def print_progress(self):
""" Print a progress bar representing the current state of the tasks.
"""
tasks_number = len(self.tasks_status)
done = sum(map(lambda x: x == 2, self.tasks_status))
working = sum(map(lambda x: x == 1, self.tasks_status))
utils.print_progress(self.print_control, tasks_number, done, working)
def import_shapefile_to_db(filepath):
connection = psycopg2.connect(host=DB_HOSTNAME, database="census_uk", user="******", password="******")
cursor = connection.cursor(cursor_factory=psycopg2.extras.DictCursor)
count = 0
shp = fiona.open(filepath)
nb_tracts = len(shp)
for feature in shp:
type = feature['type']
id = feature['id']
geom = shape(feature['geometry'])
if geom.geom_type == "Polygon":
geom = MultiPolygon([geom])
prop = feature['properties']
geo_code = prop['geo_code']
label = prop['label']
query_string = """INSERT INTO tracts
(geo_code, geom)
VALUES (%s, ST_GeomFromText(%s, %s))
ON CONFLICT DO NOTHING;"""
data = (geo_code, geom.wkt, EPSG)
cursor.execute(query_string, data)
count += 1
if count % 100 == 0:
utils.print_progress("Done: %.2f" % (100.0 * count / nb_tracts))
# if count == 10:
# break
connection.commit()
def calc_rama(grof, xtcf, btime, etime):
u = Universe(grof, xtcf)
resname_query = 'resname GLY or resname VAL or resname PRO'
atoms = u.selectAtoms(resname_query)
resname = atoms.resnames()[0] # [0] because .resnames() returns a list of one element
resid = atoms.resids()[0] # [0] because .resnames() returns a list of one element
phi_query = ('(resname ACE and name C) or '
'(resname GLY or resname VAL or resname PRO and '
'(name N or name CA or name C))')
psi_query = ('(resname GLY or resname VAL or resname PRO and (name N or name CA or name C or name NT)) or '
'(resname NH2 and name N)')
# MDAnalysis will convert the unit of length to angstrom, though in Gromacs the unit is nm
phi = u.selectAtoms(phi_query)
psi = u.selectAtoms(psi_query)
for _ in phi.atoms:
print _
for _ in psi.atoms:
print _
for ts in u.trajectory:
if btime > ts.time:
continue
if etime > 0 and etime < ts.time:
break
yield '{0:.3f} {1:.3f} {2}-{3}\n'.format(
phi.dihedral(), psi.dihedral(), resname, resid)
U.print_progress(ts)
def __gen_hist__(plot_details,verbose=False):
'''
generate single histogram
only runs on samples with an input file defined,
ie. does not loop through daughters
not really designed to be called by analysers
'''
log.debug( 'in get_hist for %s' % plot_details.sample.name )
## add the details from the sample
#plot_details += plot_details.sample.plot_details
s = plot_details.sample
vd = plot_details.var_details
sel = plot_details.get_selector()
weights = plot_details.get_weights()
target_lumi = plot_details.target_lumi
if not s.is_active():
log.warn('failed to gen hist %s for sample: %s' % (vd.name,s.name) )
return None
## create hist
h = plot_details.new_hist(s)
h.samples = s
## initialise sample
s.initialise()
## return empty hist if no events
if not s.tree.GetEntries(): return h
s.switch_on_branches()
## selection
event_list = sel.select(s) if sel else None
## initialise variables
s.prepare( plot_details )
## process events
entries = event_list.GetN() if sel else s.tree.GetEntries()
for i in xrange(entries):
ientry = event_list.GetEntry(i) if sel else i
s.tree.GetEntry(ientry)
## calculate event weight
weight = weights.weight() if weights else 1.
## fill hists
val = vd.var.calc_vals()[0]
h.Fill(val,weight)
frac = float(i)/float(entries) if entries else 0.0
if verbose: utils.print_progress(frac,title = '%s: '%s.name)
if verbose: utils.clear_progress()
#s.style_hist(h)
if target_lumi: s.scale_hist(h,target_lumi)
return h
def extend_balancing_classes(X, y, aug_intensity=0.5, counts=None):
num_classes = 43
_, class_counts = np.unique(y, return_counts=True)
max_c = max(class_counts)
total = max_c * num_classes if counts is None else np.sum(counts)
X_extended = np.empty([0, X.shape[1], X.shape[2], X.shape[3]],
dtype=X.dtype)
y_extended = np.empty([0], dtype=y.dtype)
print("Extending dataset using augmented data (intensity = {})".format(
aug_intensity))
for c, c_count in zip(range(num_classes), class_counts):
max_c = max_c if counts is None else counts[c]
X_source = (X[y == c] / 255.).astype(np.float32)
y_source = y[y == c]
X_extended = np.append(X_extended, X_source, axis=0)
for i in range((max_c // c_count) - 1):
batch_iterator = AugmentedSignsBatchIterator(
batch_size=X_source.shape[0], p=1.0, intensity=aug_intensity)
for x_batch, _ in batch_iterator(X_source, y_source):
X_extended = np.append(X_extended, x_batch, axis=0)
utils.print_progress(X_extended.shape[0], total)
batch_iterator = AugmentedSignsBatchIterator(batch_size=max_c %
c_count,
p=1.0,
intensity=aug_intensity)
for x_batch, _ in batch_iterator(X_source, y_source):
X_extended = np.append(X_extended, x_batch, axis=0)
utils.print_progress(X_extended.shape[0], total)
break
added = X_extended.shape[0] - y_extended.shape[0]
y_extended = np.append(y_extended, np.full((added), c, dtype=int))
return ((X_extended * 255.).astype(np.uint8), y_extended)
def load_features(feature_store, is_blind):
def _make_id(scanId, viewpointId):
return scanId + '_' + viewpointId
# if the tsv file for image features is provided
if feature_store:
tsv_fieldnames = ['scanId', 'viewpointId', 'image_w', 'image_h', 'vfov', 'features']
features = {}
with open(feature_store, "r") as tsv_in_file:
print('Reading image features file %s' % feature_store)
reader = list(csv.DictReader(tsv_in_file, delimiter='\t', fieldnames=tsv_fieldnames))
total_length = len(reader)
print('Loading image features ..')
