Evidence map›Paper›PMID 32129827›Full record

ArticleBioinformatics (Oxford, England)2020

Supervised learning is an accurate method for network-based gene classification.

Renming Liu, Christopher A Mancuso, Anna Yannakopoulos, Kayla A Johnson, Arjun Krishnan

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

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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

5 authors.

Renming LiuDepartment of Computational Mathematics, Science and Engineering.
Christopher A MancusoDepartment of Computational Mathematics, Science and Engineering.
Anna YannakopoulosDepartment of Computational Mathematics, Science and Engineering.
Kayla A JohnsonDepartment of Computational Mathematics, Science and Engineering.
Arjun KrishnanDepartment of Computational Mathematics, Science and Engineering.

Funding

Resolving and understanding the genomic basis of heterogeneous complex traits and diseasesR35GM128765 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI KRISHNAN, ARJUN · 2018 to 2022
$2.0M
Incorporating molecular network knowledge into predictive data-driven modelsF32GM134595 · NIGMS · MICHIGAN STATE UNIVERSITY · PI MANCUSO, CHRISTOPHER ANDREW · 2019 to 2022
$202k
NIGMS NIH HHS F32 GM134595NIGMS NIH HHS R35 GM128765
6 · The paper itself

Abstract

backgroundAssigning every human gene to specific functions, diseases and traits is a grand challenge in modern genetics. Key to addressing this challenge are computational methods, such as supervised learning and label propagation, that can leverage molecular interaction networks to predict gene attributes. In spite of being a popular machine-learning technique across fields, supervised learning has been applied only in a few network-based studies for predicting pathway-, phenotype- or disease-associated genes. It is unknown how supervised learning broadly performs across different networks and diverse gene classification tasks, and how it compares to label propagation, the widely benchmarked canonical approach for this problem.

resultsIn this study, we present a comprehensive benchmarking of supervised learning for network-based gene classification, evaluating this approach and a classic label propagation technique on hundreds of diverse prediction tasks and multiple networks using stringent evaluation schemes. We demonstrate that supervised learning on a gene's full network connectivity outperforms label propagaton and achieves high prediction accuracy by efficiently capturing local network properties, rivaling label propagation's appeal for naturally using network topology. We further show that supervised learning on the full network is also superior to learning on node embeddings (derived using node2vec), an increasingly popular approach for concisely representing network connectivity. These results show that supervised learning is an accurate approach for prioritizing genes associated with diverse functions, diseases and traits and should be considered a staple of network-based gene classification workflows. AVAILABILITY AND IMPLEMENTATION: The datasets and the code used to reproduce the results and add new gene classification methods have been made freely available. CONTACT: arjun@msu.edu. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Computational BiologyGene Regulatory NetworksHumansSupervised Machine Learning

Identifiers

PMID32129827
PMCPMC7267831

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.