Tandem Repeats Finder (TRF) — command-line tool for locating and displaying tandem repeats in DNA sequences. Detects microsatellites (STRs), minisatellites, and larger tandem duplications using a prob
Use with AI
Install the MCP server or CLI to instantly fetch Tandem Repeats Finder (TRF) documentation:
Install command
claude mcp add biocontext7 -- npx @biocontext7/mcpOr share this page: biocontext7.com/tools/trf
Ensembl Compara — comparative genomics database and API from EMBL-EBI providing pairwise and multiple whole-genome alignments, gene trees, protein families, orthologues, paralogues, and synteny region
1 shared topic • 3 shared operations
Ensembl REST API — HTTP/JSON web service for programmatic access to Ensembl genomic data without installing local databases. Supports gene/transcript/protein lookup by stable ID or gene symbol, sequen
1 shared topic • 3 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 • 3 shared operations
Use when working with Sei — the FunctionLab sequence-to-activity deep learning framework for predicting chromatin profiles and regulatory activity from DNA sequences. Sei takes 4096 bp DNA windows and
1 shared topic • 3 shared operations
Zarr — chunked, compressed N-dimensional arrays for Python with cloud-native storage. Provides hierarchical groups, pluggable compression codecs (Blosc, Zstd, Gzip), sharding for large-scale datasets,
1 shared topic • 2 shared operations