Evidence map›Paper›PMID 30589848›Full record

ArticlePloS one2018

Efficient algorithms for Longest Common Subsequence of two bucket orders to speed up pairwise genetic map comparison.

Lisa De Mattéo, Yan Holtz, Vincent Ranwez, Sèverine Bérard

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In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Lisa De MattéoISEM, Université de Montpellier, CNRS, IRD, EPHE, Montpellier, France.
Yan HoltzQueensland Brain Institute, University of Queensland, Brisbane, Australia.
Vincent RanwezAGAP, Univ Montpellier, CIRAD, INRA, Montpellier SupAgro, Montpellier, France.ORCID 0000-0002-9308-7541
Sèverine BérardISEM, Université de Montpellier, CNRS, IRD, EPHE, Montpellier, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic maps order genetic markers along chromosomes. They are, for instance, extensively used in marker-assisted selection to accelerate breeding programs. Even for the same species, people often have to deal with several alternative maps obtained using different ordering methods or different datasets, e.g. resulting from different segregating populations. Having efficient tools to identify the consistency and discrepancy of alternative maps is thus essential to facilitate genetic map comparisons. We propose to encode genetic maps by bucket order, a kind of order, which takes into account the blurred parts of the marker order while being an efficient data structure to achieve low complexity algorithms. The main result of this paper is an O(n log(n)) procedure to identify the largest agreements between two bucket orders of n elements, their Longest Common Subsequence (LCS), providing an efficient solution to highlight discrepancies between two genetic maps. The LCS of two maps, being the largest set of their collinear markers, is used as a building block to compute pairwise map congruence, to visually emphasize maker collinearity and in some scaffolding methods relying on genetic maps to improve genome assembly. As the LCS computation is a key subroutine of all these genetic map related tools, replacing the current LCS subroutine of those methods by ours -to do the exact same work but faster- could significantly speed up those methods without changing their accuracy. To ease such transition we provide all required algorithmic details in this self contained paper as well as an R package implementing them, named LCSLCIS, which is freely available at: https://github.com/holtzy/LCSLCIS.

Indexed as

AlgorithmsChromosome MappingModels, GeneticGenetic MarkersSequence Analysis, DNAGenetic Markers

Identifiers

PMID30589848
PMCPMC6320017

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.