CyteType's MCP server lets you explore your scRNA-seq results (clusters, gene expression, annotations, differential expression) directly through Claude using natural conversation. No SDK or API keys required.
MCP server URL: https://mcp.cytetype.nygen.io
Steps
- In Claude, click Customize in the left sidebar, then select Connectors.
- Click + Add Custom Connector. Give it a name (for example
CyteType), pastehttps://mcp.cytetype.nygen.io, and click Add. If it does not connect automatically, click Connect. - You will be taken to the CyteType login page. No existing account is needed; enter your email, verify with the one-time code sent to your inbox, and you will be redirected back to Claude.
- Back in Claude, open the CyteType connector menu and select Always allow from the dropdown to enable all 23 tools without per-call prompts.
- Ask Claude to connect to a job and start asking questions. Try: "Connect to my latest job and show me all clusters."
π‘ Note: Public reports work without an existing account. You still log in via email OTP, but you can immediately explore any public job ID. Authenticated users also get access to their own private, shared, and organization-visible reports.
Available tools
The connector exposes 23 tools grouped by category.
Session management (4)
connect_jobβ Connect by ID or interactively pick from your jobslist_my_jobsβ Browse all jobs you own or have access tolist_connected_jobsβ See all jobs loaded in this sessiondisconnect_jobβ Free a job's memory when you are done
Dataset exploration (8)
list_clustersβ All clusters with annotations and top markersget_cluster_detailβ Full detail for a single clusterlookup_gene_expressionβ Mean expression of genes across clustersdescribe_metadataβ Metadata schema with semantic role hintsquery_metadataβ SQL queries on cell metadata via DuckDBrun_differential_expressionβ DE analysis between cluster groupsget_cell_interactionsβ LIANA cell-cell communication datacluster_metadata_enrichmentβ Per-cluster breakdown by metadata value
Annotation introspection (6)
get_annotation_evidenceβ Gene-level evidence with literature citationsget_annotation_context_fitβ Tissue and pathway context fitget_cell_identityβ Cell state, ontology term, granular typeget_annotation_candidatesβ All candidates considered and reasoningget_candidate_gene_groupsβ Supporting and refuting gene setsget_embedding_coordinatesβ Cell coordinates for visualization
Annotation deep dive (5)
get_quality_controlβ Confidence, heterogeneity, classifier accuracyget_expert_reviewsβ Expert reviewer panel assessmentsget_neighbor_degsβ Differential genes vs. nearest neighborsget_co_expression_evidenceβ Co-expression pairs with statisticsget_pathway_detailsβ Pathway enrichment with NES scores
π‘ Tip: Connect up to 10 jobs in a single session. Call connect_job with different job IDs, then pass job_id to any tool. When only one job is connected, the parameter is optional.
Example prompts
Natural language is enough; you do not need to memorize tool names.
- Connect to my latest job and show me all clusters with their annotations and confidence levels.
- What is the expression of TP53, BRCA1, and CD8A across all clusters?
- Run DE between the T cell clusters and the macrophage clusters. Show me the top upregulated genes.
- Why was cluster 2 annotated as exhausted CD8+ T cells? Show me the evidence and what else was considered.
- Which clusters have low confidence? What did the expert reviewers flag?
- Connect to both my treatment and control jobs and compare the T cell populations.
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