Use this skill for GATK copy-number variation workflows including germline gCNV cohorts and somatic copy-ratio segmentation from WES or WGS data. Trigger on requests about CollectReadCounts, Determine
Use with AI
Install the MCP server or CLI to instantly fetch gatk-cnv documentation:
Install command
claude mcp add biocontext7 -- npx @biocontext7/mcpOr share this page: biocontext7.com/tools/gatk-cnv
The GTEx Pipeline is a standardized RNA-seq processing pipeline for the TOPMed project. It enables reproducible and harmonized analysis of gene expression, generating aligned reads, QC metrics, and bo
1 shared topic • 3 shared operations
Ensembl Database — EMBL-EBI's comprehensive genome annotation database covering 300+ species with gene models, variants, regulatory features, and comparative genomics. Query via REST API at rest.ensem
1 shared topic • 2 shared operations
IGV (Integrative Genomics Viewer) — high-performance Java desktop application for interactive visualization and exploration of genomic data. Supports BAM/CRAM alignments, VCF variants, BED/GFF annotat
1 shared topic • 2 shared operations
Qualimap — platform-independent quality control tool for next-generation sequencing alignment data. Provides BAM QC (coverage, insert size, GC content, mapping quality), RNA-seq QC (gene body coverage
1 shared topic • 2 shared operations
Sarek — nf-core Nextflow pipeline for germline and somatic variant calling from whole-genome sequencing (WGS), whole-exome sequencing (WES), and targeted sequencing data. Supports multiple variant cal
1 shared topic • 2 shared operations