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
/story-cover
Story cover
网文封面生成。分析书名题材,生成专业封面图。
/story-deslop
Story deslop
网文去AI味。检测并清除文本中的AI写作痕迹,让文字回归自然。
/story-import
Story import
逆向导入已有小说。将已写好的小说反向解析为标准项目目录结构。
/story-long-analyze
Story long analyze
长篇网文拆文。深度拆解爆款长篇小说的黄金三章、人设、爽点、节奏。
/story-long-scan
Story long scan
长篇网文扫榜。分析起点、番茄、晋江等平台排行数据,提炼市场趋势。
/story-long-write
Story long write
长篇网文写作。从大纲到正文,辅助长篇网络小说的创作。
/story-review
Story review
多视角对抗式审查。使用多个 Agent 对作品进行多维度审稿。
/story-setup
Story setup
网文写作环境部署与检查。部署 hooks、rules、agents、项目指令等基础设施;传入 check 只检查不改动。
/story-short-analyze
Story short analyze
短篇网文拆文。拆解爆款短篇的故事核、结构、情感线和反转设计。
/story-short-scan
Story short scan
短篇网文扫榜。分析知乎盐言、番茄短篇等平台热门数据。
/story-short-write
Story short write
短篇网文写作。辅助短篇小说创作,从构思到成稿。
/story
Story
网文工具箱路由入口。根据模糊意图自动分发到对应的写作、拆文或扫榜工具。
/browser-cdp
Browser cdp
浏览器操控。通过 CDP 复用 Chrome 登录态执行浏览器自动化。
/story-cover
Story cover
小说封面生成。根据书名、作者名和题材生成专业网文封面。
/story-deslop
Story deslop
网文去 AI 味。检测并清理模板化、解释腔和过度工整表达。
/story-import
Story import
逆向导入已有小说,将成稿或半成品解析为可续写项目。
/story-long-analyze
Story long analyze
长篇网文拆文,分析黄金三章、人设、爽点和长线节奏。
/story-long-scan
Story long scan
长篇网文扫榜,分析起点、番茄、晋江等平台趋势。
/story-long-write
Story long write
长篇网文写作,从选题、大纲到逐章正文和持续追踪。
/story-review
Story review
多视角小说审查;ZCode 项目 agents 不可用时自动降级 solo。
Make any song you can imagine
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