Guides Qdrant query volume scaling. Use when someone asks 'query returns too many results', 'scroll performance', 'large limit values', 'paginating search results', 'fetching many vectors', or 'high cardinality results'.
npx skills add https://github.com/qdrant/skills --skill qdrant-scaling-query-volume
Problem: When a query has a large limit (e.g. 1000) and there are multiple shards (e.g. 10), naively each shard must return the full 1000 results — totaling 10,000 scored points transferred and merged. This is wasteful since data is randomly distributed across auto-shards.
Instead of asking every shard for the full limit, ask each shard for a smaller limit computed via Poisson distribution statistics, then merge. This is safe because auto-sharding guarantees random, independent data distribution.
The strategy trades a small probability of slightly incomplete results for a large reduction in inter-shard data transfer, especially for high-limit queries across many shards. The 1.2x safety factor and the 99.9% Poisson threshold keep the error rate very low — comparable to inaccuracies already introduced by approximate vector indices like HNSW.
Efficient database search tool for bioRxiv preprint server. Use this skill when searching for life sciences preprints by keywords, authors, date ranges, or categories, retrieving paper metadata, downloading PDFs, or conducting literature reviews.
Access BRENDA enzyme database via SOAP API. Retrieve kinetic parameters (Km, kcat), reaction equations, organism data, and substrate-specific enzyme information for biochemical research and metabolic pathway analysis.
Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.
Query NCBI ClinVar for variant clinical significance. Search by gene/position, interpret pathogenicity classifications, access via E-utilities API or FTP, annotate VCFs, for genomic medicine.
Access COSMIC cancer mutation database. Query somatic mutations, Cancer Gene Census, mutational signatures, gene fusions, for cancer research and precision oncology. Requires authentication.
Query Ensembl genome database REST API for 250+ species. Gene lookups, sequence retrieval, variant analysis, comparative genomics, orthologs, VEP predictions, for genomic research.
Query openFDA API for drugs, devices, adverse events, recalls, regulatory submissions (510k, PMA), substance identification (UNII), for FDA regulatory data analysis and safety research.
Query NCBI Gene via E-utilities/Datasets API. Search by symbol/ID, retrieve gene info (RefSeqs, GO, locations, phenotypes), batch lookups, for gene annotation and functional analysis.
Take qdrant/qdrant-scaling-query-volume from the repository into ~/.claude/skills for personal
use, or into .claude/skills inside a project.
The agent identifies a skill by the name field in its header. Two skills with the
same name cannot sit side by side — one of them will be ignored.