Acceleration of short and long DNA read mapping without loss of accuracy using suffix array.
Bioinformatics
; 30(23): 3396-8, 2014 Dec 01.
Article
em En
| MEDLINE
| ID: mdl-25143289
UNLABELLED: HPG Aligner applies suffix arrays for DNA read mapping. This implementation produces a highly sensitive and extremely fast mapping of DNA reads that scales up almost linearly with read length. The approach presented here is faster (over 20× for long reads) and more sensitive (over 98% in a wide range of read lengths) than the current state-of-the-art mappers. HPG Aligner is not only an optimal alternative for current sequencers but also the only solution available to cope with longer reads and growing throughputs produced by forthcoming sequencing technologies. AVAILABILITY AND IMPLEMENTATION: https://github.com/opencb/hpg-aligner.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Alinhamento de Sequência
/
Análise de Sequência de DNA
/
Sequenciamento de Nucleotídeos em Larga Escala
Limite:
Animals
/
Humans
Idioma:
En
Revista:
Bioinformatics
Assunto da revista:
INFORMATICA MEDICA
Ano de publicação:
2014
Tipo de documento:
Article