Evidence map›Paper›PMID 34965857›Full record

ArticleAlgorithms for molecular biology : AMB2021

An improved approximation algorithm for the reversal and transposition distance considering gene order and intergenic sizes.

Klairton L Brito, Andre R Oliveira, Alexsandro O Alexandrino, Ulisses Dias, Zanoni Dias

Open access · goldAbstract read
In one paragraph

Article in Algorithms for molecular biology : AMB, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.0field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 8 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Klairton L BritoInstitute of Computing, University of Campinas, 1251 Albert Einstein Ave., 13083-852, Campinas, Brazil. klairton@ic.unicamp.br.ORCID http://orcid.org/0000-0001-5287-2925
Andre R OliveiraInstitute of Computing, University of Campinas, 1251 Albert Einstein Ave., 13083-852, Campinas, Brazil.ORCID http://orcid.org/0000-0002-0568-1859
Alexsandro O AlexandrinoInstitute of Computing, University of Campinas, 1251 Albert Einstein Ave., 13083-852, Campinas, Brazil.ORCID http://orcid.org/0000-0002-6320-9747
Ulisses DiasSchool of Technology, University of Campinas, 1888 Paschoal Marmo St., 13484-332, Limeira, Brazil.ORCID http://orcid.org/0000-0002-4763-3046
Zanoni DiasInstitute of Computing, University of Campinas, 1251 Albert Einstein Ave., 13083-852, Campinas, Brazil.ORCID http://orcid.org/0000-0003-3333-6822
Universidade Estadual de Campinas (UNICAMP) · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 140272/2020-8Conselho Nacional de Desenvolvimento Científico e Tecnológico 425340/2016-3Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 001Fundação de Amparo à Pesquisa do Estado de São Paulo 2013/08293-7Fundação de Amparo à Pesquisa do Estado de São Paulo 2015/11937-9Fundação de Amparo à Pesquisa do Estado de São Paulo 2017/12646-3Fundação de Amparo à Pesquisa do Estado de São Paulo 2019/27331-3
6 · The paper itself

Abstract

backgroundIn the comparative genomics field, one of the goals is to estimate a sequence of genetic changes capable of transforming a genome into another. Genome rearrangement events are mutations that can alter the genetic content or the arrangement of elements from the genome. Reversal and transposition are two of the most studied genome rearrangement events. A reversal inverts a segment of a genome while a transposition swaps two consecutive segments. Initial studies in the area considered only the order of the genes. Recent works have incorporated other genetic information in the model. In particular, the information regarding the size of intergenic regions, which are structures between each pair of genes and in the extremities of a linear genome. RESULTS AND

conclusionsIn this work, we investigate the SORTING BY INTERGENIC REVERSALS AND TRANSPOSITIONS problem on genomes sharing the same set of genes, considering the cases where the orientation of genes is known and unknown. Besides, we explored a variant of the problem, which generalizes the transposition event. As a result, we present an approximation algorithm that guarantees an approximation factor of 4 for both cases considering the reversal and transposition (classic definition) events, an improvement from the 4.5-approximation previously known for the scenario where the orientation of the genes is unknown. We also present a 3-approximation algorithm by incorporating the generalized transposition event, and we propose a greedy strategy to improve the performance of the algorithms. We performed practical tests adopting simulated data which indicated that the algorithms, in both cases, tend to perform better when compared with the best-known algorithms for the problem. Lastly, we conducted experiments using real genomes to demonstrate the applicability of the algorithms.

Indexed as

Approximation algorithmsGenome rearrangement eventsIntergenic regions

Identifiers

PMID34965857
PMCPMC8717661
OpenAlexW4200239892

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.