Bridging the Omics Divide: A Modular Relational Approach to Multi-Layer Biological Data Management
Background: Rapid growth of high-throughput molecular data demands systems for efficient retrieval, integration, and scalability across omics layers. Traditional file-based workflows hinder cross-modal analysis and reproducibility because of fragmented storage and ad-hoc querying. Few existing tools for genomic variation data prioritize modular multi-omics integration. We developed vcf2db, a sample-centric relational framework modeling each omics modality as a distinct but linkable component centered on biological samples. This study evaluates whether this design delivers competitive genomic retrieval while enabling extension to additional molecular layers. Results: We implemented a proof-of-concept genomic schema and ingestion pipeline for annotated VCF data using the European subset of the 1000 Genomes Project (502 samples, 25 million variants). We benchmarked it against three established VCF-oriented tools on seven retrieval tasks: coordinate filtering, annotation-driven queries, genotype extraction, and aggregation. Under controlled conditions, vcf2db performed strongly on selective queries, often outperforming other systems for coordinate and annotation filters, and remained usable for genotype retrieval. Aggregation-heavy tasks were less efficient, indicating optimization targets. We also validated modular extensibility by adding a synthetic transcriptomic layer without modifying genomic tables, linking layers via shared sample identifiers. Conclusion: vcf2db supports cross-layer retrieval directly as SQL queries anchored on shared sample identifiers, enabling integrated multi-omics access that is difficult with file-based approaches.