def __init__(self,a,b):
self.a=a
self.b=b
self.dir=None
self.setDir()
subtrArray = sp.dstack([self.a,-self.b]).sum(2)
self.length = sp.sqrt(sp.sum([n**2 for n in subtrArray]))
def jplot2d(*args):
arg=' -2D -l SOUTH '
i=0
while (i<len(args)):
i_arg=0
q=False
arg_txt=True
while ((len(args)>(i_arg+i+1)) & arg_txt):
if (type(args[i+i_arg+1]) is str):
i_arg+=1
arg=arg+' '+args[i+i_arg]
else:
arg_txt=False
name='.'+str(scipy.stats.random_integers(10000))+'.plot.tmp'
if ((len(args[i])==scipy.size(args[i]))):
a=scipy.dstack((scipy.arange(1,scipy.size(args[i])+1),args[i]))[0]
scipy.io.write_array(name,a)
else:
scipy.io.write_array(name,args[i])
i+=i_arg+1
arg=arg+' '+name
os.system('java -cp jmathplot.jar org.math.plot.PlotPanel '+arg)
def maskplot(index, data, mask, color='black', styles=['solid', 'dotted']):
""" Creates a plot with masked-out intervals in dotted or custom line style,
non-masked segments in dashed or custom line style, all in given color.
Built from the example at
http://matplotlib.org/examples/pylab_examples/multicolored_line.html
"""
points = sp.array([index, data]).T.reshape(-1, 1, 2)
segments = sp.concatenate([points[:-1], points[1:]], axis=1)
mask = mask.reshape(-1, 1)
mask = (sp.ones_like(mask) - mask).astype(bool)
mask = sp.hstack((mask, mask))
mask = sp.dstack((mask, mask))
mask = mask[1:]
#print segments.shape, mask.shape
mask1 = sp.ma.masked_where(mask, segments)
mask2 = sp.ma.masked_where(
(-mask.astype(float)+1.).astype(bool), segments)
ls1 = LineCollection(
mask1,
colors=color,
linestyles=styles[0])
ls2 = LineCollection(
mask2,
colors=colorConverter.to_rgba(color),
linestyles=styles[1])
return ls1, ls2
def process(self, sbmp):
"""Core function"""
if sbmp == None:
# Oversize required
return self.size
# reverse height and width under advice
(ws, hs, ps) = shape = (sbmp.GetHeight(), sbmp.GetWidth(), 3)
simg = wx.ImageFromBitmap(sbmp)
sarray = scipy.array(scipy.fromstring(simg.GetData(), 'uint8'), self.dtype) / 255.0
sarray = scipy.rollaxis(scipy.reshape(sarray, shape), 2)
self.shape = sarray.shape
tarray = (self.withGPU if self.gpgpu else self.withCPU)(sarray)
mm = (sarray.min(), sarray.max(), tarray.min(), tarray.max())
#print '\t', sarray.shape, tarray.shape,
print type(sarray[0,0,0]), type(tarray[0,0,0]), mm
tarray = numpy.nan_to_num(tarray)
tarray /= max(tarray.max(), self.coefficient)
tarray = scipy.array((tarray * 255.0).tolist(), 'uint8')
tarray = scipy.dstack(tarray)
timg = wx.EmptyImage(ws, hs)
timg .SetData(tarray.tostring())
self.tbmp = timg.ConvertToBitmap()
return self.tbmp
def jplot2d(*args):
arg = ' -2D -l SOUTH '
i = 0
while (i < len(args)):
i_arg = 0
q = False
arg_txt = True
while ((len(args) > (i_arg + i + 1)) & arg_txt):
if (type(args[i + i_arg + 1]) is str):
i_arg += 1
arg = arg + ' ' + args[i + i_arg]
else:
arg_txt = False
name = '.' + str(scipy.stats.random_integers(10000)) + '.plot.tmp'
if ((len(args[i]) == scipy.size(args[i]))):
a = scipy.dstack(
(scipy.arange(1,
scipy.size(args[i]) + 1), args[i]))[0]
scipy.io.write_array(name, a)
else:
scipy.io.write_array(name, args[i])
i += i_arg + 1
arg = arg + ' ' + name
os.system('java -cp jmathplot.jar org.math.plot.PlotPanel ' + arg)
def __init__(self, a, b):
self.a = a
self.b = b
self.dir = None
self.setDir()
subtrArray = sp.dstack([self.a, -self.b]).sum(2)
self.length = sp.sqrt(sp.sum([n**2 for n in subtrArray]))
def square_lattice(L):
'''
Generates an array of points making up a square LxL lattice.
:param L: the dimension of the square lattice.
'''
x = sp.linspace(0, L, L + 1)
coord_arrays = sp.meshgrid(x, x)
polygon = (sp.dstack(coord_arrays))
polygon = sp.reshape(polygon, ((L + 1)**2, 2))
return polygon
def __init__(self, train, T=10.0, grid_size=0.1):
"""Constructor for PredPol object.
Args:
train: a pandas DataFrame where each row is an observed crime, used
to learn the model parameters. Must contain at least the following
columns:
t: numeric, indicating the time of the crime. All values must be
less than the `T` supplied as an argument to this constructor.
x: numeric, indicating the horizontal position of the crime.
y: numeric, indicating the vertical position of the crime.
For numerical safety (avoiding overflows), it's recommended that t,
x, and y are all normalized to have relatively small values.
T: float, indicating the maximum `t` value in the _combined_ train
and test set of data.
grid_size: float, indicating the level of discretization/total
number of grid cells in the PredPol model. Smaller grid sizes have
more grid cells.
Returns: an initialized PredPol object before fitting parameter values.
"""
self.train = train
self.T = T
self.height = train.y.max()
self.width = train.x.max()
self.grid_size = grid_size
# Generate the center of each grid cell
x_vals = sp.arange(0, self.width, self.grid_size)
y_vals = sp.arange(0, self.height, self.grid_size)
diff = round(self.grid_size / 2,
-int(math.floor(math.log10(self.grid_size))) + 1)
x_vals += diff
y_vals += diff
xs, ys = sp.meshgrid(x_vals, y_vals)
# print(xs)
# print(ys)
self.grid_cells = sp.vstack(sp.dstack((xs, ys)))
self.grid_cells = pd.DataFrame(self.grid_cells, columns=['x', 'y'])
self.interpolator = RegularGridInterpolator(
points=(x_vals, y_vals),
values=sp.arange(1,
len(self.grid_cells) + 1).reshape(
(len(y_vals), len(x_vals))).transpose(),
method='nearest',
bounds_error=False,
fill_value=None)
self.eta = None
self.omega = None
self.sigma = None
def square_lattice(L):
'''
Generates an array of points making up a square LxL lattice.
:param L: the dimension of the square lattice.
'''
x = sp.linspace(0,L,L+1)
coord_arrays = sp.meshgrid(x,x)
polygon = (sp.dstack(coord_arrays))
polygon = sp.reshape(polygon,((L+1)**2,2))
return polygon
def __init__(self,
loc1,
loc2,
scale1,
scale2,
xmin,
xmax,
npts=100,
plot=False):
#Sample spacec for plotting and interpolating
x_eval_space = sp.linspace(xmin, xmax, npts)
y_eval_space = sp.linspace(xmin, xmax, npts)
if plot: print('Done with linspace')
x_eval, y_eval = sp.meshgrid(x_eval_space, y_eval_space)
xy_eval = sp.dstack((x_eval, y_eval))
if plot: print('Done with dstack')
#Create a bimodal pdf
bimodal_pdf = pdf(xy_eval, mean=loc1, cov=scale1)*0.5 + \
pdf(xy_eval, mean=loc2, cov=scale2)*0.5
if plot: print('Done with pdf')
bimodal_cdf = cdf(xy_eval, mean=loc1, cov=scale1)*0.5 + \
cdf(xy_eval, mean=loc2, cov=scale2)*0.5
if plot: print('Done with cdf')
#Make sure the cdf is bounded before interpolating the inverse
bimodal_cdf[-1, -1] = 1
bimodal_cdf[-1, 0] = 0
self.ppfx = interpolate.interp1d(bimodal_cdf[-1, :], x_eval_space)
self.ppfix = interpolate.interp1d(x_eval_space, sp.arange(npts))
if plot: print('Done building interpolator')
#Store the data
self.x_eval = x_eval
self.y_eval = y_eval
self.x_eval_space = x_eval_space
self.y_eval_space = y_eval_space
self.bimodal_pdf = bimodal_pdf
self.bimodal_cdf = bimodal_cdf
return
def _compare_evolutions(self,
evolution1,
evolution2,
*,
primary_to_secondary=False,
flip=True,
min_age=-scipy.inf,
max_age=scipy.inf):
"""
Require the two evolutions match for a, and primary Lconv & Lrad.
Args:
evolution1: The first of the two evolutions to compare.
evolution2: The second of the two evolutions to compare.
primary_to_secondary: If False compares the evolution of the
primary object in both evolutions, otherwise compares the
evolution of the primary in evolution1 to the evolution of the
secondary in evolution2.
flip: If true, also calls itself with the two evolutions swapped.
min_age: Discrepancies at ages before this are ignored.
min_age: Discrepancies at ages after this are ignored.
"""
def output_failing(data):
"""Output to stdout the discrepant evolutions."""
