数据处理
数据转换、清洗与 ETL
ultrapilot
Yeachan-Heo
Parallel autopilot with file ownership partitioning
aigcpanel-skills
modstart-lib
通过 AigcPanel Pro 内置 HTTP 接口调用本地 AI 模型。当需要列出可用模型、调用模型生成内容、或查询任务结果时使用本技能。适用场景：自动化脚本调用 AI 模型、外部程序集成 AigcPanel Pro、批量处理任务。
fastmcp-client-cli
PrefectHQ
Query and invoke tools on MCP servers using fastmcp list and fastmcp call. Use when you need to discover what tools a server offers, call tools, or integrate MCP servers into workflows.
flux-best-practices
black-forest-labs
Comprehensive guide for BFL FLUX image generation models. Covers prompting, T2I, I2I, structured JSON, hex colors, typography, multi-reference editing, and model-specific best practices for FLUX.2 and FLUX.1 families.
camoufox-cli
Bin-Huang
Anti-detect browser automation CLI for AI agents. Use when the user needs to interact with websites with bot detection, CAPTCHAs, or anti-bot blocks, including navigating pages, filling forms, clicking buttons, taking screenshots, extracting data, testing web apps, or automating any browser task that requires bypassing fingerprint checks.
testing-standards
DaveSkender
Testing conventions for Stock Indicators. Use for test naming (MethodName_StateUnderTest_ExpectedBehavior), FluentAssertions patterns, precision requirements, and test base class selection.
formatter-development
biomejs
Guide for implementing formatting rules using Biome's IR-based formatter infrastructure. Use when working on formatters for JavaScript, CSS, JSON, HTML, or other languages. Examples:<example>User needs to implement formatting for a new syntax node</example><example>User wants to handle comments in formatted output</example><example>User is comparing Biome's formatting against Prettier</example>
rule-options
biomejs
Guide for implementing configurable options for lint rules and assists. Use when rules need user-configurable behavior. Examples:<example>User wants to add options to a lint rule</example><example>User needs to implement JSON deserialization for rule config</example><example>User is testing rule behavior with different options</example>
1k-code-review-pr
OneKeyHQ
Structured PR code review checklist for OneKey monorepo. Use when reviewing PRs to identify build issues, script problems, CI workflow gaps, and documentation inconsistencies. Focuses on actionable feedback with priority levels and specific fix suggestions. 代码审查. Code Review PR.
implementing-figma-designs
OneKeyHQ
Implements Figma designs 1:1 using OneKey component library (还原设计稿).
perf-optimizer
OneKeyHQ
"Systematic performance optimization and regression debugging for OneKey mobile app (iOS). Use when: (1) Fixing performance regressions - when metrics like tokensStartMs, tokensSpanMs, or functionCallCount have regressed and need to be brought back to normal levels, (2) Improving baseline performance - when there's a need to optimize cold start time or reduce function call overhead, (3) User requests performance optimization/improvement/debugging for the app's startup or home screen refresh flow."
react-best-practices
OneKeyHQ
React and Next.js performance optimization guidelines from Vercel Engineering. This skill should be used when writing, reviewing, or refactoring React/Next.js code to ensure optimal performance patterns. Triggers on tasks involving React components, Next.js pages, data fetching, bundle optimization, or performance improvements.
tooluniverse-phylogenetics
mims-harvard
Production-ready phylogenetics and sequence analysis skill for alignment processing, tree analysis, and evolutionary metrics. Computes treeness, RCV, treeness/RCV, parsimony informative sites, evolutionary rate, DVMC, tree length, alignment gap statistics, GC content, and bootstrap support using PhyKIT, Biopython, and DendroPy. Performs NJ/UPGMA/parsimony tree construction, Robinson-Foulds distance, Mann-Whitney U tests, and batch analysis across gene families. Integrates with ToolUniverse for sequence retrieval (NCBI, UniProt, Ensembl) and tree annotation. Use when processing FASTA/PHYLIP/Nexus/Newick files, computing phylogenetic metrics, comparing taxa groups, or answering questions about alignments, trees, parsimony, or molecular evolution.
devtu-fix-tool
mims-harvard
Fix failing ToolUniverse tools by diagnosing test failures, identifying root causes, implementing fixes, and validating solutions. Use when ToolUniverse tools fail tests, return errors, have schema validation issues, or when asked to debug or fix tools in the ToolUniverse framework.
tooluniverse-gwas-snp-interpretation
mims-harvard
Interpret genetic variants (SNPs) from GWAS studies by aggregating evidence from multiple databases (GWAS Catalog, Open Targets Genetics, ClinVar). Retrieves variant annotations, GWAS trait associations, fine-mapping evidence, locus-to-gene predictions, and clinical significance. Use when asked to interpret a SNP by rsID, find disease associations for a variant, assess clinical significance, or answer questions like "What diseases is rs429358 associated with?" or "Interpret rs7903146".
