Evidence map›Paper›PMID 42909365›Full record

ArticleNAR genomics and bioinformatics2026

ModCRElib: a standalone package to model

Patrick Gohl, Oriol Fornes, Patricia M Bota, Alberto Meseguer, Jaume Bonet, Ruben Molina-Fernández, Joan Planas-Iglesias, Altair C Hernández, Oriol Gallego, Narcis Fernandez-Fuentes and 1 more

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2026. 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

11 authors.

Patrick GohlDepartment of Medicine and Life Sciences, (Structural Bioinformatics Group-GRIB), Universitat Pompeu Fabra, Barcelona, Catalonia 08003, Spain.
Oriol FornesCentre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, Department of Medical Genetics, University of British Columbia, Vancouver, BC V5Z 4H4, Canada.ORCID https://orcid.org/0000-0001-7479-2563
Patricia M BotaDepartment of Medicine and Life Sciences, (Structural Bioinformatics Group-GRIB), Universitat Pompeu Fabra, Barcelona, Catalonia 08003, Spain.
Alberto MeseguerDepartment of Medicine and Life Sciences, (Structural Bioinformatics Group-GRIB), Universitat Pompeu Fabra, Barcelona, Catalonia 08003, Spain.
Jaume BonetDepartment of Medicine and Life Sciences, (Structural Bioinformatics Group-GRIB), Universitat Pompeu Fabra, Barcelona, Catalonia 08003, Spain.
Ruben Molina-FernándezDepartment of Medicine and Life Sciences, (Structural Bioinformatics Group-GRIB), Universitat Pompeu Fabra, Barcelona, Catalonia 08003, Spain.
Joan Planas-IglesiasLoschmidt Laboratories, Department of Experimental Biology and RECETOX, Faculty of Science, Masaryk University, Brno 625 00, Czech Republic.
Altair C HernándezBiophysics in Cell Biology, Department of Medicine and Life Sciences, Universitat Pompeu Fabra, Barcelona, Catalonia 08005, Spain.
Oriol GallegoBiophysics in Cell Biology, Department of Medicine and Life Sciences, Universitat Pompeu Fabra, Barcelona, Catalonia 08005, Spain.
Narcis Fernandez-FuentesDepartment of Medicine and Life Sciences, (Structural Bioinformatics Group-GRIB), Universitat Pompeu Fabra, Barcelona, Catalonia 08003, Spain.ORCID https://orcid.org/0000-0002-6421-1080
Baldomero OlivaDepartment of Medicine and Life Sciences, (Structural Bioinformatics Group-GRIB), Universitat Pompeu Fabra, Barcelona, Catalonia 08003, Spain.ORCID https://orcid.org/0000-0003-0702-0250

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ModCRElib package provides various tools for the analysis and modelling of transcription factor (TF)-DNA and regulatory complex inter-protein interactions. It takes structural information on these interactions to predict TF-binding motifs, generate binding profiles along DNA sequences that score the binding affinity, predict TF-binding sites, and model the structure of higher order regulatory complexes. It is capable of working with a variety of input data formats and sources. The user may follow the analysis pipeline as outlined in the documentation or the user can make use of any of the multiple functionalities in an isolated manner. The package takes the service offered by the ModCRE server and enables users to apply its tools in an unrestricted and customizable manner. In this paper we provide five example uses of ModCRElib. This includes (i) TF-binding affinity prediction, (ii) TF ensemble pattern of bindings (aggregation of motifs), (iii) characterization of specificity in TF-binding sites along target DNA sequences, (iv) modelling TF bound to predicted binding sites, and (v) the generation of statistical potential derived scoring profiles of TF interacting with DNA.

Indexed as

Regulatory Elements, TranscriptionalSoftwareTranscription FactorsBinding SitesDNAProtein BindingDNATranscription Factors

Identifiers

PMID42909365
PMCPMC13684267

What OpenQuestion holds

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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.