def _convert_feature_stats(self, fstats, aln):
tmp_fstats = []
for row in range(len(AMINO_ACID_GROUPS.keys())):
tmp_row = []
for segment in self.common_segments:
tmp_row.append([[
str(x),
str(int(x / 10)) if x != 0 else -1,
] for x in fstats[segment][row]])
tmp_fstats.append(tmp_row)
aln.feature_stats = tmp_fstats
def score_protein(self, pcf):
prot_score = 0.0
consensus_match = OrderedDict([(x, [])
for x in self.relevant_segments])
for segment in self.relevant_segments:
tmp = []
signature_map = np.absolute(
self.signature_matrix_filtered[segment]).argmax(axis=0)
resi = Residue.objects.filter(
protein_segment__slug=segment,
protein_conformation=pcf,
generic_number__label__in=self.relevant_gn[self.schemes[0][0]]
[segment].keys(),
)
for idx, pos in enumerate(
self.relevant_gn[self.schemes[0][0]][segment].keys()):
feat = signature_map[idx]
feat_abr = list(AMINO_ACID_GROUPS.keys())[feat]
feat_name = list(AMINO_ACID_GROUP_NAMES.values())[feat]
val = self.signature_matrix_filtered[segment][feat][idx]
try:
res = resi.get(generic_number__label=pos)
r_name = res.amino_acid if res.amino_acid != 'Gap' else '_'
if feat in self.residue_to_feat[res.amino_acid]:
prot_score += val
tmp.append([
feat_abr, feat_name, val, "green", res.amino_acid,
pos
]) if val > 0 else tmp.append([
feat_abr, feat_name, val, "white", res.amino_acid,
pos
])
else:
#David doesn't want the negative values in the score
# prot_score -= val
tmp.append([
feat_abr, feat_name, val, "red", res.amino_acid,
pos
]) if val > 0 else tmp.append([
feat_abr, feat_name, val, "white", res.amino_acid,
pos
])
except (exceptions.ObjectDoesNotExist,
exceptions.MultipleObjectsReturned):
prot_score -= val
tmp.append([feat_abr, feat_name, val, "red", '_', pos
]) if val > 0 else tmp.append([
feat_abr, feat_name, val, "white", '_', pos
])
consensus_match[segment] = tmp
return (prot_score / 100, consensus_match)
def find_relevant_gns(self):
"""
Find the set of generic residue positions meeting the cutoff.
"""
matrix_consensus = OrderedDict()
for segment in self.segments:
segment_consensus = []
signature_map = self.diff_matrix[segment].argmax(axis=0)
# Update mapping to prefer features with fewer amino acids
signature_map = self._assign_preferred_features(
signature_map, segment, self.diff_matrix)
for col, pos in enumerate(list(signature_map)):
if self.diff_matrix[segment][pos][col] >= self.cutoff:
segment_consensus.append(self.diff_matrix[segment][:, col])
for scheme in self.schemes:
gnum = list(
self.common_gn[scheme[0]][segment].items())[col]
try:
self.relevant_gn[scheme[0]][segment][
gnum[0]] = gnum[1]
except KeyError:
self.relevant_gn[
scheme[0]][segment] = OrderedDict()
self.relevant_gn[scheme[0]][segment][
gnum[0]] = gnum[1]
segment_consensus = np.array(segment_consensus).T
if segment_consensus.shape != (0, ):
matrix_consensus[segment] = segment_consensus
self.signature_matrix_filtered = matrix_consensus
self.relevant_segments = OrderedDict([
(x[0], self.relevant_gn[self.schemes[0][0]][x[0]].keys())
for x in self.signature_matrix_filtered.items()
])
signature = OrderedDict([(x[0], []) for x in matrix_consensus.items()])
for segment in self.relevant_segments:
signature_map = self.signature_matrix_filtered[segment].argmax(
axis=0)
signature_map = self._assign_preferred_features(
signature_map, segment, self.signature_matrix_filtered)
tmp = np.array(self.signature_matrix_filtered[segment])
for col, pos in enumerate(list(signature_map)):
signature[segment].append([
list(AMINO_ACID_GROUPS.keys())[pos],
list(AMINO_ACID_GROUP_NAMES.values())[pos], tmp[pos][col],
int(tmp[pos][col] / 20) + 5
])
self.signature_consensus = signature
def find_relevant_gns(self):
matrix_consensus = OrderedDict()
for segment in self.segments:
print(segment)
segment_consensus = []
signature_map = np.absolute(
self.diff_matrix[segment]).argmax(axis=0)
for col, pos in enumerate(list(signature_map)):
if abs(self.diff_matrix[segment][pos][col]) > self.cutoff:
