Evidence map›Paper›PMID 39497039›Full record

ArticleBMC bioinformatics2024

PangeBlocks: customized construction of pangenome graphs via maximal blocks.

Jorge Avila Cartes, Paola Bonizzoni, Simone Ciccolella, Gianluca Della Vedova, Luca Denti

Abstract read
In one paragraph

Article in BMC bioinformatics, 2024. 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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1 · What the graph read from it

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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

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jorge Avila CartesDepartment of Informatics, Systems, and Communications, University of Milano - Bicocca, Viale Sarca, 20126, Milano, Italy.
Paola BonizzoniDepartment of Informatics, Systems, and Communications, University of Milano - Bicocca, Viale Sarca, 20126, Milano, Italy. paola.bonizzoni@unimib.it.
Simone CiccolellaDepartment of Informatics, Systems, and Communications, University of Milano - Bicocca, Viale Sarca, 20126, Milano, Italy.
Gianluca Della VedovaDepartment of Informatics, Systems, and Communications, University of Milano - Bicocca, Viale Sarca, 20126, Milano, Italy.
Luca DentiDepartment of Informatics, Systems, and Communications, University of Milano - Bicocca, Viale Sarca, 20126, Milano, Italy.

Funding

European Union's Horizon 2020 Research and Innovation Staff Exchange programme 872539H2020 Marie Skłodowska-Curie Actions 956229Ministero dell'Istruzione, dell'Università e della Ricerca 2022YRB97K
6 · The paper itself

Abstract

backgroundThe construction of a pangenome graph is a fundamental task in pangenomics. A natural theoretical question is how to formalize the computational problem of building an optimal pangenome graph, making explicit the underlying optimization criterion and the set of feasible solutions. Current approaches build a pangenome graph with some heuristics, without assuming some explicit optimization criteria. Thus it is unclear how a specific optimization criterion affects the graph topology and downstream analysis, like read mapping and variant calling.

resultsIn this paper, by leveraging the notion of maximal block in a Multiple Sequence Alignment (MSA), we reframe the pangenome graph construction problem as an exact cover problem on blocks called Minimum Weighted Block Cover (MWBC). Then we propose an Integer Linear Programming (ILP) formulation for the MWBC problem that allows us to study the most natural objective functions for building a graph. We provide an implementation of the ILP approach for solving the MWBC and we evaluate it on SARS-CoV-2 complete genomes, showing how different objective functions lead to pangenome graphs that have different properties, hinting that the specific downstream task can drive the graph construction phase.

conclusionWe show that a customized construction of a pangenome graph based on selecting objective functions has a direct impact on the resulting graphs. In particular, our formalization of the MWBC problem, based on finding an optimal subset of blocks covering an MSA, paves the way to novel practical approaches to graph representations of an MSA where the user can guide the construction.

Indexed as

SARS-CoV-2AlgorithmsCOVID-19Genome, ViralGenomicsHumansProgramming, LinearSequence AlignmentInteger linear programmingMaximal blocksPangenome graphsVariation graph construction

Identifiers

PMID39497039
PMCPMC11533710

What Socratic 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 Socratic graph.