def setUpClass(cls):
super(EventDetectTests, cls).setUpClass()
cls.HOME = '/'.join(os.path.abspath(__file__).split("/")[:-4])
cls.dna_file = os.path.join(cls.HOME, "tests/minion_test_reads/canonical_ecoli_R9/miten_PC_20160820_FNFAD20259_MN17223_mux_scan_AMS_158_R9_WGA_Ecoli_08_20_16_83098_ch138_read23_strand.fast5")
cls.rna_file = os.path.join(cls.HOME,
"tests/minion_test_reads/RNA_edge_cases/DEAMERNANOPORE_20170922_FAH26525_MN16450_sequencing_run_MA_821_R94_NA12878_mRNA_09_22_17_67136_read_61_ch_151_strand.fast5")
dna_handle = Fast5(cls.dna_file, 'r+')
rna_handle = Fast5(cls.rna_file, 'r+')
cls.dna_handle = dna_handle.create_copy("test_dna.fast5")
cls.rna_handle = rna_handle.create_copy("test_rna.fast5")
def test_rna_reads(self):
with tempfile.TemporaryDirectory() as tempdir:
template_model = os.path.join(
self.HOME, "models/testModelR9p4_5mer_acgt_RNA.model")
args = create_signalAlignment_args(
alignment_file=self.rna_bam,
bwa_reference=self.rna_reference,
forward_reference=self.rna_reference,
in_templateHmm=template_model,
path_to_bin=self.path_to_bin,
destination=tempdir,
embed=True,
delete_tmp=False)
in_rna_file = os.path.join(
self.test_dir_rna,
"DEAMERNANOPORE_20170922_FAH26525_MN16450_sequencing_run_MA_821_R94_NA12878_mRNA_09_22_17_67136_read_36_ch_218_strand.fast5"
)
final_args = merge_dicts([args, dict(in_fast5=in_rna_file)])
handle = SignalAlignment(**final_args)
handle.run()
fh = pysam.FastaFile(self.rna_reference)
f5fh = Fast5(in_rna_file)
sa_events = f5fh.get_signalalign_events()
for i, event in enumerate(sa_events):
kmer = fh.fetch(reference="rna_fake",
start=event["reference_index"],
end=event["reference_index"] + 5)[::-1]
self.assertEqual(event["path_kmer"].decode(), kmer)
self.assertEqual(event["reference_kmer"].decode(), kmer)
in_rna_file = os.path.join(
self.test_dir_rna,
"DEAMERNANOPORE_20170922_FAH26525_MN16450_sequencing_run_MA_821_R94_NA12878_mRNA_09_22_17_67136_read_61_ch_151_strand.fast5"
)
final_args = merge_dicts([args, dict(in_fast5=in_rna_file)])
handle = SignalAlignment(**final_args)
handle.run()
rev_c = ReverseComplement()
f5fh = Fast5(in_rna_file)
sa_events = f5fh.get_signalalign_events()
for i, event in enumerate(sa_events):
kmer = fh.fetch(reference="rna_fake",
start=event["reference_index"],
end=event["reference_index"] + 5)[::-1]
rev_kmer = rev_c.reverse_complement(kmer)
self.assertEqual(event["path_kmer"].decode(), rev_kmer)
self.assertEqual(event["reference_kmer"].decode(), kmer)
def create_minknow_events_from_fast5(fast5_path,
window_lengths=(3, 6),
thresholds=(1.4, 9.0),
peak_height=0.2):
"""Create events with ('start', 'length', 'mean', 'stdv', 'model_state', 'move', 'p_model_state') fields from
fast5 file. The 'model_state', 'move' and 'p_model_state' are all empty
:param fast5_path: path to fast5 file
:param window_lengths: Length 2 list of window lengths across
raw data from which `t_stats` are derived
:param thresholds: Length 2 list of thresholds on t-statistics
:param peak_height: Absolute height a peak in signal must rise below
previous and following minima to be considered relevant
"""
assert os.path.isfile(fast5_path), "File does not exist: {}".format(
fast5_path)
f5fh = Fast5(fast5_path, read='r+')
signal = f5fh.get_read(raw=True, scale=True)
# read_id = bytes.decode(f5fh.raw_attributes['read_id'])
sampling_freq = f5fh.sample_rate
