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A compilation and categorization of next-generation sequencing resources

ngs_backbone

Tool namengs_backbone
URLhttp://bioinf.comav.upv.es/ngs_backbone/index.html
Important features1. It is capable of cleaning reads, de novo assembly or mapping against a reference and annotate SNPs, SSRs, ORFs. 2. Used in transcriptome analysis and sometimes in genome analysis.
Citations
Year of publicationNot available
Rank by usage frequency100
Comments
FunctionDe novo assembler, SNP discovery
CategoryDownloadable
LicenseAGPL
Status
Input file formatFASTA, FASTQ
Output file formatBAM, VCF, GFF
Operating systemUnix,linux
Operating language
PlatformSanger, Illumina/Solexa, Roche 454
Maintained by M. Hackenberg, G. Barturen and J.L. Oliver
Downloadable file format
Submission file format

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