def objective(trial):
iris = load_iris()
X, y = cudf.DataFrame(pd.DataFrame(
iris.data.astype('float32'))), cudf.DataFrame(
pd.DataFrame(iris.target.astype('float32')))
solver = trial.suggest_categorical("solver", ["qn"])
C = trial.suggest_uniform("C", 0.0, 1.0)
if solver == "qn":
penalty = trial.suggest_categorical("penalty", ["l1", "l2"])
else:
# 'penalty' parameter isn't relevant for this solver,
# so we always specify 'l2' as the dummy value.
penalty = "l2"
classifier = LogisticRegression(max_iter=200,
solver=solver,
C=C,
penalty=penalty)
X_train, X_valid, y_train, y_valid = train_test_split(X, y)
classifier.fit(X_train, y_train)
score = classifier.score(X_valid, y_valid)
return score
def train(self, train_df, eval_df, params=None):
train_df, eval_df = cudf.DataFrame(train_df), cudf.DataFrame(eval_df)
x_train, y_train, x_eval, y_eval = train_df.drop(columns=[self.label]), train_df[self.label], \
eval_df.drop(columns=[self.label]), eval_df[self.label],
if params is None:
use_params = deepcopy(self.opt_params)
else:
use_params = deepcopy(params)
self.clf = LogisticRegression(**use_params)
self.clf.fit(X=x_train, y=y_train)
preds = self.clf.predict(X=x_eval)
output = self.get_loss(y_pred=preds, y=y_eval)
return output
def run_log_reg(scaled_df):
raw_train_arr = []
raw_test_arr = []
# Init metrics
metrics = ['accuracy', 'f1', 'roc_auc_ovr']
# Set c vals and penalty
C_vals = range(-8, 5)
C_vals = [10**val for val in C_vals]
penalty = ['none', 'l1', 'l2']
# Init params
params = {'penalty': penalty, 'C': C_vals}
# Over five trials
for i in range(5):
# Train test split
X_train, X_test, y_train, y_test = train_test_split(
scaled_df.iloc[:, :-1], scaled_df.y, train_size=5000)
# Init clf
clf = LogisticRegression()
# Init gridsearch and run
search_results = GridSearchCV(clf,
params,
scoring=metrics,
refit=False)
search_results.fit(X_train, y_train)
# Get results and organize
results = pd.DataFrame(search_results.cv_results_['params'])
results['mean_accuracy'] = search_results.cv_results_[
'mean_test_accuracy']
results['mean_f1'] = search_results.cv_results_['mean_test_f1']
results['mean_auc'] = search_results.cv_results_[
'mean_test_roc_auc_ovr']
# Get optimal clfs
opt_acc_inf = results.sort_values(by='mean_accuracy',
ascending=False).iloc[0]
opt_f1_inf = results.sort_values(by='mean_f1', ascending=False).iloc[0]
opt_auc_inf = results.sort_values(by='mean_auc',
ascending=False).iloc[0]
# Init optimal clfs
opt_acc_clf = LogisticRegression(C=opt_acc_inf.C,
penalty=opt_acc_inf.penalty,
max_iter=100000)
opt_f1_clf = LogisticRegression(C=opt_f1_inf.C,
penalty=opt_f1_inf.penalty,
max_iter=100000)
opt_auc_clf = LogisticRegression(C=opt_auc_inf.C,
penalty=opt_auc_inf.penalty,
max_iter=100000)
# Fit clfs
opt_acc_clf.fit(X_train, y_train)
opt_f1_clf.fit(X_train, y_train)
opt_auc_clf.fit(X_train, y_train)
# Get train and test metrics
train_score_acc = opt_acc_clf.score(X_train, y_train)
train_score_f1 = f1_score(y_train, opt_f1_clf.predict(X_train))
train_score_auc = roc_auc_score(y_train, opt_auc_clf.predict(X_train))
test_score_acc = opt_acc_clf.score(X_test, y_test)
test_score_f1 = f1_score(y_test, opt_f1_clf.predict(X_test))
test_score_auc = roc_auc_score(y_test, opt_auc_clf.predict(X_test))
raw_train_arr.append(
