Evidence map›Paper›PMID 30401727›Full record

ArticleEMBO molecular medicine2018

Detection of cell-free DNA fragmentation and copy number alterations in cerebrospinal fluid from glioma patients.

Florent Mouliere, Richard Mair, Dineika Chandrananda, Francesco Marass, Christopher G Smith, Jing Su, James Morris, Colin Watts, Kevin M Brindle, Nitzan Rosenfeld

Abstract read
In one paragraph

Article in EMBO molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers.

0numbers the graph read from it
0cells of the map it votes in
115citing 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

115 citing papers in PubMed.

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  17. Advances in laboratory medicine · 2025
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55 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Florent MouliereCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK f.mouliere@vumc.nl kmb1001@cam.ac.uk nitzan.rosenfeld@cruk.cam.ac.uk.ORCID 0000-0001-7043-0514
Richard MairCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
Dineika ChandranandaCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.ORCID 0000-0002-8834-9500
Francesco MarassCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
Christopher G SmithCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
Jing SuCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
James MorrisCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
Colin WattsInstitute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.
Kevin M BrindleCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK f.mouliere@vumc.nl kmb1001@cam.ac.uk nitzan.rosenfeld@cruk.cam.ac.uk.ORCID 0000-0003-3883-6287
Nitzan RosenfeldCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK f.mouliere@vumc.nl kmb1001@cam.ac.uk nitzan.rosenfeld@cruk.cam.ac.uk.ORCID 0000-0002-2825-4788

Funding

Cancer Research UK 16465Cancer Research UK 17242Cancer Research UK 20240Cancer Research UK A11906Cancer Research UK A16465Cancer Research UK A17242Cancer Research UK A20240
6 · The paper itself

Abstract

Glioma is difficult to detect or characterize using current liquid biopsy approaches. Detection of cell-free tumor DNA (cftDNA) in cerebrospinal fluid (CSF) has been proposed as an alternative to detection in plasma. We used shallow whole-genome sequencing (sWGS, at a coverage of < 0.4×) of cell-free DNA from the CSF of 13 patients with primary glioma to determine somatic copy number alterations and DNA fragmentation patterns. This allowed us to determine the presence of cftDNA in CSF without any prior knowledge of point mutations present in the tumor. We also showed that the fragmentation pattern of cell-free DNA in CSF is different from that in plasma. This low-cost screening method provides information on the tumor genome and can be used to target those patients with high levels of cftDNA for further larger-scale sequencing, such as by whole-exome and whole-genome sequencing.

Indexed as

DNA FragmentationCerebrospinal FluidCirculating Tumor DNAGliomaHumansWhole Genome SequencingCirculating Tumor DNAcell‐free DNAcerebrospinal fluidfragmentationgliomashallow WGS

Identifiers

PMID30401727
PMCPMC6284385

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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.