Descubre Habilidades de Claude para data science & ml. Explora 53 habilidades y encuentra las capacidades perfectas para tus flujos de trabajo de IA.
Provides comprehensive tools for astronomical data analysis, including coordinate transformations, unit conversions, and FITS file manipulation.
Builds and trains machine learning models on genomic interval data to generate embeddings for regions, single cells, and metadata.
Manages annotated data matrices for single-cell genomics and large-scale biological datasets using the Python AnnData framework.
Processes DICOM medical imaging files for metadata extraction, pixel data manipulation, and secure patient data anonymization.
Minimizes experimental bias by implementing structured blinding protocols and objectivity standards for scientific research studies.
Systematically refines and validates research tools through multi-phase iterative testing and rigorous data-driven evaluation.
Interprets and reports statistical findings with accuracy, prioritizing effect sizes and confidence intervals over simple p-value significance.
Automates the translation of MetaTrader 5 (MQL5) indicators into validated Python implementations for algorithmic trading.
Guides the selection, assumption checking, and interpretation of statistical hypothesis tests for rigorous research data analysis.
Automates experiment tracking and backtest logging using the MLflow Python API and QuantStats metrics.
Calculates statistical power and determines optimal sample sizes to ensure experimental designs meet rigorous scientific and funding standards.
Implements rigorous random assignment procedures for scientific experiments to minimize selection bias and meet CONSORT standards.
Evaluates methodological quality and potential biases in research studies using industry-standard frameworks for systematic reviews.
Creates and optimizes elizaOS knowledge bases using RAG, smart chunking strategies, and semantic search integration.
Conducts quantitative synthesis by pooling effect sizes across multiple research studies to calculate summary effects and assess statistical heterogeneity.
Conducts detailed subgroup analyses to examine effect moderation, explore dataset heterogeneity, and identify differential outcomes across specific populations.
Accesses the Human Metabolome Database (HMDB) to retrieve detailed chemical properties, biomarker data, and spectral information for over 220,000 metabolites.
Integrates the Times Square notebook execution system into web applications using established patterns for data fetching, real-time updates, and URL management.
Integrates differential methylation and gene expression datasets to identify coordinated epigenetic regulation patterns and classify regulatory relationships.
Performs genome-wide DNA methylation analysis to characterize patterns, genomic feature distributions, and sample similarities from sequencing data.
Implements optimized document splitting and processing workflows for Retrieval-Augmented Generation (RAG) systems.
Automates the creation and management of robust data pipelines using Hamilton DAGs and the FlowerPower framework.
Calculates and interprets standardized effect sizes to quantify the practical significance of research findings beyond statistical significance.
Evaluates the robustness of research findings by testing how conclusions change under varying analytical assumptions and data conditions.
Systematically applies eligibility criteria during literature screenings to ensure rigorous and reproducible study selection in research workflows.
Generates standardized PRISMA 2020-compliant flow diagrams to document the study selection process in systematic literature reviews.
Designs methodologically rigorous scientific experiments and research studies following NIH rigor standards and best practices.
Generates publication-quality data visualizations and scientific figures following academic design and statistical best practices.
Generates structured evidence synthesis matrices to organize, compare, and analyze research data across multiple studies.
Filters raw BAM files by removing mitochondrial reads, PCR duplicates, and blacklisted regions to prepare genomic data for peak calling.
Scroll for more results...