-
Notifications
You must be signed in to change notification settings - Fork 0
/
feature_extractor.py
452 lines (357 loc) · 17.3 KB
/
feature_extractor.py
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
119
120
121
122
123
124
125
126
127
128
129
130
131
132
133
134
135
136
137
138
139
140
141
142
143
144
145
146
147
148
149
150
151
152
153
154
155
156
157
158
159
160
161
162
163
164
165
166
167
168
169
170
171
172
173
174
175
176
177
178
179
180
181
182
183
184
185
186
187
188
189
190
191
192
193
194
195
196
197
198
199
200
201
202
203
204
205
206
207
208
209
210
211
212
213
214
215
216
217
218
219
220
221
222
223
224
225
226
227
228
229
230
231
232
233
234
235
236
237
238
239
240
241
242
243
244
245
246
247
248
249
250
251
252
253
254
255
256
257
258
259
260
261
262
263
264
265
266
267
268
269
270
271
272
273
274
275
276
277
278
279
280
281
282
283
284
285
286
287
288
289
290
291
292
293
294
295
296
297
298
299
300
301
302
303
304
305
306
307
308
309
310
311
312
313
314
315
316
317
318
319
320
321
322
323
324
325
326
327
328
329
330
331
332
333
334
335
336
337
338
339
340
341
342
343
344
345
346
347
348
349
350
351
352
353
354
355
356
357
358
359
360
361
362
363
364
365
366
367
368
369
370
371
372
373
374
375
376
377
378
379
380
381
382
383
384
385
386
387
388
389
390
391
392
393
394
395
396
397
398
399
400
401
402
403
404
405
406
407
408
409
410
411
412
413
414
415
416
417
418
419
420
421
422
423
424
425
426
427
428
429
430
431
432
433
434
435
436
437
438
439
440
441
442
443
444
445
446
447
448
449
450
451
452
import string, sys
import math
import pandas as pd
from pandas import DataFrame
import numpy as np
from sklearn.feature_extraction.text import TfidfVectorizer, CountVectorizer
def jaccard_similarity(query, document):
intersection = set(query).intersection(set(document))
union = set(query).union(set(document))
return len(intersection)/len(union)
def term_frequency(term, tokenized_document):
return tokenized_document.count(term)
def sublinear_term_frequency(term, tokenized_document):
count = tokenized_document.count(term)
if count == 0:
return 0
return 1 + math.log(count)
def augmented_term_frequency(term, tokenized_document):
max_count = max([term_frequency(t, tokenized_document) for t in tokenized_document])
return (0.5 + ((0.5 * term_frequency(term, tokenized_document))/max_count))
def inverse_document_frequencies(tokenized_documents):
idf_values = {}
all_tokens_set = set([item for sublist in tokenized_documents for item in sublist])
for tkn in all_tokens_set:
contains_token = map(lambda doc: tkn in doc, tokenized_documents)
idf_values[tkn] = 1 + math.log(len(tokenized_documents)/(sum(contains_token)))
return idf_values
def tfidf(documents, tokenize):
tokenized_documents = [tokenize(d) for d in documents]
idf = inverse_document_frequencies(tokenized_documents)
tfidf_documents = []
for document in tokenized_documents:
doc_tfidf = []
for term in idf.keys():
tf = sublinear_term_frequency(term, document)
doc_tfidf.append(tf * idf[term])
tfidf_documents.append(doc_tfidf)
return tfidf_documents
def cosine_similarity(vector1, vector2):
dot_product = sum(p*q for p,q in zip(vector1, vector2))
magnitude = math.sqrt(sum([val**2 for val in vector1])) * math.sqrt(sum([val**2 for val in vector2]))
if not magnitude:
return 0
return dot_product/magnitude
##########################################################
# --- interpret TF-IDF
def top_features_in_doc(Xtr, features, row_id, top_n=25):
"""
Top tfidf features in specific document (matrix row)
Memo
----
1. np.squeeze()
Remove single-dimensional entries from the shape of an array.
"""
row = np.squeeze(Xtr[row_id].toarray())
return top_tfidf_features(row, features, top_n)
def top_tfidf_features(row, features, top_n=25):
"""
Get top n tfidf values in row and return their corresponding feature names.