for i in range(max(d.shape[0] for d in data)):
print(
(
'%25.16e %25.16e' % tuple(data[0][i])
if i < data[0].shape[0] else
(51 * ' ')
)
+
' '
+
(
'%25.16e %25.16e' % tuple(data[1][i])
if i < data[1].shape[0] else
(51 * ' ')
)
)
for quantity_name in [
('semimajor', 'semimajor'),
('envelope_angmom', 'primary_envelope_angmom'),
('core_angmom', 'primary_core_angmom')
]:
with self.subTest(quantity=quantity_name[0], flipped=not flip):
if primary_to_secondary:
quantity = [
getattr(
evolution1, quantity_name[0],
getattr(evolution1, quantity_name[1], None)
),
getattr(
evolution2,
(
(
'' if quantity_name[0] == 'semimajor'
else 'secondary_'
)
+
quantity_name[0]
)
)
]
else:
quantity = [
getattr(evol, quantity_name[0],
getattr(evol, quantity_name[1], None))
for evol in [evolution1, evolution2]
]
age_within_range = [
scipy.logical_and(evol.age[:-1] > min_age,
evol.age[:-1] < max_age)
for evol in [evolution1, evolution2]
]
acceptable_ages = scipy.logical_and(
age_within_range[0],
scipy.logical_and(
(evolution1.age[:-1] - evolution1.age[1:]) < 0,
scipy.isfinite(quantity[0][:-1])
)
)
interp_quantity = InterpolatedUnivariateSpline(
evolution1.age[:-1][acceptable_ages],
quantity[0][:-1][acceptable_ages]
)
max_difference = scipy.nanmax(
scipy.fabs(
quantity[1][:-1][age_within_range[1]]
-
interp_quantity(evolution2.age[:-1][age_within_range[1]])
)
)
max_error = max(
(
scipy.nanmax(quantity[1][:-1][age_within_range[1]])
-
scipy.nanmin(quantity[1][:-1][age_within_range[1]])
) * 5e-3,
1e-10 * scipy.nanmean(quantity[1][:-1][age_within_range[1]])
)
if max_difference > max_error:
output_failing(
[
scipy.dstack(
(
evolution1.age[:-1][age_within_range[0]],
quantity[0][:-1][age_within_range[0]]
)
)[0],
scipy.dstack(
(
evolution2.age[:-1][age_within_range[1]],
quantity[1][:-1][age_within_range[1]]
)
)[0]
]
)
self.assertLessEqual(max_difference, max_error)
if flip:
self._compare_evolutions(evolution2,
evolution1,
primary_to_secondary=primary_to_secondary,
min_age=min_age,
max_age=max_age,
flip=False)
def verify_all_events(ev,
strain_idx=None,
list_bam=None,
event_type=None,
CFG=None,
out_fn=None):
# (ev, counts) = verify_all_events(ev, strain_idx, list_bam, event_type, CFG) ;
### set parameters if called by rproc
if strain_idx is None:
PAR = ev
ev = PAR['ev']
strain_idx = PAR['strain_idx']
list_bam = PAR['list_bam']
if 'out_fn' in PAR:
out_fn = PAR['out_fn']
event_type = PAR['event_type']
CFG = PAR['CFG']
### verify the events if demanded
if CFG['verify_alt_events']:
prune_tag = ''
if CFG['do_prune']:
prune_tag = '_pruned'
validate_tag = ''
if CFG['validate_splicegraphs']:
validate_tag = '.validated'
(genes, inserted) = cPickle.load(
open('%s/spladder/genes_graph_conf%i.%s%s%s.pickle' %
(CFG['out_dirname'], CFG['confidence_level'],
CFG['merge_strategy'], validate_tag, prune_tag)))
fn_count = '%s/spladder/genes_graph_conf%i.%s%s%s.count.pickle' % (
CFG['out_dirname'], CFG['confidence_level'], CFG['merge_strategy'],
validate_tag, prune_tag)
### load count index data from hdf5
IN = h5py.File(fn_count, 'r')
gene_ids_segs = IN['gene_ids_segs'][:]
gene_ids_edges = IN['gene_ids_edges'][:]
### sort events by gene idx
s_idx = sp.argsort([x.gene_idx for x in ev])
ev = ev[s_idx]
old_idx = sp.argsort(s_idx)
### find gene idx boundaries
assert (isequal(gene_ids_segs, sp.sort(gene_ids_segs)))
assert (isequal(gene_ids_edges, sp.sort(gene_ids_edges)))
tmp, genes_f_idx_segs = sp.unique(gene_ids_segs, return_index=True)
genes_l_idx_segs = sp.r_[genes_f_idx_segs[1:] - 1,
gene_ids_segs.shape[0]]
tmp, genes_f_idx_edges = sp.unique(gene_ids_edges, return_index=True)
genes_l_idx_edges = sp.r_[genes_f_idx_edges[1:] - 1,
gene_ids_edges.shape[0]]
gr_idx_segs = 0
gr_idx_edges = 0
counts = []
for i in range(ev.shape[0]):
g_idx = ev[i].gene_idx
### there are no edges present in the event
if gene_ids_edges.shape[0] == 0:
ver, info = verify_empty(event_type)
counts.append(sp.array([info]))
ev[i].verified = sp.array(ev[i].verified)
continue
while gene_ids_segs[genes_f_idx_segs[gr_idx_segs]] < g_idx:
gr_idx_segs += 1
assert (gene_ids_segs[genes_f_idx_segs[gr_idx_segs]] == g_idx)
while gene_ids_edges[genes_f_idx_edges[gr_idx_edges]] < g_idx:
gr_idx_edges += 1
if gr_idx_edges > g_idx:
ver, info = verify_empty(event_type)
counts.append(sp.array([info]))
ev[i].verified = sp.array(ev[i].verified)
continue
assert (gene_ids_edges[genes_f_idx_edges[gr_idx_edges]] == g_idx)
### laod relevant count data from HDF5
segments = IN['segments'][
genes_f_idx_segs[gr_idx_segs]:genes_l_idx_segs[gr_idx_segs] +
1, strain_idx]
seg_pos = IN['seg_pos'][
genes_f_idx_segs[gr_idx_segs]:genes_l_idx_segs[gr_idx_segs] +
1, strain_idx]
edges = IN['edges'][genes_f_idx_edges[gr_idx_edges]:
genes_l_idx_edges[gr_idx_edges] + 1,
strain_idx]
edge_idx = IN['edge_idx'][genes_f_idx_edges[gr_idx_edges]:
genes_l_idx_edges[gr_idx_edges] + 1]
for s_idx in range(len(strain_idx)):
print '%i/%i\r' % (s_idx, len(strain_idx))
# ev_tmp.subset_strain(s_idx) ### TODO
if event_type == 'exon_skip':
ver, info = verify_exon_skip(
ev[i], genes[g_idx], segments[:, s_idx].T,
sp.c_[edge_idx, edges[:, s_idx]], CFG)
elif event_type in ['alt_3prime', 'alt_5prime']:
ver, info = verify_alt_prime(
ev[i], genes[g_idx], segments[:, s_idx].T,
sp.c_[edge_idx, edges[:, s_idx]], CFG)
elif event_type == 'intron_retention':
ver, info = verify_intron_retention(
ev[i], genes[g_idx], segments[:, s_idx].T,
sp.c_[edge_idx,
edges[:, s_idx]], seg_pos[:, s_idx].T, CFG)
elif event_type == 'mult_exon_skip':
ver, info = verify_mult_exon_skip(
ev[i], genes[g_idx], segments[:, s_idx].T,
sp.c_[edge_idx, edges[:, s_idx]], CFG)
elif event_type == 'mutex_exons':
ver, info = verify_mutex_exons(
ev[i], genes[g_idx], segments[:, s_idx].T,
sp.c_[edge_idx, edges[:, s_idx]], CFG)
ev[i].verified.append(ver)
if s_idx == 0:
counts.append(sp.array([info]))
else:
counts[-1] = sp.r_[counts[-1], sp.array([info])]
ev[i].verified = sp.array(ev[i].verified, dtype='bool')
IN.close()
counts = sp.dstack(counts)
ev = ev[old_idx]
counts = counts[:, :, old_idx]
if out_fn is not None:
cPickle.dump((ev, counts), open(out_fn, 'w'))
return (ev, counts)
def velocity_field(self):
"""Current calculated velocity field across simulated grid points."""
return scipy.dstack((self._u_int, self._v_int))
matpyDir = '/home/dell/Desktop/sarvaswa/objectness-release-v2.2/Trial_Pascal/testSet/exp1/salprop-v1.0/matpy/' imgFile = matpyDir + 'imgFile.png' colorTextureFile = matpyDir + 'colorTextureFile.mat' #Loading Image and defining parameters img = imread(imgFile) imgLab = cvtColor(img, COLOR_BGR2LAB) L = imgLab[:, :, 0] sigma = 0.5 #TEXTURE FEATURES #LoG Computation on L channel of LAB Image LoG1 = nd.gaussian_laplace(L, sigma) LoG2 = nd.gaussian_laplace(L, 2 * sigma) LoG3 = nd.gaussian_laplace(L, 4 * sigma) LoG = dstack((LoG1, LoG2, LoG3)) LoG = average(LoG, axis=2) #Gaussian Filter Computation on L,A,B channels of LAB Image G1 = nd.gaussian_filter(L, sigma) G2 = nd.gaussian_filter(L, 2 * sigma) G3 = nd.gaussian_filter(L, 4 * sigma) #DoG Computation on L channel of LAB Image DoG1 = G2 - G1 DoG2 = G3 - G2 DoG = dstack((DoG1, DoG2)) DoG = average(DoG, axis=2) #Generate Features using above computed matrices feat = dstack((DoG, LoG))
def verify_all_events(ev,
strain_idx=None,
list_bam=None,
event_type=None,
CFG=None,
out_fn=None):
# (ev, counts) = verify_all_events(ev, strain_idx, list_bam, event_type, CFG) ;
### set parameters if called by rproc
if strain_idx is None:
PAR = ev
ev = PAR['ev']
strain_idx = PAR['strain_idx']
list_bam = PAR['list_bam']
if 'out_fn' in PAR:
out_fn = PAR['out_fn']
event_type = PAR['event_type']
CFG = PAR['CFG']
### verify the events if demanded
if CFG['verify_alt_events']:
prune_tag = ''
if CFG['do_prune']:
prune_tag = '_pruned'
validate_tag = ''
if CFG['validate_splicegraphs']:
validate_tag = '.validated'
(genes, inserted) = cPickle.load(
open('%s/spladder/genes_graph_conf%i.%s%s%s.pickle' %
(CFG['out_dirname'], CFG['confidence_level'],
CFG['merge_strategy'], validate_tag, prune_tag)))
fn_count = '%s/spladder/genes_graph_conf%i.%s%s%s.count.hdf5' % (
CFG['out_dirname'], CFG['confidence_level'], CFG['merge_strategy'],
validate_tag, prune_tag)
### load count index data from hdf5
IN = h5py.File(fn_count, 'r')
if os.path.exists(fn_count + '.quick_ids_segs'):
gene_ids_segs = cPickle.load(
open(fn_count + '.quick_ids_segs', 'r'))
else:
gene_ids_segs = IN['gene_ids_segs'][:]
if os.path.exists(fn_count + '.quick_ids_edges'):
gene_ids_edges = cPickle.load(
open(fn_count + '.quick_ids_edges', 'r'))
else:
gene_ids_edges = IN['gene_ids_edges'][:]
if os.path.exists(fn_count + '.quick_edge_idx'):
edge_idx = cPickle.load(open(fn_count + '.quick_edge_idx', 'r'))
else:
edge_idx = IN['edge_idx'][:]
### sort events by gene idx
s_idx = sp.argsort([x.gene_idx for x in ev])
ev = ev[s_idx]
old_idx = sp.argsort(s_idx)
### find gene idx boundaries
counts = []
for i in range(ev.shape[0]):
g_idx = ev[i].gene_idx
### there are no edges present in the event
if gene_ids_edges.shape[0] == 0:
ver, info = verify_empty(event_type)
counts.append(sp.array([info]))
ev[i].verified = sp.array(ev[i].verified, dtype='bool')
continue
gr_idx_segs = sp.where(gene_ids_segs == g_idx)[0]
gr_idx_edges = sp.where(gene_ids_edges == g_idx)[0]
if gr_idx_edges.shape[0] == 0:
ver, info = verify_empty(event_type)
counts.append(sp.array([info]))
ev[i].verified = sp.array(ev[i].verified, dtype='bool')
continue
### laod relevant count data from HDF5
segments = sp.atleast_2d(
IN['segments'][gr_idx_segs, :])[:, strain_idx]
seg_pos = sp.atleast_2d(IN['seg_pos'][gr_idx_segs, :])[:,
strain_idx]
edges = sp.atleast_2d(IN['edges'][gr_idx_edges, :])[:, strain_idx]
curr_edge_idx = edge_idx[gr_idx_edges]
for s_idx in range(len(strain_idx)):
#sys.stdout.write('.')
#if s_idx > 0 and s_idx % 50 == 0:
# sys.stdout.write('%i\n' % s_idx)
# ev_tmp.subset_strain(s_idx) ### TODO
if event_type == 'exon_skip':
ver, info = verify_exon_skip(
ev[i], genes[g_idx], segments[:, s_idx].T,
sp.c_[curr_edge_idx, edges[:, s_idx]], CFG)
elif event_type in ['alt_3prime', 'alt_5prime']:
ver, info = verify_alt_prime(
ev[i], genes[g_idx], segments[:, s_idx].T,
sp.c_[curr_edge_idx, edges[:, s_idx]], CFG)
elif event_type == 'intron_retention':
ver, info = verify_intron_retention(
ev[i], genes[g_idx], segments[:, s_idx].T,
sp.c_[curr_edge_idx,
edges[:, s_idx]], seg_pos[:, s_idx].T, CFG)
elif event_type == 'mult_exon_skip':
ver, info = verify_mult_exon_skip(
ev[i], genes[g_idx], segments[:, s_idx].T,
sp.c_[curr_edge_idx, edges[:, s_idx]], CFG)
elif event_type == 'mutex_exons':
ver, info = verify_mutex_exons(
ev[i], genes[g_idx], segments[:, s_idx].T,
sp.c_[curr_edge_idx, edges[:, s_idx]], CFG)
ev[i].verified.append(ver)
if s_idx == 0:
counts.append(sp.array([info]))
else:
counts[-1] = sp.r_[counts[-1], sp.array([info])]
ev[i].verified = sp.array(ev[i].verified, dtype='bool')
IN.close()
counts = sp.dstack(counts)
ev = ev[old_idx]
counts = counts[:, :, old_idx]
if out_fn is not None:
cPickle.dump((ev, counts), open(out_fn, 'w'), -1)
return (ev, counts)
sp.shape(Velocity1L_t)[1],
axis=1), [t for t in range(2,
sp.shape(Velocity1L_t)[1])], 1)
E_i_val = d_test['arr_4'][:numSamples]
E_f_val = d_test['arr_5'][:numSamples]
p_x_i_val = d_test['arr_6'][:numSamples]
p_x_f_val = d_test['arr_7'][:numSamples]
p_y_i_val = d_test['arr_8'][:numSamples]
p_y_f_val = d_test['arr_9'][:numSamples]
#===============================================================================================================
# Collect Input and Output for Network
#===============================================================================================================
# Dimensions of (samples, timesteps, features)
input_Arr = sp.dstack(
(Position1L_firstSecond, Velocity1L_firstSecond, dt_Arr))[:, 0, :]
target_Arr = sp.dstack((Position1L_firstSecond, Velocity1L_firstSecond))[:,
1, :]
input_Arr_val = sp.dstack(
(Position1L_firstSecond_val, Velocity1L_firstSecond_val, dt_Arr_val))[:,
0, :]
target_Arr_val = sp.dstack(
(Position1L_firstSecond_val, Velocity1L_firstSecond_val))[:, 1, :]
#===============================================================================================================
# Network
#===============================================================================================================
