发现data science & ml类别的 Claude 技能。浏览 61 个技能,找到适合您 AI 工作流程的完美功能。
Queries and retrieves comprehensive genomic data from NCBI Gene using E-utilities and Datasets APIs for scientific analysis.
Facilitates direct REST API access to the Kyoto Encyclopedia of Genes and Genomes for biological pathway analysis and molecular mapping.
Performs comprehensive statistical testing, hypothesis verification, and research data modeling using Python's scientific ecosystem.
Evaluates the rigor of scientific research by analyzing methodology, statistical validity, and potential biases using standardized frameworks like GRADE and Cochrane.
Generates 50+ page, consulting-grade market research reports with professional LaTeX formatting and data-driven strategic frameworks.
Integrates OMERO microscopy data management with Python for advanced image analysis, metadata handling, and automated screening workflows.
Automates electronic lab notebook management through the LabArchives REST API for research documentation, data backups, and tool integration.
Generates publication-quality scientific diagrams and architectural schematics using AI-driven iterative refinement and quality auditing.
Manages large-scale N-dimensional arrays with chunking, compression, and cloud-native storage integration.
Performs fast, scalable non-linear dimensionality reduction for visualization, clustering, and high-dimensional data analysis.
Facilitates systems biology research by querying the Reactome REST API for pathway analysis, gene mapping, and molecular interactions.
Analyzes mass spectrometry data using Python bindings for OpenMS to process complex proteomics and metabolomics workflows.
Queries the NHGRI-EBI GWAS Catalog for SNP-trait associations, genetic variants, and summary statistics to support genetic epidemiology and polygenic risk score development.
Automates laboratory liquid handling workflows by writing Python-based Protocol API v2 scripts for Opentrons Flex and OT-2 robots.
Access and analyze genomic variant clinical significance data from NCBI's ClinVar archive.
Facilitates collaborative research ideation and hypothesis generation for scientists and academic researchers.
Generates publication-quality statistical graphics and complex data visualizations using a high-level, dataset-oriented Python interface.
Facilitates advanced molecular analysis and cheminformatics workflows including property calculation, substructure searching, and 3D coordinate generation.
Accesses comprehensive pharmacogenomics data including gene-drug interactions, CPIC guidelines, and allele functions for precision medicine.
Accesses the European Nucleotide Archive (ENA) to retrieve DNA/RNA sequences, raw reads, and genome assemblies for bioinformatics pipelines.
Facilitates drug discovery and therapeutic machine learning with curated datasets, ADMET benchmarks, and molecular optimization oracles.
Performs comprehensive biological data analysis including sequence manipulation, phylogenetics, and microbial ecology statistics.
Accesses and queries the Catalogue of Somatic Mutations in Cancer (COSMIC) to retrieve high-quality genomic data for precision oncology and cancer research.
Automates R&D data management by integrating Claude with the Benchling platform for biological entity tracking, inventory control, and lab notebook documentation.
Accesses and analyzes over 200 million AI-predicted protein structures for bioinformatics and structural biology research.
Queries the ChEMBL database to retrieve bioactive molecule data, drug targets, and bioactivity measurements for medicinal chemistry.
Provides direct REST API access to UniProt for protein sequence retrieval, identifier mapping, and comprehensive functional annotation searches.
Accesses the comprehensive BRENDA enzyme database to retrieve kinetic parameters, biochemical reactions, and metabolic pathway data.
Facilitates programmatic access to the ClinicalTrials.gov API v2 to search, filter, and export global clinical study data for research and patient matching.
Conducts real-time academic research, literature reviews, and technical documentation lookups with automated model selection and proper citations.
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