Memo
----
1. np.argsort() returns the indices of the ordering
"""
topn_ids = np.argsort(row)[::-1][:top_n] # x[::-1] puts x in reversed order
top_feats = [(features[i], row[i]) for i in topn_ids]
df = pd.DataFrame(top_feats)
df.columns = ['feature', 'score']
return df
def top_mean_features(Xtr, features, grp_ids=None, min_tfidf=0.1, top_n=25):
"""
Input
Xtr: TF-IDF-transformed feature representation where each row corresponds to
a document ID and each column corresponds to a token (or n-grams in general)
features: the set of vocabulatry over which a TF-IDF score is computed for each
document
Return the top n features that on average are most important amongst documents in rows
indentified by indices in grp_ids.
"""
if grp_ids:
D = Xtr[grp_ids].toarray()
else:
D = Xtr.toarray()
D[D < min_tfidf] = 0
tfidf_means = np.mean(D, axis=0)
return top_tfidf_features(tfidf_means, features, top_n)
def top_median_features(Xtr, features, grp_ids=None, min_tfidf=0.1, top_n=25):
if grp_ids:
D = Xtr[grp_ids].toarray()
else:
D = Xtr.toarray()
D[D < min_tfidf] = 0
tfidf_means = np.median(D, axis=0)
return top_tfidf_features(tfidf_means, features, top_n)
def top_features_by_class(Xtr, y, features, min_tfidf=0.1, top_n=25):
"""
Return a list of dfs, where each df holds top_n features and their mean tfidf value
calculated across documents with the same class label.
"""
dfs = []
labels = np.unique(y)
for label in labels:
ids = np.where(y==label)
feats_df = top_mean_features(Xtr, features, ids, min_tfidf=min_tfidf, top_n=top_n)
feats_df.label = label
dfs.append(feats_df)
return dfs
def plot_tfidf_classfeats_h(dfs):
"""
Plot the data frames returned by the function top_features_by_class().
"""
fig = plt.figure(figsize=(12, 9), facecolor="w")
x = np.arange(len(dfs[0]))
for i, df in enumerate(dfs):
ax = fig.add_subplot(1, len(dfs), i+1)
ax.spines["top"].set_visible(False)
ax.spines["right"].set_visible(False)
ax.set_frame_on(False)
ax.get_xaxis().tick_bottom()
ax.get_yaxis().tick_left()
ax.set_xlabel("Mean Tf-Idf Score", labelpad=16, fontsize=14)
ax.set_title("label = " + str(df.label), fontsize=16)
ax.ticklabel_format(axis='x', style='sci', scilimits=(-2,2))
ax.barh(x, df.tfidf, align='center', color='#3F5D7D')
ax.set_yticks(x)
ax.set_ylim([-1, x[-1]+1])
yticks = ax.set_yticklabels(df.feature)
plt.subplots_adjust(bottom=0.09, right=0.97, left=0.15, top=0.95, wspace=0.52)
plt.show()
##########################################################
def eval_topn_features(df_seq, topn=3, **kargs):
col_key = kargs.get('col_key', 'Patient_id')
col_doc = kargs.get('col_doc', 'ICD10') # options: 'drug_code'
assert set([col_key, col_doc]) <= set(df_seq.columns)
col_topn = kargs.get('col_topn', 'Primary')
# place_holder = kargs.pop('place_holder', 'X')
sep = kargs.pop('sep', " ") # top N feature/code separator
n_examples = kargs.pop('n_test_examples', 10)
topn_global = kargs.pop('topn_global', 10) # show most important features in global scope (i.e. across documents)
verbose = kargs.get('verbose', 1)
pids = df_seq[col_key].values
docs = df_seq.set_index(col_key)[col_doc].to_dict()
corpus = np.array([docs[pid] for pid in pids])
Nd, Np = len(docs), len(pids)
ngram_range = (1, 1)
stop_words = []
tokenizer = lambda doc: doc.split(" ")
model = TfidfVectorizer(analyzer='word', tokenizer=tokenizer, ngram_range=ngram_range,
