dc.creator | SOBREIRA, Tiago J. P. | |
dc.creator | GRUBER, Arthur | |
dc.date.accessioned | 2012-10-20T03:26:54Z | |
dc.date.accessioned | 2018-07-04T15:37:01Z | |
dc.date.available | 2012-10-20T03:26:54Z | |
dc.date.available | 2018-07-04T15:37:01Z | |
dc.date.created | 2012-10-20T03:26:54Z | |
dc.date.issued | 2008 | |
dc.identifier | BIOINFORMATICS, v.24, n.15, p.1676-1680, 2008 | |
dc.identifier | 1367-4803 | |
dc.identifier | http://producao.usp.br/handle/BDPI/28564 | |
dc.identifier | 10.1093/bioinformatics/btn283 | |
dc.identifier | http://dx.doi.org/10.1093/bioinformatics/btn283 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1625207 | |
dc.description.abstract | Motivation: DNA assembly programs classically perform an all-against-all comparison of reads to identify overlaps, followed by a multiple sequence alignment and generation of a consensus sequence. If the aim is to assemble a particular segment, instead of a whole genome or transcriptome, a target-specific assembly is a more sensible approach. GenSeed is a Perl program that implements a seed-driven recursive assembly consisting of cycles comprising a similarity search, read selection and assembly. The iterative process results in a progressive extension of the original seed sequence. GenSeed was tested and validated on many applications, including the reconstruction of nuclear genes or segments, full-length transcripts, and extrachromosomal genomes. The robustness of the method was confirmed through the use of a variety of DNA and protein seeds, including short sequences derived from SAGE and proteome projects. | |
dc.language | eng | |
dc.publisher | OXFORD UNIV PRESS | |
dc.relation | Bioinformatics | |
dc.rights | Copyright OXFORD UNIV PRESS | |
dc.rights | restrictedAccess | |
dc.title | Sequence-specific reconstruction from fragmentary databases using seed sequences: implementation and validation on SAGE, proteome and generic sequencing data | |
dc.type | Artículos de revistas | |