Welcome to WGDI’s Documentation!¶
Description¶
WGDI (Whole-Genome Duplication Integrated analysis) is a Python-based command-line tool designed to facilitate comprehensive analysis of recursive polyploidization events and cross-species genome alignments. It supports three main workflows:
Polyploid inference
Hierarchical inference of genomic homology
Ancestral chromosome karyotyping
These workflows improve the detection of whole-genome duplications (WGD) and the characterization of WGD-related events based on high-quality chromosome-level genomes. Importantly, WGDI can extract complete synteny blocks and aid in the reconstruction of detailed karyotype evolution. The toolkit is freely available on GitHub: GitHub.
Table of Contents¶
- Introduction
- Installation
- Usage
- Dotplot
- Improved collinearity
- Non-synonymous (Ka) and synonymous (Ks)
- BlockInfo
- Correspondence
- BlockKs
- KsPeaks
- PeaksFit
- KsFigure
- Polyploid classification
- Ancestral_karyotype
- Ancestral_karyotype_repertoire
- karyotype_mapping
- Karyotype
- Shared_fusions
- Fusion_positions_database
- Fusions_detection
- Alignment
- Alignmenttrees
- Retain
- P-index
- Circos
- Examples
- Changelog
Citing WGDI¶
If you use WGDI in your work, please cite the following publication:
Sun, P., Jiao, B., Yang, Y., Shan, L., Li, T., Li, X., ... & Liu, J. (2022).
WGDI: A user-friendly toolkit for evolutionary analyses of whole-genome duplications and ancestral karyotypes.
Molecular Plant, 15(12), 1841-1851. https://doi.org/10.1016/j.molp.2022.10.018
Contact¶
For any questions or suggestions, feel free to contact Pengchuan Sun via email: sunpengchuan@gmail.com or submit changes on our GitHub repository.