min_df=0, smooth_idf=True, lowercase=False, stop_words=stop_words)
Xtr = model.fit_transform(corpus)
assert Xtr.shape[0] == len(pids), f"number of rows in Xtr {Xtr.shape[0]} not equal to num of (unique) patients {len(pids)}"
if verbose: print(f"(eval_topn_features) Nd: {Nd}, dim(Xtr): {Xtr.shape}, size(vocab): {len(model.vocabulary_)}")
fset = model.get_feature_names()
if verbose: print(f"... example feature names (n={len(fset)}=?={len(model.vocabulary_)}):\n{fset[:50]}\n{fset[-50:]}\n")
test_indices = np.random.choice(range(Nd), n_examples, replace=False)
top_features = []
for i in range(Xtr.shape[0]):
df_doc = top_features_in_doc(Xtr, features=fset, row_id=i, top_n=topn)
# "remove" features whose scores are 0 (and replace them with a placeholder)
df_doc = df_doc[df_doc['score'] > 0]
assert not df_doc.empty, f"top N({topn}) features all have zero scores?\n{df_doc}\n"
# columns: feature, score
topfs = sep.join(df_doc['feature'].values)
top_features.append( topfs )
if verbose and (i in test_indices):
print("--- doc #{} ---\n{}".format(i, df_doc.to_string(index=True)))
print("...... top N({}) features: {}\n".format(topn, topfs))
df_topn_local = DataFrame({col_key: pids, col_topn: top_features}, columns=[col_key, col_topn])
df_topn_global = top_mean_features(Xtr, fset, grp_ids=None, min_tfidf=0.1, top_n=topn_global)
if verbose:
print("(eval_topn_features) top N features overall across all docs ...")
print("... doc(mean):\n{}\n".format(df_topn_global.to_string(index=True)))
return df_topn_local, df_topn_global
def demo_tfidf_diagnosis(df_seq=None):
import os
from data_pipeline import load_data
from utils import Diagnosis
col_key = 'Patient_id'
col_date = 'Diag_date'
col_code = 'ICD10'
col_intv = 'History'
n_samples = 1000
tLoad = True
if df_seq is None:
df_diag, df_treat, df_res = load_data(input_dir=os.getcwd(), verbose=False)
diag = Diagnosis(df_diag) # create a Diagnosis object
if tLoad:
df_seq = diag.load(dtype='seq') # load the pre-computed sequence data, because it's take a minute or two to sequence the data
else:
df_seq = diag.sequence(tFilterByICD=True, tFilterByLength=False)
# note: set tFilterByICD to True to only include valid (well-formatted) ICD10 codes
# set tFilterByLength to False to include the entire d-sequence for each patient
# Say you want to focus on only the most recent 100 days of diagnoses, then pass
# n_days_lookback=100
else:
assert not df_seq.empty
pids = df_seq[col_key].values
docs = df_seq.set_index(col_key)[col_code].to_dict()
corpus = np.array([docs[pid] for pid in pids])
Nd, Np = len(docs), len(pids)
ngram_range = (1, 1)
stop_words = []
tokenizer = lambda doc: doc.split(" ")
model = TfidfVectorizer(analyzer='word', tokenizer=tokenizer, ngram_range=ngram_range,
min_df=0, smooth_idf=True, lowercase=False, stop_words=stop_words)
Xtr = model.fit_transform(corpus)
analyzer = model.build_analyzer()
print("(demo_tfidf_diagnosis) ngram_range: {} => {}".format(ngram_range, analyzer("D64.9")))
print(f"... Nd: {Nd}, dim(Xtr): {Xtr.shape}, size(vocab): {len(model.vocabulary_)}")
assert Xtr.shape[0] == len(pids), f"number of rows in Xtr {Xtr.shape[0]} not equal to num of (unique) patients {len(pids)}"
fset = model.get_feature_names()
assert sum(1 for w in stop_words if w in fset) == 0, "Found stop words in the feature set!"