[train_score_acc, train_score_f1, train_score_auc])
raw_test_arr.append([test_score_acc, test_score_f1, test_score_auc])
# Create dataframe from results
raw_train_arr = np.array(raw_train_arr).reshape(5, 3)
raw_test_arr = np.array(raw_test_arr).reshape(5, 3)
raw_train_df = pd.DataFrame(data=raw_train_arr,
columns=['accuracy', 'f1', 'auc'])
raw_test_df = pd.DataFrame(data=raw_test_arr,
columns=['accuracy', 'f1', 'auc'])
# Return results
return raw_train_df, raw_test_df
from cuml.svm import SVC
else:
from sklearn.svm import SVC
model = SVC(**alg.input_variables.__dict__)
elif alg.name == 'GaussianNaiveBayes':
from sklearn.naive_bayes import GaussianNB
model = GaussianNB(**alg.input_variables.__dict__)
warn_not_gpu_support(alg)
elif alg.name == 'LogisticRegression':
if NVIDIA_RAPIDS_ENABLED:
# nvidia rapids version should be higher than v0.13
# if version.parse(cuml.__version__) > version.parse("0.13"):
from cuml.linear_model import LogisticRegression
else:
from sklearn.linear_model import LogisticRegression
model = LogisticRegression(**alg.input_variables.__dict__)
elif alg.name == 'AdaBoost' and alg.type == 'classification':
from sklearn.ensemble import AdaBoostClassifier
model = AdaBoostClassifier(**alg.input_variables.__dict__)
warn_not_gpu_support(alg)
elif alg.name == 'GradientBoosting' and alg.type == 'classification':
from sklearn.ensemble import GradientBoostingClassifier
model = GradientBoostingClassifier(**alg.input_variables.__dict__)
warn_not_gpu_support(alg)
elif alg.name == 'RandomForest' and alg.type == 'classification':
if NVIDIA_RAPIDS_ENABLED:
from cuml.ensemble import RandomForestClassifier
else:
from sklearn.ensemble import RandomForestClassifier
model = RandomForestClassifier(**alg.input_variables.__dict__)
elif alg.name == 'XGBoost' and alg.type == 'classification':
def rank_genes_groups(
X,
labels, # louvain results
var_names,
groups=None,
reference='rest',
n_genes=100,
**kwds,
):
"""
Rank genes for characterizing groups.
Parameters
----------
X : cupy.ndarray of shape (n_cells, n_genes)
The cellxgene matrix to rank genes
labels : cudf.Series of size (n_cells,)
Observations groupings to consider
var_names : cudf.Series of size (n_genes,)
Names of genes in X
groups : Iterable[str] (default: 'all')
Subset of groups, e.g. ['g1', 'g2', 'g3'], to which comparison
shall be restricted, or 'all' (default), for all groups.
reference : str (default: 'rest')
If 'rest', compare each group to the union of the rest of the group.
If a group identifier, compare with respect to this group.
n_genes : int (default: 100)
The number of genes that appear in the returned tables.
"""
#### Wherever we see "adata.obs[groupby], we should just replace w/ the groups"
import time
start = time.time()
# for clarity, rename variable
if groups == 'all':
groups_order = 'all'
elif isinstance(groups, (str, int)):
raise ValueError('Specify a sequence of groups')
else:
groups_order = list(groups)
if isinstance(groups_order[0], int):
groups_order = [str(n) for n in groups_order]
if reference != 'rest' and reference not in set(groups_order):
groups_order += [reference]
if (reference != 'rest' and reference not in set(labels.cat.categories)):
cats = labels.cat.categories.tolist()
raise ValueError(
f'reference = {reference} needs to be one of groupby = {cats}.')
