浏览所有 Claude 技能
探索我们完整的 Claude 技能集合，扩展 AI 代理的能力。
MarkItDown Document Converter
Converts diverse file formats including PDFs, Office documents, and media into LLM-optimized Markdown for seamless data ingestion.
BioServices Bioinformatics Tool
Provides programmatic access to over 40 bioinformatics web services for automated biological data retrieval and pathway analysis.
STRING Database & PPI Analysis
Queries the STRING database for protein-protein interaction networks, functional enrichment, and biological pathway analysis.
ReportLab PDF Generation
Generates professional, production-grade PDF documents including reports, invoices, and data visualizations using the ReportLab Python toolkit.
UMAP Dimensionality Reduction
Performs high-performance nonlinear dimensionality reduction for data visualization and clustering preprocessing using the UMAP algorithm.
PyTorch Geometric (PyG)
Develops and trains Graph Neural Networks (GNNs) for analyzing irregular data structures and relational datasets.
DeepChem Molecular ML & Drug Discovery
Facilitates molecular property prediction and drug discovery through specialized machine learning models and chemical data featurization.
ChEMBL Drug Discovery
Queries the ChEMBL database for bioactive molecules, drug targets, and medicinal chemistry bioactivity data.
Research Information Lookup
Researches academic literature, technical documentation, and scientific data with automatic model selection and citation support.
TorchDrug for Molecular Science
Empowers Claude to perform graph-based drug discovery, molecular property prediction, and protein modeling using the TorchDrug framework.
PDB Database Explorer
Accesses and analyzes 3D protein and nucleic acid structures from the RCSB Protein Data Bank for structural biology and drug discovery.
NCBI Gene Database Skill
Queries the NCBI Gene database to retrieve comprehensive genetic information, sequences, and functional annotations for biological research.
Scientific Critical Thinking
Evaluates research rigor, methodology, and statistical validity using standardized frameworks like GRADE and Cochrane ROB.
deepTools NGS Analysis
Processes and analyzes high-throughput sequencing data to generate publication-quality genomic visualizations and quality control reports.
Transformers for Claude Code
Integrates Hugging Face Transformers to load, fine-tune, and run inference on thousands of pre-trained AI models across multiple modalities.
USPTO Intellectual Property Database
Accesses and analyzes comprehensive USPTO patent and trademark data for intellectual property research and prior art discovery.
ClinVar Database Assistant
Queries the NCBI ClinVar database to retrieve, interpret, and process human genetic variant clinical significance data.
PyLabRobot Laboratory Automation
Automates laboratory equipment and workflows using a hardware-agnostic Python interface for liquid handlers, plate readers, and more.
KEGG Database Explorer
Accesses the KEGG REST API to perform biological pathway analysis, gene mapping, and molecular interaction research.
CZ CELLxGENE Census Genomics
Accesses and analyzes over 61 million standardized single-cell genomics records from the CZ CELLxGENE Discover census.
Scientific Visualization
Generates journal-ready scientific figures and multi-panel layouts following publication-quality standards.
Scientific Peer Review & Critical Evaluation
Conducts systematic, rigorous reviews of scientific manuscripts and grant proposals by evaluating methodology, statistics, and reporting standards.
Opentrons Lab Automation
Automates laboratory workflows by writing and simulating Opentrons Python Protocol API v2 for Flex and OT-2 robots.
Protocols.io Integration
Manages scientific protocols on protocols.io, enabling discovery, creation, publication, and collaborative lab documentation.
Ensembl Genomic Database Integration
Accesses and queries the Ensembl REST API for genomic research, gene annotation, and variant analysis across 250+ species.
Scientific Hypothesis Generation
Generates testable scientific hypotheses and detailed experimental designs based on observations and literature evidence.
ENA Genomics Data Access
Access and retrieve comprehensive nucleotide sequence data and metadata from the European Nucleotide Archive (ENA).
GWAS Database (NHGRI-EBI)
Queries the NHGRI-EBI GWAS Catalog to retrieve genetic variant associations, study metadata, and polygenic risk score data.
Open Targets Database
Queries the Open Targets Platform to identify and prioritize therapeutic drug targets using genetic, omic, and clinical evidence.
Scientific Critical Thinking
Evaluates scientific research rigor, methodology, and statistical validity using evidence-based frameworks like GRADE and Cochrane.
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