start_time = f5fh.raw_attributes['start_time']
#
event_table = create_minknow_event_table(signal,
sampling_freq,
start_time,
window_lengths=window_lengths,
thresholds=thresholds,
peak_height=peak_height)
return event_table, f5fh
def setUpClass(cls):
super(Fast5Test, cls).setUpClass()
cls.HOME = '/'.join(os.path.abspath(__file__).split("/")[:-4])
fast5_file = os.path.join(
cls.HOME,
"tests/minion_test_reads/canonical_ecoli_R9/miten_PC_20160820_FNFAD20259_MN17223_mux_scan_AMS_158_R9_WGA_Ecoli_08_20_16_83098_ch138_read23_strand.fast5"
)
fast5handle = Fast5(fast5_file, 'r+')
cls.fast5handle = fast5handle.create_copy("test.fast5")
def remove_sa_analyses(fast5):
"""Remove signalalign analyses from a fast5 file"""
assert os.path.exists(fast5), "Fast5 path does not exist".format(fast5)
fh = Fast5(fast5, read='r+')
counter = 0
for analyses in [x for x in list(fh["Analyses"].keys()) if "SignalAlign" in x]:
fh.delete(os.path.join("Analyses", analyses))
counter += 1
fh.close()
return counter
def run_alignment_comparison(self, src_file_path, dna=True):
# copy file to tmp directory
file_name = os.path.basename(src_file_path)
file_path = os.path.join(self.tmp_directory, file_name)
shutil.copy(src_file_path, file_path)
# pre-alignment work
with closing(Fast5(file_path, read='r+')) as fast5_handle:
nuc_sequence = fast5_handle.get_fastq(
analysis="Basecall_1D", section="template").split()[2]
dest = fast5_handle.get_analysis_events_path_new(
self.UNIT_TEST_NAME)
#todo verify we don't need this
# fast5_handle.ensure_path(dest)
# run kmeralign
model_file = self.dna_template_model_file if dna else self.rna_model_file
status = self.run_kmeralign_exe(file_path, nuc_sequence, model_file,
dest)
self.assertEqual(status, 0, "error aligning file {}".format(file_name))
with closing(Fast5(file_path, read='r')) as fast5_handle:
new_events = fast5_handle.get_custom_analysis_events(
self.UNIT_TEST_NAME)
if dna:
old_events = fast5_handle.get_custom_analysis_events(
fast5_handle.__default_basecall_1d_analysis__)
else:
old_events = fast5_handle.get_resegment_basecall()
# og_events = fast5_handle.get_custom_analysis_events(fast5_handle.__default_basecall_1d_analysis__)
print("\nComparing {} events from {}".format(
"DNA" if dna else "RNA", file_name))
start_diff_avg, mean_diff_avg, std_diff_avg = self.compare_event_alignment(
old_events, new_events)
self.assertLess(mean_diff_avg, 1.0,
"Aligned event means are too varied")
self.assertLess(std_diff_avg, 1.0,
"Aligned event stds are too varied")
self.assertLess(start_diff_avg, 0.001,
"Aligned event start times are too varied")
def open(self):
if self.is_open: return True
try:
self.fastFive = Fast5(self.filename, 'r+')
self.is_open = True
return True
except Exception as e:
self.close()
self.logError(
"[NanoporeRead:open] ERROR opening {filename}, {e}".format(
filename=self.filename, e=e))
return False
def test_embed_with_both(self):
signal_file_reads = os.path.join(self.HOME,
"tests/minion_test_reads/pUC/")
template_model = os.path.join(
self.HOME, "models/testModelR9_5mer_acegt_template.model")
complement_model = os.path.join(
self.HOME, "models/testModelR9_5mer_acegt_complement.model")
puc_reference = os.path.join(self.HOME,
"tests/test_sequences/pUC19_SspI.fa")
signal_file_guide_alignment = os.path.join(
self.HOME, "tests/minion_test_reads/pUC/puc.bam")
with tempfile.TemporaryDirectory() as tempdir:
new_dir = os.path.join(tempdir, "new_dir")
if os.path.exists(new_dir):
shutil.rmtree(new_dir)
working_folder = FolderHandler()
working_folder.open_folder(os.path.join(tempdir, "test_dir"))
shutil.copytree(signal_file_reads, new_dir)
args = create_signalAlignment_args(
alignment_file=signal_file_guide_alignment,
bwa_reference=puc_reference,
forward_reference=puc_reference,
in_templateHmm=template_model,
path_to_bin=self.path_to_bin,
destination=working_folder.path,
embed=True,
output_format="both",
filter_reads=0,
twoD_chemistry=True,
in_complementHmm=complement_model,
delete_tmp=True)
final_args = merge_dicts([
args,
dict(in_fast5=os.path.join(
new_dir,
"makeson_PC_20160807_FNFAD20242_MN17284_sequencing_run_MA_470_R9_pUC_g_PCR_BC_08_07_16_93165_ch1_read176_strand.fast5"
))
])
handle = SignalAlignment(**final_args)
handle.run()
f5fh = Fast5(
os.path.join(
new_dir,
"makeson_PC_20160807_FNFAD20242_MN17284_sequencing_run_MA_470_R9_pUC_g_PCR_BC_08_07_16_93165_ch1_read176_strand.fast5"
))
mea = f5fh.get_signalalign_events(mea=True)
sam = f5fh.get_signalalign_events(sam=True)
self.assertEqual(mea[0]["raw_start"], 2879)
self.assertEqual(sam[0], "0")
self.assertEqual(len(os.listdir(working_folder.path)), 2)
def setUpClass(cls):
super(BandedAlignmentTests, cls).setUpClass()
cls.HOME = '/'.join(os.path.abspath(__file__).split("/")[:-4])
cls.rna_model_file = os.path.join(
cls.HOME, "models/testModelR9p4_5mer_acgt_RNA.model")
cls.dna_template_model_file = os.path.join(
cls.HOME, "models/testModelR9p4_5mer_acegt_template.model")
cls.rna_model = HmmModel(model_file=cls.rna_model_file)
cls.dna_model = HmmModel(model_file=cls.dna_template_model_file)
cls.dna_fast5_path = os.path.join(
cls.HOME,
"tests/minion_test_reads/1D/LomanLabz_PC_20161025_FNFAB42699_MN17633_sequencing_run_20161025_E_coli_native_450bps_82361_ch112_read108_strand.fast5"
)
cls.dna_handle = Fast5(cls.dna_fast5_path)
def resegment_reads(fast5_path, params, speedy=False, overwrite=False):
"""Re-segment and create anchor alignment from previously base-called fast5 file
:param fast5_path: path to fast5 file
:param params: event detection parameters
:param speedy: boolean option for speedyStatSplit or minknow
:param overwrite: overwrite a previous event re-segmented event table
:param name: name of key where events table will be placed (Analyses/'name'/Events)
:return True when completed
"""
assert os.path.isfile(fast5_path), "File does not exist: {}".format(fast5_path)
name = "ReSegmentBasecall_00{}"
# create Fast5 object
f5fh = Fast5(fast5_path, read='r+')
# gather previous event detection
old_event_table = f5fh.get_basecall_data()
# assert check_event_table_time(old_event_table), "Old event is not consistent"
read_id = bytes.decode(f5fh.raw_attributes['read_id'])
sampling_freq = f5fh.sample_rate
start_time = f5fh.raw_attributes['start_time']
# pick event detection algorithm
signal = f5fh.get_read(raw=True, scale=True)
if speedy:
event_table = create_speedy_event_table(signal, sampling_freq, start_time, **params)
params = merge_dicts([params, {"event_detection": "speedy_stat_split"}])
else:
event_table = create_minknow_event_table(signal, sampling_freq, start_time, **params)
params = merge_dicts([params, {"event_detection": "minknow_event_detect"}])
keys = ["nanotensor version", "time_stamp"]
values = ["0.2.0", TimeStamp().posix_date()]
