GenomicRanges — Bioconductor R package for representing, manipulating, and analyzing genomic intervals (GRanges, GRangesList). Provides operations for finding overlaps (findOverlaps, subsetByOverlaps)
Use with AI
Install the MCP server or CLI to instantly fetch GenomicRanges documentation:
Install command
claude mcp add biocontext7 -- npx @biocontext7/mcpOr share this page: biocontext7.com/tools/genomicranges
ENCODE tools provide access to the Encyclopedia of DNA Elements data, including genomic functional elements, ChIP-seq, RNA-seq, and ATAC-seq data. Facilitates data retrieval, query, and analysis for e
3 shared topics • 2 shared operations
AlleleSeq — pipeline for detecting allele-specific expression (ASE) and allele-specific binding (ASB) from RNA-seq and ChIP-seq data at heterozygous SNP positions. Constructs a personal diploid genome
3 shared topics • 1 shared operation
Use when working with Gviz, the Bioconductor R package for plotting genomic coordinates, annotations, signal tracks, read alignments, and sequence context in genome-browser-style figures. Covers core
3 shared topics • 1 shared operation
libBigWig — C library and pyBigWig Python bindings for reading and writing BigWig and BigBed binary indexed genome browser track files. Use when users need to extract signal values, interval statistic
3 shared topics • 1 shared operation
pyBigWig is a Python library for reading and writing bigWig and bigBed files, the standard binary genome-browser signal formats. Use when users need to query per-base coverage or signal values from bi
3 shared topics • 1 shared operation