Use when working with GenomicAlignments, GAlignments, GAlignmentPairs, summarizeOverlaps(), summarizeJunctions(), coverage() on BAM files, splice junction counting, paired-end alignment import, or Bio
Use with AI
Install the MCP server or CLI to instantly fetch GenomicAlignments documentation:
Install command
claude mcp add biocontext7 -- npx @biocontext7/mcpOr share this page: biocontext7.com/tools/genomicalignments
bedGraphToBigWig converts bedGraph coverage files to bigWig binary format for genome browsers (UCSC, IGV, WashU Epigenome Browser). Essential for ChIP-seq, ATAC-seq, RNA-seq, and WGBS coverage tracks.
1 shared topic • 1 shared operation
FusionCatcher — tool for detecting somatic fusion genes, translocations, and chimeric transcripts from RNA-seq data. Identifies known and novel gene fusions in tumor and normal samples using multiple
1 shared topic • 1 shared operation
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 • 1 shared operation
RASQUAL (Robust Allele Specific QUantification and quality controL) — joint QTL mapping tool that integrates total read counts and allele-specific reads for cis-regulatory variant discovery. Detects i
1 shared topic • 1 shared operation
salmon — Fast, bias-aware transcript quantification from RNA-seq data using selective alignment to the transcriptome. Supports bulk RNA-seq (mapping-based and alignment-based modes), single-cell RNA-s
1 shared topic • 1 shared operation