groups_order, groups_masks = select_groups(labels, groups_order)
original_reference = reference
n_vars = len(var_names)
# for clarity, rename variable
n_genes_user = n_genes
# make sure indices are not OoB in case there are less genes than n_genes
if n_genes_user > X.shape[1]:
n_genes_user = X.shape[1]
# in the following, n_genes is simply another name for the total number of genes
n_genes = X.shape[1]
n_groups = groups_masks.shape[0]
ns = cp.zeros(n_groups, dtype=int)
for imask, mask in enumerate(groups_masks):
ns[imask] = cp.where(mask)[0].size
if reference != 'rest':
ireference = cp.where(groups_order == reference)[0][0]
reference_indices = cp.arange(n_vars, dtype=int)
rankings_gene_scores = []
rankings_gene_names = []
# Perform LogReg
# if reference is not set, then the groups listed will be compared to the rest
# if reference is set, then the groups listed will be compared only to the other groups listed
from cuml.linear_model import LogisticRegression
reference = groups_order[0]
if len(groups) == 1:
raise Exception(
'Cannot perform logistic regression on a single cluster.')
grouping_mask = labels.astype('int').isin(cudf.Series(groups_order))
grouping = labels.loc[grouping_mask]
X = X[grouping_mask.
values, :] # Indexing with a series causes issues, possibly segfault
y = labels.loc[grouping]
clf = LogisticRegression(**kwds)
clf.fit(X.get(), grouping.to_array().astype('float32'))
scores_all = cp.array(clf.coef_).T
for igroup, group in enumerate(groups_order):
if len(groups_order) <= 2: # binary logistic regression
scores = scores_all[0]
else:
scores = scores_all[igroup]
partition = cp.argpartition(scores, -n_genes_user)[-n_genes_user:]
partial_indices = cp.argsort(scores[partition])[::-1]
global_indices = reference_indices[partition][partial_indices]
rankings_gene_scores.append(scores[global_indices].get(
)) ## Shouldn't need to take this off device
rankings_gene_names.append(var_names[global_indices].to_pandas())
if len(groups_order) <= 2:
break
groups_order_save = [str(g) for g in groups_order]
if (len(groups) == 2):
groups_order_save = [g for g in groups_order if g != reference]
print("Ranking took (GPU): " + str(time.time() - start))
start = time.time()
scores = np.rec.fromarrays(
[n for n in rankings_gene_scores],
dtype=[(rn, 'float32') for rn in groups_order_save],
)
names = np.rec.fromarrays(
[n for n in rankings_gene_names],
dtype=[(rn, 'U50') for rn in groups_order_save],
)
print("Preparing output np.rec.fromarrays took (CPU): " +
str(time.time() - start))
print("Note: This operation will be accelerated in a future version")
return scores, names, original_reference
def rank_genes_groups(
X,
labels, # louvain results
var_names,
groupby=str,
groups=None,
reference='rest',
n_genes=100,
key_added=None,
layer=None,
**kwds,
):
#### Wherever we see "adata.obs[groupby], we should just replace w/ the groups"
import time
start = time.time()
# for clarity, rename variable
if groups == 'all':
groups_order = 'all'
elif isinstance(groups, (str, int)):
raise ValueError('Specify a sequence of groups')
else:
groups_order = list(groups)
if isinstance(groups_order[0], int):
groups_order = [str(n) for n in groups_order]
if reference != 'rest' and reference not in set(groups_order):
groups_order += [reference]
if (reference != 'rest' and reference not in set(labels.cat.categories)):
cats = labels.cat.categories.tolist()
raise ValueError(
f'reference = {reference} needs to be one of groupby = {cats}.')
