Evidence map›Paper›PMID 22992218›Full record

ArticleAlgorithms for molecular biology : AMB2012

Parsimonious reconstruction of network evolution.

Rob Patro, Emre Sefer, Justin Malin, Guillaume Marçais, Saket Navlakha, Carl Kingsford

Abstract read
In one paragraph

Article in Algorithms for molecular biology : AMB, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Ancestral Reconstruction.PLoS computational biology · 2016
    Article
  7. Bayesian inference for duplication-mutation with complementarity network models.Journal of computational biology : a journal of computational molecular cell biology · 2015
    Article
  8. Article
  9. 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

6 authors.

Rob PatroCenter for Bioinformatics and Computational Biology, University of Maryland, College Park, MD 20742, USA. rob@cs.umd.edu.
Emre Sefer
Justin Malin
Guillaume Marçais
Saket Navlakha
Carl Kingsford

Funding

Reliable Assembler for Whole Genome Shotgun Data.R01HG002945 · NHGRI · UNIV OF MARYLAND, COLLEGE PARK · PI YORKE, JAMES A · 2003 to 2013
$2.1M
Accurate Computational Detection of Influenza ReassortmentsR21AI085376 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI KINGSFORD, CARLETON LEE · 2010 to 2011
$369k
NHGRI NIH HHS R01 HG002945NIAID NIH HHS R21 AI085376
6 · The paper itself

Abstract

unlabelled

backgroundUnderstanding the evolution of biological networks can provide insight into how their modular structure arises and how they are affected by environmental changes. One approach to studying the evolution of these networks is to reconstruct plausible common ancestors of present-day networks, allowing us to analyze how the topological properties change over time and to posit mechanisms that drive the networks' evolution. Further, putative ancestral networks can be used to help solve other difficult problems in computational biology, such as network alignment.

resultsWe introduce a combinatorial framework for encoding network histories, and we give a fast procedure that, given a set of gene duplication histories, in practice finds network histories with close to the minimum number of interaction gain or loss events to explain the observed present-day networks. In contrast to previous studies, our method does not require knowing the relative ordering of unrelated duplication events. Results on simulated histories and real biological networks both suggest that common ancestral networks can be accurately reconstructed using this parsimony approach. A software package implementing our method is available under the Apache 2.0 license at http://cbcb.umd.edu/kingsford-group/parana.

conclusionsOur parsimony-based approach to ancestral network reconstruction is both efficient and accurate. We show that considering a larger set of potential ancestral interactions by not assuming a relative ordering of unrelated duplication events can lead to improved ancestral network inference.

Identifiers

PMID22992218
PMCPMC3492119

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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.