglengths = dict()
return cumval, fraglengths
def unified_anib(infiles, org_lengths):
"""Calculate ANIb for files in input directory.
- infiles - paths to each input file
- org_lengths - dictionary of input sequence lengths, keyed by sequence
Calculates ANI by the ANIb method, as described in Goris et al. (2007)
Int J Syst Evol Micr 57: 81-91. doi:10.1099/ijs.0.64483-0. There are
some minor differences depending on whether BLAST+ or legacy BLAST
(BLASTALL) methods are used.
All FASTA format files (selected by suffix) in the input directory are
used to construct BLAST databases, placed in the output directory.
Each file's contents are also split into sequence fragments of length
options.fragsize, and the multiple FASTA file that results written to
the output directory. These are BLASTNed, pairwise, against the
databases.
The BLAST output is interrogated for all fragment matches that cover
at least 70% of the query sequence, with at least 30% nucleotide
identity over the full length of the query sequence. This is an odd
choice and doesn't correspond to the twilight zone limit as implied by
Goris et al. We persist with their definition, however. Only these
qualifying matches contribute to the total aligned length, and total
aligned sequence identity used to calculate ANI.
The results are processed to give matrices of aligned sequence length
(aln_lengths.tab), similarity error counts (sim_errors.tab), ANIs
(perc_ids.tab), and minimum aligned percentage (perc_aln.tab) of
each genome, for each pairwise comparison. These are written to the
output directory in plain text tab-separated format.
"""
logger.info("Running %s", args.method)
blastdir = os.path.join(args.outdirname, ALIGNDIR[args.method])
logger.info("Writing BLAST output to %s", blastdir)
# Build BLAST databases and run pairwise BLASTN
if not args.skip_blastn:
# Make sequence fragments
logger.info("Fragmenting input files, and writing to %s",
args.outdirname)
# Fraglengths does not get reused with BLASTN
fragfiles, fraglengths = anib.fragment_fasta_files(
infiles, blastdir, args.fragsize)
# Export fragment lengths as JSON, in case we re-run with --skip_blastn
with open(os.path.join(blastdir, 'fraglengths.json'), 'w') as outfile:
json.dump(fraglengths, outfile)
# Which executables are we using?
#if args.method == "ANIblastall":
# format_exe = args.formatdb_exe
# blast_exe = args.blastall_exe
#else:
# format_exe = args.makeblastdb_exe
# blast_exe = args.blastn_exe
# Run BLAST database-building and executables from a jobgraph
logger.info("Creating job dependency graph")
jobgraph = anib.make_job_graph(
infiles, fragfiles,
anib.make_blastcmd_builder(args.method, blastdir))
#jobgraph = anib.make_job_graph(infiles, fragfiles, blastdir,
# format_exe, blast_exe, args.method,
# jobprefix=args.jobprefix)
if args.scheduler == 'multiprocessing':
logger.info("Running jobs with multiprocessing")
logger.info("Running job dependency graph")
cumval = run_mp.run_dependency_graph(jobgraph, logger=logger)
if 0 < cumval:
logger.warning(
"At least one BLAST run failed. " + "%s may fail.",
args.method)
else:
logger.info("All multiprocessing jobs complete.")
else:
run_sge.run_dependency_graph(jobgraph, logger=logger)
logger.info("Running jobs with SGE")
else:
# Import fragment lengths from JSON
if args.method == "ANIblastall":
with open(os.path.join(blastdir, 'fraglengths.json'),
'rU') as infile:
fraglengths = json.load(infile)
else:
fraglengths = None
logger.warning("Skipping BLASTN runs (as instructed)!")
# Process pairwise BLASTN output
logger.info("Processing pairwise %s BLAST output.", args.method)
try:
data = anib.process_blast(blastdir,
org_lengths,
fraglengths=fraglengths,
mode=args.method)
except ZeroDivisionError:
logger.error("One or more BLAST output files has a problem.")
if not args.skip_blastn:
if 0 < cumval:
logger.error("This is possibly due to BLASTN run failure, " +
"please investigate")
else:
logger.error("This is possibly due to a BLASTN comparison " +
"being too distant for use.")
logger.error(last_exception())
if not args.nocompress:
logger.info("Compressing/deleting %s", blastdir)
compress_delete_outdir(blastdir)
# Return processed BLAST data
return data
def calculate_anim(infiles, org_lengths):
"""Returns ANIm result dataframes for files in input directory.
