NegBioDB / migrations_depmap /001_ge_initial_schema.sql
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NegBioDB final: 4 domains, fully audited
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-- NegBioDB Gene Essentiality (GE) Domain — Initial Schema
-- Migration 001: Core tables for DepMap CRISPR/RNAi gene essentiality negatives
--
-- Design decisions:
-- - Asymmetric pairs: gene + cell_line (not symmetric like PPI)
-- - Separate genes/cell_lines tables (separate DB from DTI/CT/PPI)
-- - Confidence tiers: gold/silver/bronze (same framework as DTI/CT/PPI)
-- - PRISM bridge tables: cross-domain link to DTI via InChIKey/ChEMBL
-- - Dedup: UNIQUE on (gene_id, cell_line_id, screen_id, source_db)
-- - Reference flags on genes table for common essential / nonessential sets
-- ============================================================
-- Common Layer tables (same as DTI/CT/PPI)
-- ============================================================
CREATE TABLE IF NOT EXISTS schema_migrations (
version TEXT PRIMARY KEY,
applied_at TEXT DEFAULT (strftime('%Y-%m-%dT%H:%M:%SZ', 'now'))
);
CREATE TABLE IF NOT EXISTS dataset_versions (
dataset_id INTEGER PRIMARY KEY AUTOINCREMENT,
name TEXT NOT NULL,
version TEXT NOT NULL,
source_url TEXT,
download_date TEXT,
file_hash TEXT,
row_count INTEGER,
notes TEXT,
created_at TEXT DEFAULT (strftime('%Y-%m-%dT%H:%M:%SZ', 'now'))
);
-- ============================================================
-- Domain-specific tables: Gene Essentiality
-- ============================================================
-- Genes table
CREATE TABLE genes (
gene_id INTEGER PRIMARY KEY AUTOINCREMENT,
entrez_id INTEGER UNIQUE,
gene_symbol TEXT NOT NULL,
ensembl_id TEXT,
description TEXT,
is_common_essential INTEGER DEFAULT 0,
is_reference_nonessential INTEGER DEFAULT 0,
created_at TEXT DEFAULT (strftime('%Y-%m-%dT%H:%M:%SZ', 'now')),
updated_at TEXT DEFAULT (strftime('%Y-%m-%dT%H:%M:%SZ', 'now'))
);
CREATE INDEX idx_genes_symbol ON genes(gene_symbol);
CREATE INDEX idx_genes_entrez ON genes(entrez_id) WHERE entrez_id IS NOT NULL;
-- Cell lines table
CREATE TABLE cell_lines (
cell_line_id INTEGER PRIMARY KEY AUTOINCREMENT,
model_id TEXT NOT NULL UNIQUE,
ccle_name TEXT,
stripped_name TEXT,
lineage TEXT,
primary_disease TEXT,
subtype TEXT,
sex TEXT,
primary_or_metastasis TEXT,
sample_collection_site TEXT,
created_at TEXT DEFAULT (strftime('%Y-%m-%dT%H:%M:%SZ', 'now')),
updated_at TEXT DEFAULT (strftime('%Y-%m-%dT%H:%M:%SZ', 'now'))
);
CREATE INDEX idx_cell_lines_ccle ON cell_lines(ccle_name) WHERE ccle_name IS NOT NULL;
CREATE INDEX idx_cell_lines_stripped ON cell_lines(stripped_name) WHERE stripped_name IS NOT NULL;
CREATE INDEX idx_cell_lines_lineage ON cell_lines(lineage) WHERE lineage IS NOT NULL;
-- Screen configurations
CREATE TABLE ge_screens (
screen_id INTEGER PRIMARY KEY AUTOINCREMENT,
source_db TEXT NOT NULL CHECK (source_db IN (
'depmap', 'project_score', 'demeter2')),
depmap_release TEXT NOT NULL,
screen_type TEXT NOT NULL CHECK (screen_type IN ('crispr', 'rnai')),
library TEXT,
algorithm TEXT,
notes TEXT,
created_at TEXT DEFAULT (strftime('%Y-%m-%dT%H:%M:%SZ', 'now'))
);
CREATE UNIQUE INDEX idx_ge_screens_source
ON ge_screens(source_db, depmap_release, screen_type);
-- Core fact table: GE negative results (non-essential gene-cell_line pairs)
CREATE TABLE ge_negative_results (
result_id INTEGER PRIMARY KEY AUTOINCREMENT,
gene_id INTEGER NOT NULL REFERENCES genes(gene_id),
cell_line_id INTEGER NOT NULL REFERENCES cell_lines(cell_line_id),
screen_id INTEGER REFERENCES ge_screens(screen_id),
gene_effect_score REAL,
dependency_probability REAL,
evidence_type TEXT NOT NULL CHECK (evidence_type IN (
'crispr_nonessential',
'rnai_nonessential',
'multi_screen_concordant',
'reference_nonessential',
'context_nonessential')),
confidence_tier TEXT NOT NULL CHECK (confidence_tier IN (