attributes = merge_dicts([params, dict(zip(keys, values)), f5fh.raw_attributes])
if f5fh.is_read_rna():
old_event_table = index_to_time(old_event_table, sampling_freq=sampling_freq, start_time=start_time)
# set event table
new_event_table = create_anchor_kmers(new_events=event_table, old_events=old_event_table)
f5fh.set_new_event_table(name, new_event_table, attributes, overwrite=overwrite)
# gather new sequence
sequence = sequence_from_events(new_event_table)
if f5fh.is_read_rna():
sequence = ReverseComplement().reverse(sequence)
sequence = sequence.replace("T", "U")
quality_scores = '!'*len(sequence)
fastq = create_fastq_line(read_id+" :", sequence, quality_scores)
# set fastq
f5fh.set_fastq(name, fastq)
return f5fh
def embed_eventalign_events(fast5_dir, reference, output_dir, threads=1, overwrite=False):
"""Call eventalign and embed events"""
event_generator = get_eventalign_events(fast5_dir,
reference,
output_dir,
threads=threads,
overwrite=overwrite)
attributes = None
for template, complement, fast5path in event_generator:
print(fast5path)
print("template", template)
if template or complement:
handle = Fast5(fast5path, read='r+')
handle.set_eventalign_table(template=template, complement=complement, meta=attributes, overwrite=True)
else:
print("{} did not align".format(fast5path))
return True
def mea_alignment_from_signal_align(fast5_path, events=None):
"""Get the maximum expected alignment from a nanopore read fast5 file which has signalalign data
:param fast5_path: path to fast5 file
:param events: directly pass events in via a numpy array
"""
if events is None:
assert os.path.isfile(fast5_path)
fileh = Fast5(fast5_path)
events = fileh.get_signalalign_events()
posterior_matrix, shortest_ref_per_event, event_matrix = get_mea_params_from_events(
events)
# get mea alignment
mea_alignments = maximum_expected_accuracy_alignment(
posterior_matrix, shortest_ref_per_event)
# get raw index values from alignment data structure
best_path = get_indexes_from_best_path(mea_alignments)
# corrected_path = fix_path_indexes(best_path)
final_event_table = get_events_from_path(event_matrix, best_path)
return final_event_table
def generate_events_and_alignment(
fast5_path,
nucleotide_sequence,
nucleotide_qualities=None,
event_detection_params=None,
event_detection_strategy=None,
save_to_fast5=True,
overwrite=False,
analysis_identifier=Fast5.__default_basecall_1d_analysis__,
):
assert os.path.isfile(fast5_path), "File does not exist: {}".format(
fast5_path)
# create Fast5 object
f5fh = Fast5(fast5_path, read='r+')
read_id = bytes.decode(f5fh.raw_attributes['read_id'])
sampling_freq = f5fh.sample_rate
start_time = f5fh.raw_attributes['start_time']
success = False
# event detection prep
if event_detection_strategy is None:
event_detection_strategy = EVENT_DETECT_MINKNOW
if event_detection_params is None:
event_detection_params = get_default_event_detection_params(
event_detection_strategy)
# detect events
if event_detection_strategy == EVENT_DETECT_SPEEDY:
signal = f5fh.get_read(raw=True, scale=True)
event_table = create_speedy_event_table(signal, sampling_freq,
start_time,
**event_detection_params)
event_detection_params = merge_dicts(
[event_detection_params, {
"event_detection": "speedy_stat_split"
}])
elif event_detection_strategy == EVENT_DETECT_MINKNOW:
signal = f5fh.get_read(raw=True, scale=True)
