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"""
Train Class1 pan-allele models.
"""
import argparse
import os
import signal
import sys
import time
import traceback
import random
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from functools import partial
import numpy
import pandas
import yaml
from sklearn.metrics.pairwise import cosine_similarity
from sklearn.model_selection import StratifiedKFold
from mhcnames import normalize_allele_name
import tqdm # progress bar
tqdm.monitor_interval = 0 # see https://github.com/tqdm/tqdm/issues/481
from .class1_affinity_predictor import Class1AffinityPredictor
from .class1_neural_network import Class1NeuralNetwork
from .common import configure_logging, set_keras_backend
from .parallelism import (
add_worker_pool_args,
worker_pool_with_gpu_assignments_from_args,
call_wrapped_kwargs)
from .hyperparameters import HyperparameterDefaults
from .allele_encoding import AlleleEncoding
from .encodable_sequences import EncodableSequences
from .regression_target import to_ic50, from_ic50
# To avoid pickling large matrices to send to child processes when running in
# parallel, we use this global variable as a place to store data. Data that is
# stored here before creating the thread pool will be inherited to the child
# processes upon fork() call, allowing us to share large data with the workers
# via shared memory.
GLOBAL_DATA = {}
# Note on parallelization:
# It seems essential currently (tensorflow==1.4.1) that no processes are forked
# after tensorflow has been used at all, which includes merely importing
# keras.backend. So we must make sure not to use tensorflow in the main process
# if we are running in parallel.
parser = argparse.ArgumentParser(usage=__doc__)
parser.add_argument(
"--data",
metavar="FILE.csv",
required=True,
help=(
"Training data CSV. Expected columns: "
"allele, peptide, measurement_value"))
parser.add_argument(
"--pretrain-data",
metavar="FILE.csv",
help=(
"Pre-training data CSV. Expected columns: "
"allele, peptide, measurement_value"))
parser.add_argument(
"--out-models-dir",
metavar="DIR",
required=True,
help="Directory to write models and manifest")
parser.add_argument(
"--hyperparameters",
metavar="FILE.json",
required=True,
help="JSON or YAML of hyperparameters")
parser.add_argument(
"--held-out-measurements-per-allele-fraction-and-max",
type=float,
metavar="X",
nargs=2,
default=[0.25, 100],
help="Fraction of measurements per allele to hold out, and maximum number")
parser.add_argument(
"--ignore-inequalities",
action="store_true",
default=False,
help="Do not use affinity value inequalities even when present in data")
parser.add_argument(
"--ensemble-size",
type=int,
metavar="N",
required=True,
help="Ensemble size, i.e. how many models to retain the final predictor. "
"In the current implementation, this is also the number of training folds.")
parser.add_argument(
"--num-replicates",
type=int,
metavar="N",
default=1,
help="Number of replicates per (architecture, fold) pair to train.")
parser.add_argument(
"--max-epochs",
type=int,
metavar="N",
help="Max training epochs. If specified here it overrides any 'max_epochs' "
"specified in the hyperparameters.")
parser.add_argument(
"--allele-sequences",
metavar="FILE.csv",
help="Allele sequences file.")
parser.add_argument(
"--save-interval",
type=float,
metavar="N",
default=60,
help="Write models to disk every N seconds. Only affects parallel runs; "
"serial runs write each model to disk as it is trained.")
parser.add_argument(
"--verbosity",
type=int,
help="Keras verbosity. Default: %(default)s",
default=0)
add_worker_pool_args(parser)
def assign_folds(df, num_folds, held_out_fraction, held_out_max):
result_df = pandas.DataFrame(index=df.index)
for fold in range(num_folds):
result_df["fold_%d" % fold] = True
for (allele, sub_df) in df.groupby("allele"):
medians = sub_df.groupby("peptide").measurement_value.median()
low_peptides = medians[medians < medians.median()].index.values
high_peptides = medians[medians >= medians.median()].index.values
held_out_count = int(
min(len(medians) * held_out_fraction, held_out_max))
held_out_low_count = min(
len(low_peptides),
int(held_out_count / 2))
held_out_high_count = min(
len(high_peptides),
held_out_count - held_out_low_count)
held_out_low = pandas.Series(low_peptides).sample(n=held_out_low_count)
held_out_high = pandas.Series(high_peptides).sample(n=held_out_high_count)
held_out_peptides = set(held_out_low).union(set(held_out_high))
result_df.loc[
sub_df.index[sub_df.peptide.isin(held_out_peptides)],
"fold_%d" % fold
] = False
