Evidence map›Paper›PMID 38676570›Full record

ArticleBioinformatics (Oxford, England)2024

RecGraph: recombination-aware alignment of sequences to variation graphs.

Jorge Avila Cartes, Paola Bonizzoni, Simone Ciccolella, Gianluca Della Vedova, Luca Denti, Xavier Didelot, Davide Cesare Monti, Yuri Pirola

Open access · goldAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

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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

8 authors at 2 institutions in 2 countries.

Jorge Avila CartesDepartment of Informatics, Systems and Communication, University of Milano - Bicocca. Viale Sarca 336, Milano 20126, Italy.
Paola BonizzoniDepartment of Informatics, Systems and Communication, University of Milano - Bicocca. Viale Sarca 336, Milano 20126, Italy.ORCID 0000-0001-7289-4988
Simone CiccolellaDepartment of Informatics, Systems and Communication, University of Milano - Bicocca. Viale Sarca 336, Milano 20126, Italy.ORCID 0000-0002-6469-4887
Gianluca Della VedovaDepartment of Informatics, Systems and Communication, University of Milano - Bicocca. Viale Sarca 336, Milano 20126, Italy.ORCID 0000-0001-5584-3089
Luca DentiDepartment of Informatics, Systems and Communication, University of Milano - Bicocca. Viale Sarca 336, Milano 20126, Italy.ORCID 0000-0001-8786-2276
Xavier DidelotDepartment of Statistics and School of Life Sciences, University of Warwick, Coventry CV4 7AL, United Kingdom.ORCID 0000-0003-1885-500X
Davide Cesare MontiDepartment of Informatics, Systems and Communication, University of Milano - Bicocca. Viale Sarca 336, Milano 20126, Italy.ORCID 0009-0004-1710-5500
Yuri PirolaDepartment of Informatics, Systems and Communication, University of Milano - Bicocca. Viale Sarca 336, Milano 20126, Italy.ORCID 0000-0002-8479-7592
University of Milano-Bicocca · ITUniversity of Warwick · GB

Funding

European Union's Horizon 2020 Research and Innovation Staff Exchange
6 · The paper itself

Abstract

motivationBacterial genomes present more variability than human genomes, which requires important adjustments in computational tools that are developed for human data. In particular, bacteria exhibit a mosaic structure due to homologous recombinations, but this fact is not sufficiently captured by standard read mappers that align against linear reference genomes. The recent introduction of pangenomics provides some insights in that context, as a pangenome graph can represent the variability within a species. However, the concept of sequence-to-graph alignment that captures the presence of recombinations has not been previously investigated.

resultsIn this paper, we present the extension of the notion of sequence-to-graph alignment to a variation graph that incorporates a recombination, so that the latter are explicitly represented and evaluated in an alignment. Moreover, we present a dynamic programming approach for the special case where there is at most a recombination-we implement this case as RecGraph. From a modelling point of view, a recombination corresponds to identifying a new path of the variation graph, where the new arc is composed of two halves, each extracted from an original path, possibly joined by a new arc. Our experiments show that RecGraph accurately aligns simulated recombinant bacterial sequences that have at most a recombination, providing evidence for the presence of recombination events. AVAILABILITY AND IMPLEMENTATION: Our implementation is open source and available at https://github.com/AlgoLab/RecGraph.

Indexed as

AlgorithmsGenome, BacterialRecombination, GeneticSequence AlignmentGenomicsHumansSequence Analysis, DNASoftware

Identifiers

PMID38676570
PMCPMC11256948
OpenAlexW4395958438

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.