Explora nuestra colección completa de Habilidades de Claude que extienden las capacidades de los agentes de IA.
Integrates Hugging Face Transformers to load, fine-tune, and run inference on thousands of pre-trained AI models across multiple modalities.
Evaluates research rigor, methodology, and statistical validity using standardized frameworks like GRADE and Cochrane ROB.
Accesses global statistical data from Data Commons for demographic, economic, and environmental analysis.
Performs high-performance nonlinear dimensionality reduction for data visualization and clustering preprocessing using the UMAP algorithm.
Develops and trains Graph Neural Networks (GNNs) for analyzing irregular data structures and relational datasets.
Queries the NCBI Gene database to retrieve comprehensive genetic information, sequences, and functional annotations for biological research.
Facilitates molecular property prediction and drug discovery through specialized machine learning models and chemical data featurization.
Performs automated differential gene expression analysis on bulk RNA-seq data using the PyDESeq2 framework.
Implements comprehensive machine learning workflows using scikit-learn, covering data preprocessing, model training, evaluation, and pipeline deployment.
Predicts accurate 3D protein-ligand binding poses using diffusion-based deep learning for computational drug discovery.
Empowers Claude to design, generate, and analyze protein sequences and structures using ESM3 and ESM C evolutionary scale models.
Performs advanced time series machine learning tasks including classification, forecasting, and anomaly detection using scikit-learn compatible APIs.
Evaluates scientific research rigor, methodology, and statistical validity using evidence-based frameworks like GRADE and Cochrane.
Streamlines deep learning development by organizing PyTorch code into scalable, high-performance Lightning modules and data pipelines.
Analyzes whole-slide images and multiparametric imaging data for advanced computational pathology and machine learning workflows.
Generates comprehensive, compliant clinical documentation including case reports, diagnostic findings, and regulatory trial summaries.
Accesses and analyzes 3D protein and nucleic acid structures from the RCSB Protein Data Bank for structural biology and drug discovery.
Queries the Open Targets Platform to identify and prioritize therapeutic drug targets using genetic, omic, and clinical evidence.
Scales Python data science workflows using parallel and distributed computing for larger-than-memory datasets.
Performs advanced statistical hypothesis testing, regression analysis, and Bayesian modeling with automated assumption checking and APA-style reporting.
Analyzes single-cell omics data using deep generative models for batch correction, multi-omic integration, and probabilistic modeling.
Performs comprehensive exploratory data analysis and generates detailed reports for over 200 scientific file formats.
Evaluates scientific manuscripts and grant proposals using a systematic toolkit for methodology, statistics, and reporting standards.
Manages large-scale N-dimensional arrays with chunking, compression, and cloud-native storage for scientific computing.
Queries the NHGRI-EBI GWAS Catalog to retrieve genetic variant associations, study metadata, and polygenic risk score data.
Applies unsupervised machine learning models to genomic interval data for region embeddings, single-cell analysis, and similarity searches.
Generates testable scientific hypotheses and detailed experimental designs based on observations and literature evidence.
Performs comprehensive survival analysis and time-to-event modeling using the scikit-survival library in Python.
Drafts, structures, and refines professional scientific manuscripts using standardized research formats and reporting guidelines.
Accesses the world's leading protein sequence and functional information resource via the UniProt REST API.
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