- infiles - paths to each input file
- org_lengths - dictionary of input sequence lengths, keyed by sequence
Finds ANI by the ANIm method, as described in Richter et al (2009)
Proc Natl Acad Sci USA 106: 19126-19131 doi:10.1073/pnas.0906412106.
All FASTA format files (selected by suffix) in the input directory
are compared against each other, pairwise, using NUCmer (which must
be in the path). NUCmer output is stored in the output directory.
The NUCmer .delta file output is parsed to obtain an alignment length
and similarity error count for every unique region alignment between
the two organisms, as represented by the sequences in the FASTA files.
These are processed to give matrices of aligned sequence lengths,
average nucleotide identity (ANI) percentages, coverage (aligned
percentage of whole genome), and similarity error cound for each pairwise
comparison.
"""
logger.info("Running ANIm")
logger.info("Generating NUCmer command-lines")
deltadir = os.path.join(args.outdirname, ALIGNDIR['ANIm'])
logger.info("Writing nucmer output to %s", deltadir)
# Schedule NUCmer runs
if not args.skip_nucmer:
joblist = anim.generate_nucmer_jobs(infiles,
args.outdirname,
nucmer_exe=args.nucmer_exe,
jobprefix=args.jobprefix)
if args.scheduler == 'multiprocessing':
logger.info("Running jobs with multiprocessing")
if args.workers is None:
logger.info("(using maximum number of available " +
"worker threads)")
else:
logger.info("(using %d worker threads, if available)",
args.workers)
cumval = run_mp.run_dependency_graph(joblist,
workers=args.workers,
logger=logger)
logger.info("Cumulative return value: %d", cumval)
if 0 < cumval:
logger.warning("At least one NUCmer comparison failed. " +
"ANIm may fail.")
else:
logger.info("All multiprocessing jobs complete.")
else:
logger.info("Running jobs with SGE")
logger.info("Jobarray group size set to %d", args.sgegroupsize)
run_sge.run_dependency_graph(joblist,
logger=logger,
jgprefix=args.jobprefix,
sgegroupsize=args.sgegroupsize)
else:
logger.warning("Skipping NUCmer run (as instructed)!")
# Process resulting .delta files
logger.info("Processing NUCmer .delta files.")
results = anim.process_deltadir(deltadir, org_lengths, logger=logger)
if results.zero_error: # zero percentage identity error
if not args.skip_nucmer and args.scheduler == 'multiprocessing':
if 0 < cumval:
logger.error("This has possibly been a NUCmer run failure, " +
"please investigate")
logger.error(last_exception())
sys.exit(1)
else:
logger.error("This is possibly due to a NUCmer comparison " +
"being too distant for use. Please consider " +
"using the --maxmatch option.")
logger.error("This is alternatively due to NUCmer run " +
"failure, analysis will continue, but please " +
"investigate.")
if not args.nocompress:
logger.info("Compressing/deleting %s", deltadir)
compress_delete_outdir(deltadir)
# Return processed data from .delta files
return results
def calculate_anim(args: Namespace, infiles: List[Path],
org_lengths: Dict) -> pyani_tools.ANIResults:
"""Return ANIm result dataframes for files in input directory.
:param args: Namespace, command-line arguments
:param logger: logging object
:param infiles: list of paths to each input file
:param org_lengths: dict, input sequence lengths, keyed by sequence
Finds ANI by the ANIm method, as described in Richter et al (2009)
Proc Natl Acad Sci USA 106: 19126-19131 doi:10.1073/pnas.0906412106.
All FASTA format files (selected by suffix) in the input directory
are compared against each other, pairwise, using NUCmer (which must
be in the path). NUCmer output is stored in the output directory.
