LLM Mart Basic
@llm-mart · Joined Jun 2026
Generate proper ENCODE citations for publications, grants, and presentations. Use when the user needs to cite ENCODE data, create bibliography entries, write acknowledgment sections, or ensure compliance with ENCODE data use policy.
Guide for annotating ENCODE regulatory variants with ClinVar clinical significance. Use when users need to check if variants in ENCODE peaks have clinical associations, find pathogenic variants in regulatory regions, or assess variant clinical impact. Trigger on: ClinVar, clinica
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
/do-issue
do-issue
Implement issues (GitHub/GitLab/Bitbucket) using progressive analyze-specify-plan-implement workflow
/fix-pr
fix-pr
Address PR/MR review feedback by reading comments, implementing fixes, and resolving threads. GitHub and GitLab support.
/fix-workflow
fix-workflow
Retrospective analysis and improvement of workflow components with self-evolving patterns
/fixit
fixit
Fix broken functionality from pasted error output, stack traces, or
/git-catchup
git-catchup
Summarize recent git history since a baseline with structured analysis of what changed, why, and what to watch for.
/merge-docs
Merge docs
Consolidate ephemeral LLM-generated markdown into permanent documentation.
/pr-review
pr-review
Review pull requests with scope validation, code analysis, and line comments. Supports GitHub PRs and GitLab MRs.
/prepare-pr
prepare-pr
Prepare a PR end-to-end by updating documentation, running tests, dogfooding checks, and validating with code review.
/resolve-threads
resolve-threads
Batch-resolve unresolved PR/MR review threads via GraphQL API (GitHub/GitLab)
/sync-capabilities
Sync capabilities
Detect and fix drift between plugin.json registrations and capabilities reference documentation
/update-ci
Update ci
Update pre-commit hooks and CI/CD workflows based on recent project changes
/update-dependencies
update-dependencies
Scan and update dependencies across all ecosystems with conflict detection
/update-docs
Update docs
Update project documentation with consolidation, debloating, AI slop detection, capabilities sync, and accuracy verification.
/update-plugins
Update plugins
Audit and sync plugin.json registrations with actual disk contents. Detects missing or stale skills, commands, agents, hooks.
/update-tests
update-tests
Review and update test coverage using TDD/BDD methodology with quality validation. Generates tests for changed code.
/update-tutorial
update-tutorial
Generate or update tutorials with VHS and Playwright recordings
/update-version
Update version
Bump project versions using git-workspace-review and version-updates skills.
/validate-pr
validate-pr
Generate and self-execute a diff-derived test plan for a PR. Reads
/doc-generate
doc-generate
Generate new documentation with human-quality writing.
/doc-polish
doc-polish
Clean up AI-generated content and improve documentation quality.
Make any song you can imagine
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