# Training existing model. Comment out if you do not wish to do this.
# model = load_model("trainedModel_temp.hd5")
is_candidate = sp.zeros(is_candidate.shape[0], dtype='bool')
is_candidate[keep_idx] = 1
pickle.dump(is_candidate, open(candidate_out_step3, 'wb'), -1)
### report found candidates without checking for nearby variants
event_pos = sp.array([EV['event_pos'][i, :] for i in keep_idx])
gene_idx = sp.array([EV['gene_idx'][i] for i in keep_idx], dtype='int')
gene_strand = sp.array([EV['gene_strand'][i] for i in gene_idx])
gene_ids = sp.array([EV['gene_names'][i] for i in gene_idx])
gene_names = sp.array([un.get_ID(_, lookup=lookup) for _ in gene_ids])
is_coding = sp.array(
['coding' if _ in coding_genes else 'non-coding' for _ in gene_ids])
event_chr = sp.array([EV['gene_chr'][i] for i in gene_idx])
### number of candidates per gene
gene_mult_dict = dict(sp.dstack(sp.unique(gene_ids, return_counts=True))[0, :])
gene_mult = sp.array([gene_mult_dict[_] for _ in gene_ids])
s_idx = sp.argsort(delta_psi)[::-1]
# 0 1 2--7 8 9 10 11 12 13 14 15 16 17 18 19
res = sp.c_[keep_idx, event_chr, event_pos, gene_ids, gene_names, delta_psi,
gene_strand, is_coding, cov_mean, cov_max, affected, non_affected,
gene_mult, affected_files, non_affected_files, affected_donors,
non_affected_donors][s_idx, :]
sp.savetxt(os.path.join(BASEDIR_AS, 'alternative_splicing',
'exonization_candidates_C2.txt'),
res,
fmt='%s',
delimiter='\t')
### continue overlapping to variants in a nearby window
def verify_all_events(ev, strain_idx=None, list_bam=None, event_type=None, CFG=None, out_fn=None):
# (ev, counts) = verify_all_events(ev, strain_idx, list_bam, event_type, CFG) ;
### set parameters if called by rproc
if strain_idx is None:
PAR = ev
ev = PAR["ev"]
strain_idx = PAR["strain_idx"]
list_bam = PAR["list_bam"]
if "out_fn" in PAR:
out_fn = PAR["out_fn"]
event_type = PAR["event_type"]
CFG = PAR["CFG"]
### verify the events if demanded
if CFG["verify_alt_events"]:
prune_tag = ""
if CFG["do_prune"]:
prune_tag = "_pruned"
validate_tag = ""
if CFG["validate_splicegraphs"]:
validate_tag = ".validated"
if CFG["merge_strategy"] == "single":
(genes, inserted) = cPickle.load(
open(
"%s/spladder/genes_graph_conf%i.%s%s%s.pickle"
% (CFG["out_dirname"], CFG["confidence_level"], CFG["samples"][strain_idx], validate_tag, prune_tag)
)
)
fn_count = "%s/spladder/genes_graph_conf%i.%s%s%s.count.hdf5" % (
CFG["out_dirname"],
CFG["confidence_level"],
CFG["samples"][strain_idx],
validate_tag,
prune_tag,
)
else:
(genes, inserted) = cPickle.load(
open(
"%s/spladder/genes_graph_conf%i.%s%s%s.pickle"
% (CFG["out_dirname"], CFG["confidence_level"], CFG["merge_strategy"], validate_tag, prune_tag)
)
)
fn_count = "%s/spladder/genes_graph_conf%i.%s%s%s.count.hdf5" % (
CFG["out_dirname"],
CFG["confidence_level"],
CFG["merge_strategy"],
validate_tag,
prune_tag,
)
### load count index data from hdf5
IN = h5py.File(fn_count, "r")
if os.path.exists(fn_count + ".quick_ids_segs"):
gene_ids_segs = cPickle.load(open(fn_count + ".quick_ids_segs", "r"))
else:
gene_ids_segs = IN["gene_ids_segs"][:]
if os.path.exists(fn_count + ".quick_ids_edges"):
gene_ids_edges = cPickle.load(open(fn_count + ".quick_ids_edges", "r"))
else:
gene_ids_edges = IN["gene_ids_edges"][:]
if os.path.exists(fn_count + ".quick_edge_idx"):
edge_idx = cPickle.load(open(fn_count + ".quick_edge_idx", "r"))
else:
edge_idx = IN["edge_idx"][:]
### sort events by gene idx
s_idx = sp.argsort([x.gene_idx for x in ev])
ev = ev[s_idx]
old_idx = sp.argsort(s_idx)
counts = []
for i in range(ev.shape[0]):
# sys.stdout.write('.')
# if i > 0 and i % 50 == 0:
# sys.stdout.write('%i (%i)\n' % (i, ev.shape[0]))
# sys.stdout.flush()
g_idx = ev[i].gene_idx
ev[i].verified = [] ### TODO: maybe solve that differently
### there are no edges present in the event
if gene_ids_edges.shape[0] == 0:
ver, info = verify_empty(event_type)
counts.append(sp.array([info]))
ev[i].verified = sp.array(ev[i].verified, dtype="bool")
continue
gr_idx_segs = sp.where(gene_ids_segs == g_idx)[0]
gr_idx_edges = sp.where(gene_ids_edges == g_idx)[0]
if gr_idx_edges.shape[0] == 0:
ver, info = verify_empty(event_type)
counts.append(sp.array([info]))
ev[i].verified = sp.array(ev[i].verified, dtype="bool")
continue
### laod relevant count data from HDF5
segments = sp.atleast_2d(IN["segments"][gr_idx_segs, :])[:, strain_idx]
seg_pos = sp.atleast_2d(IN["seg_pos"][gr_idx_segs, :])[:, strain_idx]
edges = sp.atleast_2d(IN["edges"][gr_idx_edges, :])[:, strain_idx]
curr_edge_idx = edge_idx[gr_idx_edges]
for s_idx in range(len(strain_idx)):
# sys.stdout.write('.')
# if s_idx > 0 and s_idx % 50 == 0:
# sys.stdout.write('%i (%i)\n' % (s_idx, len(strain_idx)))
# ev_tmp.subset_strain(s_idx) ### TODO
# sys.stdout.flush()
if event_type == "exon_skip":
ver, info = verify_exon_skip(
ev[i], genes[g_idx], segments[:, s_idx].T, sp.c_[curr_edge_idx, edges[:, s_idx]], CFG
)
elif event_type in ["alt_3prime", "alt_5prime"]:
ver, info = verify_alt_prime(
ev[i], genes[g_idx], segments[:, s_idx].T, sp.c_[curr_edge_idx, edges[:, s_idx]], CFG
)
elif event_type == "intron_retention":
ver, info = verify_intron_retention(
ev[i],
genes[g_idx],
segments[:, s_idx].T,
sp.c_[curr_edge_idx, edges[:, s_idx]],
seg_pos[:, s_idx].T,
CFG,
)
elif event_type == "mult_exon_skip":
ver, info = verify_mult_exon_skip(
ev[i], genes[g_idx], segments[:, s_idx].T, sp.c_[curr_edge_idx, edges[:, s_idx]], CFG
)
elif event_type == "mutex_exons":
ver, info = verify_mutex_exons(
ev[i], genes[g_idx], segments[:, s_idx].T, sp.c_[curr_edge_idx, edges[:, s_idx]], CFG
)
ev[i].verified.append(ver)
if s_idx == 0:
counts.append(sp.array([info]))
else:
counts[-1] = sp.r_[counts[-1], sp.array([info])]
ev[i].verified = sp.array(ev[i].verified, dtype="bool")
IN.close()
counts = sp.dstack(counts)
ev = ev[old_idx]
counts = counts[:, :, old_idx]
if out_fn is not None:
cPickle.dump((ev, counts), open(out_fn, "w"), -1)
return (ev, counts)
def no_weave(a):
b = sp.dstack(a)
return b.sum(axis=2)
def verify_all_events(ev, strain_idx=None, list_bam=None, event_type=None, options=None, out_fn=None):
### set parameters if called by rproc
if strain_idx is None:
PAR = ev
ev = PAR['ev']
strain_idx = PAR['strain_idx']
list_bam = PAR['list_bam']
if 'out_fn' in PAR:
out_fn = PAR['out_fn']
event_type = PAR['event_type']
options = PAR['options']
### verify the events if demanded
if options.verify_alt_events:
prune_tag = ''
if options.do_prune:
prune_tag = '_pruned'
validate_tag = ''
if options.validate_sg:
validate_tag = '.validated'
if options.merge == 'single':
(genes, inserted) = pickle.load(open('%s/spladder/genes_graph_conf%i.%s%s%s.pickle' % (options.outdir, options.confidence, options.samples[strain_idx], validate_tag, prune_tag), 'rb'))
fn_count = '%s/spladder/genes_graph_conf%i.%s%s%s.count.hdf5' % (options.outdir, options.confidence, options.samples[strain_idx], validate_tag, prune_tag)
else:
(genes, inserted) = pickle.load(open('%s/spladder/genes_graph_conf%i.%s%s%s.pickle' % (options.outdir, options.confidence, options.merge, validate_tag, prune_tag), 'rb'))
fn_count = '%s/spladder/genes_graph_conf%i.%s%s%s.count.hdf5' % (options.outdir, options.confidence, options.merge, validate_tag, prune_tag)
### load count index data from hdf5
IN = h5py.File(fn_count, 'r')
if os.path.exists(fn_count + '.quick_ids_segs'):
gene_ids_segs = pickle.load(open(fn_count + '.quick_ids_segs', 'rb'))
else:
gene_ids_segs = IN['gene_ids_segs'][:]
pickle.dump(gene_ids_segs, open(fn_count + '.quick_ids_segs', 'wb'), -1)
if os.path.exists(fn_count + '.quick_ids_edges'):
gene_ids_edges = pickle.load(open(fn_count + '.quick_ids_edges', 'rb'))
else:
gene_ids_edges = IN['gene_ids_edges'][:]
pickle.dump(gene_ids_edges, open(fn_count + '.quick_ids_edges', 'wb'), -1)
if os.path.exists(fn_count + '.quick_edge_idx'):
edge_idx = pickle.load(open(fn_count + '.quick_edge_idx', 'rb'))
else:
edge_idx = IN['edge_idx'][:]
pickle.dump(edge_idx, open(fn_count + '.quick_edge_idx', 'wb'), -1)
### sort events by gene idx
s_idx = sp.argsort([x.gene_idx for x in ev])
ev = ev[s_idx]
old_idx = sp.argsort(s_idx)
counts = []
for i in range(ev.shape[0]):
sys.stdout.write('.')
if i > 0 and i % 50 == 0:
sys.stdout.write('%i (%i)\n' % (i, ev.shape[0]))
sys.stdout.flush()
g_idx = ev[i].gene_idx
ev[i].verified = [] ### TODO: maybe solve that differently
### there are no edges present in the event
if gene_ids_edges.shape[0] == 0:
ver, info = verify_empty(event_type)
counts.append(sp.array([info]))
ev[i].verified = sp.array(ev[i].verified, dtype='bool')
continue
gr_idx_segs = sp.where(gene_ids_segs == g_idx)[0]
gr_idx_edges = sp.where(gene_ids_edges == g_idx)[0]
if gr_idx_edges.shape[0] == 0:
ver, info = verify_empty(event_type)
counts.append(sp.array([info]))
ev[i].verified = sp.array(ev[i].verified, dtype='bool')
continue
if isinstance(strain_idx, int):
strain_idx = [strain_idx]
### laod relevant count data from HDF5
segments = sp.atleast_2d(IN['segments'][gr_idx_segs, :])[:, strain_idx]
seg_pos = sp.atleast_2d(IN['seg_pos'][gr_idx_segs, :])[:, strain_idx]
edges = sp.atleast_2d(IN['edges'][gr_idx_edges, :])[:, strain_idx]
curr_edge_idx = edge_idx[gr_idx_edges]
for s_idx in range(len(strain_idx)):
#if s_idx > 0 and s_idx % 50 == 0:
# sys.stdout.write('%i (%i)\n' % (s_idx, len(strain_idx)))
# ev_tmp.subset_strain(s_idx) ### TODO
#sys.stdout.flush()
if event_type == 'exon_skip':
ver, info = verify_exon_skip(ev[i], genes[g_idx], segments[:, s_idx].T, sp.c_[curr_edge_idx, edges[:, s_idx]], options)
elif event_type in ['alt_3prime', 'alt_5prime']:
ver, info = verify_alt_prime(ev[i], genes[g_idx], segments[:, s_idx].T, sp.c_[curr_edge_idx, edges[:, s_idx]], options)
elif event_type == 'intron_retention':
ver, info = verify_intron_retention(ev[i], genes[g_idx], segments[:, s_idx].T, sp.c_[curr_edge_idx, edges[:, s_idx]], seg_pos[:, s_idx].T, options)
elif event_type == 'mult_exon_skip':
ver, info = verify_mult_exon_skip(ev[i], genes[g_idx], segments[:, s_idx].T, sp.c_[curr_edge_idx, edges[:, s_idx]], options)
elif event_type == 'mutex_exons':
ver, info = verify_mutex_exons(ev[i], genes[g_idx], segments[:, s_idx].T, sp.c_[curr_edge_idx, edges[:, s_idx]], options)
ev[i].verified.append(ver)
if s_idx == 0:
counts.append(sp.array([info], dtype='float'))
else:
counts[-1] = sp.r_[counts[-1], sp.array([info], dtype='float')]
ev[i].verified = sp.array(ev[i].verified, dtype='bool')
IN.close()
counts = sp.dstack(counts)
ev = ev[old_idx]
counts = counts[:, :, old_idx]
if out_fn is not None:
pickle.dump((ev, counts), open(out_fn, 'wb'), -1)
return (ev, counts)
def __init__(self,coordlist,paramlist,times = None,sensor_loc = sp.zeros(3),ver =0,coordvecs =
None,paramnames=None,species=None,velocity=None):
""" This constructor function will use create an instance of the IonoContainer class
using either cartisian or spherical coordinates depending on which ever the user prefers.
