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A compilation and categorization of next-generation sequencing resources

galign

Tool namegalign
URLhttp://shahamlab.rockefeller.edu/galign
Important features1. Used for SNP discovery. 2. Has alignment method, SNP search, deletion search, simple SNP, Format convert, genome assemble, identifies polymorphisms between sequence reads obtained using Illumina/Solexa technology and a reference genome.
CitationsShaham S. galign: a tool for rapid genome polymorphism discovery. PLoS One. 2009 Sep 25; 4(9):e7188. PubMed PMID: 19779626; PubMed Central PMCID: PMC2746318
Year of publication2009
Rank by usage frequency100
Comments
FunctionSNP discovery
CategoryFree, Downloadable
LicenseGPL
Status
Input file format
Output file formattext file
Operating systemMacOSX Intel
Operating language
PlatformIllumina/Solexa
Maintained by
Downloadable file format
Submission file format

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