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Glama

Related Servers

Alternatives to BRaVa MCP

No user-submitted related servers found.

    Related Servers

    • A
      license
      C
      quality
      F
      maintenance
      Provides AI-powered access to major biological databases for GWAS and bioinformatics research. Enables natural language queries for protein, gene, variant, pathway, and drug discovery analysis.
      44
      1
      MIT
    • A
      license
      Not graded
      quality
      D
      maintenance
      Enables real-time pharmacogenomics analysis, including variant clinical significance, drug-gene interactions, and dosing guidelines, by connecting to ClinVar, PharmGKB, gnomAD, and other databases.
      1
      MIT
    • A
      license
      A
      quality
      D
      maintenance
      Enables AI-driven pharmacogenomic analysis by querying structured genetic variant, drug response, and disease risk data. Supports natural language questions about medications, traits, and health risks based on user genome data, with privacy-first local execution.
      16
      47 npm
      12
      MIT
    • A
      license
      Not graded
      quality
      D
      maintenance
      Enables AI agents to query clinical genomics databases, retrieve supporting literature, analyze population genetics, and visualize biological pathways.
      18
      MIT

    TDQS

    A4/5.0

    Scored across 4 tools

    Disambiguation5/5

    Each tool has a distinct role: schema provides metadata and pitfalls, query runs arbitrary SQL, gene_phenotype_detail performs cross-ancestry replication analysis, and variants retrieves single-variant results. There is no overlap in functionality, and descriptions clearly differentiate use cases.

    Naming Consistency4/5

    All tool names use lowercase and underscores, but they mix single-word verbs ('query', 'schema') and descriptive multi-word nouns ('gene_phenotype_detail', 'variants'). While the style is consistent (underscore_case), the pattern varies between imperative and descriptive, which is acceptable but not perfectly uniform.

    Tool Count5/5

    Four tools are appropriate for a specialized genomic data server. Schema is a mandatory prerequisite, query enables flexible exploration, gene_phenotype_detail addresses the server's primary analysis use case, and variants provides deeper variant-level data. The count is compact and focused without being insufficient.

    Completeness4/5

    The server covers the main workflows: understanding the schema, running analytical SQL queries, performing replication checks, and accessing variant-level results. It lacks explicit tools for listing available traits or genes, but these can be obtained via query. The set is functionally complete for its domain, with minor gaps.

    Maintenance

    ActivitySlowing
    ResponsivenessNo issues