segment_consensus.append(self.diff_matrix[segment][:, col])
for scheme in self.schemes:
gnum = list(
self.common_gn[scheme[0]][segment].items())[col]
try:
self.relevant_gn[scheme[0]][segment][
gnum[0]] = gnum[1]
except:
self.relevant_gn[
scheme[0]][segment] = OrderedDict()
self.relevant_gn[scheme[0]][segment][
gnum[0]] = gnum[1]
segment_consensus = np.array(segment_consensus).T
if segment_consensus != []:
matrix_consensus[segment] = segment_consensus
self.signature_matrix_filtered = matrix_consensus
self.relevant_segments = OrderedDict([
(x[0], self.relevant_gn[self.schemes[0][0]][x[0]].keys())
for x in self.signature_matrix_filtered.items()
])
signature = OrderedDict([(x[0], []) for x in matrix_consensus.items()])
for segment in self.relevant_segments:
signature_map = np.absolute(
self.signature_matrix_filtered[segment]).argmax(axis=0)
tmp = np.array(self.signature_matrix_filtered[segment])
for col, pos in enumerate(list(signature_map)):
signature[segment].append([
list(AMINO_ACID_GROUPS.keys())[pos],
list(AMINO_ACID_GROUP_NAMES.values())[pos], tmp[pos][col],
int(tmp[pos][col] / 20) + 5
])
self.signature_consensus = signature
def __init__(self):
self.aln_pos = Alignment()
self.aln_neg = Alignment()
self.features_normalized_pos = OrderedDict()
self.features_normalized_neg = OrderedDict()
self.features_frequency_difference = OrderedDict()
self.features_frequency_diff_display = []
self.freq_cutoff = 30
self.common_gn = OrderedDict()
self.feature_preference = prepare_aa_group_preference()
self.group_lengths = dict([
(x, len(y)) for x, y in enumerate(AMINO_ACID_GROUPS.values())
])
self.default_column = np.array([
((y.startswith('-') or y == '_') and y != '--'
and not y.startswith('-_') and 100) or 0
for y in AMINO_ACID_GROUPS.keys()
])
def calculate_signature(self):
"""
Calculates the feature frequency difference between two protein sets.
Generates the full differential matrix as well as maximum difference for a position (for scatter plot).
"""
for sid, segment in enumerate(self.aln_neg.segments):
self.features_normalized_pos[segment] = np.array(
[[x[0] for x in feat[sid]]
for feat in self.aln_pos.feature_stats],
dtype='int')
self.features_normalized_neg[segment] = np.array(
[[x[0] for x in feat[sid]]
for feat in self.aln_neg.feature_stats],
dtype='int')
for segment in self.aln_neg.segments:
#TODO: get the correct default numering scheme from settings
for idx, res in enumerate(
self.common_gn[self.common_schemes[0][0]][segment].keys()):
if res not in self.aln_pos.generic_numbers[
self.common_schemes[0][0]][segment].keys():
self.features_normalized_pos[segment] = np.insert(
self.features_normalized_pos[segment], idx, 0, axis=1)
# Set 100% occurence for a gap feature
self.features_normalized_pos[segment][-1, idx] = 100
elif res not in self.aln_neg.generic_numbers[
self.common_schemes[0][0]][segment].keys():
self.features_normalized_neg[segment] = np.insert(
self.features_normalized_neg[segment], idx, 0, axis=1)
# Set 100% occurence for a gap feature
self.features_normalized_neg[segment][-1, idx] = 100
# now the difference
self.features_frequency_difference[segment] = np.subtract(
self.features_normalized_pos[segment],
self.features_normalized_neg[segment])
self._convert_feature_stats(self.features_normalized_pos, self.aln_pos)
self._convert_feature_stats(self.features_normalized_neg, self.aln_neg)
# Version with display data
for row in range(len(AMINO_ACID_GROUPS.keys())):
tmp_row = []
for segment in self.aln_neg.segments:
#first item is the real value,
# second is the assignmnent of color (via css)
# 0 - red, 5 - yellow, 10 - green
#third item is a tooltip
tmp_row.append([[
x,
int(x / 20) + 5, "{} - {}".format(
self.features_normalized_pos[segment][row][y],
self.features_normalized_neg[segment][row][y])
] for y, x in enumerate(
self.features_frequency_difference[segment][row])])
self.features_frequency_diff_display.append(tmp_row)