print("Training points per fold")
print(result_df.sum())
print("Test points per fold")
print((~result_df).sum())
return result_df
def pretrain_data_iterator(
filename,
master_allele_encoding,
peptides_per_chunk=1024):
empty = pandas.read_csv(filename, index_col=0, nrows=0)
usable_alleles = [
c for c in empty.columns
if c in master_allele_encoding.allele_to_sequence
]
print("Using %d / %d alleles" % (len(usable_alleles), len(empty.columns)))
print("Skipped alleles: ", [
c for c in empty.columns
if c not in master_allele_encoding.allele_to_sequence
])
allele_encoding = AlleleEncoding(
numpy.tile(usable_alleles, peptides_per_chunk),
borrow_from=master_allele_encoding)
synthetic_iter = pandas.read_csv(
filename, index_col=0, chunksize=peptides_per_chunk)
for (k, df) in enumerate(synthetic_iter):
if len(df) != peptides_per_chunk:
continue
df = df[usable_alleles]
encodable_peptides = EncodableSequences(
numpy.repeat(
df.index.values,
len(usable_alleles)))
yield (allele_encoding, encodable_peptides, df.stack().values)
def run(argv=sys.argv[1:]):
global GLOBAL_DATA
# On sigusr1 print stack trace
print("To show stack trace, run:\nkill -s USR1 %d" % os.getpid())
signal.signal(signal.SIGUSR1, lambda sig, frame: traceback.print_stack())
args = parser.parse_args(argv)
args.out_models_dir = os.path.abspath(args.out_models_dir)
configure_logging(verbose=args.verbosity > 1)
hyperparameters_lst = yaml.load(open(args.hyperparameters))
assert isinstance(hyperparameters_lst, list)
print("Loaded hyperparameters list:")
pprint.pprint(hyperparameters_lst)
allele_sequences = pandas.read_csv(
args.allele_sequences, index_col=0).sequence
df = pandas.read_csv(args.data)
print("Loaded training data: %s" % (str(df.shape)))
df = df.loc[
(df.peptide.str.len() >= 8) & (df.peptide.str.len() <= 15)
]
print("Subselected to 8-15mers: %s" % (str(df.shape)))
df = df.loc[~df.measurement_value.isnull()]
print("Dropped NaNs: %s" % (str(df.shape)))
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df = df.loc[df.allele.isin(allele_sequences.index)]
print("Subselected to alleles with sequences: %s" % (str(df.shape)))
if args.ignore_inequalities and "measurement_inequality" in df.columns:
print("Dropping measurement_inequality column")
del df["measurement_inequality"]
# Allele names in data are assumed to be already normalized.
print("Training data: %s" % (str(df.shape)))
(held_out_fraction, held_out_max) = (
args.held_out_measurements_per_allele_fraction_and_max)
folds_df = assign_folds(
df=df,
num_folds=args.ensemble_size,
held_out_fraction=held_out_fraction,
held_out_max=held_out_max)
allele_encoding = AlleleEncoding(
alleles=allele_sequences.index.values,
allele_to_sequence=allele_sequences.to_dict())
GLOBAL_DATA["train_data"] = df
GLOBAL_DATA["folds_df"] = folds_df
GLOBAL_DATA["allele_encoding"] = allele_encoding
GLOBAL_DATA["args"] = args
if not os.path.exists(args.out_models_dir):
print("Attempting to create directory: %s" % args.out_models_dir)
os.mkdir(args.out_models_dir)
print("Done.")
predictor = Class1AffinityPredictor(
metadata_dataframes={
'train_data': df,
'training_folds': folds_df,
})
serial_run = args.num_jobs == 1
work_items = []
for (h, hyperparameters) in enumerate(hyperparameters_lst):
if 'n_models' in hyperparameters:
raise ValueError("n_models is unsupported")
if args.max_epochs:
hyperparameters['max_epochs'] = args.max_epochs
for fold in range(args.ensemble_size):
for replicate in range(args.num_replicates):
work_dict = {
'architecture_num': h,
'num_architectures': len(hyperparameters_lst),
'fold_num': fold,
'num_folds': args.ensemble_size,
'replicate_num': replicate,
'num_replicates': args.num_replicates,
'hyperparameters': hyperparameters,
'pretrain_data_filename': args.pretrain_data,
'verbose': args.verbosity,
'progress_print_interval': None if not serial_run else 5.0,
'predictor': predictor if serial_run else None,
'save_to': args.out_models_dir if serial_run else None,
}
work_items.append(work_dict)
start = time.time()
worker_pool = worker_pool_with_gpu_assignments_from_args(args)
if worker_pool:
print("Processing %d work items in parallel." % len(work_items))
# The estimated time to completion is more accurate if we randomize
# the order of the work.
random.shuffle(work_items)
results_generator = worker_pool.imap_unordered(
partial(call_wrapped_kwargs, train_model),
work_items,
chunksize=1)
unsaved_predictors = []
last_save_time = time.time()
for new_predictor in tqdm.tqdm(results_generator, total=len(work_items)):
unsaved_predictors.append(new_predictor)
if time.time() > last_save_time + args.save_interval:
# Save current predictor.
save_start = time.time()
new_model_names = predictor.merge_in_place(unsaved_predictors)
predictor.save(
args.out_models_dir,
model_names_to_write=new_model_names,
write_metadata=False)
print(
"Saved predictor (%d models total) including %d new models "
"in %0.2f sec to %s" % (
len(predictor.neural_networks),
len(new_model_names),
time.time() - save_start,
args.out_models_dir))
unsaved_predictors = []
last_save_time = time.time()
predictor.merge_in_place(unsaved_predictors)
else:
# Run in serial. In this case, every worker is passed the same predictor,
# which it adds models to, so no merging is required. It also saves
# as it goes so no saving is required at the end.
for _ in tqdm.trange(len(work_items)):
item = work_items.pop(0) # want to keep freeing up memory
work_predictor = train_model(**item)
assert work_predictor is predictor
assert not work_items
print("Saving final predictor to: %s" % args.out_models_dir)
predictor.save(args.out_models_dir) # write all models just to be sure
print("Done.")
print("*" * 30)
training_time = time.time() - start
print("Trained affinity predictor with %d networks in %0.2f min." % (
len(predictor.neural_networks), training_time / 60.0))
print("*" * 30)
if worker_pool:
worker_pool.close()
worker_pool.join()
print("Predictor written to: %s" % args.out_models_dir)
def train_model(
architecture_num,
num_architectures,
fold_num,
num_folds,
replicate_num,
num_replicates,
hyperparameters,
pretrain_data_filename,
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verbose=None,
progress_print_interval=None,
predictor=None,
save_to=None):
if predictor is None:
predictor = Class1AffinityPredictor()
df = GLOBAL_DATA["train_data"]
folds_df = GLOBAL_DATA["folds_df"]
allele_encoding = GLOBAL_DATA["allele_encoding"]
args = GLOBAL_DATA["args"]
numpy.testing.assert_equal(len(df), len(folds_df))
train_data = df.loc[
folds_df["fold_%d" % fold_num]
].sample(frac=1.0)
train_peptides = EncodableSequences(train_data.peptide.values)
train_alleles = AlleleEncoding(
train_data.allele.values, borrow_from=allele_encoding)
train_target = from_ic50(train_data.measurement_value)
model = Class1NeuralNetwork(**hyperparameters)
progress_preamble = (
"[%2d / %2d folds] "
"[%2d / %2d architectures] "
"[%4d / %4d replicates] " % (
fold_num + 1,
num_folds,
architecture_num + 1,
num_architectures,
replicate_num + 1,
num_replicates))
if pretrain_data_filename:
iterator = pretrain_data_iterator(pretrain_data_filename, allele_encoding)
original_hyperparameters = dict(model.hyperparameters)
model.hyperparameters['minibatch_size'] = len(next(iterator)[-1])
model.hyperparameters['max_epochs'] = 1
model.hyperparameters['validation_split'] = 0.0
model.hyperparameters['random_negative_rate'] = 0.0
model.hyperparameters['random_negative_constant'] = 0
scores = []
best_score = float('inf')
best_score_epoch = 0
for (epoch, (alleles, peptides, affinities)) in enumerate(iterator):
# Fit one epoch.
start = time.time()
model.fit(
peptides=peptides,
affinities=affinities,
allele_encoding=alleles)
fit_time = time.time() - start
start = time.time()
predictions = model.predict(
train_peptides,
allele_encoding=train_alleles)
assert len(predictions) == len(train_data)
print("Prediction histogram:")
print(
pandas.Series(
dict([k, v] for (v, k) in zip(*numpy.histogram(predictions)))))
for (inequality, func) in [(">", numpy.minimum), ("<", numpy.maximum)]:
mask = train_data.measurement_inequality == inequality
predictions[mask.values] = func(
predictions[mask.values],
train_data.loc[mask].measurement_value.values)
score = numpy.mean((from_ic50(predictions) - train_target)**2)
score_time = time.time() - start
print(
progress_preamble,
"PRETRAIN epoch %d [%d values, %0.2f sec]. "
"Score [%0.2f sec.]: %f" % (
epoch, len(affinities), fit_time, score_time, score))
scores.append(score)
if score < best_score:
print("New best score", score)
best_score = score
best_score_epoch = epoch
if epoch - best_score_epoch > pretrain_patience:
print("Stopping pretraining")
break
model.hyperparameters = original_hyperparameters
if model.hyperparameters['learning_rate']:
model.hyperparameters['learning_rate'] /= 10
else:
model.hyperparameters['learning_rate'] = 0.0001
model.fit(
train_peptides,
train_data.measurement_value,
inequalities=(
train_data.measurement_inequality.values
if "measurement_inequality" in train_data.columns else None),
progress_preamble=progress_preamble,
progress_print_interval=progress_print_interval,
verbose=verbose)
predictor.class1_pan_allele_models.append(model)
predictor.clear_cache()
return predictor
if __name__ == '__main__':
run()