groups_order, groups_masks = select_groups(labels, groups_order)
original_reference = reference
n_vars = len(var_names)
# for clarity, rename variable
n_genes_user = n_genes
# make sure indices are not OoB in case there are less genes than n_genes
if n_genes_user > X.shape[1]:
n_genes_user = X.shape[1]
# in the following, n_genes is simply another name for the total number of genes
n_genes = X.shape[1]
n_groups = groups_masks.shape[0]
ns = cp.zeros(n_groups, dtype=int)
for imask, mask in enumerate(groups_masks):
ns[imask] = cp.where(mask)[0].size
if reference != 'rest':
ireference = cp.where(groups_order == reference)[0][0]
reference_indices = cp.arange(n_vars, dtype=int)
rankings_gene_scores = []
rankings_gene_names = []
rankings_gene_logfoldchanges = []
rankings_gene_pvals = []
rankings_gene_pvals_adj = []
# if 'log1p' in adata.uns_keys() and adata.uns['log1p']['base'] is not None:
# expm1_func = lambda x: np.expm1(x * np.log(adata.uns['log1p']['base']))
# else:
# expm1_func = np.expm1
# Perform LogReg
# if reference is not set, then the groups listed will be compared to the rest
# if reference is set, then the groups listed will be compared only to the other groups listed
from cuml.linear_model import LogisticRegression
reference = groups_order[0]
if len(groups) == 1:
raise Exception(
'Cannot perform logistic regression on a single cluster.')
grouping_mask = labels.astype('int').isin(cudf.Series(groups_order))
grouping = labels.loc[grouping_mask]
X = X[grouping_mask.
values, :] # Indexing with a series causes issues, possibly segfault
y = labels.loc[grouping]
clf = LogisticRegression(**kwds)
clf.fit(X.get(), grouping.to_array().astype('float32'))
scores_all = cp.array(clf.coef_).T
for igroup, group in enumerate(groups_order):
if len(groups_order) <= 2: # binary logistic regression
scores = scores_all[0]
else:
scores = scores_all[igroup]
partition = cp.argpartition(scores, -n_genes_user)[-n_genes_user:]
partial_indices = cp.argsort(scores[partition])[::-1]
global_indices = reference_indices[partition][partial_indices]
rankings_gene_scores.append(scores[global_indices].get(
)) ## Shouldn't need to take this off device
rankings_gene_names.append(var_names[global_indices].to_pandas())
if len(groups_order) <= 2:
break
groups_order_save = [str(g) for g in groups_order]
if (len(groups) == 2):
groups_order_save = [g for g in groups_order if g != reference]
print("Ranking took (GPU): " + str(time.time() - start))
start = time.time()
scores = np.rec.fromarrays(
[n for n in rankings_gene_scores],
dtype=[(rn, 'float32') for rn in groups_order_save],
)
names = np.rec.fromarrays(
[n for n in rankings_gene_names],
dtype=[(rn, 'U50') for rn in groups_order_save],
)
print("Preparing output np.rec.fromarrays took (CPU): " +
str(time.time() - start))
print("Note: This operation will be accelerated in a future version")
return scores, names, original_reference
TargetEncodeTransform(columns=[
'nom_7',
]),
TargetEncodeTransform(columns=[
'nom_8',
]),
TargetEncodeTransform(columns=[
'nom_9',
]),
# TargetEncodeTransform(columns=['ord_0',]),
# TargetEncodeTransform(columns=['ord_1',]),
# TargetEncodeTransform(columns=['ord_2',]),
# TargetEncodeTransform(columns=['ord_3',]),
# TargetEncodeTransform(columns=['ord_4',]),
# TargetEncodeTransform(columns=['ord_5',]),
LogisticRegression(),
)
pipe.fit(X, y)
y_pred = pipe.predict(X)
param_grid = {"logisticregression__C": [1, 2, 3, 4, 5, 6]}
rscv = RandomizedSearchCV(pipe,
param_distributions=param_grid,
scoring=make_scorer(roc_auc_gpu,
greater_is_better=True),
cv=kf,
verbose=6,
random_state=Config.RANDOM_STATE,
n_iter=1)
model = rscv.fit(X, y)
print(pipe)