Skip to main content
Glama

Related Servers

Alternatives to EVEE MCP Server

No user-submitted related servers found.

    Related Servers

    • A
      license
      B
      quality
      D
      maintenance
      Enables AI-powered genomic variant analysis including variant impact prediction, regulatory element discovery, and batch variant scoring. Currently operates in mock mode as a proof-of-concept awaiting the public release of Google DeepMind's AlphaGenome API.
      20
      9 npm
      2
      MIT
    • A
      license
      B
      quality
      D
      maintenance
      Provides a programmatic interface to the Genome Aggregation Database (gnomAD) API across versions v2.1.1, v3.1.2, and v4.1.0. It enables users to query gene metadata, variant information, population frequencies, and ClinVar data through a unified schema.
      12
      6
      Apache 2.0
    • A
      license
      Not graded
      quality
      A
      maintenance
      Look up variant allele frequencies by ancestry, gene loss-of-function constraint, gene variant lists, and sequencing coverage over gnomAD — with ClinVar significance joined in — via MCP.
      44 npm
      1
      Apache 2.0
    • 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

    TDQS

    A4.5/5.0

    Scored across 6 tools

    Disambiguation5/5

    Each tool has a clearly distinct purpose: search_variants for lookup, get_variant for comprehensive info, compare_variants for side-by-side comparison, get_variant_annotations for deep probes, get_variant_disruptions for top disruptions, and wait_for_variant_analysis for polling. No overlapping functionality.

    Naming Consistency5/5

    All tool names follow the verb_noun pattern in snake_case consistently (e.g., compare_variants, get_variant_annotations). The naming is predictable and easy to understand.

    Tool Count5/5

    With 6 tools, the server covers the core workflows of variant lookup, detailed retrieval, comparison, annotation analysis, disruption ranking, and async waiting. This is well-scoped for a specialized domain without being too few or too many.

    Completeness4/5

    The tool set covers essential operations: search, retrieve, compare, deep annotations, disruptions, and async polling. A minor gap is the lack of a tool to list all variants for a given gene (search_variants only returns up to 6 autocomplete results), but for targeted variant analysis, the surface is sufficiently complete.

    Maintenance

    ActivityInactive
    ResponsivenessUnresponsive