Evidence map›Paper›PMID 29281963›Full record

ArticleBMC bioinformatics2017

Improved high-dimensional prediction with Random Forests by the use of co-data.

Dennis E Te Beest, Steven W Mes, Saskia M Wilting, Ruud H Brakenhoff, Mark A van de Wiel

Abstract read
In one paragraph

Article in BMC bioinformatics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Penalized regression with multiple sources of prior effects.Bioinformatics (Oxford, England) · 2023
    Article
  5. Article
  6. Semi-supervised empirical Bayes group-regularized factor regression.Biometrical journal. Biometrische Zeitschrift · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Learning from a lot: Empirical Bayes for high-dimensional model-based prediction.Scandinavian journal of statistics, theory and applications · 2019
    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

5 authors.

Dennis E Te BeestDepartment of Epidemiology and Biostatistics, VU University Medical Center, Amsterdam, 1007 MB, The Netherlands.
Steven W MesDepartment of Otolaryngology-Head and Neck Surgery, VU University Medical Center, Amsterdam, 1007 MB, The Netherlands.
Saskia M WiltingDepartment of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, 3015 CE, The Netherlands.
Ruud H BrakenhoffDepartment of Otolaryngology-Head and Neck Surgery, VU University Medical Center, Amsterdam, 1007 MB, The Netherlands.
Mark A van de WielDepartment of Epidemiology and Biostatistics, VU University Medical Center, Amsterdam, 1007 MB, The Netherlands. mark.vdwiel@vumc.nl.

Funding

European Research Council 322986FP7 Ideas: European Research Council (BE) 611425Horizon 2020 Framework Programme 689715
6 · The paper itself

Abstract

backgroundPrediction in high dimensional settings is difficult due to the large number of variables relative to the sample size. We demonstrate how auxiliary 'co-data' can be used to improve the performance of a Random Forest in such a setting.

resultsCo-data are incorporated in the Random Forest by replacing the uniform sampling probabilities that are used to draw candidate variables by co-data moderated sampling probabilities. Co-data here are defined as any type information that is available on the variables of the primary data, but does not use its response labels. These moderated sampling probabilities are, inspired by empirical Bayes, learned from the data at hand. We demonstrate the co-data moderated Random Forest (CoRF) with two examples. In the first example we aim to predict the presence of a lymph node metastasis with gene expression data. We demonstrate how a set of external p-values, a gene signature, and the correlation between gene expression and DNA copy number can improve the predictive performance. In the second example we demonstrate how the prediction of cervical (pre-)cancer with methylation data can be improved by including the location of the probe relative to the known CpG islands, the number of CpG sites targeted by a probe, and a set of p-values from a related study.

conclusionThe proposed method is able to utilize auxiliary co-data to improve the performance of a Random Forest.

Indexed as

AlgorithmsDatabases as TopicBayes TheoremHumansNeoplasmsROC CurveTime FactorsClassificationDNA copy numberGene expressionMethylationPrior informationRandom forest

Identifiers

PMID29281963
PMCPMC5745983

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.