LLM Mart Basic
@llm-mart · Joined Jun 2026
Compare ENCODE experiments across different biosamples, tissues, or cell lines to identify tissue-specific regulatory patterns. Use when the user wants cross-tissue comparison, cell-type comparison, tissue-specific elements, differential chromatin, biosample matching, disease vs
Cross-reference ENCODE data with PubMed, bioRxiv, ClinicalTrials.gov, Open Targets, GTEx, ClinVar, GWAS Catalog, gnomAD, Ensembl, and other scientific databases. Use when the user wants to find publications, preprints, or clinical trials related to ENCODE experiments, chain ENCOD
Use ENCODE functional genomics data for disease mechanism research. Use when the user wants to connect GWAS variants to regulatory elements, annotate disease-associated loci with functional data, identify therapeutic targets from epigenomic data, build disease regulatory models,
Download ENCODE genomics files (BED, FASTQ, BAM, bigWig, etc.) to the user's machine. Use when the user wants to download data files from ENCODE experiments.
Query the Ensembl REST API for regulatory feature annotations, variant effect prediction (VEP), coordinate liftover, gene lookups, and cross-references. Use when the user needs to annotate variants with VEP (consequence, CADD, REVEL, SpliceAI), check Ensembl Regulatory Build over
Build comprehensive epigenomic profiles for tissues or cell types using ENCODE data. Use when the user wants to characterize chromatin states, assemble histone modification panels, create epigenomic landscapes, run ChromHMM segmentation, identify super-enhancers or bivalent domai
Analyze ENCODE functional genomics screens including CRISPR screens, MPRA (Massively Parallel Reporter Assays), and STARR-seq. Find screen data in ENCODE, process results, identify functional elements, and integrate with epigenomic annotations.
Search, query, and cross-reference NCBI GEO (Gene Expression Omnibus) datasets with ENCODE experiments. Use when the user wants to find GEO accessions for ENCODE experiments, search GEO for complementary datasets, download GEO metadata or series matrices, cross-reference ENCODE a
Query gnomAD (Genome Aggregation Database) for population allele frequencies, gene constraint scores, and variant annotations to interpret ENCODE regulatory variants. Use when the user needs allele frequencies for variants in ENCODE regulatory elements, wants to assess gene const
Guide for integrating GTEx tissue expression data with ENCODE regulatory elements. Use when users need to check if a gene is expressed in a tissue, correlate regulatory elements with expression, or validate ENCODE findings against GTEx. Trigger on: GTEx, tissue expression, gene e
Guide for integrating NHGRI-EBI GWAS Catalog associations with ENCODE regulatory data. Use when users need to find GWAS variants in ENCODE peaks, connect regulatory elements to disease associations, or prioritize functional variants using ENCODE annotations. Trigger on: GWAS, gen
Build comprehensive chromatin contact maps by aggregating Hi-C loop calls (BEDPE) across multiple ENCODE experiments, donors, and labs. Use when the user wants to answer "what regions are in 3D contact in my tissue?" by creating a union catalog of chromatin loops. Handles resolut
Build comprehensive histone mark maps by aggregating narrowPeak data across multiple ENCODE experiments, donors, and labs. Use when the user wants to answer "where is this histone mark present in my tissue?" by combining peak calls from multiple studies into a union peak set with
Plan and execute integrative analysis combining multiple ENCODE experiments for cross-dataset or multi-omic workflows. Use when the user wants to combine experiments, perform cross-dataset comparison, multi-omic integration, peak overlap analysis, differential binding, signal cor
Guide for using JASPAR transcription factor binding profiles with ENCODE ChIP-seq data. Use when users need to find TF binding motifs in ENCODE peaks, validate ChIP-seq targets with known motifs, or scan regulatory regions for TF binding potential. Trigger on: JASPAR, motif datab
Convert genomic coordinates between assembly versions (GRCh37/hg19 to GRCh38/hg38, mm9 to mm10). Guides UCSC liftOver for BED files, CrossMap for VCF/bigWig, and handles unmapped regions with provenance logging.
Build comprehensive DNA methylation maps by aggregating WGBS (Whole Genome Bisulfite Sequencing) data across multiple ENCODE experiments, donors, and labs. Use when the user wants to answer "where is DNA methylated/unmethylated in my tissue?" by combining per-CpG methylation data
Guide for de novo and known motif enrichment analysis of ENCODE ChIP-seq and ATAC-seq peaks using HOMER and MEME Suite. Use when users need to discover TF binding motifs in peaks, validate ChIP-seq targets, or find co-binding partners. Trigger on: motif analysis, HOMER, MEME, de
Integrate multiple ENCODE data types (RNA-seq, ATAC-seq, Histone ChIP-seq, TF ChIP-seq) for a tissue/cell type to build a comprehensive regulatory landscape. Use when the user wants to answer "what are the enhancers, promoters, and regulatory elements active in my tissue, and whi
Guide for annotating ENCODE peaks with genomic features using ChIPseeker and GREAT. Use when users need to assign peaks to genes, determine genomic feature distribution (promoter, intron, intergenic), or perform gene ontology enrichment of peak-associated genes. Trigger on: peak
/vet
Vet
Vet the staged change: run the implement-review review loop (short alias)
/learn
Learn
Extract a learning from the recent conversation and add it to the appropriate instruction file
/learn
Learn
Extract a learning from the recent conversation and add it to the appropriate instruction file
/create-pipeline
create-pipeline
Create a new pipeline from a task description. Fans out agent, skill, and hook scaffolding in parallel, then integrates into the routing system.
/d
D
Jev-first router: A/B variant of /do. One TypeSafe call replaces the manifest read; falls back to /do when unavailable or unconfident.
/do
Do
Smart router: classify requests and route to the correct agent + skill
/generate-claudemd
Generate claudemd
Generate project-specific CLAUDE.md from repo analysis.
/github-notifications
Github notifications
Triage GitHub notifications: fetch, classify, report actions needed.
/github-profile-rules
Github profile rules
`github-profile-rules` — extract programming rules and coding conventions from a GitHub user's public profile via API.
/gm-brilliant-implementation
Gm brilliant implementation
Run the complete 34-stage implementation workflow for a large, multi-system, multi-wave, or CPU-delegated 5 Star Booker GM program.
/install
Install
Plan, then apply, the VexJoy Agent install with the vexinstall engine
/pr-review
Pr review
Comprehensive PR review using specialized agents, with automatic retro knowledge capture
/reddit-moderate
Reddit moderate
Reddit moderation: fetch modqueue, classify content, take mod actions
/retro
Retro
Learning system interface: stats, search, graduate learnings. Backed by learning.db (SQLite + FTS5).
/system-upgrade
system-upgrade
Systematic upgrade pipeline for adapting agents, skills, and hooks when Claude Code ships updates, user goals change, or retro learnings accumulate.
/full-equity-research
Full equity research
agentii.full-equity-research — the spec 046 kit command. Use the Skill tool to run agentii:full-equity-research on this workspace.
/synthesize
Synthesize
agentii.synthesize — the spec 046 kit command. Use the Skill tool to run agentii:synthesize on this workspace.
/agent-diversity-review
Agent diversity review
Run the Agent Diversity Review gate and emit the result table
/create-specialist-agent
Create specialist agent
Scaffold a new spawnable specialist agent def and register it in the agent taxonomy
/customer-changelog-check
Customer changelog check
Audit whether user-visible changes in the current session have matching CHANGELOG.md entries; report MISSING with suggested lines; --fix auto-appends
Make any song you can imagine
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