"Nomad" matching MCP servers:

A local MCP server for agentic remote development that enables code sync via rsync, SSH command execution, and long-running task management in remote tmux sessions.

A nomad MCP Server (modelcontextprotocol)

Exposes a HashiCorp Nomad cluster as MCP tools for AI agents, enabling read-only inspection of jobs, allocations, nodes, and deployments, with optional write operations like stopping jobs, scaling task groups, restarting allocations, and registering jobs.

The Nomad Stays MCP Server provides access to a curated database of remote-work-friendly accommodations around the world. This API supports both the Model Context Protocol (MCP) for AI assistants and standard REST endpoints for direct integration.

Enables LLM control of ETC Eos Family lighting consoles via OSC, allowing operation of cues, levels, subs, macros, and the full Eos command line.

Enables geographic parity analysis with 26 read-only tools covering purchasing power, salary localization, cost of living, nomad visas, tax residency, FIRE planning, and relocation costs.

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.

Enables AI assistants to query genetic variant data, gene constraints, and population genetics information from the gnomAD (Genome Aggregation Database) through its GraphQL API. Supports searching for genes and variants, retrieving constraint scores, analyzing population frequencies, and accessing genomic coverage data.

Enables querying the gnomAD genome aggregation database for variant, gene, and region information.

Enables secure, authenticated access to Nomai's tools via Google OAuth 2.1, with email allowlisting for access control.

Enables read-only research into parsed SEC events keyed by CIK and CUSIP, including 8-K items, Form 144, Form D, FTD series, XBRL facts, Form 4 insider trades, and 13F filings.

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.

A read-only MCP gateway foundation for Korean public data, exposing bounded public-data capabilities to MCP clients with explicit provider isolation and honest status.