event_table = create_minknow_event_table(signal, sampling_freq,
start_time,
**event_detection_params)
event_detection_params = merge_dicts([
event_detection_params, {
"event_detection": "minknow_event_detect"
}
])
elif event_detection_strategy == EVENT_DETECT_SCRAPPIE:
event_table = create_scrappie_event_table(fast5_path, sampling_freq)
event_detection_params = merge_dicts([
event_detection_params, {
"event_detection": "scrappie_event_detect"
}
])
else:
raise Exception(
"PROGRAMMER ERROR: unknown resegment strat {}: expected {}".format(
event_detection_strategy, [
EVENT_DETECT_SPEEDY, EVENT_DETECT_MINKNOW,
EVENT_DETECT_SCRAPPIE
]))
# gather attributes
keys = ["nanotensor version", "time_stamp"]
values = ["0.2.0", TimeStamp().posix_date()]
attributes = merge_dicts(
[event_detection_params,
dict(zip(keys, values)), f5fh.raw_attributes])
# do the alignment
# todo do_alignment(events, nucleotide_sequence)
# success = evaluate_success()
# save to fast5 (if appropriate)
saved_location = None
if save_to_fast5:
fastq = create_fastq_line(
read_id, nucleotide_sequence,
"*" if nucleotide_qualities is None else nucleotide_qualities)
saved_location = save_event_table_and_fastq(
f5fh,
event_table,
fastq,
attributes=attributes,
overwrite=overwrite,
analysis_identifier=analysis_identifier)
# close
f5fh.close()
return success, event_table, saved_location
def resegment_reads(fast5_path,
params=None,
speedy=False,
overwrite=True,
analysis_path="ReSegmentBasecall_000"):
"""Re-segment and create anchor alignment from previously base-called fast5 file
:param fast5_path: path to fast5 file
:param params: event detection parameters
:param speedy: boolean option for speedyStatSplit or minknow
:param overwrite: overwrite a previous event re-segmented event table
:param analysis_path: name of key where events table will be placed (Analyses/'name'/Events)
:return True when completed
"""
assert os.path.isfile(fast5_path), "File does not exist: {}".format(
fast5_path)
# create Fast5 object and sanity check
f5fh = Fast5(fast5_path, read='r+')
if not f5fh.has_basecall_data():
f5fh.close()
return None
# gather previous event detection
old_event_table = f5fh.get_basecall_data()
read_id = bytes.decode(f5fh.raw_attributes['read_id'])
sampling_freq = f5fh.sample_rate
start_time = f5fh.raw_attributes['start_time']
# get params
if params is None:
params = get_default_event_detection_params(
EVENT_DETECT_SPEEDY if speedy else EVENT_DETECT_MINKNOW)
# pick event detection algorithm
signal = f5fh.get_read(raw=True, scale=True)
if speedy:
event_table = create_speedy_event_table(signal, sampling_freq,
start_time, **params)
params = merge_dicts(
[params, {
"event_detection": "speedy_stat_split"
}])
else:
event_table = create_minknow_event_table(signal, sampling_freq,
start_time, **params)
params = merge_dicts(
[params, {
"event_detection": "minknow_event_detect"
}])
# metadata
keys = ["nanotensor version", "time_stamp"]
values = ["0.2.0", TimeStamp().posix_date()]
attributes = merge_dicts(
[params, dict(zip(keys, values)), f5fh.raw_attributes])
# do resegmentation
if f5fh.is_read_rna():
old_event_table = index_to_time(old_event_table,
sampling_freq=sampling_freq,
start_time=start_time)
new_event_table = create_anchor_kmers(new_events=event_table,
old_events=old_event_table)
# get destination in fast5
#todo find latest location? ie: save_event_table_and_fastq(..)
