tiledbvcf
CommunityGenomic variant data storage and retrieval.
AuthorRowtion
Version1.0.0
Installs0
System Documentation
What problem does it solve?
This Skill addresses the challenge of efficiently storing, querying, and analyzing large-scale genomic variant data, which is often cumbersome with traditional VCF/BCF formats.
Core Features & Use Cases
- Scalable Storage: Ingest and store VCF/BCF data using TileDB's sparse array technology for efficient access.
- Efficient Querying: Perform rapid queries across genomic regions and samples, ideal for population genomics.
- Incremental Updates: Add new samples to existing datasets without costly re-processing.
- Use Case: Researchers can quickly query allele frequencies for specific genes across thousands of samples or export subsets of variant data for downstream analysis.
Quick Start
Use the tiledbvcf skill to create a new dataset and ingest samples from 'sample1.vcf.gz' and 'sample2.vcf.gz'.
Dependency Matrix
Required Modules
tiledb-pytiledbvcf-pypandaspyarrownumpy
Components
scriptsreferences
💻 Claude Code Installation
Recommended: Let Claude install automatically. Simply copy and paste the text below to Claude Code.
Please help me install this Skill: Name: tiledbvcf Download link: https://github.com/Rowtion/Bioclaw/archive/main.zip#tiledbvcf Please download this .zip file, extract it, and install it in the .claude/skills/ directory.
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