for i, item in enumerate(reader):
image_h = int(item['image_h'])
image_w = int(item['image_w'])
vfov = int(item['vfov'])
long_id = _make_id(item['scanId'], item['viewpointId'])
features[long_id] = np.frombuffer(base64.b64decode(item['features']),
dtype=np.float32).reshape((36, 2048))
if is_blind:
features[long_id] = np.random.rand(36, 2048)
print_progress(i + 1, total_length, prefix='Progress:',
suffix='Complete', bar_length=50)
else:
print('Image features not provided')
features = None
image_w = 640
image_h = 480
vfov = 60
return features, (image_w, image_h, vfov)
def image_curation(num_threads=24):
subsets = ['train', 'val']
for subset in subsets:
subdir = join(base_path, subset)
with open(join(base_path, subset, 'list.txt')) as f:
videos = f.readlines()
if debug:
videos = videos[:20]
n_videos = len(videos)
"""
for video in videos:
crop_video(subdir, subset, video.replace("\n", ""))
"""
with futures.ProcessPoolExecutor(max_workers=num_threads) as executor:
fs = [
executor.submit(crop_video, subdir, subset,
video.replace("\n", "")) for video in videos
]
for i, f in enumerate(futures.as_completed(fs)):
utils.print_progress(i,
n_videos,
prefix=subset,
suffix='Done ',
barLength=40)
def count_interactions(A):
logger.debug('loading {0}'.format(A.grof))
univ = Universe(A.grof)
logger.debug('loaded {0}'.format(A.grof))
pro_atoms = univ.selectAtoms(
'protein and not resname ACE and not resname NH2')
pl = pro_atoms.residues.numberOfResidues()
# +1: for missing resname ACE, such that it's easier to proceed in the next
# step
logger.debug('loading {0}, {1}'.format(A.grof, A.xtcf))
u = Universe(A.grof, A.xtcf)
logger.debug('loaded {0}, {1}'.format(A.grof, A.xtcf))
# Just for reference to the content of query when then code was first
# written and used
# query = ('(resname PRO and (name CB or name CG or name CD)) or'
# '(resname VAL and (name CG1 or name CG2)) or'
# '(resname GLY and name CA) or'
# '(resname ALA and name CB)')
query = A.query
atoms = u.selectAtoms(query)
logger.info('Number of atoms selected: {0}'.format(atoms.numberOfAtoms()))
# MDAnalysis will convert the unit of length to angstrom, though in Gromacs
# the unit is nm
cutoff = A.cutoff * 10
nres_away = A.nres_away
btime = A.btime
etime = A.etime
nframe = 0
unun_map = None
for ts in u.trajectory:
if btime > ts.time:
continue
if etime > 0 and etime < ts.time:
break
nframe += 1
map_ = np.zeros((pl + 1, pl + 1)) # map for a single frame
for i, ai in enumerate(atoms):
ai_resid = ai.resid
for j, aj in enumerate(atoms):
aj_resid = aj.resid
# to avoid counting the same pair twices,
# the 2 resid cannot be neigbors
if i < j and aj_resid - ai_resid >= nres_away:
d = np.linalg.norm(ai.pos - aj.pos)
if d <= cutoff:
# -1: resid in MDAnalysis starts from 1
map_[ai_resid - 1][aj_resid - 1] += 1
if unun_map is None:
unun_map = map_
else:
unun_map = unun_map + map_
utils.print_progress(ts)
sys.stdout.write("\n")
return unun_map / float(nframe)
def image_curation(num_threads=24):
subsets = os.listdir(train_base_path)
for subset in subsets:
subdir = join(train_base_path, subset)
videos = os.listdir(subdir)
if debug:
videos = videos[:1]
n_videos = len(videos)
"""
for video in videos:
crop_video(subdir, subset, video)
"""
with futures.ProcessPoolExecutor(max_workers=num_threads) as executor:
fs = [
executor.submit(crop_video, subdir, subset, video)
for video in videos
]
for i, f in enumerate(futures.as_completed(fs)):
utils.print_progress(i,
n_videos,
prefix=subset,
suffix='Done ',
barLength=40)
def count_interactions(grof, xtcf, btime, etime, cutoff):
cutoff = cutoff * 10 # * 10: convert from nm to angstrom to work with MDAnalysis
u = Universe(grof, xtcf)
query = ('(resname PRO and (name CB or name CG or name CD)) or'
'(resname VAL and (name CG1 or name CG2)) or'
'(resname GLY and name CA) or'
'(resname ALA and name CB)')
# MDAnalysis will convert the unit of length to angstrom, though in Gromacs the unit is nm
atoms = u.selectAtoms(query)
for ts in u.trajectory:
if btime > ts.time:
continue
if etime > 0 and etime < ts.time:
break
numcount = 0
for i, ai in enumerate(atoms):
