Evidence map›Paper›PMID 26060505›Full record

ArticleAlgorithms for molecular biology : AMB2015

Fair evaluation of global network aligners.

Joseph Crawford, Yihan Sun, Tijana Milenković

Abstract read
In one paragraph

Article in Algorithms for molecular biology : AMB, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

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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.

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Alignment of dynamic networks.Bioinformatics (Oxford, England) · 2017
    Article
  6. Article
  7. Local versus global biological network alignment.Bioinformatics (Oxford, England) · 2016
    Article
  8. The post-genomic era of biological network alignment.EURASIP journal on bioinformatics & systems biology · 2015
    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

3 authors.

Joseph CrawfordDepartment of Computer Science and Engineering, Interdisciplinary Center for Network Science and Applications (iCeNSA), ECK Institute for Global Health, University of Notre Dame, Notre Dame, IN 46556 USA.
Yihan SunDepartment of Computer Science and Engineering, Interdisciplinary Center for Network Science and Applications (iCeNSA), ECK Institute for Global Health, University of Notre Dame, Notre Dame, IN 46556 USA ; Department of Computer Science and Technology, Tsinghua University, Beijing, 100084 China ; Department of Computer Science, Carnegie Mellon University, Pittsburgh, PA 15213-3891 USA.
Tijana MilenkovićDepartment of Computer Science and Engineering, Interdisciplinary Center for Network Science and Applications (iCeNSA), ECK Institute for Global Health, University of Notre Dame, Notre Dame, IN 46556 USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAnalogous to genomic sequence alignment, biological network alignment identifies conserved regions between networks of different species. Then, function can be transferred from well- to poorly-annotated species between aligned network regions. Network alignment typically encompasses two algorithmic components: node cost function (NCF), which measures similarities between nodes in different networks, and alignment strategy (AS), which uses these similarities to rapidly identify high-scoring alignments. Different methods use both different NCFs and different ASs. Thus, it is unclear whether the superiority of a method comes from its NCF, its AS, or both. We already showed on state-of-the-art methods, MI-GRAAL and IsoRankN, that combining NCF of one method and AS of another method can give a new superior method. Here, we evaluate MI-GRAAL against a newer approach, GHOST, by mixing-and-matching the methods' NCFs and ASs to potentially further improve alignment quality. While doing so, we approach important questions that have not been asked systematically thus far. First, we ask how much of the NCF information should come from protein sequence data compared to network topology data. Existing methods determine this parameter more-less arbitrarily, which could affect alignment quality. Second, when topological information is used in NCF, we ask how large the size of the neighborhoods of the compared nodes should be. Existing methods assume that the larger the neighborhood size, the better.

resultsOur findings are as follows. MI-GRAAL's NCF is superior to GHOST's NCF, while the performance of the methods' ASs is data-dependent. Thus, for data on which GHOST's AS is superior to MI-GRAAL's AS, the combination of MI-GRAAL's NCF and GHOST's AS represents a new superior method. Also, which amount of sequence information is used within NCF does not affect alignment quality, while the inclusion of topological information is crucial for producing good alignments. Finally, larger neighborhood sizes are preferred, but often, it is the second largest size that is superior. Using this size instead of the largest one would decrease computational complexity.

conclusionTaken together, our results represent general recommendations for a fair evaluation of network alignment methods and in particular of two-stage NCF-AS approaches.

Indexed as

Across-species protein function predictionNetwork alignmentNetwork similarityProtein–protein interaction networks

Identifiers

PMID26060505
PMCPMC4460690

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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.