Evidence map›Paper›PMID 31684857›Full record

ArticleBMC bioinformatics2019

Predictive modelling using pathway scores: robustness and significance of pathway collections.

Marcelo P Segura-Lepe, Hector C Keun, Timothy M D Ebbels

Abstract readEvaluation Study
In one paragraph

Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 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

3 authors.

Marcelo P Segura-LepeComputational and Systems Medicine, Department of Surgery and Cancer, Sir Alexander Fleming building, Imperial College, London, SW1 2AZ, UK.
Hector C KeunDivision of Cancer, Department of Surgery and Cancer, Imperial College London, Hammersmith Hospital Campus, W12 0NN, London, UK.
Timothy M D EbbelsComputational and Systems Medicine, Department of Surgery and Cancer, Sir Alexander Fleming building, Imperial College, London, SW1 2AZ, UK. t.ebbels@imperial.ac.uk.ORCID http://orcid.org/0000-0002-3372-8423

Funding

FP7 Science in Society 283775Medical Research Council MR/S019669/1
6 · The paper itself

Abstract

backgroundTranscriptomic data is often used to build statistical models which are predictive of a given phenotype, such as disease status. Genes work together in pathways and it is widely thought that pathway representations will be more robust to noise in the gene expression levels. We aimed to test this hypothesis by constructing models based on either genes alone, or based on sample specific scores for each pathway, thus transforming the data to a 'pathway space'. We progressively degraded the raw data by addition of noise and examined the ability of the models to maintain predictivity.

resultsModels in the pathway space indeed had higher predictive robustness than models in the gene space. This result was independent of the workflow, parameters, classifier and data set used. Surprisingly, randomised pathway mappings produced models of similar accuracy and robustness to true mappings, suggesting that the success of pathway space models is not conferred by the specific definitions of the pathway. Instead, predictive models built on the true pathway mappings led to prediction rules with fewer influential pathways than those built on randomised pathways. The extent of this effect was used to differentiate pathway collections coming from a variety of widely used pathway databases.

conclusionsPrediction models based on pathway scores are more robust to degradation of gene expression information than the equivalent models based on ungrouped genes. While models based on true pathway scores are not more robust or accurate than those based on randomised pathways, true pathways produced simpler prediction rules, emphasizing a smaller number of pathways.

Indexed as

Gene Expression ProfilingSignal TransductionComputational BiologyDatabases, FactualGene ExpressionHumansModels, StatisticalPhenotypeTranscriptomePathwaysPredictive modellingRobustness

Identifiers

PMID31684857
PMCPMC6827178

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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.