Results for “nsga2”

Query the NHGRI-EBI GWAS Catalog REST API for SNP-trait associations, retrieving variants by rs ID, disease/trait, or gene along with p-values and summary statistics. Use when investigating genome-wide association study hits, mapping a SNP or rsID to traits, building polygenic risk scores, or doing genetic epidemiology lookups. Part of the AlterLab Academic Skills suite.

Builds and debugs n8n workflows, covering nodes, RAG with vector stores, the REST API, Code node scripts, expressions, and Docker hosting.

Validate n8n expression syntax and fix common errors when writing {{}} expressions, accessing $json/$node variables, and mapping data between nodes.