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。
Streamlines high-density neural recording analysis, spike sorting, and quality metric computation for Neuropixels electrophysiology data.
Generates publication-ready scientific figures and multi-panel layouts using Matplotlib, Seaborn, and Plotly.
Queries clinical pharmacogenomics data to provide insights into gene-drug interactions, CPIC guidelines, and genetic variants for precision medicine.
Provides unified, rapid access to over 20 genomic databases and bioinformatics analysis tools for DNA and protein research.
Queries the ChEMBL database for bioactive molecules, drug targets, and bioactivity data to accelerate medicinal chemistry and drug discovery research.
Streamlines deep learning development by organizing PyTorch code into scalable, boilerplate-free LightningModules and automated training workflows.
Accesses and analyzes over 200 million AI-predicted protein structures from the AlphaFold DB for structural biology and drug discovery.
Enables advanced materials science research through crystal structure manipulation, thermodynamic analysis, and Materials Project database integration.
Streamlines biomedical data management and genomics workflow automation on the DNAnexus cloud platform.
Applies advanced machine learning techniques to chemistry, biology, and materials science for molecular property prediction and drug discovery.
Accesses the world's most comprehensive enzyme database to retrieve kinetic parameters, reaction equations, and biochemical property data.
Accesses over 230 million purchasable chemical compounds for virtual screening, drug discovery, and molecular docking studies.
Accesses and analyzes the Ensembl REST API for gene lookups, sequence retrieval, and advanced variant effect predictions in genomic research.
Performs fast non-linear dimensionality reduction and manifold learning for data visualization and clustering preprocessing.
Enables programmatic access to the RCSB Protein Data Bank for searching, retrieving, and analyzing 3D structures of biological macromolecules.
Accesses the UniProt REST API to search, retrieve, and map protein sequence and functional data directly within scientific workflows.
Manages and analyzes microscopy data programmatically using the OMERO Python API and data management platform.
Queries the NCBI ClinVar database to interpret genetic variant pathogenicity and annotate genomic data for research and medicine.
Performs professional statistical modeling, hypothesis testing, and rigorous assumption verification with publication-ready APA reporting.
Accesses the world's largest chemical database to search compounds, retrieve molecular properties, and perform structure-based searches.
Develops and optimizes quantum circuits, hybrid quantum-classical models, and molecular simulations using the PennyLane library.
Builds and deploys serverless bioinformatics pipelines using the Latch SDK and cloud infrastructure.
Accesses and analyzes over 61 million standardized single-cell genomics records from the CZ CELLxGENE Census.
Infers gene regulatory networks from transcriptomics data using high-performance algorithms like GRNBoost2 and GENIE3.
Integrates the world's most comprehensive cancer mutation database into your research workflow to query somatic mutations, signatures, and gene census data.
Accesses the Human Metabolome Database (HMDB) to retrieve comprehensive data on small molecule metabolites, clinical biomarkers, and biochemical pathways.
Streamlines access to over 40 bioinformatics web services and databases for biological data retrieval and cross-database analysis.
Analyzes protein-protein interaction networks and performs functional enrichment using the STRING database's 20 billion interactions.
Accesses and manages NCBI Gene Expression Omnibus (GEO) data for transcriptomics and functional genomics research.
Performs complex biological computation, sequence analysis, and bioinformatics workflows using the Biopython library.
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