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Next-generation sequencing in routine brain tumor diagnostics enables an integrated diagnosis and identifies actionable targets

Overview of attention for article published in Acta Neuropathologica, December 2015
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  • In the top 25% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (90th percentile)
  • Above-average Attention Score compared to outputs of the same age and source (64th percentile)

Mentioned by

news
1 news outlet
twitter
3 X users
facebook
1 Facebook page
guideline
1 clinical guideline source

Readers on

mendeley
172 Mendeley
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Article details
Title
Next-generation sequencing in routine brain tumor diagnostics enables an integrated diagnosis and identifies actionable targets
Published in
Acta Neuropathologica, December 2015
DOI 10.1007/s00401-015-1519-8
Pubmed ID
Authors
Abstract

With the number of prognostic and predictive genetic markers in neuro-oncology steadily growing, the need for comprehensive molecular analysis of neuropathology samples has vastly increased. We therefore developed a customized enrichment/hybrid-capture-based next-generation sequencing (NGS) gene panel comprising the entire coding and selected intronic and promoter regions of 130 genes recurrently altered in brain tumors, allowing for the detection of single nucleotide variations, fusions, and copy number aberrations. Optimization of probe design, library generation and sequencing conditions on 150 samples resulted in a 5-workday routine workflow from the formalin-fixed paraffin-embedded sample to neuropathological report. This protocol was applied to 79 retrospective cases with established molecular aberrations for validation and 71 prospective cases for discovery of potential therapeutic targets. Concordance of NGS compared to established, single biomarker methods was 98.0 %, with discrepancies resulting from one case where a TERT promoter mutation was not called by NGS and three ATRX mutations not being detected by Sanger sequencing. Importantly, in samples with low tumor cell content, NGS was able to identify mutant alleles that were not detectable by traditional methods. Information derived from NGS data identified potential targets for experimental therapy in 37/47 (79 %) glioblastomas, 9/10 (90 %) pilocytic astrocytomas, and 5/14 (36 %) medulloblastomas in the prospective target discovery cohort. In conclusion, we present the settings for high-throughput, adaptive next-generation sequencing in routine neuropathology diagnostics. Such an approach will likely become highly valuable in the near future for treatment decision making, as more therapeutic targets emerge and genetic information enters the classification of brain tumors.

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X Demographics

The data shown below were collected from the profiles of 3 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley demographics

Mendeley demographics

The data shown below were compiled from readership statistics for 172 Mendeley readers of this research output. Click here to see the associated Mendeley record.
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Geographical breakdown

Geographical breakdown
Country Count As %
France 1 <1%
Spain 1 <1%
Czechia 1 <1%
Canada 1 <1%
Unknown 168 98%

Demographic breakdown

Readers by professional status
Readers by professional status Count As %
Researcher 31 18%
Student > Ph. D. Student 24 14%
Student > Master 19 11%
Other 13 8%
Student > Doctoral Student 12 7%
Other 31 18%
Unknown 42 24%
Readers by discipline
Readers by discipline Count As %
Medicine and Dentistry 38 22%
Biochemistry, Genetics and Molecular Biology 33 19%
Agricultural and Biological Sciences 15 9%
Neuroscience 10 6%
Computer Science 4 2%
Other 17 10%
Unknown 55 32%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 15. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 10 October 2024.
All research outputs
#2,920,788
of 29,921,878 outputs
Outputs from Acta Neuropathologica
#661
of 2,873 outputs
Outputs of similar age
#38,839
of 408,132 outputs
Outputs of similar age from Acta Neuropathologica
#14
of 39 outputs
Altmetric has tracked 29,921,878 research outputs across all sources so far. Compared to these this one has done particularly well and is in the 90th percentile: it's in the top 10% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 2,873 research outputs from this source. They typically receive a lot more attention than average, with a mean Attention Score of 17.5. This one has done well, scoring higher than 76% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 408,132 tracked outputs that were published within six weeks on either side of this one in any source. This one has done particularly well, scoring higher than 90% of its contemporaries.
We're also able to compare this research output to 39 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 64% of its contemporaries.