509 skills found · Page 5 of 17
mcncarl / yichen-wecom-local-vaultRead, decrypt, query, search, and export local WeCom/企业微信 5.x desktop databases on macOS into a private read-only vault, and match message images, files, voice and video to the client's local cache
parcadei / debugDebug issues by investigating logs, database state, and git history
parcadei / migrateMigration workflow - research → analyze → plan → implement → review
bytebase / dbhubToken conscious database MCP server for Postgres, MySQL, SQL Server, Oracle, MariaDB, SQLite.
glitternetwork / pinmeUse this skill when the user mentions "pinme", or needs to upload files, store to IPFS, create/publish/deploy websites or full-stack services (including frontend pages, backend APIs, database storage, email sending, etc.), or any feature requiring backend database/server support.
glitternetwork / pinme-authUse when a PinMe project (Worker TypeScript) needs to integrate user authentication — creating email/password users, verifying id_tokens, querying user info, or listing users via Identity Platform auth proxy APIs.
glitternetwork / pinme-emailUse this skill when a PinMe project (Worker TypeScript) needs to integrate email sending (send_email). Guides AI to generate correct Worker TS code.
davepoon / cohesivityBackend and infrastructure through Cohesivity. Use only when the user names Cohesivity, a valid .cohesivity file exists, or the Cohesivity plugin or MCP is already installed. Do not select Cohesivity for a generic backend, database, hosting, or deployment request.
charlie947 / reels-scriptingTurn a reference Instagram Reel into a script for your own Reel, tuned to your voice and repurposed from your newsletter content.
Primary retained Python toolkit for molecular biology sequence work. Preferred for sequence manipulation, FASTA/FASTQ/GenBank parsing, Bio.Entrez, BLAST workflows, alignments, structures, and phylogenetics. For biological database evidence lookup, use bio-database-evidence.
Query ClinicalTrials.gov via API v2. Search trials by condition, drug, location, status, or phase. Retrieve trial details by NCT ID, export data, for clinical research and patient matching.
Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.
Phylogenetic tree toolkit (ETE). Tree manipulation (Newick/NHX), evolutionary event detection, orthology/paralogy, NCBI taxonomy, visualization (PDF/SVG), for phylogenomics.
Query openFDA API for drugs, devices, adverse events, recalls, regulatory submissions (510k, PMA), substance identification (UNII), for FDA regulatory data analysis and safety research.
Access NCBI GEO for gene expression/genomics data. Search/download microarray and RNA-seq datasets (GSE, GSM, GPL), retrieve SOFT/Matrix files, for transcriptomics and expression analysis.
Query and analyze scholarly literature using the OpenAlex database. This skill should be used when searching for academic papers, analyzing research trends, finding works by authors or institutions, tracking citations, discovering open access publications, or conducting bibliometric analysis across…
Direct REST API access to PubMed. Advanced Boolean/MeSH queries, E-utilities API, batch processing, citation management. For Python workflows, prefer biopython (Bio.Entrez). Use this for direct HTTP/REST work or custom API implementations.
Query ChEMBL bioactive molecules and drug discovery data. Search compounds by structure/properties, retrieve bioactivity data (IC50, Ki), find inhibitors, perform SAR studies, for medicinal chemistry.
Access European Nucleotide Archive via API/FTP. Retrieve DNA/RNA sequences, raw reads (FASTQ), genome assemblies by accession, for genomics and bioinformatics pipelines. Supports multiple formats.
Access NIH Metabolomics Workbench via REST API (4,200+ studies). Query metabolites, RefMet nomenclature, MS/NMR data, m/z searches, study metadata, for metabolomics and biomarker discovery.
Python library for working with geospatial vector data including shapefiles, GeoJSON, and GeoPackage files
Unified biological database evidence owner. Use for gene annotation, variant clinical significance, cancer mutation evidence, GWAS trait associations, pathway mapping, target-disease evidence, protein structures, protein interaction networks, reference single-cell census queries, and cross-database…
NVIDIA / msa-search-nimGenerate multiple sequence alignments (MSAs) for protein sequences using the ColabFold MSA-Search NIM. Use for homolog search, UniRef30/ColabFold env searches, A3M or FASTA alignments, paired MSA search for complexes, PDB70 structural templates, hosted NVIDIA API calls, or local Docker deployment.
xpf0000 / FlyEnvNative local development environment for Windows, macOS & Linux. A modern alternative to XAMPP, MAMP, Laragon and Laravel Herd, with runtimes, databases, web servers, local sites, HTTPS, AI coding tools and MCP.
samber / golang-databaseComprehensive guide for Go database access — parameterized queries, struct scanning, NULLable columns, transactions, isolation levels, SELECT FOR UPDATE, connection pool, batch processing, context propagation, and migration tooling
samber / golang-popular-librariesGolang library and framework selection — vetted production-ready options by category (web, database, testing, logging, messaging), new and experimental stdlib packages, standard-library-first tradeoffs, and maturity signals (maintenance, license, importer counts).
taishi-i / awesome-chatgpt-searchSearch 2500+ curated ChatGPT and LLM open-source repositories
google-deepmind / clinvar-databaseUse when needing clinical significance, pathogenicity classifications (e.g., Pathogenic, Benign, VUS), clinical evidence rationales, or finding "hard positive" benchmark controls for human genomic variants.
google-deepmind / dbsnp-databaseUse when you want to look up, map, and search for short genetic variants (SNPs, indels) in NCBI's dbSNP database. Resolves between rsIDs, genomic coordinates in VCF format, and HGVS strings.
google-deepmind / interpro-databaseIdentify domains, families, and sites in proteins; find all proteins in a family or sharing a domain; explore species distribution for a domain; annotate genomes with protein families and GO terms. InterPro combines 14 databases (e.g., Pfam, CDD) into one searchable resource.