Upload genomic data for comprehensive variant enrichment with population genetics, protein structure analysis, drug targeting, pathway analysis, and clinical evidence integration
About BAM Files: Binary Alignment Map (BAM) files contain sequenced DNA reads aligned to a reference genome. For cancer analysis, you need tumor tissue and optionally normal tissue BAM files.
Comprehensive Enrichment: Every variant is automatically enriched with population allele frequencies from 71,000+ genomes, protein structure predictions from 200 million+ proteins, drug-target interactions from 1.6 million+ compounds, protein-protein interaction networks, cancer pathway analysis, functional impact predictions, clinical evidence from curated databases, research literature citations, and therapeutic matching from FDA-approved drugs and clinical trials.
About VCF Files: Variant Call Format (VCF) files contain pre-called genetic variants. Using VCF is much faster than BAM files because variant calling has already been performed. Omics807 will directly annotate and analyze your variants.
Supported: .vcf and .vcf.gz (compressed VCF) files from any variant caller (GATK, DeepSomatic, Strelka2, etc.)
Comprehensive Enrichment: All variants are automatically enriched with population allele frequencies, protein structure predictions, drug-target interactions, protein-protein networks, cancer pathway analysis, functional impact predictions, clinical evidence, research literature, and therapeutic matching—delivering comprehensive precision medicine insights from germline filtering to actionable treatment options.