Add, extend, or review OpenAI Ads conversion tracking for purchases, signups, and other confirmed outcomes. The skill covers browser Pixel events, server-side Conversions API events, duplicate-event prevention, secret handling, and local verification with a setup report.
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Deploy a runnable prototype to the hosting service you choose, such as Sites or Vercel. Use the available deployment tool, return a working shareable URL, and identify any remaining manual steps.
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Search human genes by name or keyword through Clinical Tables and get concise results with gene IDs, symbols, and descriptions. Select the fields to display and browse results in small pages for autocomplete-style lookup.
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Prepare a Python environment for Mixpanel analysis by installing required libraries and checking credentials and connectivity. Use it for first-time setup, missing dependencies, or guidance on service account and OAuth sign-in options.
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Set up and operate NVIDIA AI-Q Blueprint locally or on your own infrastructure. Choose a deployment mode, configure credentials, check service health, troubleshoot failures, and provide a verified server address for aiq-research.
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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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Turn broad life sciences questions into focused research plans. Resolve names and identifiers for genes, diseases, or compounds, select relevant research skills, and combine evidence into a concise answer that explains uncertainty and useful follow-up analyses.
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Retrieve focused genome, assembly, and taxonomy metadata from NCBI Datasets v2, a biological data service. Get concise Markdown summaries by default, with raw JSON or text available when requested.
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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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Plan or run bulk RNA-seq processing from sequencing reads to count matrices, tables of expression counts across samples. Check sample metadata, reference consistency, read mapping, and quantification quality, and produce summaries for downstream analysis.
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Turn Notion product requirements and feature specifications into linked implementation plans and manageable tasks. Extract requirements, flag ambiguities, and keep task status, milestones, blockers, and decisions aligned as work progresses.
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Retrieve concise summaries from Reactome about biological pathways, events, participating molecules, and diagram-related data. Look up specific identifiers, search for relevant entries, or find pathways associated with an entity, and save the full response when needed.
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Find and inspect UI components in MagicPath, add them to an app, and adapt their behavior and styling. Apply themes or create and edit canvas components from code, including work based on an existing repository interface.
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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 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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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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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 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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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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Plan or run targeted DNA panel analysis using UMIs, barcodes that identify DNA molecules. Organize consensus reads, coverage checks, and low-frequency variant results with molecular support, filtering reasons, and explicit quality limitations.
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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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Prepare meeting agendas and reading materials using relevant Notion pages and supplemental research. Tailor the content to attendees and required decisions, with source links, discussion owners, time allocations, and follow-up actions.
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Retrieve focused target, disease, drug, variant, and study data from Open Targets Platform. Produce concise summaries or disease-by-source evidence matrices to compare available evidence while keeping queries and returned results compact.
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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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