for j, aj in enumerate(atoms):
# to avoid counting the same pair twices,
# the 2 resid cannot be neigbors
if i < j and abs(ai.resid - aj.resid) >= 2:
d = np.linalg.norm(ai.pos - aj.pos)
if d <= cutoff:
numcount += 1
yield '{0:10.0f}{1:8d}\n'.format(ts.time, numcount)
utils.print_progress(ts)
def calc_dihedral(grof, xtcf, btime, etime):
# xtcf=None, so if only gro file is parsed, it still works
univer = Universe(grof, xtcf)
tets = select_dihedrals(univer) # there should be a better name for tet
# Write headers, hdr: header
hdrs = []
for k, tet in enumerate(tets):
# ca1 + ca2 + (NO. peptide-bond)
hdr = (utils.swap_aa_name(tet[0].resname) +
utils.swap_aa_name(tet[-1].resname) + "{0:02d}".format(k + 1))
# hdrs.append("{0:8s}".format(hdr))
hdrs.append("{0:4s}".format(hdr))
yield '#{0:8s}{1}\n'.format('t(ps)', ' '.join(hdrs))
if not xtcf:
yield calc_dih(tets)
else:
for ts in univer.trajectory:
if btime > ts.time:
continue
if etime > 0 and etime < ts.time:
break
res = calc_dih(tets, ts.time)
yield res
utils.print_progress(ts)
def ISTA(fx, gx, gradf, proxg, params):
method_name = 'ISTA'
print_start_message(method_name)
# Parameter setup
alpha = 1 / params['Lips']
info = []
x = params['x0']
for k in range(params['maxit']):
# Perform proximal gradient step
x = proxg(x - alpha * gradf(x), alpha)
# Record convergence
F_x = fx(x) + gx(x)
info.append(F_x)
# Early stopping
if stop({'F_x': F_x}, params):
print('Early stop')
return x, info
if k % params['iter_print'] == 0:
print_progress(k, params['maxit'], F_x, fx(x), gx(x))
return x, info
def calc_dihedral(grof, xtcf, btime, etime):
# xtcf=None, so if only gro file is parsed, it still works
univer = Universe(grof, xtcf)
tets = select_dihedrals(univer) # there should be a better name for tet
# Write headers, hdr: header
hdrs = []
for k, tet in enumerate(tets):
# ca1 + ca2 + (NO. peptide-bond)
hdr = (utils.swap_aa_name(tet[0].resname) +
utils.swap_aa_name(tet[-1].resname) +
"{0:02d}".format(k+1))
# hdrs.append("{0:8s}".format(hdr))
hdrs.append("{0:4s}".format(hdr))
yield '#{0:8s}{1}\n'.format('t(ps)', ' '.join(hdrs))
if not xtcf:
yield calc_dih(tets)
else:
for ts in univer.trajectory:
if btime > ts.time:
continue
if etime > 0 and etime < ts.time:
break
res = calc_dih(tets, ts.time)
yield res
utils.print_progress(ts)
def image_curation(num_threads=24):
subset_dirs = sorted(
glob.glob(join(base_path, TRAIN_SUBSET_PREFIX + '*') + "[!zip]"))
#subset_dirs.append(join(base_path, TEST_SUBSET_PREFIX))
for subdir in subset_dirs:
videos = sorted(os.listdir((join(subdir, 'videos'))))
if debug:
videos = videos[:1]
n_videos = len(videos)
subset = subdir.split('/')[-1]
#for video in videos:
# crop_video(subdir, subset, video)
with futures.ProcessPoolExecutor(max_workers=num_threads) as executor:
fs = [
executor.submit(crop_video, subdir, subset, video)
for video in videos
]
for i, f in enumerate(futures.as_completed(fs)):
utils.print_progress(i,
n_videos,
prefix=subset,
suffix='Done ',
barLength=40)
def main(args):
"""Main function for the testing pipeline
:args: commandline arguments
:returns: None
"""
##########################################################################
# Basic settings #
##########################################################################
exp_dir = 'experiments'
model_dir = os.path.join(exp_dir, 'models')
model_file = os.path.join(model_dir, 'best.pth')
val_dataset = dataset.NCovDataset('data/', stage='val')
val_loader = torch.utils.data.DataLoader(
val_dataset, batch_size=1, shuffle=False, num_workers=11,
drop_last=False)
cov_net = model.COVNet(n_classes=args.n_classes)
if torch.cuda.is_available():
cov_net.cuda()
state = torch.load(model_file)
cov_net.load_state_dict(state.state_dict())
with torch.no_grad():
val_loss, metric_collects = evaluate_model(cov_net, val_loader)
prefix = '******Evaluate******'
utils.print_progress(mean_loss=val_loss, metric_collects=metric_collects,
prefix=prefix)
def get_atom_and_bond_features(mols, mol_ids, dist_matrices):
atom_features, bond_features = [], []
bond_idx, atom_to_m_id, bond_to_m_id = [], [], []
print('Get atom and bond features.')