The NUCmer .delta file output is parsed to obtain an alignment length
and similarity error count for every unique region alignment between
the two organisms, as represented by the sequences in the FASTA files.
These are processed to give matrices of aligned sequence lengths,
average nucleotide identity (ANI) percentages, coverage (aligned
percentage of whole genome), and similarity error cound for each pairwise
comparison.
"""
logger = logging.getLogger(__name__)
logger.info("Running ANIm")
logger.info("Generating NUCmer command-lines")
deltadir = args.outdirname / ALIGNDIR["ANIm"]
logger.info("Writing nucmer output to %s", deltadir)
# Schedule NUCmer runs
if not args.skip_nucmer:
joblist = anim.generate_nucmer_jobs(
infiles,
args.outdirname,
nucmer_exe=args.nucmer_exe,
filter_exe=args.filter_exe,
maxmatch=args.maxmatch,
jobprefix=args.jobprefix,
)
if args.scheduler == "multiprocessing":
logger.info("Running jobs with multiprocessing")
if args.workers is None:
logger.info(
"(using maximum number of available worker threads)")
else:
logger.info("(using %d worker threads, if available)",
args.workers)
cumval = run_mp.run_dependency_graph(joblist,
workers=args.workers,
logger=logger)
logger.info("Cumulative return value: %d", cumval)
if cumval > 0:
logger.warning(
"At least one NUCmer comparison failed. ANIm may fail.")
else:
logger.info("All multiprocessing jobs complete.")
else:
logger.info("Running jobs with SGE")
logger.info("Jobarray group size set to %d", args.sgegroupsize)
run_sge.run_dependency_graph(
joblist,
jgprefix=args.jobprefix,
sgegroupsize=args.sgegroupsize,
sgeargs=args.sgeargs,
)
else:
logger.warning("Skipping NUCmer run (as instructed)!")
# Process resulting .delta files
logger.info("Processing NUCmer .delta files.")
results = anim.process_deltadir(deltadir, org_lengths, logger=logger)
if results.zero_error: # zero percentage identity error
if not args.skip_nucmer and args.scheduler == "multiprocessing":
if cumval > 0:
logger.error(
"This has possibly been a NUCmer run failure, please investigate",
exc_info=True,
)
raise SystemExit(1)
logger.error(
"This is possibly due to:\n\t(i) a NUCmer comparison being too distant "
"for use (please consider using the --maxmatch option)\n\t(ii) NUCmer run "
"failure (analysis will continue, but please investigate)")
if not args.nocompress:
logger.info("Compressing/deleting %s", deltadir)
compress_delete_outdir(deltadir, logger)
# Return processed data from .delta files
return results
def calculate_anim(infiles, org_lengths):
"""Returns ANIm result dataframes for files in input directory.
- infiles - paths to each input file
- org_lengths - dictionary of input sequence lengths, keyed by sequence
Finds ANI by the ANIm method, as described in Richter et al (2009)
Proc Natl Acad Sci USA 106: 19126-19131 doi:10.1073/pnas.0906412106.
All FASTA format files (selected by suffix) in the input directory
are compared against each other, pairwise, using NUCmer (which must
be in the path). NUCmer output is stored in the output directory.
The NUCmer .delta file output is parsed to obtain an alignment length
and similarity error count for every unique region alignment between
the two organisms, as represented by the sequences in the FASTA files.
These are processed to give matrices of aligned sequence lengths,
average nucleotide identity (ANI) percentages, coverage (aligned
percentage of whole genome), and similarity error cound for each pairwise
comparison.
"""
logger.info("Running ANIm")
logger.info("Generating NUCmer command-lines")
# Schedule NUCmer runs
if not args.skip_nucmer:
joblist = anim.generate_nucmer_jobs(infiles,
args.outdirname,
nucmer_exe=args.nucmer_exe,
maxmatch=args.maxmatch)
if args.scheduler == 'multiprocessing':
logger.info("Running jobs with multiprocessing")
cumval = run_mp.run_dependency_graph(joblist,
verbose=args.verbose,
logger=logger)
logger.info("Cumulative return value: %d" % cumval)
if 0 < cumval:
logger.warning("At least one NUCmer comparison failed. " +
"ANIm may fail.")
else:
logger.info("All multiprocessing jobs complete.")
else:
logger.info("Running jobs with SGE")
run_sge.run_dependency_graph(joblist,
verbose=args.verbose,
logger=logger)
else:
logger.warning("Skipping NUCmer run (as instructed)!")
