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Scaling read aligners to hundreds of threads on general-purpose processors

MOTIVATION: General-purpose processors can now contain many dozens of processor cores and support hundreds of simultaneous threads of execution. To make best use of these threads, genomics software must contend with new and subtle computer architecture issues. We discuss some of these and propose me...

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Detalles Bibliográficos
Autores principales: Langmead, Ben, Wilks, Christopher, Antonescu, Valentin, Charles, Rone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361242/
https://www.ncbi.nlm.nih.gov/pubmed/30020410
http://dx.doi.org/10.1093/bioinformatics/bty648
Descripción
Sumario:MOTIVATION: General-purpose processors can now contain many dozens of processor cores and support hundreds of simultaneous threads of execution. To make best use of these threads, genomics software must contend with new and subtle computer architecture issues. We discuss some of these and propose methods for improving thread scaling in tools that analyze each read independently, such as read aligners. RESULTS: We implement these methods in new versions of Bowtie, Bowtie 2 and HISAT. We greatly improve thread scaling in many scenarios, including on the recent Intel Xeon Phi architecture. We also highlight how bottlenecks are exacerbated by variable-record-length file formats like FASTQ and suggest changes that enable superior scaling. AVAILABILITY AND IMPLEMENTATION: Experiments for this study: https://github.com/BenLangmead/bowtie-scaling. BOWTIE: http://bowtie-bio.sourceforge.net. BOWTIE 2: http://bowtie-bio.sourceforge.net/bowtie2. HISAT: http://www.ccb.jhu.edu/software/hisat SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.