Inputs:
coordlist - Nx3 Numpy array where N is the number of coordinates.
paramlist - NxTxP Numpy array where T is the number of times and P is the number of parameters
alternatively it could be NxP if there is only one time instance.
times - A T length numpy array where T is the number of times. This is
optional input, if not given then its just a numpy array of 0-T
sensor_loc - A numpy array of length 3 that gives the sensor location.
The default value is [0,0,0] in cartisian space.
ver - (Optional) If 0 the coordlist is in Cartisian coordinates if 1 then
coordlist is a spherical coordinates.
coordvecs - (Optional) A dictionary that holds the individual coordinate vectors.
if sphereical coordinates keys are 'r','theta','phi' if cartisian 'x','y','z'.
paramnames - This is a list or number numpy array of numbers for each parameter in the
"""
r2d = 180.0/np.pi
d2r = np.pi/180.0
# Set up the size for the time vector if its not given.
Ndims = paramlist.ndim
psizetup = paramlist.shape
if times is None:
if Ndims==3:
times = np.arange(psizetup[1])
else:
times = np.arange(1)
if Ndims==2:
paramlist = paramlist[:,np.newaxis,:]
# Assume that the
if ver==0:
X_vec = coordlist[:,0]
Y_vec = coordlist[:,1]
Z_vec = coordlist[:,2]
R_vec = sp.sqrt(X_vec**2+Y_vec**2+Z_vec**2)
Az_vec = sp.arctan2(X_vec,Y_vec)*r2d
El_vec = sp.arcsin(Z_vec/R_vec)*r2d
self.Cart_Coords = coordlist
self.Sphere_Coords = sp.array([R_vec,Az_vec,El_vec]).transpose()
if coordvecs is not None:
if set(coordvecs)!={'x','y','z'}:
raise NameError("Keys for coordvecs need to be 'x','y','z' ")
else:
coordvecs = ['x','y','z']
elif ver==1:
R_vec = coordlist[:,0]
Az_vec = coordlist[:,1]
El_vec = coordlist[:,2]
xvecmult = np.sin(Az_vec*d2r)*np.cos(El_vec*d2r)
yvecmult = np.cos(Az_vec*d2r)*np.cos(El_vec*d2r)
zvecmult = np.sin(El_vec*d2r)
X_vec = R_vec*xvecmult
Y_vec = R_vec*yvecmult
Z_vec = R_vec*zvecmult
self.Cart_Coords = sp.column_stack((X_vec,Y_vec,Z_vec))
self.Sphere_Coords = coordlist
if coordvecs is not None:
if set(coordvecs)!={'r','theta','phi'}:
raise NameError("Keys for coordvecs need to be 'r','theta','phi' ")
else:
coordvecs = ['r','theta','phi']
# used to deal with the change in the files
if type(coordvecs)==np.ndarray:
coordvecs = [str(ic) for ic in coordvecs]
self.Param_List = paramlist
self.Time_Vector = times
self.Coord_Vecs = coordvecs
self.Sensor_loc = sensor_loc
self.Species = species
(Nloc,Nt) = paramlist.shape[:2]
#set up a Velocity measurement
if velocity is None:
self.Velocity=sp.zeros((Nloc,Nt,3))
else:
# if in sperical coordinates and you have a velocity
if velocity.ndim ==2 and ver==1:
veltup = (velocity*sp.tile(xvecmult[:,sp.newaxis],(1,Nt)),
velocity*sp.tile(yvecmult[:,sp.newaxis],(1,Nt)),
velocity*sp.tile(zvecmult[:,sp.newaxis],(1,Nt)))
self.Velocity= sp.dstack(veltup)
else:
self.Velocity=velocity
# set up a params name
if paramnames is None:
partparam = paramlist.shape[2:]
if species is not None:
paramnames = [['Ni_'+isp,'Ti_'+isp] for isp in species[:-1]]
paramnames.append(['Ne','Te'])
self.Param_Names=sp.array(paramnames,dtype=str)
else:
paramnums = np.arange(np.product(partparam))
self.Param_Names = np.reshape(paramnums,partparam)
else:
self.Param_Names = paramnames
def distance(a, b):
#Returns the distance from point a to point b. Takes any iterable class of length 3 representing X,Y,Z in cartesian coordinates. Arrays/lists/tuples all work.
subtrArray = sp.dstack([a, -b]).sum(2)
return sp.sqrt(sp.sum([n**2 for n in subtrArray]))
def quantify_from_graph(ev, strain_idx=None, event_type=None, CFG=None, out_fn=None, fn_merge=None):
# cov = quantify_from_graph(ev, strain_idx, event_type, CFG, out_fn)
### set parameters if called by rproc
if strain_idx is None:
PAR = ev
ev = PAR['ev']
strain_idx = PAR['strain_idx']
if 'out_fn' in PAR:
out_fn = PAR['out_fn']
event_type = PAR['event_type']
CFG = PAR['CFG']
if fn_merge is None:
fn_merge = get_filename('fn_out_merge_val', CFG)
if CFG['is_matlab']:
genes = scio.loadmat(fn_merge, struct_as_record=False)['genes'][0, :]
fn_count = fn_merge.replace('mat', 'count.mat')
else:
genes = cPickle.load(open(fn_merge_val, 'r'))[0]
fn_count = fn_merge.replace('pickle', 'count.hdf5')
### load count index data from hdf5
IN = h5py.File(fn_count, 'r')
gene_ids_segs = IN['gene_ids_segs'][:].astype('int')
gene_ids_edges = IN['gene_ids_edges'][:].astype('int')
if len(gene_ids_segs.shape) > 1:
gene_ids_segs = gene_ids_segs[0, :]
if len(gene_ids_edges.shape) > 1:
gene_ids_edges = gene_ids_edges[0, :]
### sort events by gene idx
s_idx = sp.argsort([x.gene_idx for x in ev])
ev = ev[s_idx]
old_idx = sp.argsort(s_idx)
### find gene idx boundaries
assert(isequal(gene_ids_segs, sp.sort(gene_ids_segs)))
assert(isequal(gene_ids_edges, sp.sort(gene_ids_edges)))
tmp, genes_f_idx_segs = sp.unique(gene_ids_segs, return_index=True)
genes_l_idx_segs = sp.r_[genes_f_idx_segs[1:] - 1, gene_ids_segs.shape[0]]
tmp, genes_f_idx_edges = sp.unique(gene_ids_edges, return_index=True)
genes_l_idx_edges = sp.r_[genes_f_idx_edges[1:] - 1, gene_ids_edges.shape[0]]
gr_idx_segs = 0
gr_idx_edges = 0
counts = []
for i in range(ev.shape[0]):
sys.stdout.write('.')
if i % 10 == 0:
sys.stdout.write('%i\n' % i)
sys.stdout.flush()
if CFG['is_matlab']:
offset = 1
else:
offset = 0
g_idx = ev[i].gene_idx
while gene_ids_segs[genes_f_idx_segs[gr_idx_segs]] < g_idx:
gr_idx_segs += 1
assert(gene_ids_segs[genes_f_idx_segs[gr_idx_segs]] == g_idx)
while gene_ids_edges[genes_f_idx_edges[gr_idx_edges]] < g_idx:
gr_idx_edges += 1
assert(gene_ids_edges[genes_f_idx_edges[gr_idx_edges]] == g_idx)
### laod relevant count data from HDF5
if CFG['is_matlab']:
segments = IN['segments'][strain_idx, genes_f_idx_segs[gr_idx_segs]:genes_l_idx_segs[gr_idx_segs] + 1].T
seg_pos = IN['seg_pos'][strain_idx, genes_f_idx_segs[gr_idx_segs]:genes_l_idx_segs[gr_idx_segs] + 1].astype('int')
edges = IN['edges'][strain_idx, genes_f_idx_edges[gr_idx_edges]:genes_l_idx_edges[gr_idx_edges] + 1].T
edge_idx = IN['edge_idx'][0, genes_f_idx_edges[gr_idx_edges]:genes_l_idx_edges[gr_idx_edges] + 1].astype('int')
else:
segments = IN['segments'][genes_f_idx_segs[gr_idx_segs]:genes_l_idx_segs[gr_idx_segs]+1, strain_idx]
seg_pos = IN['seg_pos'][genes_f_idx_segs[gr_idx_segs]:genes_l_idx_segs[gr_idx_segs]+1, strain_idx]
edges = IN['edges'][genes_f_idx_edges[gr_idx_edges]:genes_l_idx_edges[gr_idx_edges]+1, strain_idx]
edge_idx = IN['edge_idx'][genes_f_idx_edges[gr_idx_edges]:genes_l_idx_edges[gr_idx_edges]+1]
for s_idx in range(len(strain_idx)):
#print '%i/%i' % (s_idx, len(strain_idx))
if event_type == 'exon_skip':
cov = quantify_exon_skip(ev[i], genes[g_idx - offset], segments[:, s_idx].T, sp.c_[edge_idx, edges[:, s_idx]], CFG)
elif event_type in ['alt_3prime', 'alt_5prime']:
cov = quantify_alt_prime(ev[i], genes[g_idx - offset], segments[:, s_idx].T, sp.c_[edge_idx, edges[:, s_idx]], CFG)
elif event_type == 'intron_retention':
cov = quantify_intron_retention(ev[i], genes[g_idx - offset], segments[:, s_idx].T, sp.c_[edge_idx, edges[:, s_idx]], seg_pos[:, s_idx].T, CFG)
elif event_type == 'mult_exon_skip':
cov = quantify_mult_exon_skip(ev[i], genes[g_idx - offset], segments[:, s_idx].T, sp.c_[edge_idx, edges[:, s_idx]], CFG)
elif event_type == 'mutex_exons':
cov = quantify_mutex_exons(ev[i], genes[g_idx - offset], segments[:, s_idx].T, sp.c_[edge_idx, edges[:, s_idx]], CFG)
if s_idx == 0:
counts.append(sp.array([cov]))
else:
counts[-1] = sp.r_[counts[-1], sp.array([cov])]
IN.close()
counts = sp.dstack(counts)
### re-sort by old idx
ev = ev[old_idx]
counts = counts[:, :, old_idx]
if out_fn is not None:
cPickle.dump((ev, counts), open(out_fn, 'w'))
return (ev, counts)
def __init__(self, series1, series2, wave1, wave2, *args, **kwargs):
series = sp.vstack((series1.ravel(), series2.ravel())).T
wave = sp.dstack((wave1, wave2))
WaveletTransform.__init__(self, series, wave, *args, **kwargs)
def dsift(im,
verbose=True,
fast=True,
sizes=[4, 6, 8, 10],
step=2,
color='rgb',
floatdescriptors=False,
magnif=6,
windowsize=1.5,
contrastthreshold=0.005):
opts = Options(verbose, fast, sizes, step, color, floatdescriptors,
magnif, windowsize, contrastthreshold)
dsiftOpts = DSiftOptions(opts)
# make sure image is float, otherwise segfault
im = array(im, 'float32')
# Extract the features
imageSize = shape(im)
if im.ndim == 3:
if imageSize[2] != 3:
# "IndexError: tuple index out of range" if both if's are checked at the same time
raise ValueError("Image data in unknown format/shape")
if opts.color == 'gray':
numChannels = 1
if (im.ndim == 2):
im = vl_rgb2gray(im)
else:
numChannels = 3
if (im.ndim == 2):
im = dstack([im, im, im])
if opts.color == 'rgb':
pass
elif opts.color == 'opponent':
# from https://github.com/vlfeat/vlfeat/blob/master/toolbox/sift/vl_phow.m
# Note that the mean differs from the standard definition of opponent
# space and is the regular intesity (for compatibility with
# the contrast thresholding).
# Note also that the mean is added pack to the other two
# components with a small multipliers for monochromatic
# regions.
mu = 0.3 * im[:, :, 0] + 0.59 * im[:, :, 1] + 0.11 * im[:, :, 2]
alpha = 0.01
im = dstack([mu,
(im[:, :, 0] - im[:, :, 1]) / sqrt(2) + alpha * mu,
(im[:, :, 0] + im[:, :, 1] - 2 * im[:, :, 2]) / sqrt(6) + alpha * mu])
else:
raise ValueError('Color option ' + str(opts.color) + ' not recognized')
if opts.verbose:
great='great'
#print('{0}: color space: {1}'.format('vl_phow', opts.color))
#print('{0}: image size: {1} x {2}'.format('vl_phow', imageSize[0], imageSize[1]))
#print('{0}: sizes: [{1}]'.format('vl_phow', opts.sizes))
frames_all = []
descrs_all = []
for size_of_spatial_bins in opts.sizes:
# from https://github.com/vlfeat/vlfeat/blob/master/toolbox/sift/vl_phow.m
# Recall from VL_DSIFT() that the first descriptor for scale SIZE has
# center located at XC = XMIN + 3/2 SIZE (the Y coordinate is
# similar). It is convenient to align the descriptors at different
# scales so that they have the same geometric centers. For the
# maximum size we pick XMIN = 1 and we get centers starting from
# XC = 1 + 3/2 MAX(OPTS.SIZES). For any other scale we pick XMIN so
# that XMIN + 3/2 SIZE = 1 + 3/2 MAX(OPTS.SIZES).
# In pracrice, the offset must be integer ('bounds'), so the
# alignment works properly only if all OPTS.SZES are even or odd.
off = floor(3.0 / 2 * (max(opts.sizes) - size_of_spatial_bins)) + 1
# smooth the image to the appropriate scale based on the size
# of the SIFT bins
sigma = size_of_spatial_bins / float(opts.magnif)
ims = vl_imsmooth(im, sigma)
# extract dense SIFT features from all channels
frames = []
descrs = []
for k in range(numChannels):
size_of_spatial_bins = int(size_of_spatial_bins)
# vl_dsift does not accept numpy.int64 or similar
f_temp, d_temp = vl_dsift(data=ims[:, :, k],
step=dsiftOpts.step,
size=size_of_spatial_bins,
fast=dsiftOpts.fast,
verbose=dsiftOpts.verbose,
norm=dsiftOpts.norm,
bounds=[off, off, maxint, maxint])
frames.append(f_temp)
descrs.append(d_temp)
frames = array(frames)
descrs = array(descrs)
d_new_shape = [descrs.shape[0] * descrs.shape[1], descrs.shape[2]]
descrs = descrs.reshape(d_new_shape)
# remove low contrast descriptors
# note that for color descriptors the V component is
# thresholded
if (opts.color == 'gray') | (opts.color == 'opponent'):
contrast = frames[0][2, :]
elif opts.color == 'rgb':
contrast = mean([frames[0][2, :], frames[1][2, :], frames[2][2, :]], 0)
else:
raise ValueError('Color option ' + str(opts.color) + ' not recognized')
descrs[:, contrast < opts.contrastthreshold] = 0
# save only x,y, and the scale
frames_temp = array(frames[0][0:3, :])
padding = array(size_of_spatial_bins * ones(frames[0][0].shape))
frames_all.append(vstack([frames_temp, padding]))
descrs_all.append(array(descrs))
frames_all = hstack(frames_all)
descrs_all = hstack(descrs_all)
return frames_all, descrs_all
def __init__(self,
coordlist,
paramlist,
times=None,
sensor_loc=sp.zeros(3),
ver=0,
coordvecs=None,
paramnames=None,
species=None,
velocity=None):
""" This constructor function will use create an instance of the IonoContainer class
using either cartisian or spherical coordinates depending on which ever the user prefers.
Inputs:
coordlist - Nx3 Numpy array where N is the number of coordinates.
paramlist - NxTxP Numpy array where T is the number of times and P is the number of parameters
alternatively it could be NxP if there is only one time instance.
times - A T length numpy array where T is the number of times. This is
optional input, if not given then its just a numpy array of 0-T
sensor_loc - A numpy array of length 3 that gives the sensor location.
The default value is [0,0,0] in cartisian space.
ver - (Optional) If 0 the coordlist is in Cartisian coordinates if 1 then
coordlist is a spherical coordinates.
coordvecs - (Optional) A dictionary that holds the individual coordinate vectors.
if sphereical coordinates keys are 'r','theta','phi' if cartisian 'x','y','z'.
paramnames - This is a list or number numpy array of numbers for each parameter in the
"""
r2d = 180.0 / np.pi
d2r = np.pi / 180.0
# Set up the size for the time vector if its not given.
Ndims = paramlist.ndim
psizetup = paramlist.shape
if times is None:
if Ndims == 3:
times = np.arange(psizetup[1])
else:
times = np.arange(1)
if Ndims == 2:
paramlist = paramlist[:, np.newaxis, :]
# Assume that the
if ver == 0:
X_vec = coordlist[:, 0]
Y_vec = coordlist[:, 1]
Z_vec = coordlist[:, 2]
R_vec = sp.sqrt(X_vec**2 + Y_vec**2 + Z_vec**2)
Az_vec = sp.arctan2(X_vec, Y_vec) * r2d
El_vec = sp.arcsin(Z_vec / R_vec) * r2d
self.Cart_Coords = coordlist
self.Sphere_Coords = sp.array([R_vec, Az_vec, El_vec]).transpose()
if coordvecs is not None:
if set(coordvecs) != {'x', 'y', 'z'}:
raise NameError(
"Keys for coordvecs need to be 'x','y','z' ")
else:
coordvecs = ['x', 'y', 'z']
elif ver == 1:
R_vec = coordlist[:, 0]
Az_vec = coordlist[:, 1]
El_vec = coordlist[:, 2]
xvecmult = np.sin(Az_vec * d2r) * np.cos(El_vec * d2r)
yvecmult = np.cos(Az_vec * d2r) * np.cos(El_vec * d2r)
zvecmult = np.sin(El_vec * d2r)
X_vec = R_vec * xvecmult
Y_vec = R_vec * yvecmult
Z_vec = R_vec * zvecmult
self.Cart_Coords = sp.column_stack((X_vec, Y_vec, Z_vec))
self.Sphere_Coords = coordlist
if coordvecs is not None:
if set(coordvecs) != {'r', 'theta', 'phi'}:
raise NameError(
"Keys for coordvecs need to be 'r','theta','phi' ")
else:
coordvecs = ['r', 'theta', 'phi']
# used to deal with the change in the files
if type(coordvecs) == np.ndarray:
coordvecs = [str(ic) for ic in coordvecs]
self.Param_List = paramlist
self.Time_Vector = times
self.Coord_Vecs = coordvecs
self.Sensor_loc = sensor_loc
self.Species = species
(Nloc, Nt) = paramlist.shape[:2]
#set up a Velocity measurement
if velocity is None:
self.Velocity = sp.zeros((Nloc, Nt, 3))
else:
# if in sperical coordinates and you have a velocity
if velocity.ndim == 2 and ver == 1:
veltup = (velocity * sp.tile(xvecmult[:, sp.newaxis], (1, Nt)),
velocity * sp.tile(yvecmult[:, sp.newaxis], (1, Nt)),
velocity * sp.tile(zvecmult[:, sp.newaxis], (1, Nt)))
self.Velocity = sp.dstack(veltup)
else:
self.Velocity = velocity
# set up a params name
if paramnames is None:
partparam = paramlist.shape[2:]
if species is not None:
paramnames = [['Ni_' + isp, 'Ti_' + isp]
for isp in species[:-1]]
paramnames.append(['Ne', 'Te'])
self.Param_Names = sp.array(paramnames, dtype=str)
else:
paramnums = np.arange(np.product(partparam))
self.Param_Names = np.reshape(paramnums, partparam)
else:
self.Param_Names = paramnames
[t for t in range(1,
sp.shape(Velocity1L_t_val)[1] - 1)], 1)
# dt_Arr_val=sp.repeat(d_test['arr_17'][:numSamples,sp.newaxis],T,axis=1)
E_i_val = d_test['arr_4'][:numSamples]
E_f_val = d_test['arr_5'][:numSamples]
p_x_i_val = d_test['arr_6'][:numSamples]
p_x_f_val = d_test['arr_7'][:numSamples]
p_y_i_val = d_test['arr_8'][:numSamples]
p_y_f_val = d_test['arr_9'][:numSamples]
#===============================================================================================================
# Collect Input and Output for Network
#===============================================================================================================
# Dimensions of (samples, timesteps, features)
input_Arr = sp.dstack(
(Velocity1L_firstLast, Velocity2L_firstLast, m1_Arr, m2_Arr))[:, 0, :]
target_Arr = sp.dstack(
(Velocity1L_firstLast, Velocity2L_firstLast, m1_Arr, m2_Arr))[:, 1, :]
input_Arr_val = sp.dstack((Velocity1L_firstLast_val, Velocity2L_firstLast_val,
m1_Arr_val, m2_Arr_val))[:, 0, :]
target_Arr_val = sp.dstack((Velocity1L_firstLast_val, Velocity2L_firstLast_val,
m1_Arr_val, m2_Arr_val))[:, 1, :]
#===============================================================================================================
# Network
#===============================================================================================================
# # Training existing model. Comment out if you do not wish to do this.
# # model = load_model("trainedModel_temp.hd5")
#
# model = Sequential()
def verify_all_events(ev,
strain_idx=None,
list_bam=None,
event_type=None,
options=None,
out_fn=None):
### set parameters if called by rproc
if strain_idx is None:
PAR = ev
ev = PAR['ev']
strain_idx = PAR['strain_idx']
list_bam = PAR['list_bam']
if 'out_fn' in PAR:
out_fn = PAR['out_fn']
event_type = PAR['event_type']
options = PAR['options']
### verify the events if demanded
if options.verify_alt_events:
prune_tag = ''
if options.do_prune:
prune_tag = '_pruned'
validate_tag = ''
if options.validate_sg:
validate_tag = '.validated'
if options.merge == 'single':
(genes, inserted) = pickle.load(
open(
'%s/spladder/genes_graph_conf%i.%s%s%s.pickle' %
(options.outdir, options.confidence,
options.samples[strain_idx], validate_tag, prune_tag),
'rb'))
fn_count = '%s/spladder/genes_graph_conf%i.%s%s%s.count.hdf5' % (
options.outdir, options.confidence,
options.samples[strain_idx], validate_tag, prune_tag)
else:
(genes, inserted) = pickle.load(
open(
'%s/spladder/genes_graph_conf%i.%s%s%s.pickle' %
(options.outdir, options.confidence, options.merge,
validate_tag, prune_tag), 'rb'))
fn_count = '%s/spladder/genes_graph_conf%i.%s%s%s.count.hdf5' % (
options.outdir, options.confidence, options.merge,
validate_tag, prune_tag)
### load count index data from hdf5
IN = h5py.File(fn_count, 'r')
if os.path.exists(fn_count + '.quick_ids_segs'):
gene_ids_segs = pickle.load(
open(fn_count + '.quick_ids_segs', 'rb'))
else:
gene_ids_segs = IN['gene_ids_segs'][:]
pickle.dump(gene_ids_segs, open(fn_count + '.quick_ids_segs',
'wb'), -1)
if os.path.exists(fn_count + '.quick_ids_edges'):
gene_ids_edges = pickle.load(
open(fn_count + '.quick_ids_edges', 'rb'))
else:
gene_ids_edges = IN['gene_ids_edges'][:]
pickle.dump(gene_ids_edges,
open(fn_count + '.quick_ids_edges', 'wb'), -1)
if os.path.exists(fn_count + '.quick_edge_idx'):
edge_idx = pickle.load(open(fn_count + '.quick_edge_idx', 'rb'))
else:
edge_idx = IN['edge_idx'][:]
pickle.dump(edge_idx, open(fn_count + '.quick_edge_idx', 'wb'), -1)
### sort events by gene idx
s_idx = sp.argsort([x.gene_idx for x in ev])
ev = ev[s_idx]
old_idx = sp.argsort(s_idx)
counts = []
for i in range(ev.shape[0]):
sys.stdout.write('.')