for it, m_name in enumerate(mols):
print_progress(it, C.N_MOLS)
m_id, mol = mol_ids[m_name], mols[m_name]
dist_matrix = dist_matrices[m_name]
n_atoms, n_bonds = mol.GetNumAtoms(), mol.GetNumBonds()
atom_features.append(get_atom_features(mol, dist_matrix))
e_feats, b_idx = get_bond_features(mol, dist_matrix)
bond_features.append(e_feats)
bond_idx.append(b_idx)
atom_to_m_id.append(np.repeat(m_id, n_atoms))
bond_to_m_id.append(np.repeat(m_id, n_bonds))
atom_features = pd.DataFrame(np.concatenate(atom_features),
columns=C.ATOM_FEATS)
bond_features = pd.DataFrame(np.concatenate(bond_features),
columns=C.BOND_FEATS)
bond_idx = np.concatenate(bond_idx)
bond_features['idx_0'] = bond_idx[:, 0]
bond_features['idx_1'] = bond_idx[:, 1]
atom_features['molecule_id'] = np.concatenate(atom_to_m_id)
bond_features['molecule_id'] = np.concatenate(bond_to_m_id)
return atom_features, bond_features
def load_features(feature_store, whether_img_feat):
def _make_id(scanId, viewpointId):
return scanId + '_' + viewpointId
# if the tsv file for image features is provided
if feature_store and whether_img_feat:
tsv_fieldnames = ['scanId', 'viewpointId', 'image_w', 'image_h', 'vfov', 'features']
features = {}
with open(feature_store, "r") as tsv_in_file:
print('Reading image features file %s' % feature_store)
reader = list(csv.DictReader(tsv_in_file, delimiter='\t', fieldnames=tsv_fieldnames))
#reader = reader[1:]
total_length = len(reader)
print('Loading image features ..')
for i, item in enumerate(reader):
image_h = int(item['image_h'])
image_w = int(item['image_w'])
vfov = int(item['vfov'])
long_id = _make_id(item['scanId'], item['viewpointId'])
features[long_id] = np.frombuffer(base64.b64decode(item['features']),
dtype=np.float32).reshape((36, 2048))
print_progress(i + 1, total_length, prefix='Progress:',
suffix='Complete', bar_length=50)
#features['17DRP5sb8fy_10c252c90fa24ef3b698c6f54d984c5c'] = np.zeros((36, 152)
else:
print('Image features not provided')
features = None
image_w = 640
image_h = 480
vfov = 60
return features, (image_w, image_h, vfov)
def main():
raw_list = csv_to_list(csv_file)[:100]
total_len = len(raw_list)
counter = 0
result_dict = dict()
print "Commencing Web Scraping..."
start_time = time.time()
for raw_link in raw_list:
try:
raw_link = raw_link[0]
whois_link = "http://www.whois.com/whois/" + raw_link
ipaddress_link = "http://" + raw_link + ".ipaddress.com/"
whois_soup = link_to_lxmlsoup(whois_link)
ipaddress_soup = link_to_lxmlsoup(ipaddress_link)
result_dict.setdefault('Raw Link', []).append(str(raw_link))
result_dict = whois_parser(whois_soup, result_dict)
result_dict = ipaddress_parser(ipaddress_soup, result_dict)
counter, total_len = print_counter(counter, total_len)
if counter % 400 == 0:
print "Commencing 30 Second Sleep after 400 iterations"
time.sleep(30)
time_elapsed = time.time() - start_time
print_progress(time_elapsed, counter, total_len)
except:
dict_to_json(result_dict, 'output.json')
dict_to_csv(result_dict, 'output.csv')
print "Unexpected Error", sys.exc_info()[0]
raise
dict_to_json(result_dict, 'output.json')
dict_to_csv(result_dict, 'output.csv')
def read_data(data_dir, max_files=MAX_NUM_FILES):
# prepare
data = []
# sort files for reproducibility
files = os.listdir(data_dir)
files = sorted(files)
random.Random(SHUFFLE_SEED).shuffle(files)
if max_files > 0:
files = files[:int(max_files)]
print('Reading files...')
for index, file_name in enumerate(files):
if not index % PROGRESS_ITER:
print_progress(index, files)
file_path = os.path.join(data_dir, file_name)
if os.path.isfile(file_path):
# read array and parse all elements to float, keep NaNs as nan value
contents = pd.read_csv(file_path, delimiter='|').values
patient = PatientData(sequence_x=contents[:, :-1],
sequence_y=contents[:, -1:])
data.append(patient)
print_progress(len(files), files)
return data
def count_interactions(grof, xtcf, btime, etime, cutoff):
cutoff = cutoff * 10 # * 10: convert from nm to angstrom to work with MDAnalysis
u = Universe(grof, xtcf)
query = ('(resname PRO and (name CB or name CG or name CD)) or'
'(resname VAL and (name CG1 or name CG2)) or'
'(resname GLY and name CA) or'
'(resname ALA and name CB)')
# MDAnalysis will convert the unit of length to angstrom, though in Gromacs the unit is nm
atoms = u.selectAtoms(query)
for ts in u.trajectory:
if btime > ts.time:
continue
if etime > 0 and etime < ts.time:
break
numcount = 0
for i, ai in enumerate(atoms):
for j, aj in enumerate(atoms):
# to avoid counting the same pair twices,
# the 2 resid cannot be neigbors
if i < j and abs(ai.resid - aj.resid) >= 2:
d = np.linalg.norm(ai.pos - aj.pos)
if d <= cutoff:
numcount += 1
yield '{0:10.0f}{1:8d}\n'.format(ts.time, numcount)
utils.print_progress(ts)
def pretrain(self, env):
test_s, test_q_c, test_w = self._get_batch(env, config.PRETRAIN_BATCH)
last_loss = 9999.
