ArticleScientific reports2021
Empirically classifying network mechanisms.
Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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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.
The trial behind it
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Who cites it
2 citing papers in PubMed.
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Network data are often explained by assuming a generating mechanism and estimating related parameters. Without a way to test the relevance of assumed mechanisms, conclusions from such models may be misleading. Here we introduce a simple empirical approach to mechanistically classify arbitrary network data as originating from any of a set of candidate mechanisms or none of them. We tested our approach on simulated data from five of the most widely studied network mechanisms, and found it to be highly accurate. We then tested 1284 empirical networks spanning 17 different kinds of systems against these five widely studied mechanisms. We found that 387 (30%) of these empirical networks were classified as unlike any of the mechanisms, and only 1% or fewer of the networks classified as each of the mechanisms for which our approach was most sensitive. Based on this, we use Bayes' theorem to show that most of the 70% of empirical networks our approach classified as a mechanism could be false positives, because of the high sensitivity required of a test to detect rarely occurring mechanisms. Thus, it is possible that very few of our empirical networks are described by any of these five widely studied mechanisms. Additionally, 93 networks (7%) were classified as plausibly being governed by each of multiple mechanisms. This raises the possibility that some systems are governed by mixtures of mechanisms. We show that mixtures are often unidentifiable because different mixtures can produce structurally equivalent networks, but that we can still accurately predict out-of-sample functional properties.
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Registered trials
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