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biology
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clinical-trials
protein-protein-interaction
gene-essentiality
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6d1bbc7 | 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 | \section{Database Schema}
\label{app:schema}
NegBioDB uses three separate SQLite databases, one per domain, sharing common design patterns: WAL journal mode, foreign key enforcement, COALESCE-based deduplication indexes, and a four-tier confidence system (gold/silver/bronze/copper). Full DDL for all migrations is available in the repository. Below we summarize the key tables.
\subsection{DTI Domain Schema}
Two migrations: \texttt{001\_initial\_schema} (core tables) and \texttt{002\_target\_variants} (variant support).
\begin{small}
\begin{verbatim}
-- Core entity tables
compounds (compound_id PK, canonical_smiles, inchikey UNIQUE,
inchikey_connectivity, pubchem_cid, chembl_id,
molecular_weight, logp, hbd, hba, tpsa, qed, ...)
targets (target_id PK, uniprot_accession UNIQUE,
chembl_target_id, gene_symbol, target_family,
development_level CHECK IN (Tclin/Tchem/Tbio/Tdark), ...)
assays (assay_id PK, source_db, source_assay_id,
assay_format CHECK IN (biochemical/cell-based/in_vivo),
screen_type, z_factor, pubmed_id, ...)
-- Core fact table (30.5M rows)
negative_results (result_id PK, compound_id FK, target_id FK, assay_id FK,
result_type CHECK IN (hard_negative/conditional_negative/
methodological_negative/dose_time_negative/
hypothesis_negative),
confidence_tier CHECK IN (gold/silver/bronze/copper),
activity_type, activity_value, pchembl_value,
source_db, source_record_id, extraction_method, ...)
-- Dedup: UNIQUE(compound_id, target_id, COALESCE(assay_id,-1),
-- source_db, source_record_id)
-- Aggregation (for ML export)
compound_target_pairs (pair_id PK, compound_id FK, target_id FK,
num_assays, num_sources, best_confidence,
compound_degree, target_degree, ...)
-- Variant support (migration 002)
target_variants (variant_id PK, target_id FK, variant_label,
source_db, UNIQUE(target_id, variant_label, ...))
\end{verbatim}
\end{small}
\subsection{CT Domain Schema}
Two migrations: \texttt{001\_ct\_initial\_schema} (core tables) and \texttt{002\_schema\_fixes} (expert review fixes).
\begin{small}
\begin{verbatim}
-- Entity tables
interventions (intervention_id PK, intervention_type CHECK IN
(drug/biologic/device/...),
intervention_name, chembl_id, canonical_smiles,
inchikey, molecular_type, ...)
conditions (condition_id PK, condition_name, mesh_id,
icd10_code, therapeutic_area, ...)
clinical_trials (trial_id PK, source_trial_id UNIQUE,
overall_status, trial_phase, enrollment_actual,
primary_endpoint, why_stopped,
termination_type CHECK IN (clinical_failure/
administrative/external_event/unknown), ...)
-- Core fact table (132,925 rows)
trial_failure_results (result_id PK, intervention_id FK,
condition_id FK, trial_id FK,
failure_category CHECK IN (efficacy/safety/pharmacokinetic/
enrollment/strategic/regulatory/design/other),
confidence_tier CHECK IN (gold/silver/bronze/copper),
p_value_primary, effect_size, serious_adverse_events,
highest_phase_reached, result_interpretation CHECK IN
(definitive_negative/inconclusive_underpowered/
mixed_endpoints/futility_stopped/safety_stopped/
administrative),
source_db, extraction_method, ...)
-- Dedup: UNIQUE(intervention_id, condition_id,
-- COALESCE(trial_id,-1), source_db, source_record_id)
-- Junction tables
trial_interventions (trial_id FK, intervention_id FK, arm_role)
trial_conditions (trial_id FK, condition_id FK)
intervention_targets (intervention_id FK, uniprot_accession, ...)
\end{verbatim}
\end{small}
\subsection{PPI Domain Schema}
Two migrations: \texttt{001\_ppi\_initial\_schema} (core tables) and \texttt{002\_llm\_annotations} (protein annotations for LLM benchmark).
\begin{small}
\begin{verbatim}
-- Entity table
proteins (protein_id PK, uniprot_accession UNIQUE,
gene_symbol, amino_acid_sequence, sequence_length,
subcellular_location,
function_description, go_terms,
domain_annotations, ...) -- migration 002
-- Core fact table (2.23M rows)
ppi_negative_results (result_id PK, protein1_id FK, protein2_id FK,
experiment_id FK,
evidence_type CHECK IN (experimental_non_interaction/
ml_predicted_negative/low_score_negative/
compartment_separated/literature_reported),
confidence_tier CHECK IN (gold/silver/bronze/copper),
interaction_score, detection_method,
source_db, extraction_method, ...,
CHECK (protein1_id < protein2_id)) -- canonical ordering
-- Dedup: UNIQUE(protein1_id, protein2_id,
-- COALESCE(experiment_id,-1),
-- source_db, source_record_id)
-- Aggregation
protein_protein_pairs (pair_id PK, protein1_id FK, protein2_id FK,
num_experiments, num_sources, best_confidence,
protein1_degree, protein2_degree, ...,
CHECK (protein1_id < protein2_id))
-- LLM support (migration 002)
ppi_publication_abstracts (pmid PK, title, abstract, ...)
\end{verbatim}
\end{small}
\subsection{Common Design Patterns}
\begin{itemize}[nosep,leftmargin=*]
\item \textbf{Deduplication:} All fact tables use \texttt{COALESCE(fk, -1)} in UNIQUE indexes to handle NULL foreign keys (SQLite treats NULLs as distinct in UNIQUE constraints).
\item \textbf{Confidence tiers:} Four-level system across all domains: gold (systematic screens, multiple confirmations) $>$ silver (ML-derived, p-value based) $>$ bronze (computational, NLP-detected) $>$ copper (label-only).
\item \textbf{Aggregation tables:} Pre-computed pair-level statistics for ML export, avoiding expensive JOINs during dataset construction.
\item \textbf{Symmetric pairs (PPI):} \texttt{CHECK (protein1\_id $<$ protein2\_id)} enforces canonical ordering, preventing duplicate pair representations.
\item \textbf{Schema migrations:} All databases track applied migrations in a \texttt{schema\_migrations} table for reproducible upgrades.
\end{itemize}
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