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。
Generates publication-quality statistical graphics and complex data visualizations using the Seaborn Python library.
Infers gene regulatory networks from transcriptomics data using high-performance algorithms like GRNBoost2 and GENIE3.
Accesses and manages NCBI Gene Expression Omnibus (GEO) data for transcriptomics and functional genomics research.
Manages large-scale N-dimensional arrays with chunked storage, compression, and cloud-native parallel I/O.
Enables programmatic access to the RCSB Protein Data Bank for searching, retrieving, and analyzing 3D structures of biological macromolecules.
Facilitates advanced mass spectrometry data analysis using the Python interface to the OpenMS library for proteomics and metabolomics.
Solves complex single and multi-objective optimization problems using evolutionary algorithms and Pareto front analysis.
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.
Analyzes protein-protein interaction networks and performs functional enrichment using the STRING database's 20 billion interactions.
Provides a comprehensive toolkit for rigorous statistical modeling, econometric analysis, and time-series forecasting within the Claude environment.
Enables advanced materials science research through crystal structure manipulation, thermodynamic analysis, and Materials Project database integration.
Queries the NHGRI-EBI GWAS Catalog to retrieve genetic variant associations, study metadata, and genomic summary statistics.
Streamlines access to over 40 bioinformatics web services and databases for biological data retrieval and cross-database analysis.
Accesses the Human Metabolome Database (HMDB) to retrieve comprehensive data on small molecule metabolites, clinical biomarkers, and biochemical pathways.
Parses and manipulates Flow Cytometry Standard (FCS) files, converting biological data into NumPy arrays and CSV formats for scientific analysis.
Integrates the world's most comprehensive cancer mutation database into your research workflow to query somatic mutations, signatures, and gene census data.
Processes and analyzes high-performance genomic interval data for computational biology and machine learning applications.
Performs complex biological computation, sequence analysis, and bioinformatics workflows using the Biopython library.
Predicts high-accuracy 3D protein-ligand binding poses using state-of-the-art diffusion-based deep learning models.
Simulates high-performance computational fluid dynamics using pseudospectral methods and Python-based analysis.
Facilitates direct REST API access to the KEGG database for biological pathway analysis, gene mapping, and molecular interaction research.
Simplifies molecular cheminformatics workflows by providing a Pythonic wrapper for RDKit with sensible defaults and parallel processing.
Manipulates genomic datasets including SAM, BAM, VCF, and FASTA files through a Pythonic interface to htslib.
Accesses AI-ready Therapeutics Data Commons (TDC) datasets and benchmarks for drug discovery and pharmaceutical machine learning.
Integrates NCBI Gene data access into Claude for querying sequences, functional annotations, and genomic metadata.
Develops and trains Graph Neural Networks (GNNs) for node classification, link prediction, and geometric deep learning tasks.
Performs comprehensive differential gene expression analysis from bulk RNA-seq count data using the Python implementation of DESeq2.
Manages and analyzes microscopy data programmatically using the OMERO Python API and data management platform.
Provides unified, rapid access to over 20 genomic databases and bioinformatics analysis tools for DNA and protein research.
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