Evidence map›Paper›PMID 25387159›Full record

ArticleOmics : a journal of integrative biology2014

Novel multivariate methods for integration of genomics and proteomics data: applications in a kidney transplant rejection study.

Oliver P Günther, Heesun Shin, Raymond T Ng, W Robert McMaster, Bruce M McManus, Paul A Keown, Scott J Tebbutt, Kim-Anh Lê Cao

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In one paragraph

Article in Omics : a journal of integrative biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

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0cells of the map it votes in
24citing 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

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3 · Its place in the literature

Who cites it

24 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

8 authors.

Oliver P Günther1 NCE CECR Prevention of Organ Failure (PROOF) Centre of Excellence , Vancouver, British Columbia, Canada .
Heesun Shin
Raymond T Ng
W Robert McMaster
Bruce M McManus
Paul A Keown
Scott J Tebbutt
Kim-Anh Lê Cao

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multi-omics research is a key ingredient of data-intensive life sciences research, permitting measurement of biological molecules at different functional levels in the same individual. For a complete picture at the biological systems level, appropriate statistical techniques must however be developed to integrate different 'omics' data sets (e.g., genomics and proteomics). We report here multivariate projection-based analyses approaches to genomics and proteomics data sets, using the case study of and applications to observations in kidney transplant patients who experienced an acute rejection event (n=20) versus non-rejecting controls (n=20). In this data sets, we show how these novel methodologies might serve as promising tools for dimension reduction and selection of relevant features for different analytical frameworks. Unsupervised analyses highlighted the importance of post transplant time-of-rejection, while supervised analyses identified gene and protein signatures that together predicted rejection status with little time effect. The selected genes are part of biological pathways that are representative of immune responses. Gene enrichment profiles revealed increases in innate immune responses and neutrophil activities and a depletion of T lymphocyte related processes in rejection samples as compared to controls. In all, this article offers candidate biomarkers for future detection and monitoring of acute kidney transplant rejection, as well as ways forward for methodological advances to better harness multi-omics data sets.

Indexed as

AdultBiomarkersFemaleGenomicsGraft RejectionHumansKidney TransplantationMaleMiddle AgedMultivariate AnalysisProteomicsResearch DesignBiomarkers

Identifiers

PMID25387159
PMCPMC4229708

What OpenQuestion holds

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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.