Descubre Habilidades de Claude para data science & ml. Explora 53 habilidades y encuentra las capacidades perfectas para tus flujos de trabajo de IA.
Accesses and analyzes over 61 million standardized single-cell genomics records from the CZ CELLxGENE Discover census.
Retrieves genomic, proteomic, and structural data from over 20 biological databases using a unified interface.
Scales Python data science workflows using parallel and distributed computing for larger-than-memory datasets.
Manipulates and processes DICOM medical imaging data for healthcare applications and scientific research.
Processes and analyzes complex mass spectrometry data for proteomics and metabolomics workflows using the PyOpenMS library.
Explains machine learning model predictions and feature importance using Shapley Additive exPlanations for transparent and interpretable AI.
Accesses and analyzes comprehensive FDA regulatory data for drugs, medical devices, and food safety through the openFDA API.
Applies medicinal chemistry filters and drug-likeness rules to prioritize compound libraries for autonomous discovery.
Processes and analyzes massive tabular datasets exceeding available RAM using lazy, out-of-core DataFrame operations.
Analyzes and visualizes complex graph data structures using the comprehensive Python NetworkX library.
Manipulates genomic datasets by reading and writing SAM, BAM, CRAM, VCF, and FASTA files using a Pythonic interface.
Generates professional, publication-ready clinical decision support documents and biomarker-stratified cohort analyses in LaTeX format.
Solves complex single and multi-objective optimization problems using evolutionary algorithms and Pareto front analysis.
Performs automated differential gene expression analysis on bulk RNA-seq data using the PyDESeq2 framework.
Automates the end-to-end scientific research lifecycle from data analysis and hypothesis generation to publishing LaTeX-formatted papers.
Executes complex biomedical research tasks across genomics, drug discovery, and clinical analysis using autonomous AI reasoning.
Analyzes and visualizes phylogenetic trees with support for evolutionary event detection and NCBI taxonomy integration.
Manages biological datasets with automated lineage tracking, ontology-based curation, and FAIR-compliant data lakehouse capabilities.
Accesses and integrates the world's most comprehensive database for exploring somatic mutations in human cancer into bioinformatics workflows.
Empowers Claude to design, generate, and analyze protein sequences and structures using ESM3 and ESM C evolutionary scale models.
Predicts accurate 3D protein-ligand binding poses using diffusion-based deep learning for computational drug discovery.
Provides comprehensive cheminformatics capabilities for molecular analysis, manipulation, and property calculation within Claude Code.
Performs comprehensive single-cell RNA-seq data analysis, including quality control, clustering, and visualization.
Analyzes whole-slide images and multiparametric imaging data for advanced computational pathology and machine learning workflows.
Builds and deploys specialized machine learning models for clinical healthcare data and electronic health records.
Analyzes single-cell omics data using deep generative models for batch correction, multi-omic integration, and probabilistic modeling.
Parses and manipulates Flow Cytometry Standard (FCS) files for scientific data preprocessing and analysis.
Performs high-performance nonlinear dimensionality reduction for data visualization and clustering preprocessing using the UMAP algorithm.
Performs advanced time series machine learning tasks including classification, forecasting, and anomaly detection using scikit-learn compatible APIs.
Provides AI-ready datasets and benchmarks for therapeutic machine learning and drug discovery tasks.
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