if i > 0 and i % 50 == 0:
sys.stdout.write('%i (%i)\n' % (i, ev.shape[0]))
sys.stdout.flush()
g_idx = ev[i].gene_idx
ev[i].verified = [] ### TODO: maybe solve that differently
### there are no edges present in the event
if gene_ids_edges.shape[0] == 0:
ver, info = verify_empty(event_type)
counts.append(sp.array([info]))
ev[i].verified = sp.array(ev[i].verified, dtype='bool')
continue
gr_idx_segs = sp.where(gene_ids_segs == g_idx)[0]
gr_idx_edges = sp.where(gene_ids_edges == g_idx)[0]
if gr_idx_edges.shape[0] == 0:
ver, info = verify_empty(event_type)
counts.append(sp.array([info]))
ev[i].verified = sp.array(ev[i].verified, dtype='bool')
continue
if isinstance(strain_idx, int):
strain_idx = [strain_idx]
### laod relevant count data from HDF5
segments = sp.atleast_2d(
IN['segments'][gr_idx_segs, :])[:, strain_idx]
seg_pos = sp.atleast_2d(IN['seg_pos'][gr_idx_segs, :])[:,
strain_idx]
edges = sp.atleast_2d(IN['edges'][gr_idx_edges, :])[:, strain_idx]
curr_edge_idx = edge_idx[gr_idx_edges]
for s_idx in range(len(strain_idx)):
#if s_idx > 0 and s_idx % 50 == 0:
# sys.stdout.write('%i (%i)\n' % (s_idx, len(strain_idx)))
# ev_tmp.subset_strain(s_idx) ### TODO
#sys.stdout.flush()
if event_type == 'exon_skip':
ver, info = verify_exon_skip(
ev[i], genes[g_idx], segments[:, s_idx].T,
sp.c_[curr_edge_idx, edges[:, s_idx]], options)
elif event_type in ['alt_3prime', 'alt_5prime']:
ver, info = verify_alt_prime(
ev[i], genes[g_idx], segments[:, s_idx].T,
sp.c_[curr_edge_idx, edges[:, s_idx]], options)
elif event_type == 'intron_retention':
ver, info = verify_intron_retention(
ev[i], genes[g_idx], segments[:, s_idx].T,
sp.c_[curr_edge_idx,
edges[:, s_idx]], seg_pos[:, s_idx].T, options)
elif event_type == 'mult_exon_skip':
ver, info = verify_mult_exon_skip(
ev[i], genes[g_idx], segments[:, s_idx].T,
sp.c_[curr_edge_idx, edges[:, s_idx]], options)
elif event_type == 'mutex_exons':
ver, info = verify_mutex_exons(
ev[i], genes[g_idx], segments[:, s_idx].T,
sp.c_[curr_edge_idx, edges[:, s_idx]], options)
ev[i].verified.append(ver)
if s_idx == 0:
counts.append(sp.array([info], dtype='float'))
else:
counts[-1] = sp.r_[counts[-1],
sp.array([info], dtype='float')]
ev[i].verified = sp.array(ev[i].verified, dtype='bool')
IN.close()
counts = sp.dstack(counts)
ev = ev[old_idx]
counts = counts[:, :, old_idx]
if out_fn is not None:
pickle.dump((ev, counts), open(out_fn, 'wb'), -1)
return (ev, counts)
def distance(a,b):
#Returns the distance from point a to point b. Takes any iterable class of length 3 representing X,Y,Z in cartesian coordinates. Arrays/lists/tuples all work.
subtrArray = sp.dstack([a,-b]).sum(2)
return sp.sqrt(sp.sum([n**2 for n in subtrArray]))
def quantify_from_graph(ev, strain_idx=None, event_type=None, CFG=None, out_fn=None, fn_merge=None):
# cov = quantify_from_graph(ev, strain_idx, event_type, CFG, out_fn)
### set parameters if called by rproc
if strain_idx is None:
PAR = ev
ev = PAR["ev"]
strain_idx = PAR["strain_idx"]
if "out_fn" in PAR:
out_fn = PAR["out_fn"]
event_type = PAR["event_type"]
CFG = PAR["CFG"]
if fn_merge is None:
fn_merge = get_filename("fn_out_merge_val", CFG)
if CFG["is_matlab"]:
genes = scio.loadmat(fn_merge, struct_as_record=False)["genes"][0, :]
fn_count = fn_merge.replace("mat", "count.mat")
else:
genes = cPickle.load(open(fn_merge_val, "r"))[0]
fn_count = fn_merge.replace("pickle", "count.pickle")
### load count index data from hdf5
IN = h5py.File(fn_count, "r")
gene_ids_segs = IN["gene_ids_segs"][:].astype("int")
gene_ids_edges = IN["gene_ids_edges"][:].astype("int")
if len(gene_ids_segs.shape) > 1:
gene_ids_segs = gene_ids_segs[0, :]
if len(gene_ids_edges.shape) > 1:
gene_ids_edges = gene_ids_edges[0, :]
### sort events by gene idx
s_idx = sp.argsort([x.gene_idx for x in ev])
ev = ev[s_idx]
old_idx = sp.argsort(s_idx)
### find gene idx boundaries
assert isequal(gene_ids_segs, sp.sort(gene_ids_segs))
assert isequal(gene_ids_edges, sp.sort(gene_ids_edges))
tmp, genes_f_idx_segs = sp.unique(gene_ids_segs, return_index=True)
genes_l_idx_segs = sp.r_[genes_f_idx_segs[1:] - 1, gene_ids_segs.shape[0]]
tmp, genes_f_idx_edges = sp.unique(gene_ids_edges, return_index=True)
genes_l_idx_edges = sp.r_[genes_f_idx_edges[1:] - 1, gene_ids_edges.shape[0]]
gr_idx_segs = 0
gr_idx_edges = 0
counts = []
for i in range(ev.shape[0]):
sys.stdout.write(".")
if i % 10 == 0:
sys.stdout.write("%i\n" % i)
sys.stdout.flush()
if CFG["is_matlab"]:
offset = 1
else:
offset = 0
g_idx = ev[i].gene_idx
while gene_ids_segs[genes_f_idx_segs[gr_idx_segs]] < g_idx:
gr_idx_segs += 1
assert gene_ids_segs[genes_f_idx_segs[gr_idx_segs]] == g_idx
while gene_ids_edges[genes_f_idx_edges[gr_idx_edges]] < g_idx:
gr_idx_edges += 1
assert gene_ids_edges[genes_f_idx_edges[gr_idx_edges]] == g_idx
### laod relevant count data from HDF5
if CFG["is_matlab"]:
segments = IN["segments"][strain_idx, genes_f_idx_segs[gr_idx_segs] : genes_l_idx_segs[gr_idx_segs] + 1].T
seg_pos = IN["seg_pos"][
strain_idx, genes_f_idx_segs[gr_idx_segs] : genes_l_idx_segs[gr_idx_segs] + 1
].astype("int")
edges = IN["edges"][strain_idx, genes_f_idx_edges[gr_idx_edges] : genes_l_idx_edges[gr_idx_edges] + 1].T
edge_idx = IN["edge_idx"][0, genes_f_idx_edges[gr_idx_edges] : genes_l_idx_edges[gr_idx_edges] + 1].astype(
"int"
)
else:
segments = IN["segments"][genes_f_idx_segs[gr_idx_segs] : genes_l_idx_segs[gr_idx_segs] + 1, strain_idx]
seg_pos = IN["seg_pos"][genes_f_idx_segs[gr_idx_segs] : genes_l_idx_segs[gr_idx_segs] + 1, strain_idx]
edges = IN["edges"][genes_f_idx_edges[gr_idx_edges] : genes_l_idx_edges[gr_idx_edges] + 1, strain_idx]
edge_idx = IN["edge_idx"][genes_f_idx_edges[gr_idx_edges] : genes_l_idx_edges[gr_idx_edges] + 1]
for s_idx in range(len(strain_idx)):
# print '%i/%i' % (s_idx, len(strain_idx))
if event_type == "exon_skip":
cov = quantify_exon_skip(
ev[i], genes[g_idx - offset], segments[:, s_idx].T, sp.c_[edge_idx, edges[:, s_idx]], CFG
)
elif event_type in ["alt_3prime", "alt_5prime"]:
cov = quantify_alt_prime(
ev[i], genes[g_idx - offset], segments[:, s_idx].T, sp.c_[edge_idx, edges[:, s_idx]], CFG
)
elif event_type == "intron_retention":
cov = quantify_intron_retention(
ev[i],
genes[g_idx - offset],
segments[:, s_idx].T,
sp.c_[edge_idx, edges[:, s_idx]],
seg_pos[:, s_idx].T,
CFG,
)
elif event_type == "mult_exon_skip":
cov = quantify_mult_exon_skip(
ev[i], genes[g_idx - offset], segments[:, s_idx].T, sp.c_[edge_idx, edges[:, s_idx]], CFG
)
elif event_type == "mutex_exons":
cov = quantify_mutex_exons(
ev[i], genes[g_idx - offset], segments[:, s_idx].T, sp.c_[edge_idx, edges[:, s_idx]], CFG
)
if s_idx == 0:
counts.append(sp.array([cov]))
else:
counts[-1] = sp.r_[counts[-1], sp.array([cov])]
IN.close()
counts = sp.dstack(counts)
### re-sort by old idx
ev = ev[old_idx]
counts = counts[:, :, old_idx]
if out_fn is not None:
cPickle.dump((ev, counts), open(out_fn, "w"))
return (ev, counts)
def length(self):
#Returns the length of the edge.
subtrArray = sp.dstack([self.a,-self.b]).sum(2)
return sp.sqrt(sp.sum([n**2 for n in subtrArray]))
def plotScatter(self,
file_name='scatter_ts',
out_dir='./cache',
plot_test=True,
xaxis=0,
yaxis=2,
xlab='G1 score',
ylab='G2M score',
class_labels=['G1 phase', 'S phase', 'G2M phase'],
method='RF',
decision_lines=True):
plparams = {
'backend': 'pdf',
'axes.labelsize': 14,
'text.fontsize': 14,
'legend.fontsize': 13,
'xtick.labelsize': 14,
'ytick.labelsize': 14,
'text.usetex': False
}
PL.rcParams.update(plparams)
assert self.scores != None, 'cyclone: first train the model before attempting to plot'
if not os.path.exists(out_dir):
os.makedirs(out_dir)
file_name = file_name + method + '.pdf'
if plot_test == False:
file_name = file_name + method + '_cv.pdf'
if plot_test == True:
if method == 'RF':
labs = self.labels_tst
scores = self.scores_tst
elif method == 'LR':
labs = self.labels_tst
scores = self.scoresLR_tst
elif method == 'LRall':
labs = self.labels_tst
scores = self.scoresLRall_tst
elif method == 'GNB':
labs = self.labels_tst
scores = self.scoresGNB_tst
elif method == 'SVM':
labs = self.labels_tst
scores = self.scoresSVM_tst
elif method == 'SVMrbf':
labs = self.labels_tst
scores = self.scoresSVMrbf_tst
else:
if method == 'RF':
labs = self.labels
scores = self.scores
elif method == 'LR':
labs = self.labels
scores = self.scoresLR
elif method == 'LRall':
labs = self.labels
scores = self.scoresLRall
elif method == 'GNB':
labs = self.labels
scores = self.scoresGNB
elif method == 'SVM':
labs = self.labels
scores = self.scoresSVM
elif method == 'SVMrbf':
labs = self.labels
scores = self.scoresSVMrbf
cols = [
'r', 'b', 'g', 'y', 'Crimson', 'DeepPink', 'LightSalmon', 'Lime',
'Olive'
]
cols_d = {}
cols_d['G1'] = '#1b9e77'
cols_d['S'] = '#d95f02'
cols_d['G2M'] = '#7570b3'
cols_d['mid'] = '#e7298a'
cols_d['early'] = '#e6ab02'
cols_d['late'] = '#66a61e'
labs = labs.astype('int')
lab_col = list()
fig = PL.figure(figsize=(6, 6))
ax = fig.add_subplot(111)
#ax=PL.axes([0.25,0.25,0.65,0.65])
ax.set_position([0.1, 0.1, 0.7, 0.7])
hList = list()
for iplot in range(len(labs)):
#hList.append(PL.plot(scores[iplot,xaxis],scores[iplot,yaxis],'.',markersize=15,c=cols[labs[iplot]-1], alpha=0.75))
if class_labels[labs[iplot] - 1] in cols_d.keys():
hList.append(
PL.plot(scores[iplot, xaxis],
scores[iplot, yaxis],
'.',
markersize=15,
c=cols_d[class_labels[labs[iplot] - 1]],
alpha=0.75))
else:
hList.append(
PL.plot(scores[iplot, xaxis],
scores[iplot, yaxis],
'.',
markersize=15,
c='#8c510a',
alpha=0.75))
PL.xlabel(xlab)
PL.ylabel(ylab)
if xlab == 'G1 score':
PL.xlim(xmin=0.0, xmax=.95)
x_max = 0.75
else:
x_max = scores[:, xaxis].max() #+ 0.05
PL.xlim(xmax=x_max + 0.05)
if ylab == 'G2M score':
PL.ylim(ymin=0.0, ymax=.95)
y_max = 0.75
else:
y_max = scores[:, yaxis].max() #+ 0.05
PL.ylim(ymax=y_max + 0.05)
if decision_lines == True:
x_min = 0.0
y_min = 0.0
h = 0.001
xx, yy = SP.meshgrid(SP.arange(x_min, x_max, h),
SP.arange(y_min, y_max, h))
zz = 1 - (xx + yy)
Z = SP.argmax(SP.dstack((xx, yy, zz)), 2)
PL.contour(xx, yy, Z, levels=[0, 1])
legH = list()
u_classes = SP.unique(labs)
for ileg in u_classes:
legH.append(hList[SP.where(labs == ileg)[0][0]][0])
lh = PL.legend(legH,
class_labels,
loc='upper center',
bbox_to_anchor=(0.5, 1.15),
ncol=3,
numpoints=1,
scatterpoints=1)
lh.set_frame_on(False)
ax.spines["right"].set_visible(False)
ax.spines["top"].set_visible(False)
ax.get_xaxis().tick_bottom()
PL.savefig(out_dir + '/' + file_name,
bbox_extra_artists=[lh]) #,bbox_inches='tight')
def vl_phow(im,
verbose=True,
fast=True,
sizes=[4, 6, 8, 10],
step=2,
color='rgb',
floatdescriptors=False,
magnif=6,
windowsize=1.5,
contrastthreshold=0.005):
opts = Options(verbose, fast, sizes, step, color, floatdescriptors, magnif,
windowsize, contrastthreshold)
dsiftOpts = DSiftOptions(opts)
# make sure image is float, otherwise segfault
im = array(im, 'float32')
# Extract the features
imageSize = shape(im)
if im.ndim == 3:
if imageSize[2] != 3:
# "IndexError: tuple index out of range" if both if's are checked at the same time
raise ValueError("Image data in unknown format/shape")
if opts.color == 'gray':
numChannels = 1
if (im.ndim == 2):
im = vl_rgb2gray(im)
else:
numChannels = 3
if (im.ndim == 2):
im = dstack([im, im, im])
if opts.color == 'rgb':
pass
elif opts.color == 'opponent':
