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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Search NCBI databases for literature, genes, proteins, nucleotide records, and GEO dataset descriptions. Retrieve records, summaries, or related entries through Entrez, NCBI’s database access service, and receive concise results with links to cited publications.
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Analyze marker-gene sequencing data to study microbial communities. Supports FASTQ quality checks and, with primers, metadata, and taxonomy resources, workflows that produce sequence variant tables, taxonomic assignments, diversity measurements, and plots.
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Send research questions to a running NVIDIA AI-Q Blueprint backend and receive reports with citations and source URLs preserved. Track longer research jobs, check their progress, and retrieve completed reports after a local interruption.
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Plan or run ATAC-seq analysis to identify accessible DNA regions. Check sequencing quality, align reads, detect peaks, combine evidence across replicate samples, and prepare comparisons between conditions with quality summaries and visualization tracks.
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Turn conversations and notes into structured Notion pages, including wiki entries, how-to guides, FAQs, and decision logs. Capture context and sources, connect related pages, and maintain owners and status as information changes.
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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 focused information from PubChem, including molecular formulas, molecular weights, compound descriptions, assay summaries, and substance metadata. Get concise Markdown summaries, with the option to save the full response for further use.
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Plan DNA variant detection workflows by identifying the assay and sample model, then routing to germline, cancer somatic, or molecular-barcode panel skills. It also supports focused local BAM/CRAM checks with variant files, depth summaries, and optional filters.
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Search multiple Notion pages and turn their contents into briefs, comparisons, or research reports. Organize findings by topic, flag gaps and contradictions, and create documentation in Notion with citations and source links.
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Build or review quality control workflows for single-cell and single-nucleus RNA sequencing data. Select filters from observed data, detect doublets, assign cell types, and create UMAP plots that summarize cell relationships, while recording analysis decisions and outputs.
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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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Find proteomics projects, which study proteins on a broad scale, in PRIDE Archive and summarize their metadata. Search by keyword or use a PXD accession to inspect a specific project's registered information.
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Start shotgun metagenomics workflows for mixed-community DNA reads in FASTQ files. Check read quality, remove host sequences, and profile organisms and biological functions using supported tools and databases, producing tables and visual summaries when results are available.
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Retrieve genes, genetic variants, clinical annotations, and dosing guidelines from the PharmGKB API, then turn the results into concise summaries. Save the full response when you need the underlying data.
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Search Rhea, a biochemical reaction database, using reaction IDs, compound names, enzyme classification numbers, or reaction terms. Get concise summaries of focused search results, with raw JSON available when you need machine-readable output.
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Look up structure metadata in RCSB PDB, search for entries by keyword, and retrieve sequences in FASTA, a text format for biological sequences. Receive concise summaries or short sequence previews, with raw output available on request.
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Check whether a Dynamo deployment is ready for disaggregated serving, where input processing and token generation run separately. Read-only probes inspect transport settings, GPU networking capabilities, and NIXL transfer-test readiness, then report gaps and next steps.
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Search UniProt protein records by gene or identifier and receive concise summaries. The skill supports UniProtKB, UniRef, and UniParc lookups, with optional file saving for full JSON records or FASTA, a text format for biological sequences.
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Guide the use of NVIDIA cuOpt for route planning and mathematical optimization, choosing values to minimize cost or maximize profit under constraints. Covers requirements, environment checks, installation guidance, and verification of solver results.
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Look up TPMI associations for a single genetic variant using an rsID or genome coordinates. Get a concise summary showing the queried variant, the total number of associations, and whether the displayed results are incomplete.
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Query ProteomeXchange through its PROXI API to inspect datasets, libraries, proteins, peptide forms, and spectra. Receive concise summaries focused on a dataset or identifier, and save complete responses when more detail is needed.
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Check article and file availability through the NCBI PMC Open Access service using supported article identifiers. Receive a concise metadata summary, with the option to save the original XML response when you need the full service output.
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Plan or run bulk RNA-seq analysis to find genes whose expression differs between conditions. Check sample replication, study design, batch effects, and data quality, then produce comparison tables, diagnostic plots, and ranked gene lists.
中文简介正在准备中。当前显示英语简介。