Results for “variant-query”
23 skills
k-dense-ai Tiledbvcf
Store, query, and export genomic variant data (VCF/BCF) using TileDB's sparse array technology for scalable population genomics workflows.
30.2k
alterlab-ieu Alterlab Gnomad
Query gnomAD (Genome Aggregation Database) for population allele frequencies and gene constraint scores (pLI, LOEUF) reflecting loss-of-function intolerance. Use when checking how common a variant is across populations, filtering rare-disease candidate variants, assessing variant pathogenicity, or identifying loss-of-function intolerant genes. Part of the AlterLab Academic Skills suite.
60 · bundle
michaelschecht Gnomad Database
Query gnomAD for population allele frequencies, constraint metrics, and loss-of-function intolerance. Use when interpreting variants, filtering common alleles, or prioritizing genes in rare disease workflows.
0
More results
adobe Find Test Content
Searches for existing content pages containing a specific block in AEM Edge Delivery Services, reporting URLs with occurrences and variants to help identify test content during development.
142 · bundle
georgeqle Vard Scan
Scan for viral app opportunities from trends, gaps, and user pain points
1 · bundle
livelybug Design Shotgun
Design shotgun: generate multiple AI design variants, open a comparison board, collect structured feedback, and iterate. (gstack)
0
georgeqle Vard Align
Quick feasibility and novelty check — go/no-go decision for this week's build
1 · bundle
lambenthan Variable Map
汇总某个经管实证变量在文献中的测算口径、数据来源、模型角色和项目可用性
77
welitonevoc Vexor
Vector-powered CLI for semantic file search with a Claude/Codex skill
1
jorcan Vexor
Enables semantic file search across a codebase using a vector-powered CLI, with integration for Claude and Codex agents.
0 · bundle
lambenthan Ask
对 wiki 提问，综合检索相关页面后回答，好的回答可 crystallize 回 wiki
77
lambenthan Refine
通用多轮迭代改进：对任意研究制品反复调用 /review → 解析反馈 → 修复 → 更新 wiki，直到达标
77
phoroth Vexor
Provides guidance and patterns for using a vector-powered CLI for semantic file search with Claude/Codex skills.
3
fradser Batch Grill Me
Runs a relentless interview that asks every frontier question at once, round by round. Use when the user wants to be grilled on a design or map a design tree.
580
kk20300113-png Design Shotgun
Design shotgun: generate multiple AI design variants, open a comparison board, collect structured feedback, and iterate. Standalone design exploration you can run anytime. Use when: "explore designs", "show me options", "design variants", "visual brainstorm", or "I don't like how this looks". Proactively suggest when the user describes a UI feature but hasn't seen what it could look like. (gstack)
0
lovits Ask
Ask a local external advisor CLI (Claude or Gemini) and capture a reusable artifact
0
mmehdi0606 Vexor
Vector-powered CLI for semantic file search with a Claude/Codex skill
2
lingxling Vexor
Provides guidance and patterns for using a vector-powered CLI for semantic file search with Claude and Codex skills.
253
sickn33 Vexor
Vector-powered CLI for semantic file search with a Claude/Codex skill
45.1k
ranbot-ai Vexor
Vector-powered CLI for semantic file search with a Claude/Codex skill
6
vimalinx Bcftools
Use when working with VCF/BCF variant files for indexing, manipulation, analysis, or variant calling.
0 · bundle
alterlab-ieu Alterlab Jaspar
Query JASPAR for transcription factor binding site (TFBS) profiles (PWMs/PFMs), searching by TF name, species, or class, scanning DNA sequences for binding sites, and comparing matrices. Use when doing motif analysis, regulatory genomics, transcription factor binding prediction, or interpreting regulatory/non-coding GWAS variants. Part of the AlterLab Academic Skills suite.
60 · bundle
alterlab-ieu Alterlab Clinpgx
Access ClinPGx pharmacogenomics data (the successor to PharmGKB) to query gene-drug interactions, CPIC/DPWG dosing guidelines, drug labels, and pharmacogene records. Use when interpreting pharmacogenes (CYP2D6, CYP2C19, TPMT, DPYD, SLCO1B1), looking up genotype-guided drug dosing, checking PGx drug-safety associations (e.g. HLA-B*57:01 and abacavir), or supporting precision medicine and clinical pharmacogenomics decisions. For star-allele definitions/frequencies see PharmVar; for germline/somatic variant pathogenicity see alterlab-clinvar. Part of the AlterLab Academic Skills suite.
60 · bundle