# from https://github.com/vlfeat/vlfeat/blob/master/toolbox/sift/vl_phow.m
# Note that the mean differs from the standard definition of opponent
# space and is the regular intesity (for compatibility with
# the contrast thresholding).
# Note also that the mean is added pack to the other two
# components with a small multipliers for monochromatic
# regions.
mu = 0.3 * im[:, :, 0] + 0.59 * im[:, :, 1] + 0.11 * im[:, :, 2]
alpha = 0.01
im = dstack([
mu, (im[:, :, 0] - im[:, :, 1]) / sqrt(2) + alpha * mu,
(im[:, :, 0] + im[:, :, 1] - 2 * im[:, :, 2]) / sqrt(6) +
alpha * mu
])
else:
raise ValueError('Color option ' + str(opts.color) +
' not recognized')
if opts.verbose:
print('{0}: color space: {1}'.format('vl_phow', opts.color))
print('{0}: image size: {1} x {2}'.format('vl_phow', imageSize[0],
imageSize[1]))
print('{0}: sizes: [{1}]'.format('vl_phow', opts.sizes))
frames_all = []
descrs_all = []
for size_of_spatial_bins in opts.sizes:
# from https://github.com/vlfeat/vlfeat/blob/master/toolbox/sift/vl_phow.m
# Recall from VL_DSIFT() that the first descriptor for scale SIZE has
# center located at XC = XMIN + 3/2 SIZE (the Y coordinate is
# similar). It is convenient to align the descriptors at different
# scales so that they have the same geometric centers. For the
# maximum size we pick XMIN = 1 and we get centers starting from
# XC = 1 + 3/2 MAX(OPTS.SIZES). For any other scale we pick XMIN so
# that XMIN + 3/2 SIZE = 1 + 3/2 MAX(OPTS.SIZES).
# In pracrice, the offset must be integer ('bounds'), so the
# alignment works properly only if all OPTS.SZES are even or odd.
off = floor(3.0 / 2 * (max(opts.sizes) - size_of_spatial_bins)) + 1
# smooth the image to the appropriate scale based on the size
# of the SIFT bins
sigma = size_of_spatial_bins / float(opts.magnif)
ims = vl_imsmooth(im, sigma)
# extract dense SIFT features from all channels
frames = []
descrs = []
for k in range(numChannels):
size_of_spatial_bins = int(size_of_spatial_bins)
# vl_dsift does not accept numpy.int64 or similar
f_temp, d_temp = vl_dsift(data=ims[:, :, k],
step=dsiftOpts.step,
size=size_of_spatial_bins,
fast=dsiftOpts.fast,
verbose=dsiftOpts.verbose,
norm=dsiftOpts.norm,
bounds=[off, off, maxint, maxint])
frames.append(f_temp)
descrs.append(d_temp)
frames = array(frames)
descrs = array(descrs)
d_new_shape = [descrs.shape[0] * descrs.shape[1], descrs.shape[2]]
descrs = descrs.reshape(d_new_shape)
# remove low contrast descriptors
# note that for color descriptors the V component is
# thresholded
if (opts.color == 'gray') | (opts.color == 'opponent'):
contrast = frames[0][2, :]
elif opts.color == 'rgb':
contrast = mean(
[frames[0][2, :], frames[1][2, :], frames[2][2, :]], 0)
else:
raise ValueError('Color option ' + str(opts.color) +
' not recognized')
descrs[:, contrast < opts.contrastthreshold] = 0
# save only x,y, and the scale
frames_temp = array(frames[0][0:3, :])
padding = array(size_of_spatial_bins * ones(frames[0][0].shape))
frames_all.append(vstack([frames_temp, padding]))
descrs_all.append(array(descrs))
frames_all = hstack(frames_all)
descrs_all = hstack(descrs_all)
return frames_all, descrs_all
def __init__(self, series1, series2, wave1, wave2, *args, **kwargs):
series = sp.vstack((series1.ravel(), series2.ravel())).T
wave = sp.dstack((wave1, wave2))
WaveletTransform.__init__(self, series, wave, *args, **kwargs)
def plotScatter(self, file_name = 'scatter_ts',out_dir = './cache', plot_test = True, xaxis = 0, yaxis = 2, xlab = 'G1 score', ylab = 'G2M score', class_labels = ['G1 phase','S phase','G2M phase'], method = 'RF', decision_lines=True):
plparams = {'backend': 'pdf',
'axes.labelsize': 14,
'text.fontsize': 14,
'legend.fontsize': 13,
'xtick.labelsize': 14,
'ytick.labelsize': 14,
'text.usetex': False}
PL.rcParams.update(plparams)
assert self.scores != None, 'cyclone: first train the model before attempting to plot'
if not os.path.exists(out_dir):
os.makedirs(out_dir)
file_name = file_name+method+'.pdf'
if plot_test==False:
file_name = file_name+method+'_cv.pdf'
if plot_test ==True:
if method=='RF':
labs = self.labels_tst
scores = self.scores_tst
elif method=='LR':
labs = self.labels_tst
scores = self.scoresLR_tst
elif method=='LRall':
labs = self.labels_tst
scores = self.scoresLRall_tst
elif method=='GNB':
labs = self.labels_tst
scores = self.scoresGNB_tst
elif method=='SVM':
labs = self.labels_tst
scores = self.scoresSVM_tst
elif method=='SVMrbf':
labs = self.labels_tst
scores = self.scoresSVMrbf_tst
else:
if method=='RF':
labs = self.labels
scores = self.scores
elif method=='LR':
labs = self.labels
scores = self.scoresLR
elif method=='LRall':
labs = self.labels
scores = self.scoresLRall
elif method=='GNB':
labs = self.labels
scores = self.scoresGNB
elif method=='SVM':
labs = self.labels
scores = self.scoresSVM
elif method=='SVMrbf':
labs = self.labels
scores = self.scoresSVMrbf
cols = ['r', 'b', 'g', 'y', 'Crimson', 'DeepPink','LightSalmon','Lime', 'Olive']
cols_d = {}
cols_d['G1'] = '#1b9e77'
cols_d['S'] = '#d95f02'
cols_d['G2M'] = '#7570b3'
cols_d['mid'] = '#e7298a'
cols_d['early'] = '#e6ab02'
cols_d['late'] = '#66a61e'
labs = labs.astype('int')
lab_col = list()
fig = PL.figure(figsize=(6,6))
ax = fig.add_subplot(111)
#ax=PL.axes([0.25,0.25,0.65,0.65])
ax.set_position([0.1,0.1,0.7,0.7])
hList =list()
for iplot in range(len(labs)):
#hList.append(PL.plot(scores[iplot,xaxis],scores[iplot,yaxis],'.',markersize=15,c=cols[labs[iplot]-1], alpha=0.75))
if class_labels[labs[iplot]-1] in cols_d.keys():
hList.append(PL.plot(scores[iplot,xaxis],scores[iplot,yaxis],'.',markersize=15,c=cols_d[class_labels[labs[iplot]-1]], alpha=0.75))
else:
hList.append(PL.plot(scores[iplot,xaxis],scores[iplot,yaxis],'.',markersize=15,c='#8c510a', alpha=0.75))
PL.xlabel(xlab)
PL.ylabel(ylab)
if xlab == 'G1 score':
PL.xlim(xmin = 0.0, xmax = .95)
x_max = 0.75
else:
x_max = scores[:,xaxis].max() #+ 0.05
PL.xlim(xmax = x_max+0.05)
if ylab == 'G2M score':
PL.ylim(ymin = 0.0, ymax = .95)
y_max = 0.75
else:
y_max = scores[:,yaxis].max() #+ 0.05
PL.ylim(ymax = y_max+0.05)
if decision_lines ==True:
x_min = 0.0
y_min = 0.0
h = 0.001
xx, yy = SP.meshgrid(SP.arange(x_min, x_max, h),
SP.arange(y_min, y_max, h))
zz = 1 - (xx + yy)
Z = SP.argmax(SP.dstack((xx,yy,zz)), 2)
PL.contour(xx, yy, Z, levels = [0,1])
legH=list()
u_classes = SP.unique(labs)
for ileg in u_classes:
legH.append(hList[SP.where(labs==ileg)[0][0]][0])
lh=PL.legend(legH,class_labels,loc='upper center',bbox_to_anchor=(0.5, 1.15),ncol=3, numpoints=1,scatterpoints=1)
lh.set_frame_on(False)
ax.spines["right"].set_visible(False)
ax.spines["top"].set_visible(False)
ax.get_xaxis().tick_bottom()
PL.savefig(out_dir+'/'+file_name,bbox_extra_artists=[lh])#,bbox_inches='tight')
Position2L_t_val, [t for t in range(2,
sp.shape(Velocity1L_t_val)[1])], 1)
Velocity1L_firstSecond_val = sp.delete(
Velocity1L_t_val, [t for t in range(2,
sp.shape(Velocity1L_t_val)[1])], 1)
Velocity2L_firstSecond_val = sp.delete(
Velocity2L_t_val, [t for t in range(2,
sp.shape(Velocity1L_t_val)[1])], 1)
dt_Arr_val = sp.delete(
sp.repeat(d_test['arr_17'][:numSamples, sp.newaxis],
sp.shape(Velocity1L_t_val)[1],
axis=1), [t for t in range(2,
sp.shape(Velocity1L_t_val)[1])], 1)
initial_state = sp.dstack(
(Position1L_firstSecond_val, Velocity1L_firstSecond_val))[:, 0, :]
plotThisX = [initial_state[0, 0]]
plotThisY = [initial_state[0, 1]]
statesCovered = [initial_state]
for i in range(100):
predictFromThis = sp.array(
[sp.append(statesCovered[i], dt_Arr_val[0, 0]) for j in range(1)])
prediction = model.predict(predictFromThis)
tempXArray = prediction[0, 0]
tempYArray = prediction[0, 1]
plotThisX.append(tempXArray)
plotThisY.append(tempYArray)
statesCovered.append(prediction)
plt.figure()
def armorf(x, ntrls, npts, p):
from scipy import shape, array, matrix, zeros, disp, concatenate, eye, dstack
from numpy import linalg # for inverse and Cholesky factorization;
import numpy as np
inv = linalg.inv
# Make name consistent with Matlab
# Initialization
x = matrix(x)
[L, N] = shape(x)
# L is the number of channels, N is the npts*ntrls
R0 = R0f = R0b = pf = pb = pfb = ap = bp = En = matrix(zeros((L, L, 1)))
# covariance matrix at 0,
# calculate the covariance matrix?
for i in range(ntrls):
En = En + x[:, i * npts:(i + 1) * npts] * x[:, i * npts:
(i + 1) * npts].H
ap = ap + x[:, i * npts + 1:(i + 1) * npts] * x[:, i * npts + 1:
(i + 1) * npts].H
bp = bp + x[:, i * npts:(i + 1) * npts - 1] * x[:, i * npts:
(i + 1) * npts - 1].H
ap = inv((ckchol(ap / ntrls * (npts - 1)).T).H)
bp = inv((ckchol(bp / ntrls * (npts - 1)).T).H)
for i in range(ntrls):
efp = ap * x[:, i * npts + 1:(i + 1) * npts]
ebp = bp * x[:, i * npts:(i + 1) * npts - 1]
pf = pf + efp * efp.H
pb = pb + ebp * ebp.H
pfb = pfb + efp * ebp.H
En = (ckchol(En / N).T).H
# Covariance of the noise
# Initial output variables
tmp = []
for i in range(L):
tmp.append(
[]) # In Matlab, coeff=[], and anything can be appended to that.