'gold', 'silver', 'bronze')),
source_db TEXT NOT NULL,
source_record_id TEXT NOT NULL,
extraction_method TEXT NOT NULL CHECK (extraction_method IN (
'score_threshold', 'reference_set', 'multi_source_concordance')),
created_at TEXT DEFAULT (strftime('%Y-%m-%dT%H:%M:%SZ', 'now')),
updated_at TEXT DEFAULT (strftime('%Y-%m-%dT%H:%M:%SZ', 'now'))
);
CREATE INDEX idx_ge_nr_gene ON ge_negative_results(gene_id);
CREATE INDEX idx_ge_nr_cell_line ON ge_negative_results(cell_line_id);
CREATE INDEX idx_ge_nr_pair ON ge_negative_results(gene_id, cell_line_id);
CREATE INDEX idx_ge_nr_tier ON ge_negative_results(confidence_tier);
CREATE INDEX idx_ge_nr_source ON ge_negative_results(source_db);
CREATE UNIQUE INDEX idx_ge_nr_unique_source ON ge_negative_results(
gene_id, cell_line_id,
COALESCE(screen_id, -1),
source_db);
-- ============================================================
-- Aggregation table
-- ============================================================
CREATE TABLE gene_cell_pairs (
pair_id INTEGER PRIMARY KEY AUTOINCREMENT,
gene_id INTEGER NOT NULL REFERENCES genes(gene_id),
cell_line_id INTEGER NOT NULL REFERENCES cell_lines(cell_line_id),
num_screens INTEGER NOT NULL,
num_sources INTEGER NOT NULL,
best_confidence TEXT NOT NULL,
best_evidence_type TEXT,
min_gene_effect REAL,
max_gene_effect REAL,
mean_gene_effect REAL,
gene_degree INTEGER,
cell_line_degree INTEGER,
UNIQUE(gene_id, cell_line_id)
);
CREATE INDEX idx_gcp_gene ON gene_cell_pairs(gene_id);
CREATE INDEX idx_gcp_cell_line ON gene_cell_pairs(cell_line_id);
CREATE INDEX idx_gcp_confidence ON gene_cell_pairs(best_confidence);
-- ============================================================
-- Benchmark split tables
-- ============================================================
CREATE TABLE ge_split_definitions (
split_id INTEGER PRIMARY KEY AUTOINCREMENT,
split_name TEXT NOT NULL,
split_strategy TEXT NOT NULL CHECK (split_strategy IN (
'random', 'cold_gene', 'cold_cell_line',
'cold_both', 'degree_balanced')),
description TEXT,
random_seed INTEGER,
train_ratio REAL DEFAULT 0.7,
val_ratio REAL DEFAULT 0.1,
test_ratio REAL DEFAULT 0.2,
date_created TEXT DEFAULT (strftime('%Y-%m-%dT%H:%M:%SZ', 'now')),
version TEXT DEFAULT '1.0',
UNIQUE(split_name, version)
);
CREATE TABLE ge_split_assignments (
pair_id INTEGER NOT NULL REFERENCES gene_cell_pairs(pair_id),
split_id INTEGER NOT NULL REFERENCES ge_split_definitions(split_id),
fold TEXT NOT NULL CHECK (fold IN ('train', 'val', 'test')),
PRIMARY KEY (pair_id, split_id)
);
CREATE INDEX idx_ge_splits_fold ON ge_split_assignments(split_id, fold);
-- ============================================================
-- PRISM drug sensitivity bridge tables
-- ============================================================
CREATE TABLE prism_compounds (
compound_id INTEGER PRIMARY KEY AUTOINCREMENT,
broad_id TEXT UNIQUE,
name TEXT,
smiles TEXT,
inchikey TEXT,
chembl_id TEXT,
pubchem_cid INTEGER,
mechanism_of_action TEXT,
target_name TEXT,
created_at TEXT DEFAULT (strftime('%Y-%m-%dT%H:%M:%SZ', 'now'))
);
CREATE INDEX idx_prism_inchikey ON prism_compounds(inchikey)
WHERE inchikey IS NOT NULL;
CREATE INDEX idx_prism_chembl ON prism_compounds(chembl_id)
WHERE chembl_id IS NOT NULL;
CREATE TABLE prism_sensitivity (
sensitivity_id INTEGER PRIMARY KEY AUTOINCREMENT,
compound_id INTEGER NOT NULL REFERENCES prism_compounds(compound_id),
cell_line_id INTEGER NOT NULL REFERENCES cell_lines(cell_line_id),
screen_type TEXT CHECK (screen_type IN ('primary', 'secondary')),
log_fold_change REAL,
auc REAL,
ic50 REAL,
ec50 REAL,
depmap_release TEXT,
created_at TEXT DEFAULT (strftime('%Y-%m-%dT%H:%M:%SZ', 'now'))
);
CREATE INDEX idx_prism_sens_compound ON prism_sensitivity(compound_id);
CREATE INDEX idx_prism_sens_cell_line ON prism_sensitivity(cell_line_id);
-- Record migration
INSERT INTO schema_migrations (version) VALUES ('001');