Evidence map›Paper›PMID 19646452›Full record

ArticleJournal of theoretical biology2009

Generalized lattice graphs for 2D-visualization of biological information.

H González-Díaz, L G Pérez-Montoto, A Duardo-Sanchez, E Paniagua, S Vázquez-Prieto, R Vilas, M A Dea-Ayuela, F Bolas-Fernández, C R Munteanu, J Dorado and 2 more

Abstract read
In one paragraph

Article in Journal of theoretical biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 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

12 authors.

H González-DíazDepartment of Microbiology and Parasitology, and Department of Organic Chemistry, Faculty of Pharmacy and Department of Special Public Law, Financial and Tributary Law Area, Faculty of Law, University of Santiago de Compostela (USC), 15782 Santiago de Compostela, Spain. gonzalezdiazh@yahoo.es
L G Pérez-Montoto
A Duardo-Sanchez
E Paniagua
S Vázquez-Prieto
R Vilas
M A Dea-Ayuela
F Bolas-Fernández
C R Munteanu
J Dorado
J Costas
F M Ubeira

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several graph representations have been introduced for different data in theoretical biology. For instance, complex networks based on Graph theory are used to represent the structure and/or dynamics of different large biological systems such as protein-protein interaction networks. In addition, Randic, Liao, Nandy, Basak, and many others developed some special types of graph-based representations. This special type of graph includes geometrical constrains to node positioning in space and adopts final geometrical shapes that resemble lattice-like patterns. Lattice networks have been used to visually depict DNA and protein sequences but they are very flexible. However, despite the proved efficacy of new lattice-like graph/networks to represent diverse systems, most works focus on only one specific type of biological data. This work proposes a generalized type of lattice and illustrates how to use it in order to represent and compare biological data from different sources. We exemplify the following cases: protein sequence; mass spectra (MS) of protein peptide mass fingerprints (PMF); molecular dynamic trajectory (MDTs) from structural studies; mRNA microarray data; single nucleotide polymorphisms (SNPs); 1D or 2D-Electrophoresis study of protein polymorphisms and protein-research patent and/or copyright information. We used data available from public sources for some examples but for other, we used experimental results reported herein for the first time. This work may break new ground for the application of Graph theory in theoretical biology and other areas of biomedical sciences.

Indexed as

Models, BiologicalAnimalsComputational BiologyCopyrightElectrophoresisLeishmaniaMass SpectrometryOligonucleotide Array Sequence AnalysisPolymorphism, Single NucleotideProteomicsProtozoan ProteinsRNA, MessengerSequence Analysis, ProteinProtozoan ProteinsRNA, Messenger

Identifiers

PMID19646452
PMCPMC7094121

What OpenQuestion holds

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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.