for i in range(config.PRETRAIN_EPOCHS):
utils.print_progress(i, config.PRETRAIN_EPOCHS, step=100)
# print loss
if utils.is_time(i, 100):
lr = config.PRETRAIN_LR / (1 + i / 100)
self.model.set_lr(lr)
q = self.model(test_s)
loss_c = self.model.get_loss_c(q, test_q_c, test_w)
print("\nLoss: {:.4e} LR: {:.2e}".format(loss_c.data.item(), lr))
if last_loss <= loss_c: # stop early
break
last_loss = loss_c
s, q_c, w = self._get_batch(env, config.PRETRAIN_BATCH)
self.model.train_c(s, q_c, w)
self.model_.copy_weights(self.model, rho=1.0)
def main(args_dict):
# Extract configuration
MK = args_dict['MK']
# Construct Robust Bayesian regression model
sigma = 2 * np.ones(1)
bounder = robustbayesregr.Bounder()
splitter = robustbayesregr.Splitter()
proposal = robustbayesregr.IsotropicGaussian(1, sigma)
np.random.seed(0)
x, y = robustbayesregr.generate_data(1000)
target = robustbayesregr.CauchyRegression(x, y, sigma)
# Obtain MK samples (and their corresponding MAP values) using A* sampling implementation
samples = np.empty((MK)).squeeze()
MAPs = []
for i in range(MK):
stream = astar.astar_sampling_iterator(target, proposal, bounder,
splitter)
X, G = stream.next()
samples[i] = X
MAPs.append(G[0] - EULER)
if i % 1 == 0:
print_progress('Sampled %d / %d' % (i + 1, MK))
print('')
lnZ = float(np.log(target.z()))
# Dump true ln(Z) and MAP values to JSON file
data = {'lnZ': lnZ, 'MAPs': MAPs}
savepath = 'data/astar_rbr_MK%d.json' % (MK)
json_dump(data, savepath, indent=None)
print('Saved %d samples to %s' % (len(MAPs), savepath))
def estimate_MSE_vs_alpha(transform, Ms, alphas, K):
# Without loss of generality
Z = 1
tZ = transform(Z)
# Estimate MSEs by constructing estimators K times
MSEs = np.empty((len(Ms), len(alphas)))
MSEs_stdev = np.empty((len(Ms), len(alphas)))
for Mi, M in enumerate(Ms):
# Compute means (K x alphas) in a loop, as otherwise
# this runs out of memory with K = 100,000.
means = np.empty((K, len(alphas)))
for ai, alpha in enumerate(alphas):
Ws = np.power(np.random.exponential(1.0, size=(K, M)), alpha) # (K, M)
means[:, ai] = np.mean(Ws, axis=1)
print_progress('M = %d: done %.0f%%' % (M, 100.0 * (ai+1) / len(alphas)))
print('')
g = np.power(gamma(1.0 + alphas), 1.0 / alphas) # (alphas)
tZ_hats = transform(g * np.power(means, -1.0/alphas)) # (K, alphas)
SEs = (tZ_hats - tZ) ** 2 # (K, alphas)
MSEs[Mi] = np.mean(SEs, axis=0) # (alphas)
MSEs_stdev[Mi] = np.std(SEs, axis=0) / np.sqrt(K) # (alphas)
return MSEs, MSEs_stdev
def run(self, content_urls):
responses = []
total = len(content_urls)
count = 0
start = time.time()
for url in content_urls:
rrl = utils.RequestRateLimiterFactory(self.request_rate)()
if count is 0:
print(f'[WARNING] rate_limited _call_api(): max_per_Second:{self.request_rate}')
try:
request_url = f'{url}{self.query_params}' if self.query_params is not None else url
res = rrl.make_rate_limited_request(request_url, self.request_verb, headers=self.headers)
parsed_res = self.res_callback(res=res, url=url, remaining_count=total-count, rrl=rrl)
except Exception as e:
# TODO: could provide 'skip' vs 'abandon' option for exceptions
print(f'[WARNING] Exception thrown - skipping {url}')
print(e)
parsed_res = []
count += 1
responses.append(parsed_res)
utils.print_progress(count, total, urlparse(url).hostname)
end = time.time()
print(f'{sum([len(res) for res in responses])} items scraped from {count} urls in {end-start:.2f}s.')
return responses
def ista(fx, gx, gradf, proxg, params):
method_name = 'ISTA'
print_start_message(method_name)
tic = time.time()
# Parameter setup
lmbd = params['lambda']
alpha = 1 / params['Lips']
X = params['x0']
run_details = {'X_final': None, 'conv': np.zeros(params['maxit'] + 1)}
run_details['conv'][0] = fx(params['x0']) + lmbd * gx(params['x0'])
for k in range(1, params['maxit'] + 1):
# Perform proximal gradient step
X = proxg(X - alpha * gradf(X), alpha * lmbd)
# Record convergence
run_details['conv'][k] = fx(X) + lmbd * gx(X)
if k % params['iter_print'] == 0:
print_progress(k, params['maxit'], run_details['conv'][k], fx(X),
gx(X))
run_details['X_final'] = X
print_end_message(method_name, time.time() - tic)
return run_details
def get_atom_and_bond_features(mols, mol_ids, dist_matrices): # mol_ids: {}
atom_features, bond_features = [], []
bond_idx, atom_to_m_id, bond_to_m_id = [], [], []
print('Get atom and bond features.')
