Evidence map›Paper›PMID 26780836›Full record

ArticleBMC bioinformatics2016

Algorithms for reconstruction of chromosomal structures.

Vassily Lyubetsky, Roman Gershgorin, Alexander Seliverstov, Konstantin Gorbunov

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

6 citing papers in PubMed, 15 citations in OpenAlex.

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  6. Molecular Phylogenetics 2016.BioMed research international · 2016
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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

4 authors at 1 institution in 1 country.

Vassily LyubetskyInstitute for Information Transmission Problems of the Russian Academy of Sciences (Kharkevich Institute), Bolshoi Karetnyi lane, 19, 127051, Moscow, Russia. lyubetsk@iitp.ru.
Roman GershgorinInstitute for Information Transmission Problems of the Russian Academy of Sciences (Kharkevich Institute), Bolshoi Karetnyi lane, 19, 127051, Moscow, Russia. gershr@mail.ru.
Alexander SeliverstovInstitute for Information Transmission Problems of the Russian Academy of Sciences (Kharkevich Institute), Bolshoi Karetnyi lane, 19, 127051, Moscow, Russia. slvstv@iitp.ru.
Konstantin GorbunovInstitute for Information Transmission Problems of the Russian Academy of Sciences (Kharkevich Institute), Bolshoi Karetnyi lane, 19, 127051, Moscow, Russia. gorbunov@iitp.ru.
Institute for Information Transmission Problems · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOne of the main aims of phylogenomics is the reconstruction of objects defined in the leaves along the whole phylogenetic tree to minimize the specified functional, which may also include the phylogenetic tree generation. Such objects can include nucleotide and amino acid sequences, chromosomal structures, etc. The structures can have any set of linear and circular chromosomes, variable gene composition and include any number of paralogs, as well as any weights of individual evolutionary operations to transform a chromosome structure. Many heuristic algorithms were proposed for this purpose, but there are just a few exact algorithms with low (linear, cubic or similar) polynomial computational complexity among them to our knowledge. The algorithms naturally start from the calculation of both the distance between two structures and the shortest sequence of operations transforming one structure into another. Such calculation per se is an NP-hard problem.

resultsA general model of chromosomal structure rearrangements is considered. Exact algorithms with almost linear or cubic polynomial complexities have been developed to solve the problems for the case of any chromosomal structure but with certain limitations on operation weights. The computer programs are tested on biological data for the problem of mitochondrial or plastid chromosomal structure reconstruction. To our knowledge, no computer programs are available for this model.

conclusionsExactness of the proposed algorithms and such low polynomial complexities were proved. The reconstructed evolutionary trees of mitochondrial and plastid chromosomal structures as well as the ancestral states of the structures appear to be reasonable.

Indexed as

AlgorithmsChromosome StructuresComputational BiologyComputer SimulationModels, MolecularPhylogenySoftware

Identifiers

PMID26780836
PMCPMC4717669
OpenAlexW2253805474

What OpenQuestion holds

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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.