self.signature = OrderedDict([(x, []) for x in self.aln_neg.segments])
for segment in self.aln_neg.segments:
tmp = np.array(self.features_frequency_difference[segment])
signature_map = np.absolute(tmp).argmax(axis=0)
self.signature[segment] = []
for col, pos in enumerate(list(signature_map)):
self.signature[segment].append([
list(AMINO_ACID_GROUPS.keys())[pos],
list(AMINO_ACID_GROUP_NAMES.values())[pos],
self.features_frequency_difference[segment][pos][col],
int(self.features_frequency_difference[segment][pos][col] /
20) + 5
])
features_pos = OrderedDict()
features_neg = OrderedDict()
self.features_consensus_pos = OrderedDict([
(x, []) for x in self.aln_neg.segments
])
self.features_consensus_neg = OrderedDict([
(x, []) for x in self.aln_neg.segments
])
for sid, segment in enumerate(self.aln_neg.segments):
features_pos[segment] = np.array(
[[x[0] for x in feat[sid]]
for feat in self.aln_pos.feature_stats],
dtype='int')
features_neg[segment] = np.array(
[[x[0] for x in feat[sid]]
for feat in self.aln_neg.feature_stats],
dtype='int')
features_cons_pos = np.absolute(
features_pos[segment]).argmax(axis=0)
features_cons_neg = np.absolute(
features_neg[segment]).argmax(axis=0)
for col, pos in enumerate(list(features_cons_pos)):
self.features_consensus_pos[segment].append([
list(AMINO_ACID_GROUPS.keys())[pos],
list(AMINO_ACID_GROUP_NAMES.values())[pos],
features_pos[segment][pos][col],
int(features_pos[segment][pos][col] / 20) + 5
])
for col, pos in enumerate(list(features_cons_neg)):
self.features_consensus_neg[segment].append([
list(AMINO_ACID_GROUPS.keys())[pos],
list(AMINO_ACID_GROUP_NAMES.values())[pos],
features_neg[segment][pos][col],
int(features_neg[segment][pos][col] / 20) + 5
])
self._convert_feature_stats(self.features_normalized_pos, self.aln_pos)
self._convert_feature_stats(self.features_normalized_neg, self.aln_neg)
def score_protein(self, pcf):
prot_score = 0.0
norm = 0.0
consensus_match = OrderedDict([(x, [])
for x in self.relevant_segments])
relevant_gns_total = []
for segment in self.relevant_segments:
for idx, pos in enumerate(
self.relevant_gn[self.schemes[0][0]][segment].keys()):
relevant_gns_total.append(pos)
resi = Residue.objects.filter(
protein_conformation=pcf,
generic_number__label__in=relevant_gns_total).prefetch_related(
'generic_number')
resi_dict = {}
for r in resi:
if r.generic_number:
resi_dict[r.generic_number.label] = r
for segment in self.relevant_segments:
tmp = []
signature_map = self.signature_matrix_filtered[segment].argmax(
axis=0)
signature_map = self._assign_preferred_features(
signature_map, segment, self.signature_matrix_filtered)
norm += np.sum(
np.amax(self.signature_matrix_filtered[segment], axis=0))
for idx, pos in enumerate(
self.relevant_gn[self.schemes[0][0]][segment].keys()):
feat = signature_map[idx]
feat_abr = list(AMINO_ACID_GROUPS.keys())[feat]
feat_name = list(AMINO_ACID_GROUP_NAMES.values())[feat]
val = self.signature_matrix_filtered[segment][feat][idx]
if pos in resi_dict:
res = resi_dict[pos]
if feat in self.residue_to_feat[res.amino_acid]:
if val > 0:
prot_score += val
tmp.append([
feat_abr, feat_name, val, "green", res.amino_acid,
pos
]) if val > 0 else tmp.append([
feat_abr, feat_name, val, "white", res.amino_acid,
pos
])
else:
#David doesn't want the negative values in the score
# prot_score -= val
tmp.append([
feat_abr, feat_name, val, "red", res.amino_acid,
pos
]) if val > 0 else tmp.append([
feat_abr, feat_name, val, "white", res.amino_acid,
pos
])
else:
if feat_name == 'Gap':
tmp.append([
feat_abr, feat_name, val, "green", '_', pos
]) if val > 0 else tmp.append(
[feat_abr, feat_name, val, "white", '_', pos])
prot_score += val
else:
#David doesn't want the negative values in the score
#prot_score -= val
tmp.append([
feat_abr, feat_name, val, "red", '_', pos
]) if val > 0 else tmp.append(
[feat_abr, feat_name, val, "white", '_', pos])
consensus_match[segment] = tmp
return (prot_score / 100, prot_score / norm * 100, consensus_match)