for it, m_name in enumerate(mols):
print_progress(it, C.N_MOLS)
m_id, mol = mol_ids[m_name], mols[m_name] # m_id: int
dist_matrix = dist_matrices[m_name] # 获取分子的距离矩阵
n_atoms, n_bonds = mol.GetNumAtoms(), mol.GetNumBonds() # 根据mol结构文件获取分子中 原子的个数和 键的个数
# mol.GetNumAtoms(), mol.GetNumBonds()
atom_features.append(get_atom_features(mol, dist_matrix)) # 针对每个分子文件，获取分子中原子特征
e_feats, b_idx = get_bond_features(mol, dist_matrix) # 针对每个分子文件，获取键的特征
bond_features.append(e_feats)
bond_idx.append(b_idx) # b_idx: array(n_bonds, 2)
atom_to_m_id.append(np.repeat(m_id, n_atoms)) # 根据原子个数产生对应个数的分子id, [array, array, array, ...]
bond_to_m_id.append(np.repeat(m_id, n_bonds)) # 根据键个数产生对应个数的分子id
atom_features = pd.DataFrame(
np.concatenate(atom_features), columns=C.ATOM_FEATS) # atom_features:[np.array(n_atoms*atom_feats), np.array(), ...]
bond_features = pd.DataFrame(
np.concatenate(bond_features), columns=C.BOND_FEATS) # bond_features:[np.array(n_bonds*bond_feats), np.array(), ...]
bond_idx = np.concatenate(bond_idx) # bond_idx: [np.array(n_bonds*2), np.array(), ...]
bond_features['idx_0'] = bond_idx[:,0] # 给bond_features——df添加成键原子的索引
bond_features['idx_1'] = bond_idx[:,1] #
atom_features['molecule_id'] = np.concatenate(atom_to_m_id) # 给atom_features--df添加列
bond_features['molecule_id'] = np.concatenate(bond_to_m_id) # 给bond_features--df添加列
return atom_features, bond_features # 返回 atom_features--df, bond_features--df
def __init__(
self,
opts,
features,
img_spec,
batch_size=64,
seed=10,
splits=["train"],
tokenizer=None,
):
self.env = PanoEnvBatch(features, img_spec, batch_size=batch_size)
self.data = []
self.scans = []
self.opts = opts
print("Loading {} dataset".format(splits[0]))
json_data = load_datasets(splits)
total_length = len(json_data)
# iteratively load data into system memory
for i, item in enumerate(json_data):
if not is_experiment() and i >= 20:
break # if this is in developing mode, load only a small amount of data
# Split multiple instructions into separate entries
for j, instr in enumerate(item["instructions"]):
self.scans.append(item["scan"])
new_item = dict(item)
new_item["instr_id"] = "%s_%d" % (item["path_id"], j)
new_item["instructions"] = instr
if tokenizer:
if (
"instr_encoding" not in item
): # we may already include 'instr_encoding' when generating synthetic instructions
new_item["instr_encoding"] = tokenizer.encode_sentence(
instr)
else:
new_item["instr_encoding"] = item["instr_encoding"]
self.data.append(new_item)
print_progress(
i + 1,
total_length,
prefix="Progress:",
suffix="Complete",
bar_length=50,
)
self.scans = set(self.scans)
self.splits = splits
self.seed = seed
random.seed(self.seed)
random.shuffle(self.data)
self.ix = 0
self.batch_size = batch_size
self._load_nav_graphs()
print("R2RBatch loaded with %d instructions, using splits: %s" %
(len(self.data), ",".join(splits)))
def __gen_hist__(plot_details, verbose=False):
'''
generate single histogram
only runs on samples with an input file defined,
ie. does not loop through daughters
not really designed to be called by analysers
'''
log.debug('in get_hist for %s' % plot_details.sample.name)
## add the details from the sample
#plot_details += plot_details.sample.plot_details
s = plot_details.sample
vd = plot_details.var_details
sel = plot_details.get_selector()
weights = plot_details.get_weights()
target_lumi = plot_details.target_lumi
if not s.is_active():
log.warn('failed to gen hist %s for sample: %s' % (vd.name, s.name))
return None
## create hist
h = plot_details.new_hist(s)
h.samples = s
## initialise sample
s.initialise()
## return empty hist if no events
if not s.tree.GetEntries(): return h
s.switch_on_branches()
## selection
event_list = sel.select(s) if sel else None
## initialise variables
s.prepare(plot_details)
## process events
entries = event_list.GetN() if sel else s.tree.GetEntries()
for i in xrange(entries):
ientry = event_list.GetEntry(i) if sel else i
s.tree.GetEntry(ientry)
## calculate event weight
weight = weights.weight() if weights else 1.
