'concise' 검색 결과

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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• Check Open Access availability using a PMCID
• Look up availability using a supported DOI
• Save the original XML response for later use

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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• Check TPMI associations for a variant identified by rsID
• Look up a variant using GRCh37 genome coordinates
• Save the full association response to a file

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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• Look up a human gene by symbol
• Review gene candidates matching a keyword
• Choose fields for gene search results

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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• Summarize information about a target or disease
• Look up drug, variant, or study data
• Compare disease evidence scores across data sources

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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• Check which species are listed in EVA
• Look up an archived variant by its identifier
• Inspect variants within a small genomic region

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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• Look up information for an Ensembl gene ID
• Find genes overlapping a genomic region
• Check links to related database records

Retrieve study, mutation, clinical, and sample data from cBioPortal and turn the results into concise summaries. Use it to browse studies, inspect molecular profiles, or look up mutations for specified genes.

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• Find studies by keyword
• Look up mutations for a specified gene
• Review clinical and sample information

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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• Look up a metabolite such as serotonin
• Find pathways related to glycolysis
• Search for proteins or diseases

Search chemical substances by name or ChEBI ID, retrieve compound details and structure metadata, and explore parent–child relationships in chemical classifications. Results are presented as concise summaries, with raw JSON available on request.

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• Find chemical substances by name
• Look up compound details by ChEBI ID
• Explore parent and child chemical classifications

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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• Checking the frequency of a specific genetic variant
• Retrieving gene constraint measures
• Looking up variant effects on gene transcripts

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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• Find ontology terms for a disease or trait
• Look up drugs associated with a gene
• Summarize literature and genetic evidence

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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• Browse a small set of registered HLA alleles
• Filter HLA allele records by part of a name
• Check cell metadata registered in IPD

Retrieve public collection and dataset metadata from CELLxGENE Discover and turn it into concise summaries. Use targeted collection lookups to review single-cell research data, with raw JSON available when machine-readable output is needed.

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• Review a specific single-cell data collection
• Explore available public collections
• Get collection metadata as JSON

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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• Search for studies related to RNA
• Find single-cell studies in ArrayExpress
• Retrieve study details by accession

Retrieve concise summaries from GWAS Catalog, a resource for studies linking genetic variants to traits. Look up studies, associations, genes, variants, and publications, with JSON output or saved full responses when needed.

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• Finding GWAS studies related to asthma
• Checking associations mapped to BRCA1
• Looking up genetic variants and related publications

Look up compound–target binding data in BindingDB using PDB or UniProt identifiers, or search for similar chemical structures. Receive concise summaries of matching records, with full API responses saved to a file when requested.

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• Find ligands linked to a PDB identifier
• Look up binding data for a UniProt entry
• Search for compounds with similar structures

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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• Looking up healthy wild-type expression metadata
• Searching with relationships between biological terms
• Checking whether matching data exists

Retrieve concise FinnGen association results for one genetic variant. Accepts rsID identifiers or GRCh37/GRCh38 genome coordinates, resolves the query format, and reports association counts, truncation, and optional raw output files.

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• Look up FinnGen associations for a single rsID
• Query a variant using GRCh37 or GRCh38 coordinates
• Review association counts and whether results were truncated

Retrieve public eQTL Catalogue association data, linking genes and genetic variants, along with study metadata. Filter requests to specific identifiers and receive concise Markdown summaries or raw JSON when machine-readable output is requested.

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• Look up association data for a specific gene
• Filter association results by a genetic variant
• Check study metadata in the public catalogue

Retrieve concise Genebass summaries linking a selected gene's variant group to traits across a broad association scan. Specify one Ensembl gene ID, choose a variant group, and control result counts, with optional JSON output.

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• Review trait associations for a single gene
• Request associations for a chosen variant group
• Expand the number of associations returned

Retrieve concise information about microbiome studies, samples, and habitat metadata from MGnify. Narrow requests by study or sample identifier or biome, a type of biological environment, and receive readable summaries or JSON for further processing.

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• Looking up a microbiome study by its identifier
• Summarizing metadata for a specific sample
• Browsing biological environment categories

Retrieve gene data, search downloads, and tissue or cell-line pages from Human Protein Atlas. Get concise summaries by default, with raw JSON or HTML saved to a file only when requested.

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• Look up gene data by Ensembl ID
• Review Human Protein Atlas search results
• Check tissue and cell-line pages

Look up existing predictions and protein information in the AlphaFold Protein Structure Database. Retrieve concise structure metadata, UniProt summaries, sequence summaries, and annotations, with an option to save the full response for later inspection.

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• Look up an existing protein structure prediction
• Check a UniProt summary
• Review sequence summaries and annotations

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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• Check disease and trait associations for one variant
• Look up a variant using an rsID or genome coordinates
• Save complete association results for further analysis