# Process resulting .delta files
logger.info("Processing NUCmer .delta files.")
try:
data = anim.process_deltadir(args.outdirname, org_lengths)
except ZeroDivisionError:
logger.error("One or more NUCmer output files has a problem.")
if not args.skip_nucmer:
if 0 < cumval:
logger.error("This is possibly due to NUCmer run failure, " +
"please investigate")
else:
logger.error("This is possibly due to a NUCmer comparison " +
"being too distant for use. Please consider " +
"using the --maxmatch option.")
logger.error(last_exception())
return data
def unified_anib(infiles, org_lengths):
"""Calculate ANIb for files in input directory.
- infiles - paths to each input file
- org_lengths - dictionary of input sequence lengths, keyed by sequence
Calculates ANI by the ANIb method, as described in Goris et al. (2007)
Int J Syst Evol Micr 57: 81-91. doi:10.1099/ijs.0.64483-0. There are
some minor differences depending on whether BLAST+ or legacy BLAST
(BLASTALL) methods are used.
All FASTA format files (selected by suffix) in the input directory are
used to construct BLAST databases, placed in the output directory.
Each file's contents are also split into sequence fragments of length
options.fragsize, and the multiple FASTA file that results written to
the output directory. These are BLASTNed, pairwise, against the
databases.
The BLAST output is interrogated for all fragment matches that cover
at least 70% of the query sequence, with at least 30% nucleotide
identity over the full length of the query sequence. This is an odd
choice and doesn't correspond to the twilight zone limit as implied by
Goris et al. We persist with their definition, however. Only these
qualifying matches contribute to the total aligned length, and total
aligned sequence identity used to calculate ANI.
The results are processed to give matrices of aligned sequence length
(aln_lengths.tab), similarity error counts (sim_errors.tab), ANIs
(perc_ids.tab), and minimum aligned percentage (perc_aln.tab) of
each genome, for each pairwise comparison. These are written to the
output directory in plain text tab-separated format.
"""
logger.info("Running %s" % args.method)
# Build BLAST databases and run pairwise BLASTN
if not args.skip_blastn:
# Make sequence fragments
logger.info("Fragmenting input files, and writing to %s" %
args.outdirname)
# Fraglengths does not get reused with BLASTN
fragfiles, fraglengths = anib.fragment_FASTA_files(infiles,
args.outdirname,
args.fragsize)
# Export fragment lengths as JSON, in case we re-run BLASTALL with
# --skip_blastn
if args.method == "ANIblastall":
with open(os.path.join(args.outdirname,
'fraglengths.json'), 'w') as outfile:
json.dump(fraglengths, outfile)
# Which executables are we using?
if args.method == "ANIblastall":
format_exe = args.formatdb_exe
blast_exe = args.blastall_exe
else:
format_exe = args.makeblastdb_exe
blast_exe = args.blastn_exe
# Run BLAST database-building and executables from a jobgraph
logger.info("Creating job dependency graph")
jobgraph = anib.make_job_graph(infiles, fragfiles, args.outdirname,
format_exe, blast_exe, args.method)
if args.scheduler == 'multiprocessing':
logger.info("Running jobs with multiprocessing")
logger.info("Running job dependency graph")
cumval = run_mp.run_dependency_graph(jobgraph, verbose=args.verbose,
logger=logger)
if 0 < cumval:
logger.warning("At least one BLAST run failed. " +
"%s may fail." % args.method)
else:
logger.info("All multiprocessing jobs complete.")
else:
run_sge.run_dependency_graph(jobgraph, verbose=args.verbose,
logger=logger)
logger.info("Running jobs with SGE")
else:
# Import fragment lengths from JSON
if args.method == "ANIblastall":
with open(os.path.join(args.outdirname, 'fraglengths.json'),
'rU') as infile:
fraglengths = json.load(infile)
else:
fraglengths = None
logger.warning("Skipping BLASTN runs (as instructed)!")
