Related Experiment Video
Updated: Aug 5, 2026

A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes
Published on: May 22, 2018
SynFlow: an interactive online genome structural variant viewer
Marilyne Summo1,2,3, Gaëtan Droc1,2,3, Mathieu Rouard3,4
1UMR AGAP Institut, Univ Montpellier, CIRAD, INRAE, Institut Agro, Montpellier, France.
SynFlow offers a dynamic web-based tool for interactive exploration of structural variations (SVs) in large genomic datasets. This application enhances comparative genomics by enabling real-time filtering and visualization of complex genomic events.
Area of Science:
- Genomics
- Bioinformatics
- Computational Biology
Background:
- Structural variations (SVs) are critical for genome evolution and phenotypic diversity.
- Advancements in genome assembly necessitate improved methods for SV detection and interpretation.
- Existing visualization tools for SVs are often static, limiting interactive exploration of large datasets.
Purpose of the Study:
- To develop an interactive web-based application for visualizing structural variations.
- To address the limitations of static plots in comparative genomics research.
- To provide a dynamic platform for exploring and filtering SVs in real time.
Main Methods:
- Introduction of SynFlow, a lightweight, web-based interactive application.
- Utilizing SyRI for structural variation detection.
- Developing dynamic, shareable visualizations with real-time filtering and reordering capabilities.
Main Results:
- SynFlow successfully reproduces complex static synteny plots from literature.
- The application transforms static plots into dynamic visualizations supporting deep exploration of SVs.
- SynFlow offers multiple access points: precomputed datasets, user-uploaded data, and on-the-fly analysis.
Conclusions:
- SynFlow enhances the interactive exploration of structural variations in genomics.
- The tool facilitates real-time analysis and visualization of complex genomic events.
- SynFlow provides a valuable resource for comparative genomics research.
Related Concept Videos
Evolutionary Relationships through Genome Comparisons
Genomics
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Point and Frameshift Mutations
Sanger Sequencing
Next-generation Sequencing
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features.
