Synteny Browser
Synteny Browser visualizes regions of conserved synteny between genomes to support comparative genomics analyses and identification of conserved, functionally relevant genes.
Key Features:
- Synteny visualization: Visualizes conserved syntenic regions and block-level alignments between two genomes.
- Selective display of genome features: Filters and highlights genomic features within syntenic blocks based on annotated biological attributes such as type, function, and phenotype association.
- True orientation display: Represents the orientation of the comparison genome relative to the reference within syntenic blocks.
- Gene symbol visibility: Displays gene symbols for genomic features to support identification and cross-referencing.
- Anchors visualization: Displays anchors that delineate syntenic blocks.
Scientific Applications:
- Comparative genomics (Mus musculus – Homo sapiens): Enables detailed comparisons of conserved genomic regions between laboratory mouse (Mus musculus) and human (Homo sapiens).
- Evolutionary biology: Supports analysis of conservation and rearrangement of genomic regions across species.
- Functional genomics: Facilitates identification of functionally relevant genes within conserved syntenic contexts.
- Genetic disease studies: Assists in mapping and comparing candidate loci conserved between species for disease research.
Methodology:
Implemented on a genome-agnostic software platform and operable for any two genomes when syntenic block coordinates are provided and biological feature attributes are available in standard bioinformatics file formats.
Topics
Details
- License:
- CC-BY-4.0
- Programming Languages:
- JavaScript, Python
- Added:
- 1/14/2020
- Last Updated:
- 12/27/2020
Operations
Publications
Kolishovski G, Lamoureux A, Hale P, Richardson JE, Recla JM, Adesanya O, Simons A, Kunde-Ramamoorthy G, Bult CJ. The JAX Synteny Browser for mouse-human comparative genomics. Mammalian Genome. 2019;30(11-12):353-361. doi:10.1007/s00335-019-09821-4. PMID:31776723. PMCID:PMC6892358.
PMID: 31776723
PMCID: PMC6892358
Funding: - National Human Genome Research Institute: HG000330, HG007053
- National Cancer Institute: CA034196, CA089713