print(f"... example feature names (n={len(fset)}=?={len(model.vocabulary_)}):\n{fset[:50]}\n{fset[-50:]}\n")
n_examples = 10
test_indices = np.random.choice(range(Nd), n_examples, replace=False)
for i, dvec in enumerate(Xtr):
# if i in test_indices:
# print("...... doc #[{}]:\n{}\n".format(i, dvec.toarray()))
assert np.sum(dvec) > 0
print("... size(ICD10 codes): {}".format( len(model.vocabulary_) ))
# --- interpretation
print("(demo_tfidf_diagnosis) Interpreting the TF-IDF model")
topn = 3
for i in range(Xtr.shape[0]):
df_doc = top_features_in_doc(Xtr, features=fset, row_id=i, top_n=topn)
if i in test_indices:
print("...... doc #{}:\n{}\n".format(i, df_doc.to_string(index=True)))
topn = 10
print("... top N ICD10 codes overall across all docs")
df_topn = top_mean_features(Xtr, fset, grp_ids=None, min_tfidf=0.1, top_n=top_n)
print("... doc(avg):\n{}\n".format(df_topn.to_string(index=True)))
# --- interface
# a. get the scores of individual tokens or n-grams in a given document?
print("(demo_tfidf_diagnosis) Get the scores of individual ICD10s in a given d-sequence")
df = pd.DataFrame(Xtr.toarray(), columns = model.get_feature_names())
print(df.head())
# df.to_csv(Diagnosis.get_path(dtype='tfidf'), sep='|', index=False, header=True)
return df
def demo_tfidf_transform(**kargs):
"""
Memo
----
"""
# from sklearn.feature_extraction.text import TfidfVectorizer
from sklearn.metrics.pairwise import linear_kernel
# ... compute dot product
docs = {}
docs[0] = "SMN1 GENE MUTATION ANALYSIS BLOOD TISSUE MOLECULAR GENETICS METHOD NARRATIVE"
docs[1] = "SMN1 GENE TARGETED MUTATION ANALYSIS BLOOD TISSUE MOLECULAR GENETICS METHOD"
docs[2] = "SALMON IGE AB SERUM"
docs[3] = "SCALLOP IGE AB RAST CLASS SERUM"
docs[4] = "SJOGRENS SYNDROME A EXTRACTABLE NUCLEAR AB SERUM"
docs[5] = "MYELOCYTES BLOOD"
dtest = {}
dtest[0] = "SCALLOP IGE AB RAST CLASS SERUM"
corpus = np.array([docs[i] for i in range(len(docs))])
vectorizer = CountVectorizer(decode_error="replace")
vec_train = vectorizer.fit_transform(corpus)
# -- model persistance
# # Save vectorizer.vocabulary_
# pickle.dump(vectorizer.vocabulary_,open("feature.pkl","wb"))
# # Load it later
# transformer = TfidfTransformer()
# loaded_vec = CountVectorizer(decode_error="replace",vocabulary=pickle.load(open("feature.pkl", "rb")))
# tfidf = transformer.transform(loaded_vec.fit_transform(np.array(["aaa ccc eee"])))
# vec = TfidfVectorizer()
# tfidf = vec.fit_transform()
ngram_range = (1,3)
stop_words = ['METHOD', 'CLASS']
tfidf = TfidfVectorizer(analyzer='word', ngram_range=ngram_range, min_df=0, smooth_idf=True, stop_words=stop_words)
# sublinear_tf=True? it's unlikely to observe repeated tokens in the LOINC long name or MTRT
Xtr = tfidf.fit_transform(corpus)
analyzer = tfidf.build_analyzer()
print("... ngram_range: {} => {}".format(ngram_range, analyzer("RHEUMATOID FACTOR IGA SERUM")))
# --- get feature index
part_sent = "CLASS SERUM"
feature_index = tfidf.vocabulary_.get("CLASS SERUM".lower()) # lowercase: True by default
print("... phrase: {} => {}".format(part_sent, feature_index))
# > size of the vocab
# tfidf.vocabulary_: a dictionary
print("... size(vocab): {}".format( len(tfidf.vocabulary_) ))
# -- doc vectors
# print("... d2v(train):\n{}\n".format( tfidf.to_array() ))
fset = tfidf.get_feature_names()
assert sum(1 for w in stop_words if w in fset) == 0, "Found stop words in the feature set!"