# Process pairwise BLASTN output
logger.info("Processing pairwise %s BLAST output." % args.method)
try:
data = anib.process_blast(args.outdirname, org_lengths,
fraglengths=fraglengths, mode=args.method)
except ZeroDivisionError:
logger.error("One or more BLAST output files has a problem.")
if not args.skip_blastn:
if 0 < cumval:
logger.error("This is possibly due to BLASTN run failure, " +
"please investigate")
else:
logger.error("This is possibly due to a BLASTN comparison " +
"being too distant for use.")
logger.error(last_exception())
return data
def calculate_anim(infiles, org_lengths):
"""Returns ANIm result dataframes for files in input directory.
- infiles - paths to each input file
- org_lengths - dictionary of input sequence lengths, keyed by sequence
Finds ANI by the ANIm method, as described in Richter et al (2009)
Proc Natl Acad Sci USA 106: 19126-19131 doi:10.1073/pnas.0906412106.
All FASTA format files (selected by suffix) in the input directory
are compared against each other, pairwise, using NUCmer (which must
be in the path). NUCmer output is stored in the output directory.
The NUCmer .delta file output is parsed to obtain an alignment length
and similarity error count for every unique region alignment between
the two organisms, as represented by the sequences in the FASTA files.
These are processed to give matrices of aligned sequence lengths,
average nucleotide identity (ANI) percentages, coverage (aligned
percentage of whole genome), and similarity error cound for each pairwise
comparison.
"""
logger.info("Running ANIm")
logger.info("Generating NUCmer command-lines")
deltadir = os.path.join(args.outdirname, ALIGNDIR['ANIm'])
logger.info("Writing nucmer output to %s" % deltadir)
# Schedule NUCmer runs
if not args.skip_nucmer:
joblist = anim.generate_nucmer_jobs(infiles, args.outdirname,
nucmer_exe=args.nucmer_exe,
maxmatch=args.maxmatch,
jobprefix=args.jobprefix)
if args.scheduler == 'multiprocessing':
logger.info("Running jobs with multiprocessing")
if args.workers is None:
logger.info("(using maximum number of available " +
"worker threads)")
else:
logger.info("(using %d worker threads, if available)" %
args.workers)
cumval = run_mp.run_dependency_graph(joblist,
workers=args.workers,
verbose=args.verbose,
logger=logger)
logger.info("Cumulative return value: %d" % cumval)
if 0 < cumval:
logger.warning("At least one NUCmer comparison failed. " +
"ANIm may fail.")
else:
logger.info("All multiprocessing jobs complete.")
else:
logger.info("Running jobs with SGE")
logger.info("Jobarray group size set to %d" % args.sgegroupsize)
run_sge.run_dependency_graph(joblist, verbose=args.verbose,
logger=logger,
jgprefix=args.jobprefix,
sgegroupsize=args.sgegroupsize)
else:
logger.warning("Skipping NUCmer run (as instructed)!")
# Process resulting .delta files
logger.info("Processing NUCmer .delta files.")
data = anim.process_deltadir(deltadir, org_lengths, logger=logger)
if data[-1]: # zero percentage identity error
if not args.skip_nucmer and args.scheduler == 'multiprocessing':
if 0 < cumval:
logger.error("This has possibly been a NUCmer run failure, " +
"please investigate")
logger.error(last_exception())
sys.exit(1)
else:
logger.error("This is possibly due to a NUCmer comparison " +
"being too distant for use. Please consider " +
"using the --maxmatch option.")
logger.error("This is alternatively due to NUCmer run " +
"failure, analysis will continue, but please " +
"investigate.")
if not args.nocompress:
logger.info("Compressing/deleting %s" % deltadir)
compress_delete_outdir(deltadir)
# Return processed data from .delta files
return tuple(data[:-1])
