Efficient computation of the phylogenetic likelihood function on multi-gene alignments and multi-core architectures
The continuous accumulation of sequence data, for example, due to novel wet-laboratory techniques such as pyrosequencing, coupled with the increasing popularity of multi-gene phylogenies and emerging multi-core processor architectures that face problems of cache congestion, poses new challenges with...
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Published in | Philosophical transactions of the Royal Society of London. Series B. Biological sciences Vol. 363; no. 1512; pp. 3977 - 3984 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
London
The Royal Society
27.12.2008
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Abstract | The continuous accumulation of sequence data, for example, due to novel wet-laboratory techniques such as pyrosequencing, coupled with the increasing popularity of multi-gene phylogenies and emerging multi-core processor architectures that face problems of cache congestion, poses new challenges with respect to the efficient computation of the phylogenetic maximum-likelihood (ML) function. Here, we propose two approaches that can significantly speed up likelihood computations that typically represent over 95 per cent of the computational effort conducted by current ML or Bayesian inference programs. Initially, we present a method and an appropriate data structure to efficiently compute the likelihood score on 'gappy' multi-gene alignments. By 'gappy' we denote sampling-induced gaps owing to missing sequences in individual genes (partitions), i.e. not real alignment gaps. A first proof-of-concept implementation in RAxML indicates that this approach can accelerate inferences on large and gappy alignments by approximately one order of magnitude. Moreover, we present insights and initial performance results on multi-core architectures obtained during the transition from an OpenMP-based to a Pthreads-based fine-grained parallelization of the ML function. |
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AbstractList | The continuous accumulation of sequence data, for example, due to novel wet-laboratory techniques such as pyrosequencing, coupled with the increasing popularity of multi-gene phylogenies and emerging multi-core processor architectures that face problems of cache congestion, poses new challenges with respect to the efficient computation of the phylogenetic maximum-likelihood (ML) function. Here, we propose two approaches that can significantly speed up likelihood computations that typically represent over 95 per cent of the computational effort conducted by current ML or Bayesian inference programs. Initially, we present a method and an appropriate data structure to efficiently compute the likelihood score on 'gappy' multi-gene alignments. By 'gappy' we denote sampling-induced gaps owing to missing sequences in individual genes (partitions), i.e. not real alignment gaps. A first proof-of-concept implementation in RAxML indicates that this approach can accelerate inferences on large and gappy alignments by approximately one order of magnitude. Moreover, we present insights and initial performance results on multi-core architectures obtained during the transition from an OpenMP-based to a Pthreads-based fine-grained parallelization of the ML function. The continuous accumulation of sequence data, for example, due to novel wet-laboratory techniques such as pyrosequencing, coupled with the increasing popularity of multi-gene phylogenies and emerging multi-core processor architectures that face problems of cache congestion, poses new challenges with respect to the efficient computation of the phylogenetic maximum-likelihood (ML) function. Here, we propose two approaches that can significantly speed up likelihood computations that typically represent over 95 per cent of the computational effort conducted by current ML or Bayesian inference programs. Initially, we present a method and an appropriate data structure to efficiently compute the likelihood score on ‘gappy’ multi-gene alignments. By ‘gappy’ we denote sampling-induced gaps owing to missing sequences in individual genes (partitions), i.e. not real alignment gaps. A first proof-of-concept implementation in RAxML indicates that this approach can accelerate inferences on large and gappy alignments by approximately one order of magnitude. Moreover, we present insights and initial performance results on multi-core architectures obtained during the transition from an OpenMP-based to a Pthreads-based fine-grained parallelization of the ML function. The continuous accumulation of sequence data, for example, due to novel wet-laboratory techniques such as pyrosequencing, coupled with the increasing popularity of multi-gene phylogenies and emerging multi-core processor architectures that face problems of cache congestion, poses new challenges with respect to the efficient computation of the phylogenetic maximum-likelihood (ML) function. Here, we propose two approaches that can significantly speed up likelihood computations that typically represent over 95 per cent of the computational effort conducted by current ML or Bayesian inference programs. Initially, we present a method and an appropriate data structure to efficiently compute the likelihood score on ‘gappy’ multi-gene alignments. By ‘gappy’ we denote sampling-induced gaps owing to missing sequences in individual genes (partitions), i.e. not real alignment gaps. A first proof-of-concept implementation in |
Author | Stamatakis, Alexandros Ott, Michael |
AuthorAffiliation | 1 Department of Computer Science The Exelixis Lab, Ludwig-Maximilians-Universität München Amalienstrasse 17, 80333 München, Germany 2 Department of Computer Science, Technische Universität München Boltzmannstrasse 3, 85747 Garching b. München, Germany |
AuthorAffiliation_xml | – name: 1 Department of Computer Science The Exelixis Lab, Ludwig-Maximilians-Universität München Amalienstrasse 17, 80333 München, Germany – name: 2 Department of Computer Science, Technische Universität München Boltzmannstrasse 3, 85747 Garching b. München, Germany |
Author_xml | – sequence: 1 givenname: Alexandros surname: Stamatakis fullname: Stamatakis, Alexandros email: alexandros.stamatakis@gmail.com organization: Department of Computer Science The Exelixis Lab, Ludwig-Maximilians-Universität MünchenAmalienstrasse 17, 80333 München, Germany – sequence: 2 givenname: Michael surname: Ott fullname: Ott, Michael organization: Department of Computer Science, Technische Universität MünchenBoltzmannstrasse 3, 85747 Garching b. München, Germany |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18852107$$D View this record in MEDLINE/PubMed |
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Snippet | The continuous accumulation of sequence data, for example, due to novel wet-laboratory techniques such as pyrosequencing,
coupled with the increasing... The continuous accumulation of sequence data, for example, due to novel wet-laboratory techniques such as pyrosequencing, coupled with the increasing... |
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SubjectTerms | Algorithms Architecture Branches Computational Biology - methods Computer architecture Computer Simulation Data models Datasets Genetic vectors Likelihood Functions Mathematical vectors Maximum Likelihood Multi-Core Architectures Multi-Gene Phylogenies OpenMP Phylogenetic Inference Phylogenetics Phylogeny Plant roots RAxML Sequence Alignment - methods Topology |
Title | Efficient computation of the phylogenetic likelihood function on multi-gene alignments and multi-core architectures |
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