ntSynt-viz: visualizing synteny patterns across multiple genomes
- 1Department of Basic and Translational Research, BC Cancer Research Institute , 675 W 10th Ave, BC, V5Z 1L3, Vancouver, BC ,
- 2BC Cancer Genome Sciences Centre
- 3Department of Medical Genetics, University of British Columbia , 6200 University Blvd, V6T 1Z4, Vancouver, BC ,
Abstract
With the explosion of chromosome-scale genome assemblies being generated in recent years, there is vast potential for comparative genomics analyses through detecting multi-genome synteny. While existing tools can detect synteny blocks between multiple genomes, their text-based outputs make it challenging to intuitively explore large-scale synteny patterns. Interpretable, information-rich and easy-to-use synteny visualization tools are imperative to enable important biological insights from the synteny block data output by the aforementioned utilities. Here, we present ntSynt-viz, a command-line tool for automated sorting, normalization, and plotting of multi-genome synteny blocks. We show how ntSynt-viz provides clearer and more easily interpretable chromosome painting ribbon plots compared to the state-of-the-art tools NGenomeSyn and plotsr when evaluating synteny between 14 human genomes, and compared to NGenomeSyn when comparing 9 hoverfly genomes. As plotsr is limited to comparing genomes with equal chromosome numbers, it was not applicable to the hoverfly dataset. Furthermore, we demonstrate how ntSynt-viz can also be applied to visualize syntenic patterns encoded in pangenome graphs, using a Minigraph-Cactus graph built from 16 Drosophila genomes. We expect that ntSynt-viz will provide crucial insights into large-scale synteny patterns between divergent genomes, thereby advancing research into key evolutionary questions.
Related
- END nucleases are antiphage defence systems targeting multiple phages with modified genomes
- Statistical analysis provides new insights into patterns and mechanisms of the WANCY hotspot on vertebrate mitochondrial genomes
- Microhomology-Driven Genomic Alterations in Cancer Genomes: Patterns, Prevalence, and Clinical Implications.
- XtractPAV: an automated pipeline for identifying presence-absence variations across multiple genomes
- Visualization and Characterization of Gene Group Distribution Patterns Across Genomes
BibTeX
@article{coombe2026ntsyntviz,
title = {{ntSynt-viz: visualizing synteny patterns across multiple genomes}},
author = {Lauren Coombe and René L. Warren and İnanç Birol},
journal = {Journal of Evolutionary Biology},
year = {2026},
month = sep,
doi = {10.1093/jeb/voag079},
url = {https://doi.org/10.1093/jeb/voag079},
note = {CC BY},
}
RIS
TY - JOUR
TI - ntSynt-viz: visualizing synteny patterns across multiple genomes
AU - Lauren Coombe
AU - René L. Warren
AU - İnanç Birol
PY - 2026
DA - 2026/09/03
JO - Journal of Evolutionary Biology
DO - 10.1093/jeb/voag079
UR - https://doi.org/10.1093/jeb/voag079
AB - With the explosion of chromosome-scale genome assemblies being generated in recent years, there is vast potential for comparative genomics analyses through detecting multi-genome synteny. While existing tools can detect synteny blocks between multiple genomes, their text-based outputs make it challenging to intuitively explore large-scale synteny patterns. Interpretable, information-rich and easy-to-use synteny visualization tools are imperative to enable important biological insights from the synteny block data output by the aforementioned utilities. Here, we present ntSynt-viz, a command-line tool for automated sorting, normalization, and plotting of multi-genome synteny blocks. We show how ntSynt-viz provides clearer and more easily interpretable chromosome painting ribbon plots compared to the state-of-the-art tools NGenomeSyn and plotsr when evaluating synteny between 14 human genomes, and compared to NGenomeSyn when comparing 9 hoverfly genomes. As plotsr is limited to comparing genomes with equal chromosome numbers, it was not applicable to the hoverfly dataset. Furthermore, we demonstrate how ntSynt-viz can also be applied to visualize syntenic patterns encoded in pangenome graphs, using a Minigraph-Cactus graph built from 16 Drosophila genomes. We expect that ntSynt-viz will provide crucial insights into large-scale synteny patterns between divergent genomes, thereby advancing research into key evolutionary questions.
SN - 1010-061X
SN - 1420-9101
ER -