Validate FASTQ sequencing files, run local quality checks, and interpret reports to decide whether trimming is needed. Optionally remove adapters or low-quality read ends while preserving original reads and their quality reports.
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Plan or run DNA analysis to find small genetic changes in tumors, using tumor samples alone or paired with normal tissue. Check sample pairing, contamination, data quality, filtering, and annotations that add information to detected variants.
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Find the right workflow for next-generation sequencing data by inspecting files and clarifying only missing setup details. Receive a recommended analysis skill, checks of available tools, and plans for software installation and reference data.
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Manage Mixpanel Headless login and connection settings, check credentials, and switch accounts, projects, or workspaces. Save named combinations of these settings as targets so an agent can select the intended connection together.
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Retrieve HLA alleles, forms of HLA genes, and cell metadata from the public IPD API. Filter allele records by name, limit returned items, and receive concise summaries, with raw JSON or text available on request.
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Retrieve GTEx associations between a genetic variant and gene expression in individual tissues. Supply one rsID or genome coordinate, and receive JSON with the resolved variant, association rows, counts, and warnings.
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Query Bgee for healthy wild-type gene expression metadata and receive concise summaries. The skill supports lookups that account for relationships between biological terms, keeps requests small, and saves raw results only when requested.
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Prepare 3D models for browser games by cleaning source assets, exporting GLB or glTF, and optimizing geometry and textures. It also guides collision shapes, distance-based detail levels, and runtime checks for the chosen engine.
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Look up species information and archived genetic variants in the European Variation Archive. Uses focused API requests to return concise Markdown summaries, with raw JSON available when structured data is needed for further processing.
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Retrieve focused information from CIViC for cancer variant interpretation. It uses GraphQL, a way to request specific data fields, to inspect available data structures and turn targeted evidence results into concise summaries.
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Query the ChEMBL API for molecules, biological targets, activity records, and mechanisms of action. Search by text or look up an identifier, then receive concise summaries or JSON output when machine-readable results are needed.
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Create or update Google Slides presentations using an existing deck as a design reference. It extracts colors, typography, and layouts, preserves editable slide elements, and checks rendered slides for visual problems.
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Retrieve concise Ensembl summaries for gene identifiers, genomic regions, links to related database records, and genetic variants. Use a bundled Python script to request data, limit displayed results, or save the full response when needed.
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Search BioStudies and ArrayExpress by keywords or retrieve study information using an accession, a study’s registration identifier. Returns concise summaries and can save complete API responses to a file for further inspection.
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Look up one genetic variant in BioBank Japan and get a concise summary of its associations with diseases and traits. Accepts rsIDs or genome coordinates, converts the query as needed, and can save complete results.
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Search HMDB for metabolites, proteins, diseases, or pathways and receive concise Markdown summaries. Keep searches focused on one category, with an option to save the full response when more detail is needed.
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Plan a browser game's architecture before coding. Choose an engine, separate game rules from rendering, and define input, assets, menus, saves, debugging, and performance checks within a shared design.
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Query gnomAD for variant frequencies, gene constraint measures, and effects on gene transcripts. Get concise Markdown summaries from focused requests, with options to return machine-readable JSON or save the full response to a file.
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Create HTML-based videos with animated titles, synchronized captions, narration, music-driven effects, and scene transitions. Structure scenes and timing, define a visual style, and check layouts, text contrast, and animation choreography within HyperFrames.
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Prioritizes candidate genes from GWAS, studies linking genetic variants to traits. Combines locus predictions, gene expression evidence, and rare variant support into ranked results with source attribution, confidence labels, reproducible files, and optional figures.
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Query EpiGraphDB for trait classifications, related literature, genetic evidence, and gene–drug relationships. Get concise summaries with limited result counts, or save the complete response when you need the underlying data.
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Search nucleotide or protein sequences with NCBI BLAST, check job progress, and get compact summaries of the top matches. Use the job ID to retrieve results later, or request raw output saved to a file.
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Search ClinVar and NCBI Variation for genetic variants, or look up records using VCV, RCV, SCV, and RefSNP identifiers. Get concise summaries, check identifier mappings, and save full JSON responses when needed.
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Search ClinicalTrials.gov studies by condition and recruitment status, then receive concise summaries. Use the same client to inspect API field definitions, allowed values, search areas, and field statistics, with an option to save raw responses.
中文简介正在准备中。当前显示英语简介。