Discover Agent Skills for data science & ml. Browse 61 skills for Claude, ChatGPT & Codex.
Queries the ClinicalTrials.gov API to search for medical studies, retrieve trial details, and export structured clinical research data.
Accesses and interprets the NCBI ClinVar archive to identify genomic variant clinical significance and pathogenicity classifications.
Processes and analyzes high-throughput sequencing data to generate publication-quality visualizations and quality control metrics for genomics research.
Queries and interprets genomic variant data from the NCBI ClinVar database to support clinical genetics and research workflows.
Accesses and analyzes comprehensive pharmaceutical data from DrugBank, including drug properties, interactions, targets, and chemical structures.
Interfaces with NCBI ClinVar to query, interpret, and process human genetic variant clinical significance data for genomic medicine.
Processes and analyzes high-throughput sequencing data to generate publication-quality genomic visualizations and quality control metrics.
Generates publication-quality scientific visualizations and data plots locally using Python's Matplotlib and Seaborn libraries.
Builds high-performance Retrieval-Augmented Generation systems using vector databases, semantic search, and advanced retrieval patterns.
Queries the Ensembl REST API to retrieve gene annotations, sequences, variants, and comparative genomics data for over 250 species.
Builds end-to-end MLOps pipelines for data preparation, model training, validation, and production deployment.
Provides unified Python access to over 40 bioinformatics web services and databases for integrated biological data analysis.
Trains and deploys sophisticated neural network architectures across distributed E2B sandbox environments.
Accesses and analyzes comprehensive pharmaceutical data from DrugBank including drug properties, interactions, and molecular structures.
Builds end-to-end MLOps pipelines from data preparation through model training, validation, and production deployment.
Performs constraint-based reconstruction and analysis of metabolic models using Python for systems biology and metabolic engineering.
Accesses the Catalogue of Somatic Mutations in Cancer (COSMIC) to retrieve somatic mutations, gene fusions, and mutational signatures for oncology research.
Performs 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 publication-ready LaTeX manuscripts.
Implements comprehensive evaluation strategies for LLM applications using automated metrics, human feedback, and benchmarking.
Integrates Reactome's open-source curated pathway database for biological pathway analysis, gene mapping, and systems biology research.
Generates rigorous, testable scientific hypotheses and detailed experimental designs based on observations and existing literature.
Generates professional, multi-page PDF reports with formatted text, tables, and embedded visualizations using the ReportLab library.
Processes and analyzes mass spectrometry data using Python-based spectral similarity metrics and metadata harmonization.
Searches the arXiv preprint repository for scholarly articles across various scientific and technical domains.
Integrates Benchling’s R&D platform with Claude to automate life sciences workflows, manage biological registries, and streamline lab data operations.
Trains and deploys distributed neural networks within secure E2B sandbox environments using the Flow Nexus framework.
Queries and interprets NCBI ClinVar data for human genetic variant pathogenicity and clinical significance.
Provides comprehensive cheminformatics capabilities for molecular analysis, property calculation, and 3D coordinate generation.
Automates Excel spreadsheet analysis, data manipulation, and visual reporting using Python-based data science libraries.
Scroll for more results...