tooluniverse-multi-omics-integration
mims-harvard
Integrate and analyze multiple omics datasets (transcriptomics, proteomics, epigenomics, genomics, metabolomics) for systems biology and precision medicine. Performs cross-omics correlation, multi-omics clustering (MOFA+, NMF), pathway-level integration, and sample matching. Coordinates ToolUniverse skills for expression data (RNA-seq), epigenomics (methylation, ChIP-seq), variants (SNVs, CNVs), protein interactions, and pathway enrichment. Use when analyzing multi-omics datasets, performing integrative analysis, discovering multi-omics biomarkers, studying disease mechanisms across molecular layers, or conducting systems biology research that requires coordinated analysis of transcriptome, genome, epigenome, proteome, and metabolome data.
tooluniverse-expression-data-retrieval
mims-harvard
Retrieves gene expression and omics datasets from ArrayExpress and BioStudies with gene disambiguation, experiment quality assessment, and structured reports. Creates comprehensive dataset profiles with metadata, sample information, and download links. Use when users need expression data, omics datasets, or mention ArrayExpress (E-MTAB, E-GEOD) or BioStudies (S-BSST) accessions.
tooluniverse-immune-repertoire-analysis
mims-harvard
Comprehensive immune repertoire analysis for T-cell and B-cell receptor sequencing data. Analyze TCR/BCR repertoires to assess clonality, diversity, V(D)J gene usage, CDR3 characteristics, convergence, and predict epitope specificity. Integrate with single-cell data for clonotype-phenotype associations. Use for adaptive immune response profiling, cancer immunotherapy research, vaccine response assessment, autoimmune disease studies, or repertoire diversity analysis in immunology research.
tooluniverse-drug-drug-interaction
mims-harvard
Comprehensive drug-drug interaction (DDI) prediction and risk assessment. Analyzes interaction mechanisms (CYP450, transporters, pharmacodynamic), severity classification, clinical evidence grading, and provides management strategies. Supports single drug pairs, polypharmacy analysis (3+ drugs), and alternative drug recommendations. Use when users ask about drug interactions, medication safety, polypharmacy risks, or need DDI assessment for clinical decision support.
tooluniverse-network-pharmacology
mims-harvard
Construct and analyze compound-target-disease networks for drug repurposing, polypharmacology discovery, and systems pharmacology. Builds multi-layer networks from ChEMBL, OpenTargets, STRING, DrugBank, Reactome, FAERS, and 60+ other ToolUniverse tools. Calculates Network Pharmacology Scores (0-100), identifies repurposing candidates, predicts mechanisms, and analyzes polypharmacology. Use when users ask about drug repurposing via network analysis, multi-target drug effects, compound-target-disease networks, systems pharmacology, or polypharmacology.
tooluniverse-precision-medicine-stratification
mims-harvard
Comprehensive patient stratification for precision medicine by integrating genomic, clinical, and therapeutic data. Given a disease/condition, genomic data (germline variants, somatic mutations, expression), and optional clinical parameters, performs multi-phase analysis across 9 phases covering disease disambiguation, genetic risk assessment, disease-specific molecular stratification, pharmacogenomic profiling, comorbidity/DDI risk, pathway analysis, clinical evidence and guideline mapping, clinical trial matching, and integrated outcome prediction. Generates a quantitative Precision Medicine Risk Score (0-100) with risk tier assignment (Low/Intermediate/High/Very High), treatment algorithm (1st/2nd/3rd line), pharmacogenomic guidance, clinical trial matches, and monitoring plan. Use when clinicians ask about patient risk stratification, treatment selection, prognosis prediction, or personalized therapeutic strategy across cancer, metabolic, cardiovascular, neurological, or rare diseases.
create-tooluniverse-skill
mims-harvard
Create high-quality ToolUniverse skills following test-driven, implementation-agnostic methodology. Integrates tools from ToolUniverse's 1,264+ tool library, creates missing tools when needed using devtu-create-tool, tests thoroughly, and produces skills with Python SDK + MCP support. Use when asked to create new ToolUniverse skills, build research workflows, or develop domain-specific analysis capabilities for biology, chemistry, or medicine.
tooluniverse-gwas-drug-discovery
mims-harvard
Transform GWAS signals into actionable drug targets and repurposing opportunities. Performs locus-to-gene mapping, target druggability assessment, existing drug identification, safety profile evaluation, and clinical trial matching. Use when discovering drug targets from GWAS data, finding drug repurposing opportunities from genetic associations, or translating GWAS findings into therapeutic leads.
tooluniverse-precision-oncology
mims-harvard
Provide actionable treatment recommendations for cancer patients based on molecular profile. Interprets tumor mutations, identifies FDA-approved therapies, finds resistance mechanisms, matches clinical trials. Use when oncologist asks about treatment options for specific mutations (EGFR, KRAS, BRAF, etc.), therapy resistance, or clinical trial eligibility.