Improved Algorithmic Complexity for the 3SEQ Recombination Detection Algorithm

Abstract Identifying recombinant sequences in an era of large genomic databases is challenging as it requires an efficient algorithm to identify candidate recombinants and parents, as well as appropriate statistical methods to correct for the large number of comparisons performed. In 2007, a computa...

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Veröffentlicht in:Molecular biology and evolution Jg. 35; H. 1; S. 247 - 251
Hauptverfasser: Lam, Ha Minh, Ratmann, Oliver, Boni, Maciej F
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States Oxford University Press 01.01.2018
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ISSN:0737-4038, 1537-1719, 1537-1719
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Abstract Abstract Identifying recombinant sequences in an era of large genomic databases is challenging as it requires an efficient algorithm to identify candidate recombinants and parents, as well as appropriate statistical methods to correct for the large number of comparisons performed. In 2007, a computation was introduced for an exact nonparametric mosaicism statistic that gave high-precision P values for putative recombinants. This exact computation meant that multiple-comparisons corrected P values also had high precision, which is crucial when performing millions or billions of tests in large databases. Here, we introduce an improvement to the algorithmic complexity of this computation from O(mn3) to O(mn2), where m and n are the numbers of recombination-informative sites in the candidate recombinant. This new computation allows for recombination analysis to be performed in alignments with thousands of polymorphic sites. Benchmark runs are presented on viral genome sequence alignments, new features are introduced, and applications outside recombination analysis are discussed.
AbstractList Identifying recombinant sequences in an era of large genomic databases is challenging as it requires an efficient algorithm to identify candidate recombinants and parents, as well as appropriate statistical methods to correct for the large number of comparisons performed. In 2007, a computation was introduced for an exact nonparametric mosaicism statistic that gave high-precision P values for putative recombinants. This exact computation meant that multiple-comparisons corrected P values also had high precision, which is crucial when performing millions or billions of tests in large databases. Here, we introduce an improvement to the algorithmic complexity of this computation from O(mn3) to O(mn2), where m and n are the numbers of recombination-informative sites in the candidate recombinant. This new computation allows for recombination analysis to be performed in alignments with thousands of polymorphic sites. Benchmark runs are presented on viral genome sequence alignments, new features are introduced, and applications outside recombination analysis are discussed.
Abstract Identifying recombinant sequences in an era of large genomic databases is challenging as it requires an efficient algorithm to identify candidate recombinants and parents, as well as appropriate statistical methods to correct for the large number of comparisons performed. In 2007, a computation was introduced for an exact nonparametric mosaicism statistic that gave high-precision P values for putative recombinants. This exact computation meant that multiple-comparisons corrected P values also had high precision, which is crucial when performing millions or billions of tests in large databases. Here, we introduce an improvement to the algorithmic complexity of this computation from O(mn3) to O(mn2), where m and n are the numbers of recombination-informative sites in the candidate recombinant. This new computation allows for recombination analysis to be performed in alignments with thousands of polymorphic sites. Benchmark runs are presented on viral genome sequence alignments, new features are introduced, and applications outside recombination analysis are discussed.
Identifying recombinant sequences in an era of large genomic databases is challenging as it requires an efficient algorithm to identify candidate recombinants and parents, as well as appropriate statistical methods to correct for the large number of comparisons performed. In 2007, a computation was introduced for an exact nonparametric mosaicism statistic that gave high-precision P values for putative recombinants. This exact computation meant that multiple-comparisons corrected P values also had high precision, which is crucial when performing millions or billions of tests in large databases. Here, we introduce an improvement to the algorithmic complexity of this computation from O(mn3) to O(mn2), where m and n are the numbers of recombination-informative sites in the candidate recombinant. This new computation allows for recombination analysis to be performed in alignments with thousands of polymorphic sites. Benchmark runs are presented on viral genome sequence alignments, new features are introduced, and applications outside recombination analysis are discussed.Identifying recombinant sequences in an era of large genomic databases is challenging as it requires an efficient algorithm to identify candidate recombinants and parents, as well as appropriate statistical methods to correct for the large number of comparisons performed. In 2007, a computation was introduced for an exact nonparametric mosaicism statistic that gave high-precision P values for putative recombinants. This exact computation meant that multiple-comparisons corrected P values also had high precision, which is crucial when performing millions or billions of tests in large databases. Here, we introduce an improvement to the algorithmic complexity of this computation from O(mn3) to O(mn2), where m and n are the numbers of recombination-informative sites in the candidate recombinant. This new computation allows for recombination analysis to be performed in alignments with thousands of polymorphic sites. Benchmark runs are presented on viral genome sequence alignments, new features are introduced, and applications outside recombination analysis are discussed.
Author Lam, Ha Minh
Boni, Maciej F
Ratmann, Oliver
AuthorAffiliation 4 Center for Infectious Disease Dynamics, Department of Biology, Pennsylvania State University, University Park, PA
3 MRC Centre for Outbreak Analyses and Modelling, Department of Infectious Disease Epidemiology, School of Public Health, Imperial College London, London, United Kingdom
2 Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom
1 Wellcome Trust Major Overseas Programme, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam
AuthorAffiliation_xml – name: 2 Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom
– name: 3 MRC Centre for Outbreak Analyses and Modelling, Department of Infectious Disease Epidemiology, School of Public Health, Imperial College London, London, United Kingdom
– name: 1 Wellcome Trust Major Overseas Programme, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam
– name: 4 Center for Infectious Disease Dynamics, Department of Biology, Pennsylvania State University, University Park, PA
Author_xml – sequence: 1
  givenname: Ha Minh
  surname: Lam
  fullname: Lam, Ha Minh
  organization: Wellcome Trust Major Overseas Programme, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam
– sequence: 2
  givenname: Oliver
  surname: Ratmann
  fullname: Ratmann, Oliver
  organization: MRC Centre for Outbreak Analyses and Modelling, Department of Infectious Disease Epidemiology, School of Public Health, Imperial College London, London, United Kingdom
– sequence: 3
  givenname: Maciej F
  surname: Boni
  fullname: Boni, Maciej F
  email: mfb9@psu.edu
  organization: Wellcome Trust Major Overseas Programme, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29029186$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright The Author 2017. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 2017
The Author 2017. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution.
The Author 2017. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Copyright_xml – notice: The Author 2017. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 2017
– notice: The Author 2017. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution.
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Issue 1
Keywords nonparametric
recombination
mosaic structure
Language English
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Snippet Abstract Identifying recombinant sequences in an era of large genomic databases is challenging as it requires an efficient algorithm to identify candidate...
Identifying recombinant sequences in an era of large genomic databases is challenging as it requires an efficient algorithm to identify candidate recombinants...
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StartPage 247
SubjectTerms Algorithms
Biology
Complexity
Computation
Datasets
Gene Rearrangement - genetics
Genomes
Infectious diseases
Methods
Mosaicism
Nucleotide sequence
Phylogeny
Probability
Recombinants
Recombination
Recombination, Genetic - genetics
Sequence Alignment - methods
Sequence Analysis, DNA - methods
Sequence Analysis, DNA - statistics & numerical data
Software
Statistical analysis
Statistical methods
Variables
Title Improved Algorithmic Complexity for the 3SEQ Recombination Detection Algorithm
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