print("> feature names:\n{}\n".format(fset))
for i, dvec in enumerate(Xtr):
print("> doc #[{}]:\n{}\n".format(i, dvec.toarray()))
# --- predicting new data
corpus_test = np.array([doc for i, doc in dtest.items()])
doc_vec_test = tfidf.transform(corpus_test)
print("... d2v(test):\n{}\n".format( doc_vec_test.toarray() ))
# --- interpretation
print("(demo_predict) Interpreting the TF-IDF model")
for i, dvec in enumerate(Xtr):
# top_tfidf_features(dvec, features=tfidf.get_feature_names(), top_n=10)
df = top_features_in_doc(Xtr, features=fset, row_id=i, top_n=10)
print("... doc #{}:\n{}\n".format(i, df.to_string(index=True)))
print("... top n features overall across all docs")
df = top_mean_features(Xtr, fset, grp_ids=None, min_tfidf=0.1, top_n=10)
print("... doc(avg):\n{}\n".format(df.to_string(index=True)))
# --- interface
# a. get the scores of individual tokens or n-grams in a given document?
print("> Get the scores of individual tokens or n-grams in a given document? ")
df = pd.DataFrame(Xtr.toarray(), columns = tfidf.get_feature_names())
vocab = ['salmon ige ab', 'salmon']
print(df.head())
return
def demo_tfidf(**kargs):
"""
Memo
----
TfidfVectorizer is equivalent to CountVectorizer followed by TfidfTransformer, where
CountVectorizer: Transforms text into a sparse matrix of n-gram counts.
TfidfTransformer: Performs the TF-IDF transformation from a provided matrix of counts.
"""
# import string, sys
# import math
# from sklearn.feature_extraction.text import TfidfVectorizer
tokenizer = lambda doc: doc.upper().split(" ")
document_0 = "SMN1 GENE MUTATION ANALYSIS BLOOD TISSUE MOLECULAR GENETICS METHOD NARRATIVE"
document_1 = "SMN1 GENE TARGETED MUTATION ANALYSIS BLOOD TISSUE MOLECULAR GENETICS METHOD"
document_2 = "SALMON IGE AB SERUM"
document_3 = "SCALLOP IGE AB RAST CLASS SERUM"
document_4 = "SJOGRENS SYNDROME A EXTRACTABLE NUCLEAR AB SERUM"
document_5 = "MYELOCYTES BLOOD"
document_6 = "KAPPA LIGHT CHAINS FREE 24 HOUR URINE"
all_documents = [document_0, document_1, document_2, document_3, document_4, document_5, document_6]
sklearn_tfidf = TfidfVectorizer(norm='l2', min_df=0, use_idf=True, smooth_idf=False, sublinear_tf=True, tokenizer=tokenizer)
# sublinear_tf: Apply sublinear tf scaling, i.e. replace tf with 1 + log(tf)
# smooth_idf: Smooth idf weights by adding one to document frequencies, as if an extra document
# was seen containing every term in the collection exactly once. Prevents zero divisions.
tfidf_representation = tfidf(all_documents, tokenizer)
sklearn_representation = sklearn_tfidf.fit_transform(all_documents)
# sklearn_representation: a sparse matrix
# print(tfidf_representation[0])
# print(sklearn_representation.toarray()[0].tolist())
my_tfidf_comparisons = []
for count_0, doc_0 in enumerate(tfidf_representation):
for count_1, doc_1 in enumerate(tfidf_representation):
my_tfidf_comparisons.append((cosine_similarity(doc_0, doc_1), count_0, count_1))
skl_tfidf_comparisons = []
for count_0, doc_0 in enumerate(sklearn_representation.toarray()):
for count_1, doc_1 in enumerate(sklearn_representation.toarray()):
skl_tfidf_comparisons.append((cosine_similarity(doc_0, doc_1), count_0, count_1))
for x in zip(sorted(my_tfidf_comparisons, reverse = True), sorted(skl_tfidf_comparisons, reverse = True)):
print(x)
return
def test():
# --- TF-IDF encoding
# demo_tfidf()
# --- prediction using the vectors produced by TF-IDF encoding
# demo_tfidf_transform()
# --- TF-IDF scores for d-sequences
demo_tfidf_diagnosis()
return
if __name__ == "__main__":
test()