浏览所有 Claude 技能

Reactome Pathway Analysis

Integrates the Reactome database to perform pathway enrichment, gene-pathway mapping, and molecular interaction analysis for systems biology.

Benchling R&D Integration

Automates Benchling R&D platform operations including biological sequence management, inventory tracking, and electronic lab notebook documentation.

Scientific Data Visualization

Generates publication-ready scientific figures and multi-panel layouts using Matplotlib, Seaborn, and Plotly.

PPTX Presentation Toolkit

Programmatically creates, edits, and analyzes PowerPoint presentations with support for scientific schematics and XML-level customization.

Statistical Analysis

Performs professional statistical modeling, hypothesis testing, and rigorous assumption verification with publication-ready APA reporting.

Scientific Brainstorming

Facilitates collaborative research ideation to generate hypotheses, challenge assumptions, and explore interdisciplinary connections for creative scientific problem-solving.

deepTools NGS Analysis

Streamlines high-throughput sequencing data analysis by providing tools for BAM processing, quality control, and publication-quality genomic visualizations.

ClinVar Genomic Analysis

Queries the NCBI ClinVar database to interpret genetic variant pathogenicity and annotate genomic data for research and medicine.

Bioinformatics & Genomic Data (gget)

Provides unified, rapid access to over 20 genomic databases and bioinformatics analysis tools for DNA and protein research.

GWAS Catalog Explorer

Queries the NHGRI-EBI GWAS Catalog to retrieve genetic variant associations, study metadata, and genomic summary statistics.

Plotly Scientific Visualization

Generates interactive, publication-quality scientific and statistical charts using the Plotly Python library.

Scientific Hypothesis Generation

Formulates testable, evidence-based scientific hypotheses and experimental designs from observations or literature synthesis.

Scientific Schematics

Generates publication-ready scientific diagrams and architectures with automated quality review and iterative refinement.

Scanpy Single-Cell Analysis

Performs comprehensive single-cell RNA-seq analysis workflows including quality control, normalization, clustering, and cell-type annotation.

Market Research Report Generator

Generates comprehensive, consultant-grade market research reports with professional LaTeX formatting and integrated strategic visualizations.

MarkItDown Document Converter

Converts complex documents, images, and multimedia files into clean, token-efficient Markdown for optimized LLM processing.

Clinical Decision Support

Generates professional, publication-ready clinical decision support documents and biomarker-stratified cohort analyses for pharmaceutical and clinical research.

Mass Spectrometry Analysis (Matchms)

Processes and analyzes mass spectrometry data using the Matchms library for spectral similarity and metadata harmonization.

Molfeat Molecular Featurization

Converts chemical structures into high-dimensional numerical representations for molecular machine learning and QSAR modeling.

Metabolomics Workbench Database

Accesses the NIH Metabolomics Workbench to query over 4,200 studies, standardize metabolite nomenclature, and perform mass spectrometry searches.

Matplotlib Scientific Visualization

Generates professional-grade scientific plots and data visualizations using Python's foundational Matplotlib library.

Neuropixels Neural Analysis

Streamlines high-density neural recording analysis, spike sorting, and quality metric computation for Neuropixels electrophysiology data.

NetworkX Analysis

Builds, analyzes, and visualizes complex networks and graph data structures using the comprehensive NetworkX library for Python.

TorchDrug Discovery ML

Simplifies graph-based machine learning for drug discovery, protein modeling, and molecular science using the TorchDrug framework.

Modal Serverless Python

Runs Python code in the cloud with serverless containers, autoscaling GPUs, and minimal infrastructure management.

HMDB Scientific Database Access

Accesses the Human Metabolome Database (HMDB) to retrieve comprehensive data on small molecule metabolites, clinical biomarkers, and biochemical pathways.

STRING Protein Interaction Database

Analyzes protein-protein interaction networks and performs functional enrichment using the STRING database's 20 billion interactions.

LatchBio Bioinformatics Workflows

Builds and deploys serverless bioinformatics pipelines using the Latch SDK and cloud infrastructure.

CELLxGENE Census Analysis

Accesses and analyzes over 61 million standardized single-cell genomics records from the CZ CELLxGENE Census.

COSMIC Cancer Database

Integrates the world's most comprehensive cancer mutation database into your research workflow to query somatic mutations, signatures, and gene census data.