• Aucun résultat trouvé

Biomanycores, open-source parallel code for many-core bioinformatics

N/A
N/A
Protected

Academic year: 2021

Partager "Biomanycores, open-source parallel code for many-core bioinformatics"

Copied!
2
0
0

Texte intégral

(1)

HAL Id: inria-00623390

https://hal.inria.fr/inria-00623390

Submitted on 14 Sep 2011

HAL

is a multi-disciplinary open access archive for the deposit and dissemination of sci- entific research documents, whether they are pub- lished or not. The documents may come from teaching and research institutions in France or abroad, or from public or private research centers.

L’archive ouverte pluridisciplinaire

HAL, est

destinée au dépôt et à la diffusion de documents scientifiques de niveau recherche, publiés ou non, émanant des établissements d’enseignement et de recherche français ou étrangers, des laboratoires publics ou privés.

Biomanycores, open-source parallel code for many-core bioinformatics

Mathieu Giraud, Stéphane Janot, Jean-Frédéric Berthelot, Charles Deltel, Laetitia Jourdan, Dominique Lavenier, Helene Touzet, Jean-Stéphane Varré

To cite this version:

Mathieu Giraud, Stéphane Janot, Jean-Frédéric Berthelot, Charles Deltel, Laetitia Jourdan, et al..

Biomanycores, open-source parallel code for many-core bioinformatics. Bioinformatics Open Source

Conference (BOSC 2011), 2011, Vienne, Austria. �inria-00623390�

(2)

Biomanycores, open-source parallel code for many-core bioinformatics

Mathieu Giraud

1

, St´ephane Janot

1

, Jean-Fr´ed´eric Berthelot

1

, Charles Deltel

2

, Laetitia Jourdan

1

, Dominique Lavenier

2

, H´el`ene Touzet

1

, Jean-St´ephane Varr´e

1

1LIFL, UMR CNRS 8022, Universit´e Lille 1 and INRIA Lille, France

2IRISA, UMR CNRS 6074, Universit´e Rennes 1, ENS Cachan, and INRIA Rennes, France

[email protected]

URL:http://www.biomanycores.org Licenses:Various open-source licenses

Graphics processing units (GPUs) enable efficient parallel processing at a very low cost, and are a first step towards the generalization of massively many- core architectures. Since CUDA (in 2007) and the standard OpenCL (2009), many GPU bioinformatics applications have been developed, from sequence alignment to proteomics or phylogenetics (review in [4]).

Biomanycores is a collection of bioinformatics tools, designed to bridge the gap between researches in OpenCL/CUDA high-performance computing on GPU and other “manycore processors” and usual bioinformaticians and biologists.

The main goal is to gather parallel programs and interface them with the BioJava [2], BioPerl [3] and Biopython [1] frameworks. We will also provide benchmarks to show in which cases it is worth us- ing parallel versions of the programs.

Biomanycores was presented at BOSC 2009. Since November 2010, a developer is working full-time on this project, redesigning, extending and document- ing Biomanycores. The release 1.1104 of Biomany- cores (April 15) includes applications for sequence alignment, sequence processing, and RNA folding tools. Next releases are likely to include tools for proteomics, phylogenetics and genome-wide associ- ation studies.

Biomanycores design makes it easy to alter ex- isting pipelines and scripts, in order to use a par- allel application instead of the standard one. In some cases, this leads to large improvements. For example, the complexity of the brute-force Position

Weight Matrix (PWM) scan algorithm is in O(nm), where n is the sequence length and m the matrix size. PWM performance can be measured in millions of operations per second, one operation being the scoring of one sequence character against one matrix column. While the native Biopythonsearch_pwm method peaks at 2 Mop/s, the Biomanycores GPU version (TFM-CUDA) peaks at more than 2 Gop/s, 1000 times faster, even once included the overhead due to the Python interpreter.

In the coming months, we plan to integrate new applications into Biomanycores. Moreover, we wish to receive critical feedback from BioJava, BioPerl and Biopython communities and users in order to im- prove our interfaces, and discuss further integration into these frameworks.

People who are developing CUDA or OpenCL bioinformatics code (available under a free license) are welcome to get involved in the project – we are willing to help them to integrate their code. Please contact us [email protected].

References

[1] P. J. A. Cock, T. Antao, J. T. Chang, and al. Biopython: freely available Python tools for computational molecular biology and bioinformatics.

Bioinformatics, page btp163, 2009.

[2] R. C. G. Holland, T. A. Down, M. Pocock, and al. BioJava: an open- source framework for bioinformatics.Bioinformatics, 24(18):2096–2097, 2008.

[3] J. E. Stajich, D. Block, K. Boulez, and al. The Bioperl toolkit: Perl mod- ules for the life sciences.Genome Research, 12(10):1611–1618, 2002.

[4] J.-S. Varr´e, B. Schmidt, S. Janot, and M. Giraud. Advances in Ge- nomic Sequence Analysis and Pattern Discovery, chapter Manycore high- performance computing in bioinformatics. World Scientific, 2011.

Références

Documents relatifs

In this section, we compare some deadlock-free routing algorithms for the MPPA2 NoC: XY, Hamilto- nian Odd-Even (HOE) Simple Cycle Breaking (SCB) and Turn Prohibition (TP). The

In this paper, we compare the developed tool to others in previous works, specifically in the context of many-core applications; we give a particular importance to the

ABBREVIATIONS: DIGE: Differential in Gel Electrophoresis; EBI: European Bioinfor- matics Institute; GEML: Gene Expression Markup Language; HUPO: Human Proteome Organisation;

Le passage vers le nouveau système comptable SCF conforme aux normes internationales va présenter aux entreprises Algériennes une chance pour pouvoir produire une information

Bioinformatics also enables integration of hetero- geneous high-throughput data sets produced by a given study and existing data sets using knowledge management, annotation and

(1) the proposed vectorization mechanism reduces the execution time by 55.4% (resp. multi-core) approach ; (2) the o ffl oad mode allows a faster execution on MIC than the native

Given a mapping (tasks to cores), we automatically generate code suitable for the targeted many-core architecture. This minimizes memory interferences and allows usage of a framework

Pragmatisch gesehen ist eine detaillierte Unterscheidung des Subtyps eines pleo- morphzelligen, hoch malignen Sarkoms bei den zurzeit zur Verfügung stehenden therapeutischen