NegBioDB / tests /test_ge_features.py
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"""Tests for GE omics feature computation module.
Tests gene features, cell line features, omics loading, and combined matrix building.
"""
from pathlib import Path
import numpy as np
import pandas as pd
import pytest
from negbiodb_depmap.depmap_db import get_connection, run_ge_migrations
from negbiodb_depmap.ge_features import (
build_feature_matrix,
compute_cell_line_features,
compute_gene_features,
load_omics_features,
)
MIGRATIONS_DIR = Path(__file__).parent.parent / "migrations_depmap"
@pytest.fixture
def tmp_db(tmp_path):
db_path = tmp_path / "test_ge.db"
run_ge_migrations(db_path, MIGRATIONS_DIR)
return db_path
@pytest.fixture
def populated_db(tmp_db):
"""DB with genes, cell lines, screens, negative results, and pairs."""
conn = get_connection(tmp_db)
# Genes
conn.execute(
"INSERT INTO genes (gene_id, entrez_id, gene_symbol, is_common_essential, is_reference_nonessential) "
"VALUES (1, 7157, 'TP53', 0, 0)"
)
conn.execute(
"INSERT INTO genes (gene_id, entrez_id, gene_symbol, is_common_essential, is_reference_nonessential) "
"VALUES (2, 1956, 'EGFR', 0, 1)"
)
conn.execute(
"INSERT INTO genes (gene_id, entrez_id, gene_symbol, is_common_essential, is_reference_nonessential) "
"VALUES (3, 672, 'BRCA1', 1, 0)"
)
# Cell lines
conn.execute(
"INSERT INTO cell_lines (cell_line_id, model_id, ccle_name, lineage, primary_disease) "
"VALUES (1, 'ACH-000001', 'HELA_CERVIX', 'Cervix', 'Cervical Cancer')"
)
conn.execute(
"INSERT INTO cell_lines (cell_line_id, model_id, ccle_name, lineage, primary_disease) "
"VALUES (2, 'ACH-000002', 'MCF7_BREAST', 'Breast', 'Breast Cancer')"
)
conn.execute(
"INSERT INTO cell_lines (cell_line_id, model_id, ccle_name, lineage, primary_disease) "
"VALUES (3, 'ACH-000003', 'A549_LUNG', 'Lung', 'Lung Cancer')"
)
# Screen
conn.execute(
"INSERT INTO ge_screens (screen_id, source_db, depmap_release, screen_type, algorithm) "
"VALUES (1, 'depmap', 'TEST', 'crispr', 'Chronos')"
)
# Negative results
for gid, clid, effect, dep_prob in [
(1, 1, -0.1, 0.1),
(1, 2, -0.2, 0.15),
(2, 1, -0.05, 0.05),
(2, 2, -0.3, 0.2),
(2, 3, -0.15, 0.08),
(3, 1, -0.4, 0.25),
]:
conn.execute(
"INSERT INTO ge_negative_results "
"(gene_id, cell_line_id, screen_id, gene_effect_score, dependency_probability, "
"confidence_tier, evidence_type, source_db, source_record_id, extraction_method) "
"VALUES (?, ?, 1, ?, ?, 'silver', 'crispr_nonessential', 'depmap', 'TEST', 'score_threshold')",
(gid, clid, effect, dep_prob),
)
conn.commit()
# Refresh pairs
from negbiodb_depmap.depmap_db import refresh_all_ge_pairs
refresh_all_ge_pairs(conn)
conn.commit()
conn.close()
return tmp_db
@pytest.fixture
def conn_pop(populated_db):
c = get_connection(populated_db)
yield c
c.close()
# ── Gene features ─────────────────────────────────────────────────────
class TestComputeGeneFeatures:
def test_returns_dataframe(self, conn_pop):
df = compute_gene_features(conn_pop)
assert isinstance(df, pd.DataFrame)
assert len(df) > 0
def test_gene_count(self, conn_pop):
df = compute_gene_features(conn_pop)
assert len(df) == 3 # 3 genes
def test_expected_columns(self, conn_pop):
df = compute_gene_features(conn_pop)
for col in ["mean_effect", "min_effect", "max_effect",
"is_common_essential", "is_reference_nonessential",
"rnai_concordance_fraction"]:
assert col in df.columns
def test_mean_effect_reasonable(self, conn_pop):
df = compute_gene_features(conn_pop)
# Gene 2 (EGFR) has 3 records: -0.05, -0.3, -0.15
row = df.loc[2]
assert -0.5 < row["mean_effect"] < 0.0
def test_common_essential_flag(self, conn_pop):
df = compute_gene_features(conn_pop)
assert df.loc[3, "is_common_essential"] == 1 # BRCA1
assert df.loc[1, "is_common_essential"] == 0 # TP53
# ── Cell line features ────────────────────────────────────────────────
class TestComputeCellLineFeatures:
def test_returns_dataframe(self, conn_pop):
df = compute_cell_line_features(conn_pop)
assert isinstance(df, pd.DataFrame)
assert len(df) > 0
def test_cell_line_count(self, conn_pop):
df = compute_cell_line_features(conn_pop)
assert len(df) == 3 # 3 cell lines
def test_lineage_one_hot(self, conn_pop):
df = compute_cell_line_features(conn_pop)
lineage_cols = [c for c in df.columns if c.startswith("lineage_")]
assert len(lineage_cols) == 3 # Cervix, Breast, Lung
