Evidence map›Paper›PMID 28061752›Full record

ArticleBMC genomics2017

Enumerateblood - an R package to estimate the cellular composition of whole blood from Affymetrix Gene ST gene expression profiles.

Casey P Shannon, Robert Balshaw, Virginia Chen, Zsuzsanna Hollander, Mustafa Toma, Bruce M McManus, J Mark FitzGerald, Don D Sin, Raymond T Ng, Scott J Tebbutt

Abstract read
In one paragraph

Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

10 authors.

Casey P ShannonPROOF Centre of Excellence, Vancouver, BC, Canada. casey.shannon@hli.ubc.ca.
Robert BalshawPROOF Centre of Excellence, Vancouver, BC, Canada.
Virginia ChenPROOF Centre of Excellence, Vancouver, BC, Canada.
Zsuzsanna HollanderPROOF Centre of Excellence, Vancouver, BC, Canada.
Mustafa TomaDivision of Cardiology, University of British Columbia, Vancouver, BC, Canada.
Bruce M McManusPROOF Centre of Excellence, Vancouver, BC, Canada.
J Mark FitzGeraldDepartment of Medicine, Division of Respiratory Medicine, University of British Columbia, Vancouver, BC, Canada.
Don D SinDepartment of Medicine, Division of Respiratory Medicine, University of British Columbia, Vancouver, BC, Canada.
Raymond T NgPROOF Centre of Excellence, Vancouver, BC, Canada.
Scott J TebbuttPROOF Centre of Excellence, Vancouver, BC, Canada.

Funding

CIHR
6 · The paper itself

Abstract

backgroundMeasuring genome-wide changes in transcript abundance in circulating peripheral whole blood is a useful way to study disease pathobiology and may help elucidate the molecular mechanisms of disease, or discovery of useful disease biomarkers. The sensitivity and interpretability of analyses carried out in this complex tissue, however, are significantly affected by its dynamic cellular heterogeneity. It is therefore desirable to quantify this heterogeneity, either to account for it or to better model interactions that may be present between the abundance of certain transcripts, specific cell types and the indication under study. Accurate enumeration of the many component cell types that make up peripheral whole blood can further complicate the sample collection process, however, and result in additional costs. Many approaches have been developed to infer the composition of a sample from high-dimensional transcriptomic and, more recently, epigenetic data. These approaches rely on the availability of isolated expression profiles for the cell types to be enumerated. These profiles are platform-specific, suitable datasets are rare, and generating them is expensive. No such dataset exists on the Affymetrix Gene ST platform.

resultsWe present 'Enumerateblood', a freely-available and open source R package that exposes a multi-response Gaussian model capable of accurately predicting the composition of peripheral whole blood samples from Affymetrix Gene ST expression profiles, outperforming other current methods when applied to Gene ST data.

conclusions'Enumerateblood' significantly improves our ability to study disease pathobiology from whole blood gene expression assayed on the popular Affymetrix Gene ST platform by allowing a more complete study of the various components of this complex tissue without the need for additional data collection. Future use of the model may allow for novel insights to be generated from the ~400 Affymetrix Gene ST blood gene expression datasets currently available on the Gene Expression Omnibus (GEO) website.

Indexed as

Gene Expression ProfilingMachine LearningBlood CellsGenomicsHumansModels, Statistical

Identifiers

PMID28061752
PMCPMC5219701

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LicenceCC BY
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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.