Evidence map›Paper›PMID 35788693›Full record

ArticleNPJ digital medicine2022

Cross-Platform Omics Prediction procedure: a statistical machine learning framework for wider implementation of precision medicine.

Kevin Y X Wang, Gulietta M Pupo, Varsha Tembe, Ellis Patrick, Dario Strbenac, Sarah-Jane Schramm, John F Thompson, Richard A Scolyer, Samuel Muller, Garth Tarr and 2 more

Abstract read
In one paragraph

Article in NPJ digital medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 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

12 authors.

Kevin Y X WangCharles Perkins Centre, The University of Sydney, Sydney, NSW, 2006, Australia.
Gulietta M PupoThe Westmead Institute for Medical Research, The University of Sydney, Sydney, NSW, 2006, Australia.
Varsha TembeThe Westmead Institute for Medical Research, The University of Sydney, Sydney, NSW, 2006, Australia.
Ellis PatrickCharles Perkins Centre, The University of Sydney, Sydney, NSW, 2006, Australia.
Dario StrbenacCharles Perkins Centre, The University of Sydney, Sydney, NSW, 2006, Australia.
Sarah-Jane SchrammThe Westmead Institute for Medical Research, The University of Sydney, Sydney, NSW, 2006, Australia.
John F ThompsonMelanoma Institute Australia, The University of Sydney, North Sydney, NSW, 2006, Australia.
Richard A ScolyerCharles Perkins Centre, The University of Sydney, Sydney, NSW, 2006, Australia.ORCID http://orcid.org/0000-0002-8991-0013
Samuel MullerSchool of Mathematics and Statistics, The University of Sydney, Sydney, NSW, 2006, Australia.ORCID http://orcid.org/0000-0002-3087-8127
Garth TarrSchool of Mathematics and Statistics, The University of Sydney, Sydney, NSW, 2006, Australia.ORCID http://orcid.org/0000-0002-6605-7478
Graham J MannThe Westmead Institute for Medical Research, The University of Sydney, Sydney, NSW, 2006, Australia. graham.mann@anu.edu.au.
Jean Y H YangCharles Perkins Centre, The University of Sydney, Sydney, NSW, 2006, Australia. jean.yang@sydney.edu.au.ORCID http://orcid.org/0000-0002-5271-2603

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this modern era of precision medicine, molecular signatures identified from advanced omics technologies hold great promise to better guide clinical decisions. However, current approaches are often location-specific due to the inherent differences between platforms and across multiple centres, thus limiting the transferability of molecular signatures. We present Cross-Platform Omics Prediction (CPOP), a penalised regression model that can use omics data to predict patient outcomes in a platform-independent manner and across time and experiments. CPOP improves on the traditional prediction framework of using gene-based features by selecting ratio-based features with similar estimated effect sizes. These components gave CPOP the ability to have a stable performance across datasets of similar biology, minimising the effect of technical noise often generated by omics platforms. We present a comprehensive evaluation using melanoma transcriptomics data to demonstrate its potential to be used as a critical part of a clinical screening framework for precision medicine. Additional assessment of generalisation was demonstrated with ovarian cancer and inflammatory bowel disease studies.

Identifiers

PMID35788693
PMCPMC9253123

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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.