Evidence map›Paper›PMID 23931333›Full record

ArticleJournal of computational biology : a journal of computational molecular cell biology2013

A probabilistic model of neutral and selective dynamics of protein network evolution.

Janusz Dutkowski, Jerzy Tiuryn

Abstract read
In one paragraph

Article in Journal of computational biology : a journal of computational molecular cell biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

2 authors.

Janusz DutkowskiDepartments of Medicine and Bioengineering, University of California, San Diego, California, USA.
Jerzy Tiuryn

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Comparative approaches in genomics have long relied on rigorous mathematical models of sequence evolution. Such models provide the basis for formulating and solving well-defined computational problems, in turn yielding key insights into the evolutionary processes acting on the genome. Analogous model-based approaches for analyzing biological networks are still under development. Here we describe a model-based approach for estimating the probability of network rewiring events during evolution. Our method builds on the standard duplication-and-divergence model and incorporates phylogenetic analysis to guide the comparison of protein networks across species. We apply our algorithm to study the evolution of functional modules and unconstrained network regions in seven available eukaryotic interactomes. Based on this analysis we identify a map of co-functioning protein families whose members participate in strongly conserved interactions and form major complexes and pathways in the eukaryotic cell. The proposed approach provides principled means for inferring the probability of network rewiring events, enabling insights into the conservation and divergence of protein interactions and the formation of functional modules in protein networks.

Indexed as

AlgorithmsEvolution, MolecularModels, GeneticPhylogenyGene DuplicationProteinsProteins

Identifiers

PMID23931333
PMCPMC3761421

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.