coeff = matrix(tmp)
# Coefficient matrices of the AR model
kr = matrix(tmp)
# reflection coefficients
aparr = array(ap) # Convert AP matrix to an array, so it can be dstacked
bparr = array(bp)
for m in range(p):
# Calculate the next order reflection (parcor) coefficient
ck = inv((ckchol(pf).T).H) * pfb * inv(ckchol(pb).T)
kr = concatenate((kr, ck), 1)
# Update the forward and backward prediction errors
ef = eye(L) - ck * ck.H
eb = eye(L) - ck.H * ck
# Update the prediction error
En = En * (ckchol(ef).T).H
E = (ef + eb) / 2
# Update the coefficients of the forward and backward prediction errors
Z = zeros((L, L)) # Make it easier to define this
aparr = dstack((aparr, Z))
bparr = dstack((bparr, Z))
pf = pb = pfb = Z
# Do some variable juggling to handle Python's array/matrix limitations
a = b = zeros((L, L, 0))
for i in range(m + 2):
tmpap1 = matrix(
aparr[:, :, i]
) # Need to convert back to matrix to perform operations
tmpbp1 = matrix(bparr[:, :, i])
tmpap2 = matrix(aparr[:, :, m + 1 - i])
tmpbp2 = matrix(bparr[:, :, m + 1 - i])
tmpa = inv((ckchol(ef).T).H) * (tmpap1 - ck * tmpbp2)
tmpb = inv((ckchol(eb).T).H) * (tmpbp1 - ck.H * tmpap2)
a = dstack((a, array(tmpa)))
b = dstack((b, array(tmpb)))
for k in range(ntrls):
efp = zeros((L, npts - m - 2))
ebp = zeros((L, npts - m - 2))
for i in range(m + 2):
k1 = m + 2 - i + k * npts
k2 = npts - i + k * npts
efp = efp + matrix(a[:, :, i]) * matrix(x[:, k1:k2])
ebp = ebp + matrix(b[:, :, m + 1 - i]) * matrix(
x[:, k1 - 1:k2 - 1])
pf = pf + efp * efp.H
pb = pb + ebp * ebp.H
pfb = pfb + efp * ebp.H
aparr = a
bparr = b
for j in range(p):
coeff = concatenate(
(coeff, inv(matrix(a[:, :, 0])) * matrix(a[:, :, j + 1])), 1)
return coeff, En * En.H, kr
# m2_Arr_val= sp.delete( sp.repeat(d_test['arr_16'][:numSamples,sp.newaxis],sp.shape(Velocity1L_t)[1],axis=1),
# [t for t in range(1,sp.shape(Velocity1L_t_val)[1]-1)],1)
# dt_Arr_val=sp.repeat(d_test['arr_17'][:numSamples,sp.newaxis],T,axis=1)
E_i_val = d_test['arr_4'][:numSamples]
E_f_val = d_test['arr_5'][:numSamples]
p_x_i_val = d_test['arr_6'][:numSamples]
p_x_f_val = d_test['arr_7'][:numSamples]
p_y_i_val = d_test['arr_8'][:numSamples]
p_y_f_val = d_test['arr_9'][:numSamples]
#===============================================================================================================
# Collect Input and Output for Network
#===============================================================================================================
# Dimensions of (samples, timesteps, features)
input_Arr = sp.dstack((Position1L_first, Position2L_first, Velocity1L_first,
Velocity2L_first, radius_Arr))[:, 0, :]
target_Arr = isCollision_Arr
input_Arr_val = sp.dstack(
(Position1L_first_val, Position2L_first_val, Velocity1L_first_val,
Velocity2L_first_val, radius_Arr_val))[:, 0, :]
target_Arr_val = isCollision_Arr_val
#===============================================================================================================
# Network
#===============================================================================================================
# Training existing model. Comment out if you do not wish to do this.
model = load_model("trainedModel_temp.hd5")
model = Sequential()
model.add(
def verify_all_events(ev, strain_idx=None, list_bam=None, event_type=None, CFG=None, out_fn=None):
# (ev, counts) = verify_all_events(ev, strain_idx, list_bam, event_type, CFG) ;
### set parameters if called by rproc
if strain_idx is None:
PAR = ev
ev = PAR['ev']
strain_idx = PAR['strain_idx']
list_bam = PAR['list_bam']
if 'out_fn' in PAR:
out_fn = PAR['out_fn']
event_type = PAR['event_type']
CFG = PAR['CFG']
### verify the events if demanded
if CFG['verify_alt_events']:
prune_tag = ''
if CFG['do_prune']:
prune_tag = '_pruned'
validate_tag = ''
if CFG['validate_splicegraphs']:
validate_tag = '.validated'
(genes, inserted) = cPickle.load(open('%s/spladder/genes_graph_conf%i.%s%s%s.pickle' % (CFG['out_dirname'], CFG['confidence_level'], CFG['merge_strategy'], validate_tag, prune_tag)))
fn_count = '%s/spladder/genes_graph_conf%i.%s%s%s.count.pickle' % (CFG['out_dirname'], CFG['confidence_level'], CFG['merge_strategy'], validate_tag, prune_tag)
### load count index data from hdf5
IN = h5py.File(fn_count, 'r')
gene_ids_segs = IN['gene_ids_segs'][:]
gene_ids_edges = IN['gene_ids_edges'][:]
### sort events by gene idx
s_idx = sp.argsort([x.gene_idx for x in ev])
ev = ev[s_idx]
old_idx = sp.argsort(s_idx)
### find gene idx boundaries
assert(isequal(gene_ids_segs, sp.sort(gene_ids_segs)))
assert(isequal(gene_ids_edges, sp.sort(gene_ids_edges)))
tmp, genes_f_idx_segs = sp.unique(gene_ids_segs, return_index=True)
genes_l_idx_segs = sp.r_[genes_f_idx_segs[1:] - 1, gene_ids_segs.shape[0]]
tmp, genes_f_idx_edges = sp.unique(gene_ids_edges, return_index=True)
genes_l_idx_edges = sp.r_[genes_f_idx_edges[1:] - 1, gene_ids_edges.shape[0]]
gr_idx_segs = 0
gr_idx_edges = 0
counts = []
for i in range(ev.shape[0]):
g_idx = ev[i].gene_idx
while gene_ids_segs[genes_f_idx_segs[gr_idx_segs]] < g_idx:
gr_idx_segs += 1
assert(gene_ids_segs[genes_f_idx_segs[gr_idx_segs]] == g_idx)
while gene_ids_edges[genes_f_idx_edges[gr_idx_edges]] < g_idx:
gr_idx_edges += 1
assert(gene_ids_edges[genes_f_idx_edges[gr_idx_edges]] == g_idx)
### laod relevant count data from HDF5
segments = IN['segments'][genes_f_idx_segs[gr_idx_segs]:genes_l_idx_segs[gr_idx_segs]+1, strain_idx]
seg_pos = IN['seg_pos'][genes_f_idx_segs[gr_idx_segs]:genes_l_idx_segs[gr_idx_segs]+1, strain_idx]
edges = IN['edges'][genes_f_idx_edges[gr_idx_edges]:genes_l_idx_edges[gr_idx_edges]+1, strain_idx]
edge_idx = IN['edge_idx'][genes_f_idx_edges[gr_idx_edges]:genes_l_idx_edges[gr_idx_edges]+1]
for s_idx in range(len(strain_idx)):
print '%i/%i\r' % (s_idx, len(strain_idx))
# ev_tmp.subset_strain(s_idx) ### TODO
if event_type == 'exon_skip':
ver, info = verify_exon_skip(ev[i], genes[g_idx], segments[:, s_idx].T, sp.c_[edge_idx, edges[:, s_idx]], CFG)
elif event_type in ['alt_3prime', 'alt_5prime']:
ver, info = verify_alt_prime(ev[i], genes[g_idx], segments[:, s_idx].T, sp.c_[edge_idx, edges[:, s_idx]], CFG)
elif event_type == 'intron_retention':
ver, info = verify_intron_retention(ev[i], genes[g_idx], segments[:, s_idx].T, sp.c_[edge_idx, edges[:, s_idx]], seg_pos[:, s_idx].T, CFG)
elif event_type == 'mult_exon_skip':
ver, info = verify_mult_exon_skip(ev[i], genes[g_idx], segments[:, s_idx].T, sp.c_[edge_idx, edges[:, s_idx]], CFG)
elif event_type == 'mutex_exons':
ver, info = verify_mutex_exons(ev[i], genes[g_idx], segments[:, s_idx].T, sp.c_[edge_idx, edges[:, s_idx]], CFG)
ev[i].verified.append(ver)
if s_idx == 0:
counts.append(sp.array([info]))
else:
counts[-1] = sp.r_[counts[-1], sp.array([info])]
ev[i].verified = sp.array(ev[i].verified)
IN.close()
counts = sp.dstack(counts)
ev = ev[old_idx]
counts = counts[:, :, old_idx]
if out_fn is not None:
cPickle.dump((ev, counts), open(out_fn, 'w'))
return (ev, counts)
def project(self):
self.copy(self.screen, dstack(self.scale * self.target))
if kw.get('verbose', False):
self.tell(self.screen)
self.tell()
ShowImage("RPN", self.paste)
def vl_phow(im,
verbose=False,
fast=True,
sizes=[4, 6, 8, 10],
step=2,
color='rgb',
floatdescriptors=False,
magnif=6,
windowsize=1.5,
contrastthreshold=0.005):
opts = Options(verbose, fast, sizes, step, color, floatdescriptors, magnif,
windowsize, contrastthreshold)
dsiftOpts = DSiftOptions(opts)
im = array(im, 'float32')
imageSize = shape(im)
if im.ndim == 3:
if imageSize[2] != 3:
raise ValueError("Image data in unknown format/shape")
if opts.color == 'gray':
numChannels = 1
if (im.ndim == 2):
im = vl_rgb2gray(im)
else:
numChannels = 3
if (im.ndim == 2):
im = dstack([im, im, im])
if opts.color == 'rgb':
pass
elif opts.color == 'opponent':
mu = 0.3 * im[:, :, 0] + 0.59 * im[:, :, 1] + 0.11 * im[:, :, 2]
alpha = 0.01
im = dstack([
mu, (im[:, :, 0] - im[:, :, 1]) / sqrt(2) + alpha * mu,
(im[:, :, 0] + im[:, :, 1] - 2 * im[:, :, 2]) / sqrt(6) +
alpha * mu
])
else:
raise ValueError('Color option ' + str(opts.color) +
' not recognized')
if opts.verbose:
print('{0}: color space: {1}'.format('vl_phow', opts.color))
print('{0}: image size: {1} x {2}'.format('vl_phow', imageSize[0],
imageSize[1]))
print('{0}: sizes: [{1}]'.format('vl_phow', opts.sizes))
frames_all = []
descrs_all = []
for size_of_spatial_bins in opts.sizes:
off = floor(3.0 / 2 * (max(opts.sizes) - size_of_spatial_bins)) + 1
sigma = size_of_spatial_bins / float(opts.magnif)
ims = vl_imsmooth(im, sigma)
frames = []
descrs = []
for k in range(numChannels):
size_of_spatial_bins = int(size_of_spatial_bins)
f_temp, d_temp = vl_dsift(
image=ims[:, :, k],
step=dsiftOpts.step,
size=size_of_spatial_bins,
fast=dsiftOpts.fast,
verbose=dsiftOpts.verbose,
norm=dsiftOpts.norm,
)
frames.append(f_temp.T)
descrs.append(d_temp.T)
frames = array(frames)
descrs = array(descrs)
d_new_shape = [descrs.shape[0] * descrs.shape[1], descrs.shape[2]]
descrs = descrs.reshape(d_new_shape)
if (opts.color == 'gray') | (opts.color == 'opponent'):
contrast = frames[0][2, :]
elif opts.color == 'rgb':
contrast = mean(
[frames[0][2, :], frames[1][2, :], frames[2][2, :]], 0)
else:
raise ValueError('Color option ' + str(opts.color) +
' not recognized')
descrs = descrs[:, contrast > opts.contrastthreshold]
frames = frames[0][:, contrast > opts.contrastthreshold]
frames_temp = array(frames[0:3, :])
padding = array(size_of_spatial_bins * ones(frames[0].shape))
frames_to_add = vstack([frames_temp, padding])
frames_all.append(vstack([frames_temp, padding]))
descrs_all.append(array(descrs))
frames_all = hstack(frames_all)
descrs_all = hstack(descrs_all)
return frames_all.T[:, :2], descrs_all.T
damaged_pixels = sp.where(mask == 1)
'''
Se hace la interpolacion con Spline para cada capa de la imagen y luego se
unen para visualizar el Spline "total".
'''
splR = inter.SmoothBivariateSpline(good_pixels[0], good_pixels[1],
stamp[good_pixels[0], good_pixels[1], 0])
splG = inter.SmoothBivariateSpline(good_pixels[0], good_pixels[1],
stamp[good_pixels[0], good_pixels[1], 1])
splB = inter.SmoothBivariateSpline(good_pixels[0], good_pixels[1],
stamp[good_pixels[0], good_pixels[1], 2])
new_img = sp.dstack([
splR(stamp_xy[0], stamp_xy[1]),
splG(stamp_xy[0], stamp_xy[1]),
splB(stamp_xy[0], stamp_xy[1])
])
plt.imshow(new_img)
'''
Se arregla la imagen cambiando los pixeles muertos por los nuevos pixeles aproximados.
'''
fxdR = img[:, :, 0]
fxdG = img[:, :, 1]
fxdB = img[:, :, 2]
fxdR[damaged_pixels[0],
damaged_pixels[1]] = new_img[damaged_pixels_stamp[0],
damaged_pixels_stamp[1], 0]
fxdG[damaged_pixels[0],