destination = f5fh._join_path(f5fh.__base_analysis__, analysis_path)
f5fh.set_event_table(destination,
new_event_table,
attributes,
overwrite=overwrite)
# gather new sequence
sequence = sequence_from_events(new_event_table)
if f5fh.is_read_rna():
sequence = ReverseComplement().reverse(sequence)
sequence = sequence.replace("T", "U")
quality_scores = '!' * len(sequence)
fastq = create_fastq_line(read_id + " :", sequence, quality_scores)
# set fastq
f5fh.set_fastq(destination, fastq, overwrite=overwrite)
return f5fh
def test_embed(self):
signal_file_reads = os.path.join(
self.HOME, "tests/minion_test_reads/no_event_data_1D_ecoli")
template_model = os.path.join(
self.HOME, "models/testModelR9p4_5mer_acegt_template.model")
ecoli_reference = os.path.join(
self.HOME, "tests/test_sequences/E.coli_K12.fasta")
signal_file_guide_alignment = os.path.join(
self.HOME, "tests/minion_test_reads/oneD_alignments.sam")
with tempfile.TemporaryDirectory() as tempdir:
new_dir = os.path.join(tempdir, "new_dir")
working_folder = FolderHandler()
working_folder.open_folder(os.path.join(tempdir, "test_dir"))
shutil.copytree(signal_file_reads, new_dir)
args = create_signalAlignment_args(
alignment_file=signal_file_guide_alignment,
bwa_reference=ecoli_reference,
forward_reference=ecoli_reference,
in_templateHmm=template_model,
path_to_bin=self.path_to_bin,
destination=working_folder.path,
embed=True)
final_args = merge_dicts([
args,
dict(in_fast5=os.path.join(
new_dir,
"LomanLabz_PC_20161025_FNFAB42699_MN17633_sequencing_run_20161025_E_coli_native_450bps_82361_ch6_read347_strand.fast5"
))
])
handle = SignalAlignment(**final_args)
handle.run()
f5fh = Fast5(
os.path.join(
new_dir,
"LomanLabz_PC_20161025_FNFAB42699_MN17633_sequencing_run_20161025_E_coli_native_450bps_82361_ch6_read347_strand.fast5"
))
mea = f5fh.get_signalalign_events(mea=True)
sam = f5fh.get_signalalign_events(sam=True)
self.assertEqual(mea[0]["raw_start"], 153)
self.assertEqual(sam[0], "9")
self.assertEqual(len(os.listdir(working_folder.path)), 1)
self.assertEqual(
sorted(os.listdir(working_folder.path))[0],
"9e4d14b1-8167-44ef-9fdb-5c29dd0763fd.sm.backward.tsv")
# DNA WITH events
signal_file_reads = os.path.join(self.HOME,
"tests/minion_test_reads/1D")
template_model = os.path.join(
self.HOME, "models/testModelR9p4_5mer_acegt_template.model")
ecoli_reference = os.path.join(
self.HOME, "tests/test_sequences/E.coli_K12.fasta")
signal_file_guide_alignment = os.path.join(
self.HOME, "tests/minion_test_reads/oneD_alignments.sam")
with tempfile.TemporaryDirectory() as tempdir:
new_dir = os.path.join(tempdir, "new_dir")
working_folder = FolderHandler()
working_folder.open_folder(os.path.join(tempdir, "test_dir"))
shutil.copytree(signal_file_reads, new_dir)
args = create_signalAlignment_args(
alignment_file=signal_file_guide_alignment,
bwa_reference=ecoli_reference,
forward_reference=ecoli_reference,
in_templateHmm=template_model,
path_to_bin=self.path_to_bin,
destination=working_folder.path,
embed=True)
final_args = merge_dicts([
args,
dict(in_fast5=os.path.join(
new_dir,
"LomanLabz_PC_20161025_FNFAB42699_MN17633_sequencing_run_20161025_E_coli_native_450bps_82361_ch6_read347_strand.fast5"
))
])
handle = SignalAlignment(**final_args)
handle.run()
f5fh = Fast5(
os.path.join(
new_dir,
"LomanLabz_PC_20161025_FNFAB42699_MN17633_sequencing_run_20161025_E_coli_native_450bps_82361_ch6_read347_strand.fast5"
))
mea = f5fh.get_signalalign_events(mea=True)
sam = f5fh.get_signalalign_events(sam=True)
self.assertEqual(mea[0]["raw_start"], 153)
self.assertEqual(sam[0], "9")
self.assertEqual(len(os.listdir(working_folder.path)), 1)
self.assertEqual(
sorted(os.listdir(working_folder.path))[0],
"9e4d14b1-8167-44ef-9fdb-5c29dd0763fd.sm.backward.tsv")