## fill hists
val = vd.var.calc_vals()[0]
h.Fill(val, weight)
frac = float(i) / float(entries) if entries else 0.0
if verbose: utils.print_progress(frac, title='%s: ' % s.name)
if verbose: utils.clear_progress()
#s.style_hist(h)
if target_lumi: s.scale_hist(h, target_lumi)
return h
def count_interactions(A):
logger.debug('loading {0}'.format(A.grof))
univ = Universe(A.grof)
logger.debug('loaded {0}'.format(A.grof))
pro_atoms = univ.selectAtoms('protein and not resname ACE and not resname NH2')
pl = pro_atoms.residues.numberOfResidues()
# +1: for missing resname ACE, such that it's easier to proceed in the next
# step
logger.debug('loading {0}, {1}'.format(A.grof, A.xtcf))
u = Universe(A.grof, A.xtcf)
logger.debug('loaded {0}, {1}'.format(A.grof, A.xtcf))
# Just for reference to the content of query when then code was first
# written and used
# query = ('(resname PRO and (name CB or name CG or name CD)) or'
# '(resname VAL and (name CG1 or name CG2)) or'
# '(resname GLY and name CA) or'
# '(resname ALA and name CB)')
query = A.query
atoms = u.selectAtoms(query)
logger.info('Number of atoms selected: {0}'.format(atoms.numberOfAtoms()))
# MDAnalysis will convert the unit of length to angstrom, though in Gromacs
# the unit is nm
cutoff = A.cutoff * 10
nres_away = A.nres_away
btime = A.btime
etime = A.etime
nframe = 0
unun_map = None
for ts in u.trajectory:
if btime > ts.time:
continue
if etime > 0 and etime < ts.time:
break
nframe += 1
map_ = np.zeros((pl+1, pl+1)) # map for a single frame
for i, ai in enumerate(atoms):
ai_resid = ai.resid
for j, aj in enumerate(atoms):
aj_resid = aj.resid
# to avoid counting the same pair twices,
# the 2 resid cannot be neigbors
if i < j and aj_resid - ai_resid >= nres_away:
d = np.linalg.norm(ai.pos - aj.pos)
if d <= cutoff:
# -1: resid in MDAnalysis starts from 1
map_[ai_resid-1][aj_resid-1] += 1
if unun_map is None:
unun_map = map_
else:
unun_map = unun_map + map_
utils.print_progress(ts)
sys.stdout.write("\n")
return unun_map / float(nframe)
def generate_svg_stack(dataset_name, X, classIds, n, data_size):
outfile = '../data/imgs/{}.svg'.format(dataset_name)
with open(outfile, "w") as svgFile:
svgFile.write(svgMetaData)
for i in range(n):
utils.print_progress(i, n)
figData = generate_figure_data(X[i], classIds[i], data_size)
svgFile.write(svgImgTag.format(i, i, figData))
svgFile.write("</svg>")
def train(self, inputs, targets, lr=1, batch_size=30, epochs=100, plot=False, kernel='linear'):
self.batch_size = batch_size
# init the kernel
self.set_kernel(kernel)
# set optimization method (Gradient Descent)
self.optimization = tf.train.GradientDescentOptimizer(lr)
self.training_step = self.optimization.minimize(self.loss)
self.init = tf.global_variables_initializer()
self.session.run(self.init)
# set training data
train_inputs, train_target = inputs, targets
# performance tracking
train_loss_result, train_accuracy_result = [], []
# for each epoch
for i in range(epochs):
# generate random indexes for each batch
batch_index = np.random.choice(len(train_inputs), size=batch_size)
self.session.run(self.training_step, feed_dict={self.inputs: train_inputs[batch_index],
self.target: train_target[:, batch_index]})
# if plotting, record every epoch
if plot:
# record accuracy
train_accuracy, train_loss = self.generate_step_tracking_data(
train_inputs[batch_index], train_target[:, batch_index])
train_accuracy_result.append(train_accuracy)
train_loss_result.append(train_loss)
if (i+1) % (epochs / 5) == 0:
# if not plotting, get intermittent accuracy and loss
if not plot:
# record accuracy
train_accuracy, train_loss = self.generate_step_tracking_data(
train_inputs[batch_index], train_target[:, batch_index])
utl.print_progress(i, epochs, train_loss, train_accuracy)
# plot results
if plot:
if not self.features == 2:
print('Plotting only supported for 2 feature data sets... skipping output')
else:
utl.plot_loss(train_loss_result)
utl.plot_accuracy(train_accuracy_result)
grid = utl.generate_grid(train_inputs)
grid_predictions = self.session.run(self.prediction, feed_dict={self.inputs: train_inputs[batch_index],
self.target: train_target[:, batch_index],
self.grid: grid})
# plot the result grid
utl.plot_result(grid_predictions, inputs, targets)
# commit data points for the last support vectors used
self.support_vector_data = [train_inputs[batch_index], train_target[:, batch_index]]
def evaluate_checkpoint(P, postfix, data, word2id, checkpoint_fname, epoch,
device):
"""
"""
# Check for checkpoints
_ = load_checkpoint(P, model, opt, device, checkpoint_fname)
response_filename = "{}response_str_{}.txt".format(P.EVAL_DIR, postfix)
if os.path.isfile(response_filename):
print("Skipping {}, it does already exist.".format(response_filename))
return
saver_response_str = sentences_saver(response_filename)
print()
total_decoder_loss = 0
total_saliency_loss = 0
start_time = time()
for batch_num, batch in enumerate(data):
# Get batch
input, target, templates, target_saliencies = unpack_batch(
batch, device)
saliency, response = model(input, target, templates)
decoder_target = [t[1:] for t in target] # Cut <BOS> from target
decoder_loss = torch.stack([
decoder_loss_fn(res, tar)
for res, tar in zip(response, decoder_target)
]).mean()
if P.USE_BILINEAR:
