SNP-VISTA
SNP-VISTA aids in analyses of the following types of data: A. Large-scale re-sequence data of disease-related genes for discovery of associated and/or causative alleles (GeneSNP-VISTA). B. Massive amounts of ecogenomics data for studying homologous recombination in microbial populations (EcoSNP-VISTA). The main features and capabilities of SNP-VISTA are: 1) Mapping of SNPs to gene structure; 2) classification of SNPs, based on their location in the gene, frequency of occurrence in samples and allele composition; 3) clustering, based on user-defined subsets of SNPs, highlighting haplotypes as well as recombinant sequences; 4) integration of protein conservation visualization; and 5) display of automatically calculated recombination points that are user-editable. The main strength of SNP-VISTA is its graphical interface and use of visual representations, which support interactive exploration and hence better understanding of large-scale SNPs data.
- Short Name / Acronym:
- SNP-VISTA
- Project Type:
- Open Source, No Publicly Available Repository
- Site Accession Number:
- 3844
- Software Type:
- Scientific
- License(s):
- Other
- Programming Language(s):
- GNU C++compiler
- Research Organization:
- Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States)
- Sponsoring Organization:
- USDOEPrimary Award/Contract Number:AC02-05CH11231
- DOE Contract Number:
- AC02-05CH11231
- Code ID:
- 73223
- OSTI ID:
- 1247304
- Country of Origin:
- United States
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