Google DeepMind

Search arxiv by topic, filter by recency and citation count, and get a ranked summary of which papers are most relevant and most cited in your domain.

Searches OpenAlex for peer-reviewed papers and preprints matching your query, returning title, authors, abstract, and citation count so you can spot the foundational work fast.

Queries PubMed Central, retrieves abstracts and citations, and synthesizes findings across multiple papers into a single evidence summary.

Queries Europe PMC for peer-reviewed papers, preprints, and citations matching your topic. Returns abstracts, links, and publication metadata you can filter or export.

Searches bioRxiv for recent preprints matching your query, summarizes the abstracts and key methods, and flags which ones overlap or contradict each other.

Takes a repetitive process you run weekly and breaks it into discrete steps, dependencies, and decision points—then outputs a structured workflow file ready to automate.

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Queries NIH and FDA trial registries to surface active studies, enrollment criteria, and outcome summaries for a given condition or molecule.

Connects Claude to a live Postgres instance so you can ask questions about your data in plain English and get results without writing SQL.

Fetches AlphaFold protein structures by gene or accession ID and analyzes folding stability, binding sites, and mutation effects without needing a biotech lab.

Queries PubChem to retrieve molecular weight, structure, safety info, and synonyms for any chemical compound by name or identifier.

Queries the National Center for Biotechnology Information API to retrieve DNA, RNA, and protein sequences by accession number or gene name for analysis or research.

Searches the OpenFDA database for drug interactions, adverse events, and safety recalls. Returns structured data on any medication or adverse event you name.

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Searches UniProt for protein metadata, sequences, and functional annotations without leaving Claude. Returns structured data ready to analyze or visualize.

Queries the ClinVar database to find what diseases a genetic variant is linked to, with confidence levels and clinical significance from published research.

Searches the ChEMBL database for molecular structures, chemical properties, and bioactivity records across millions of compounds and assays.

Queries a protein sequence against public databases and returns ranked matches with alignment scores, enabling rapid identification of homologs and functional analogs.

Takes a set of protein sequences, performs multiple sequence alignment, and highlights conserved domains, variable regions, and clinically significant mutations.

Connects to the Ensembl database to retrieve gene sequences, variant annotations, and protein information without writing SQL or API calls yourself.

Searches the Open Targets database for genetic associations, protein interactions, and clinical trial data linked to a disease or drug target.

Connects to dbSNP and returns clinical summaries, allele frequencies, and linked studies for a given variant or gene region.

Queries the EMBL-EBI Ontology Lookup Service to resolve gene names, protein identifiers, disease codes, and experimental method terms with their canonical definitions.

A lightweight in-memory key-value store for caching strings, lists, and simple objects during a conversation or workflow — no database setup required.

Queries the InterPro database to identify conserved domains, functional regions, and known annotations for any protein sequence or accession number.

Searches the Human Protein Atlas for expression patterns, subcellular localization, and disease associations across tissue types and cell lines.

Searches the Reactome database for protein interactions, cellular pathways, and disease mechanisms. Returns citations and experimental evidence for each result.

Upload a protein structure or sequence and discover similar ones across millions of known proteins, ranked by structural similarity. Returns PDB IDs and alignment scores.

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Connect to a PostgreSQL, MySQL, or SQLite database and ask questions in plain English. Returns structured results and can write safe read-only queries on your behalf.

Searches the gnomAD database for allele frequencies, variant impact, and population-specific genetic data across millions of sequenced genomes.

Search the GTEx database for how a gene is expressed across human tissues, cell types, and conditions. Returns normalized expression levels and statistical confidence.

Searches JASPAR for DNA binding motifs, retrieves consensus sequences, and returns position weight matrices for gene regulation research or bioinformatics workflows.

Takes a raw customer database with PII and applies encryption protocols, anonymization rules, and access logs so sensitive data stays protected in compliance with privacy standards.

Maps transcription factor binding sites across a genome sequence using UCSC conservation data, surfacing high-confidence regulatory regions and their functional annotations.

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