Evidence map›Paper›PMID 25302942›Full record

ArticlePloS one2014

Reconstruction of ancestral gene orders using probabilistic and gene encoding approaches.

Ning Yang, Fei Hu, Lingxi Zhou, Jijun Tang

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In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

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10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ning YangSchool of Automation, Northwestern Polytechnical University, Xi'an, shaanxi, China.
Fei HuTianjin Key Laboratory of Cognitive Computing and Application, Tianjin University, Tianjin, China; Department of Computer Science and Engineering, University of South Carolina, Columbia, South Carolina, United States of America.
Lingxi ZhouTianjin Key Laboratory of Cognitive Computing and Application, Tianjin University, Tianjin, China; Department of Computer Science and Engineering, University of South Carolina, Columbia, South Carolina, United States of America.
Jijun TangTianjin Key Laboratory of Cognitive Computing and Application, Tianjin University, Tianjin, China; Department of Computer Science and Engineering, University of South Carolina, Columbia, South Carolina, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current tools used in the reconstruction of ancestral gene orders often fall into event-based and adjacency-based methods according to the principles they follow. Event-based methods such as GRAPPA are very accurate but with extremely high complexity, while more recent methods based on gene adjacencies such as InferCARsPro is relatively faster, but often produces an excessive number of chromosomes. This issue is mitigated by newer methods such as GapAdj, however it sacrifices a considerable portion of accuracy. We recently developed an adjacency-based method in the probabilistic framework called PMAG to infer ancestral gene orders. PMAG relies on calculating the conditional probabilities of gene adjacencies that are found in the leaf genomes using the Bayes' theorem. It uses a novel transition model which accounts for adjacency changes along the tree branches as well as a re-rooting procedure to prevent any information loss. In this paper, we improved PMAG with a new method to assemble gene adjacencies into valid gene orders, using an exact solver for traveling salesman problem (TSP) to maximize the overall conditional probabilities. We conducted a series of simulation experiments using a wide range of configurations. The first set of experiments was to verify the effectiveness of our strategy of using the better transition model and re-rooting the tree under the targeted ancestral genome. PMAG was then thoroughly compared in terms of three measurements with its four major competitors including InferCARsPro, GapAdj, GASTS and SCJ in order to assess their performances. According to the results, PMAG demonstrates superior performance in terms of adjacency, distance and assembly accuracies, and yet achieves comparable running time, even all TSP instances were solved exactly. PMAG is available for free at http://phylo.cse.sc.edu.

Indexed as

Computer SimulationEvolution, MolecularGene OrderModels, GeneticModels, StatisticalPhylogenyAlgorithmsAnimalsGene RearrangementGenomeHumans

Identifiers

PMID25302942
PMCPMC4193752

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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.