ragtag

RagTag: Reference-guided genome scaffolding and assembly refinement suite

RagTag performs reference-guided scaffolding and enhancement of genome assemblies. Its component RaGOO orders and orients contigs using Minimap2 alignments to construct chromosome-scale pseudomolecules and improve assembly accuracy and completeness.


Key Features:

  • Reference-guided scaffolding: Orders and orients contigs against a reference genome to generate chromosome-scale assemblies.
  • Pseudomolecule construction: Builds contiguous sequences approximating full chromosomes from assembled contigs.
  • Structural variant detection: Identifies structural variants, including variants spanning sequencing gaps, after assembly.
  • Minimap2 integration: Leverages Minimap2 for rapid and sensitive sequence alignment during contig placement.

Scientific Applications:

  • De novo genome assembly refinement: Applied to tomato (M82 reference cultivar) assemblies for accurate contig ordering and orientation.
  • Pan-genome structural variation analysis: Detected structural variants across 103 Arabidopsis thaliana accessions using newly assembled pseudomolecules.

Methodology:

RaGOO aligns assembled contigs to a reference genome using Minimap2, clusters and orders contigs by alignment coordinates, orients them to match the reference, and concatenates them into chromosome-scale pseudomolecules. Post-scaffolding, it analyzes alignments to identify structural variants, including those spanning sequencing gaps.

Topics

Details

License:
MIT
Tool Type:
command-line tool
Programming Languages:
Python
Added:
9/29/2021
Last Updated:
11/24/2024

Operations

Publications

Alonge M, Soyk S, Ramakrishnan S, Wang X, Goodwin S, Sedlazeck FJ, Lippman ZB, Schatz MC. RaGOO: fast and accurate reference-guided scaffolding of draft genomes. Genome Biology. 2019;20(1). doi:10.1186/s13059-019-1829-6. PMID:31661016. PMCID:PMC6816165.

PMID: 31661016
PMCID: PMC6816165
Funding: - National Science Foundation: DBI-1350041, IOS-1445025, IOS-1732253, MCB180087 - National Institutes of Health: R01-HG006677, UM1 HG008898