Skills that structure how sources are gathered, weighed and cited.
31 skills · browse every category
Research
Standardized methods for checking and storing private keys without chat history exposure.
Restoration, dating, and attribution analysis for Ancient Greek and Latin inscriptions.
Access biology and medical preprint metadata directly from bioRxiv and medRxiv repositories.
Genetic and clinical data retrieval for drug discovery and disease association analysis.
Scientific paper search and full-text retrieval for research discovery on arXiv.
Access to open-access life science literature, citations, and full-text files from Europe PMC.
Biomolecular structure discovery via automated database interaction.
Homologue identification using high-speed sequence alignment tools and databases.
Scientific literature retrieval and cross-database linking from the NCBI archives.
Multiple sequence alignment for proteins using the EBI Clustal Omega web service.
Chemical data retrieval for molecular properties, hazard info, and structural research.
Pathway analysis, gene identifier mapping, and biological knowledge retrieval.
Retrieve evolutionary constraint data and transcription factor sites from UCSC archives.
Retrieval of protein metadata, functional annotations, and sequence records from UniProt.
Protein-protein interaction data retrieval and functional enrichment analysis via CLI.
Retrieve population allele frequencies and gene constraint metrics from gnomAD.
Access regulatory genomics data from the ENCODE registry using GraphQL and REST queries.
Protein domain and family lookups via the integrated InterPro database interface.
Access median RNA expression levels and eQTL variant data from 54 human tissue sites.
Access structured registry data from ClinicalTrials.gov using API-linked search tools.
Predict genomic variant impacts on gene expression and regulatory elements with precision.
Transcription factor binding profiles and position matrices from the JASPAR database.
Academic database queries for research papers, authors, and citation metrics.
Structural insights from AlphaFold Database using specific UniProt Accession IDs.
Clinical pathogenicity classifications and interpretation evidence for human genomic variants.
Genetic variant lookups for rsIDs, genomic coordinates, and HGVS nomenclature strings.
Gene ontology and functional annotation lookup via the QuickGO API.
Gene annotation, ID mapping, and genomic sequence retrieval from the Ensembl REST API.
Access protein abundance and spatial data from the Human Protein Atlas repository.
3D protein structure alignment against large-scale database repositories.
Access bioactive molecule data, chemical structures, and assay results for drug research.