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BMC Genomics ; 14 Suppl 1: S13, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23369189

RESUMEN

With the introduction of next-generation sequencing (NGS) technologies, we are facing an exponential increase in the amount of genomic sequence data. The success of all medical and genetic applications of next-generation sequencing critically depends on the existence of computational techniques that can process and analyze the enormous amount of sequence data quickly and accurately. Unfortunately, the current read mapping algorithms have difficulties in coping with the massive amounts of data generated by NGS.We propose a new algorithm, FastHASH, which drastically improves the performance of the seed-and-extend type hash table based read mapping algorithms, while maintaining the high sensitivity and comprehensiveness of such methods. FastHASH is a generic algorithm compatible with all seed-and-extend class read mapping algorithms. It introduces two main techniques, namely Adjacency Filtering, and Cheap K-mer Selection.We implemented FastHASH and merged it into the codebase of the popular read mapping program, mrFAST. Depending on the edit distance cutoffs, we observed up to 19-fold speedup while still maintaining 100% sensitivity and high comprehensiveness.


Asunto(s)
Mapeo Cromosómico , Programas Informáticos , Algoritmos , Bases de Datos Genéticas , Genoma Humano , Secuenciación de Nucleótidos de Alto Rendimiento , Humanos , Alineación de Secuencia
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