def test_disease_one_hot(self, conn_pop):
df = compute_cell_line_features(conn_pop)
disease_cols = [c for c in df.columns if c.startswith("disease_")]
assert len(disease_cols) == 3
# ── Omics features ───────────────────────────────────────────────────
class TestLoadOmicsFeatures:
def test_empty_when_no_files(self):
result = load_omics_features()
assert result == {}
def test_expression_loading(self, tmp_path):
# Create synthetic expression matrix
data = {"TP53": [5.0, 3.0], "EGFR": [2.0, 4.0]}
df = pd.DataFrame(data, index=["ACH-000001", "ACH-000002"])
expr_file = tmp_path / "expression.csv"
df.to_csv(expr_file, index_label="")
result = load_omics_features(expression_file=expr_file)
assert len(result) > 0
assert ("ACH-000001", "TP53") in result
assert result[("ACH-000001", "TP53")][0] == 5.0 # expression dim
def test_cn_loading(self, tmp_path):
data = {"TP53": [2.0]}
df = pd.DataFrame(data, index=["ACH-000001"])
cn_file = tmp_path / "cn.csv"
df.to_csv(cn_file, index_label="")
result = load_omics_features(cn_file=cn_file)
assert ("ACH-000001", "TP53") in result
assert result[("ACH-000001", "TP53")][1] == 2.0 # CN dim
def test_mutation_loading(self, tmp_path):
data = {"TP53": [1.0], "EGFR": [0.0]}
df = pd.DataFrame(data, index=["ACH-000001"])
mut_file = tmp_path / "mutations.csv"
df.to_csv(mut_file, index_label="")
result = load_omics_features(mutation_file=mut_file)
assert ("ACH-000001", "TP53") in result
assert result[("ACH-000001", "TP53")][2] == 1.0 # mutation dim
def test_combined_3_dims(self, tmp_path):
# All 3 omics files
for fname, data in [
("expr.csv", {"G1": [5.0]}),
("cn.csv", {"G1": [2.0]}),
("mut.csv", {"G1": [1.0]}),
]:
df = pd.DataFrame(data, index=["ACH-000001"])
df.to_csv(tmp_path / fname, index_label="")
result = load_omics_features(
expression_file=tmp_path / "expr.csv",
cn_file=tmp_path / "cn.csv",
mutation_file=tmp_path / "mut.csv",
)
vec = result[("ACH-000001", "G1")]
assert len(vec) == 3
assert vec[0] == 5.0
assert vec[1] == 2.0
assert vec[2] == 1.0
def test_gene_symbol_filter(self, tmp_path):
data = {"TP53": [5.0], "EGFR": [3.0], "BRCA1": [1.0]}
df = pd.DataFrame(data, index=["ACH-000001"])
expr_file = tmp_path / "expression.csv"
df.to_csv(expr_file, index_label="")
result = load_omics_features(
expression_file=expr_file,
gene_symbols=["TP53", "EGFR"],
)
keys = [k[1] for k in result.keys()]
assert "TP53" in keys
assert "EGFR" in keys
def test_model_id_filter(self, tmp_path):
data = {"TP53": [5.0, 3.0]}
df = pd.DataFrame(data, index=["ACH-000001", "ACH-000002"])
expr_file = tmp_path / "expression.csv"
df.to_csv(expr_file, index_label="")
result = load_omics_features(
expression_file=expr_file,
model_ids=["ACH-000001"],
)
model_ids = [k[0] for k in result.keys()]
assert "ACH-000001" in model_ids
assert "ACH-000002" not in model_ids
# ── Build feature matrix ─────────────────────────────────────────────
class TestBuildFeatureMatrix:
def test_basic_matrix(self, conn_pop):
pairs_df = pd.DataFrame({
"gene_id": [1, 2],
"cell_line_id": [1, 2],
"gene_symbol": ["TP53", "EGFR"],
"model_id": ["ACH-000001", "ACH-000002"],
})
X = build_feature_matrix(conn_pop, pairs_df)
assert isinstance(X, np.ndarray)
assert X.shape[0] == 2
assert X.shape[1] > 0
def test_no_nan(self, conn_pop):
pairs_df = pd.DataFrame({
"gene_id": [1],
"cell_line_id": [1],
"gene_symbol": ["TP53"],
"model_id": ["ACH-000001"],
})
X = build_feature_matrix(conn_pop, pairs_df)
assert not np.isnan(X).any()
def test_with_omics(self, conn_pop, tmp_path):
# Create simple omics
data = {"TP53": [5.0]}
df = pd.DataFrame(data, index=["ACH-000001"])
expr_file = tmp_path / "expression.csv"
df.to_csv(expr_file, index_label="")
omics = load_omics_features(expression_file=expr_file)
pairs_df = pd.DataFrame({
"gene_id": [1],
"cell_line_id": [1],
"gene_symbol": ["TP53"],
"model_id": ["ACH-000001"],
})
X = build_feature_matrix(conn_pop, pairs_df, omics_features=omics)
assert X.shape[0] == 1
# Should have gene features + cell line features + 3 omics dims
assert X.shape[1] > 10
def test_unknown_gene_zeros(self, conn_pop):
pairs_df = pd.DataFrame({
"gene_id": [999],
"cell_line_id": [1],
"gene_symbol": ["FAKE"],
"model_id": ["ACH-000001"],
})
X = build_feature_matrix(conn_pop, pairs_df)
assert X.shape[0] == 1
# Gene features should be zero since gene_id 999 doesn't exist