Evidence map›Paper›PMID 26482909›Full record

ArticleScientific reports2015

Genome-wide DNA methylation detection by MethylCap-seq and Infinium HumanMethylation450 BeadChips: an independent large-scale comparison.

Tim De Meyer, Pierre Bady, Geert Trooskens, Sebastian Kurscheid, Jocelyne Bloch, Johan M Kros, Johannes A Hainfellner, Roger Stupp, Mauro Delorenzi, Monika E Hegi and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 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

11 authors.

Tim De MeyerDept. of Mathematical Modelling, Statistics and Bioinformatics, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.
Pierre BadyLab. of Brain Tumor Biology and Genetics, Department of Clinical Neurosciences, University Hospital Lausanne, Lausanne, Switzerland.
Geert TrooskensDept. of Mathematical Modelling, Statistics and Bioinformatics, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.
Sebastian KurscheidLab. of Brain Tumor Biology and Genetics, Department of Clinical Neurosciences, University Hospital Lausanne, Lausanne, Switzerland.
Jocelyne BlochNeurosurgery, Department of Clinical Neurosciences, University Hospital Lausanne, Lausanne, Switzerland.
Johan M KrosDivision of Neuropathology, University Hospital Rotterdam, Rotterdam, The Netherlands.
Johannes A HainfellnerInstitute of Neurology, Medical University of Vienna, Vienna, Austria.
Roger StuppNeurosurgery, Department of Clinical Neurosciences, University Hospital Lausanne, Lausanne, Switzerland.
Mauro DelorenziSwiss Institute of Bioinformatics, Lausanne, Switzerland.
Monika E HegiLab. of Brain Tumor Biology and Genetics, Department of Clinical Neurosciences, University Hospital Lausanne, Lausanne, Switzerland.
Wim Van CriekingeDept. of Mathematical Modelling, Statistics and Bioinformatics, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two cost-efficient genome-scale methodologies to assess DNA-methylation are MethylCap-seq and Illumina's Infinium HumanMethylation450 BeadChips (HM450). Objective information regarding the best-suited methodology for a specific research question is scant. Therefore, we performed a large-scale evaluation on a set of 70 brain tissue samples, i.e. 65 glioblastoma and 5 non-tumoral tissues. As MethylCap-seq coverages were limited, we focused on the inherent capacity of the methodology to detect methylated loci rather than a quantitative analysis. MethylCap-seq and HM450 data were dichotomized and performances were compared using a gold standard free Bayesian modelling procedure. While conditional specificity was adequate for both approaches, conditional sensitivity was systematically higher for HM450. In addition, genome-wide characteristics were compared, revealing that HM450 probes identified substantially fewer regions compared to MethylCap-seq. Although results indicated that the latter method can detect more potentially relevant DNA-methylation, this did not translate into the discovery of more differentially methylated loci between tumours and controls compared to HM450. Our results therefore indicate that both methodologies are complementary, with a higher sensitivity for HM450 and a far larger genome-wide coverage for MethylCap-seq, but also that a more comprehensive character does not automatically imply more significant results in biomarker studies.

Indexed as

DNA MethylationEpigenesis, GeneticEpigenomicsGenome-Wide Association StudyAllelesCase-Control StudiesComputational BiologyCpG IslandsGlioblastomaHumansMolecular Sequence AnnotationSensitivity and Specificity

Identifiers

PMID26482909
PMCPMC4612737

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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.