# Only when the bilinear is used, there is a sailency loss.
saliency_loss = torch.stack([
saliency_loss_fn(sal, true_sal)
for sal, true_sal in zip(saliency, target_saliencies)
]).mean()
total_saliency_loss += saliency_loss.item()
total_decoder_loss += decoder_loss.item()
for inp, templ, targ in zip(input, templates, target):
response, _ = model.respond(device,
word2id, [inp], [templ],
max_length=50)
# Write the results to txt files
saver_response_str.store_sentence(word2id.id2string(response))
print_progress("Evaluating: ", P, epoch - 1, batch_num, len(data),
total_saliency_loss / (batch_num + 1),
total_decoder_loss / (batch_num + 1), start_time)
print()
saver_response_str.write_to_file()
def run(self, filename):
firmwarefilename = filename
name = firmwarefilename.remove(".new.dat")
transferfilename = name + ".transfer.list"
if not os.path.exists(transferfilename):
print(f"Couldn't find needed {transferfilename}.")
exit(0)
with open(transferfilename, 'r') as tfr:
with open(firmwarefilename, 'rb') as qr:
version = int(tfr.readline().replace("\n", ""))
if version > 3:
print(f"Error, version {str(version)} not supported.")
exit(0)
with open(name + ".bin", "wb") as qw:
totalblocks = int(tfr.readline().replace("\n", ""))
blocksize = 4096
buffersize = 0x200000
ip = tfr.readline()
command = ip.split(" ")[0]
ip = ip.split(" ")[1]
values = ip.split(",")
print_progress(0,
100,
prefix='Progress:',
suffix='Complete',
bar_length=50)
if command == "new":
count = int(values[0])
old = 0
for i in range(0, count / 2):
start = int(values[1 + (i * 2)])
end = int(values[2 + (i * 2)])
length = (end - start) * blocksize
for pos in range(0, (blocksize * start), 4096):
qw.write(b"\x00" * 4096)
total = length
while length > 0:
size = buffersize
if size > length:
size = length
buffer = qr.read(size)
qw.write(buffer)
length -= size
prog = int(
float(i) / float(total) * float(100))
if (prog > old):
print_progress(prog,
100,
prefix='Progress:',
suffix='Complete',
bar_length=50)
old = prog
elif command == "erase":
pass
def main():
# get all image names
images = glob.glob('{}/*.jpg'.format(PATH_TO_IMAGES))
for i, image in enumerate(images):
rotate_image(image, 'right')
rotate_image(image, 'left')
rotate_image(image)
print_progress((i + 1) / len(images))
print('\nRotated {} images'.format(len(images)))
def clear_table(db, name_arr=[]):
print('Cleaning Tables')
c = db.cursor()
total = len(name_arr)
count = 0
for n in name_arr:
count += 1
c.execute("DELETE FROM " + n)
c.execute("ALTER TABLE " + n + " AUTO_INCREMENT = 1")
print_progress(count, total)
db.commit()
def sequence_spacing(grof, xtcf, btime, etime, peptide_length, atom_sel):
u = Universe(grof, xtcf)
# this selection part should be better customized
# here, only have been backbone atoms are used, u.selectAtoms doesn't
# include Hydrogen atoms
# REMMEMBER: ARGS verification should be done in main ONLY!
# range works like this:
# in MDAnalysis, resid starts from 1, in sequence_spacing.py, we don't count
# the C- and N- termini, so it's from 2 to peptide_len+2
residues = [u.selectAtoms(atom_sel.format(i)) for i in range(2, peptide_length + 2)]
ijdist_dict = {}
for ts in u.trajectory:
# btime, etime defaults to 0, if etime is 0, loop till the end of the
# trajectory
if btime > ts.time:
continue
if etime > 0 and etime < ts.time:
break
# the good stuff
for i, resi in enumerate(residues):
for j, resj in enumerate(residues):
# to remove duplicate since resi & resj are within the same peptide
if i < j:
dij = abs(i - j)
d_atomi_atomj = []
# loop through every atom in both residues
for atomi in resi:
for atomj in resj:
d_atomi_atomj.append(
np.linalg.norm(atomi.pos - atomj.pos))
# add the result to the dictionary
ij_dist = np.average(d_atomi_atomj) # distance between i and j
if dij not in ijdist_dict.keys():
ijdist_dict[dij] = [ij_dist]
else:
ijdist_dict[dij].append(ij_dist)
utils.print_progress(ts)
return ijdist_dict
if search_term:
params["jql"] = params["jql"] + " AND text~'%s'" % search_term
if ticket_id:
params["jql"] = params["jql"] + " AND issue='%s'" % ticket_id
params["maxResults"] = config._MAX_SEARCH_RESULTS
params["fields"] = ["summary",]
search_result = utils.get_request_auth(config._SEARCH, params)
if "issues" in search_result and len(search_result["issues"]) != 0:
print("\nTicket found:")
issues = search_result["issues"]
for issue in issues:
print("%s -> %s" % (issue["key"], issue["fields"]["summary"]))
print("\nWould you liket to tag/label the above ticket(s) with '%s'?" % search_term)
prompt = input("Proceed? [y/n] ")
if prompt == "n":
pass
elif prompt == "y":
for index, issue in enumerate(issues, start=1):
payload = utils.add_label_payload(search_term)
if utils.put_request_auth(config._ISSUE_BY_KEY % issue["key"], payload):
utils.print_progress(index, len(issues))
else:
print("\nNo tickets")
print("\n\nSee you next time!")
print("Have a good day!")
