Evidence map›Paper›PMID 40746377›Full record

ArticleNAR genomics and bioinformatics2025

An nf-core framework for the systematic comparison of alternative modeling tools: the multiple sequence alignment case study.

Luisa Santus, Jose Espinosa-Carrasco, Leon Rauschning, Júlia Mir-Pedrol, Igor Trujnara, Alessio Vignoli, Leila Mansouri, Athanasios Baltzis, Evan W Floden, Paolo Di Tommaso and 6 more

Abstract readComparative Study
In one paragraph

Article in NAR genomics and bioinformatics, 2025. 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
–field-weighted citation impact
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.

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

16 authors.

Luisa SantusCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Dr. Aiguader 88, 08003 Barcelona, Spain.ORCID https://orcid.org/0000-0002-5992-0771
Jose Espinosa-CarrascoCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Dr. Aiguader 88, 08003 Barcelona, Spain.ORCID https://orcid.org/0000-0002-1541-042X
Leon RauschningCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Dr. Aiguader 88, 08003 Barcelona, Spain.ORCID https://orcid.org/0000-0002-1756-9311
Júlia Mir-PedrolCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Dr. Aiguader 88, 08003 Barcelona, Spain.ORCID https://orcid.org/0000-0001-6104-9260
Igor TrujnaraCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Dr. Aiguader 88, 08003 Barcelona, Spain.ORCID https://orcid.org/0000-0002-8735-5976
Alessio VignoliCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Dr. Aiguader 88, 08003 Barcelona, Spain.ORCID https://orcid.org/0000-0001-7131-2915
Leila MansouriCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Dr. Aiguader 88, 08003 Barcelona, Spain.ORCID https://orcid.org/0000-0001-8442-9709
Athanasios BaltzisCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Dr. Aiguader 88, 08003 Barcelona, Spain.ORCID https://orcid.org/0000-0002-7495-1218
Evan W FlodenSeqera, Carrer de Marià Aguiló, 28, 08005 Barcelona, Spain.ORCID https://orcid.org/0000-0002-5431-190X
Paolo Di TommasoSeqera, Carrer de Marià Aguiló, 28, 08005 Barcelona, Spain.ORCID https://orcid.org/0000-0003-3220-0253
Edgar GarrigaLife Sciences Department, Barcelona Supercomputing Center, Barcelona, 08034 Catalonia, Spain.ORCID https://orcid.org/0000-0002-9861-5294
Adam GudyśFaculty of Automatic Control, Electronics and Computer Science, Silesian University of Technology, Akademicka 16, 44-100 Gliwice, Poland.ORCID https://orcid.org/0000-0002-5508-0090
Sebastian DeorowiczFaculty of Automatic Control, Electronics and Computer Science, Silesian University of Technology, Akademicka 16, 44-100 Gliwice, Poland.ORCID https://orcid.org/0000-0002-9496-733X
Cameron GilchristSchool of Biological Sciences, Seoul National University, 08826 Seoul, South Korea.ORCID https://orcid.org/0000-0001-7798-427X
Martin SteineggerSchool of Biological Sciences, Seoul National University, 08826 Seoul, South Korea.ORCID https://orcid.org/0000-0001-8781-9753
Cedric NotredameCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Dr. Aiguader 88, 08003 Barcelona, Spain.ORCID https://orcid.org/0000-0003-1461-0988

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The computational complexity of many key bioinformatics problems has resulted in numerous alternative heuristic solutions, where no single approach consistently outperforms all others. This creates difficulties for users trying to identify the most suitable tool for their dataset and for developers managing and evaluating alternative methods. As data volumes grow, deploying these methods becomes increasingly difficult, highlighting the need for standardized frameworks for seamless tool deployment and comparison in high-performance computing (HPC) environments. Multiple sequence aligners (MSAs) rank among the most commonly employed modeling techniques in bioinformatics, playing a crucial role in applications such as protein structure prediction, phylogenetic reconstruction, and variant effect prediction. MSAs are NP-hard problems, which makes them a major example of computational challenges where heuristic solutions are essential. Here, we present a pilot design of an nf-core framework for streamlined tool deployment and rigorous performance evaluation focusing on the MSA software ecosystem. While showcased with the integration of popular MSA tools and designed to directly benefit the MSA community, we also present the framework as a proof of principle for the broader bioinformatics community. nf-core/multiplesequencealign is free open-source software available at https://nf-co.re/multiplesequencealign.

Indexed as

Computational BiologySequence AlignmentSoftwareAlgorithms

Identifiers

PMID40746377
PMCPMC12311786

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.