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CVE: an R package for interactive variant prioritisation in precision oncology

Overview of attention for article published in BMC Medical Genomics, May 2017
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45 Mendeley
Title
CVE: an R package for interactive variant prioritisation in precision oncology
Published in
BMC Medical Genomics, May 2017
DOI 10.1186/s12920-017-0261-6
Pubmed ID
Authors

Andreas Mock, Suzanne Murphy, James Morris, Francesco Marass, Nitzan Rosenfeld, Charlie Massie

Abstract

An increasing number of precision oncology programmes are being launched world-wide. To support this development, we present the Cancer Variant Explorer (CVE), an R package with an interactive Shiny web browser interface. Leveraging Oncotator and the Drug Gene Interaction Database, CVE offers exploration of variants within single or multiple tumour exomes to identify drivers, resistance mechanisms and to assess druggability. We present example applications including the analysis of an individual patient and a cohort-wide study, and provide a first extension of CVE by adding a tumour-specific co-expression network. The CVE package allows interactive variant prioritisation to expedite the analysis of cancer sequencing studies. Our framework also includes the prioritisation of druggable targets, allows exploratory analysis of tissue specific networks and is extendable for specific applications by virtue of its modular design. We encourage the use of CVE within translational research studies and molecular tumour boards. The CVE package is available via Bioconductor ( http://bioconductor.org/packages/CVE/ ).

X Demographics

X Demographics

The data shown below were collected from the profiles of 4 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 45 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Taiwan 1 2%
Unknown 44 98%

Demographic breakdown

Readers by professional status Count As %
Researcher 18 40%
Student > Ph. D. Student 10 22%
Other 5 11%
Student > Bachelor 3 7%
Student > Master 2 4%
Other 2 4%
Unknown 5 11%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 13 29%
Agricultural and Biological Sciences 7 16%
Medicine and Dentistry 6 13%
Computer Science 4 9%
Design 2 4%
Other 8 18%
Unknown 5 11%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. 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 05 March 2018.
All research outputs
#13,555,965
of 22,977,819 outputs
Outputs from BMC Medical Genomics
#506
of 1,229 outputs
Outputs of similar age
#160,214
of 313,676 outputs
Outputs of similar age from BMC Medical Genomics
#10
of 17 outputs
Altmetric has tracked 22,977,819 research outputs across all sources so far. This one is in the 39th percentile – i.e., 39% of other outputs scored the same or lower than it.
So far Altmetric has tracked 1,229 research outputs from this source. They receive a mean Attention Score of 4.8. This one has gotten more attention than average, scoring higher than 56% 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 313,676 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 47th percentile – i.e., 47% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 17 others from the same source and published within six weeks on either side of this one. This one is in the 41st percentile – i.e., 41% of its contemporaries scored the same or lower than it.