Evidence map›Paper›PMID 33351828›Full record

ArticlePloS one2020

Multi-resolution visualization and analysis of biomolecular networks through hierarchical community detection and web-based graphical tools.

Paolo Perlasca, Marco Frasca, Cheick Tidiane Ba, Jessica Gliozzo, Marco Notaro, Mario Pennacchioni, Giorgio Valentini, Marco Mesiti

Abstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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.

Paolo PerlascaAnacletoLab, Department of Computer Science, University of Milan, Milan, Italy.ORCID 0000-0001-6674-2822
Marco FrascaAnacletoLab, Department of Computer Science, University of Milan, Milan, Italy.
Cheick Tidiane BaAnacletoLab, Department of Computer Science, University of Milan, Milan, Italy.ORCID 0000-0002-4035-7464
Jessica GliozzoNeuroradiology Unit, IRCCS San Raffaele Hospital, Milan, Italy.ORCID 0000-0001-7629-8112
Marco NotaroAnacletoLab, Department of Computer Science, University of Milan, Milan, Italy.ORCID 0000-0003-4309-2200
Mario PennacchioniAnacletoLab, Department of Computer Science, University of Milan, Milan, Italy.
Giorgio ValentiniAnacletoLab, Department of Computer Science, University of Milan, Milan, Italy.ORCID 0000-0002-5694-3919
Marco MesitiAnacletoLab, Department of Computer Science, University of Milan, Milan, Italy.ORCID 0000-0001-5701-0080

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The visual exploration and analysis of biomolecular networks is of paramount importance for identifying hidden and complex interaction patterns among proteins. Although many tools have been proposed for this task, they are mainly focused on the query and visualization of a single protein with its neighborhood. The global exploration of the entire network and the interpretation of its underlying structure still remains difficult, mainly due to the excessively large size of the biomolecular networks. In this paper we propose a novel multi-resolution representation and exploration approach that exploits hierarchical community detection algorithms for the identification of communities occurring in biomolecular networks. The proposed graphical rendering combines two types of nodes (protein and communities) and three types of edges (protein-protein, community-community, protein-community), and displays communities at different resolutions, allowing the user to interactively zoom in and out from different levels of the hierarchy. Links among communities are shown in terms of relationships and functional correlations among the biomolecules they contain. This form of navigation can be also combined by the user with a vertex centric visualization for identifying the communities holding a target biomolecule. Since communities gather limited-size groups of correlated proteins, the visualization and exploration of complex and large networks becomes feasible on off-the-shelf computer machines. The proposed graphical exploration strategies have been implemented and integrated in UNIPred-Web, a web application that we recently introduced for combining the UNIPred algorithm, able to address both integration and protein function prediction in an imbalance-aware fashion, with an easy to use vertex-centric exploration of the integrated network. The tool has been deeply amended from different standpoints, including the prediction core algorithm. Several tests on networks of different size and connectivity have been conducted to show off the vast potential of our methodology; moreover, enrichment analyses have been performed to assess the biological meaningfulness of detected communities. Finally, a CoV-human network has been embedded in the system, and a corresponding case study presented, including the visualization and the prediction of human host proteins that potentially interact with SARS-CoV2 proteins.

Indexed as

InternetAlgorithmsCOVID-19HumansMetabolic Networks and PathwaysProteinsSARS-CoV-2Proteins

Identifiers

PMID33351828
PMCPMC7755227

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.