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CANEapp: a user-friendly application for automated next generation transcriptomic data analysis

Overview of attention for article published in BMC Genomics, January 2016
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About this Attention Score

  • Good Attention Score compared to outputs of the same age (74th percentile)
  • Good Attention Score compared to outputs of the same age and source (74th percentile)

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8 X users
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1 Facebook page

Citations

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13 Dimensions

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71 Mendeley
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2 CiteULike
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Title
CANEapp: a user-friendly application for automated next generation transcriptomic data analysis
Published in
BMC Genomics, January 2016
DOI 10.1186/s12864-015-2346-y
Pubmed ID
Authors

Dmitry Velmeshev, Patrick Lally, Marco Magistri, Mohammad Ali Faghihi

Abstract

Next generation sequencing (NGS) technologies are indispensable for molecular biology research, but data analysis represents the bottleneck in their application. Users need to be familiar with computer terminal commands, the Linux environment, and various software tools and scripts. Analysis workflows have to be optimized and experimentally validated to extract biologically meaningful data. Moreover, as larger datasets are being generated, their analysis requires use of high-performance servers. To address these needs, we developed CANEapp (application for Comprehensive automated Analysis of Next-generation sequencing Experiments), a unique suite that combines a Graphical User Interface (GUI) and an automated server-side analysis pipeline that is platform-independent, making it suitable for any server architecture. The GUI runs on a PC or Mac and seamlessly connects to the server to provide full GUI control of RNA-sequencing (RNA-seq) project analysis. The server-side analysis pipeline contains a framework that is implemented on a Linux server through completely automated installation of software components and reference files. Analysis with CANEapp is also fully automated and performs differential gene expression analysis and novel noncoding RNA discovery through alternative workflows (Cuffdiff and R packages edgeR and DESeq2). We compared CANEapp to other similar tools, and it significantly improves on previous developments. We experimentally validated CANEapp's performance by applying it to data derived from different experimental paradigms and confirming the results with quantitative real-time PCR (qRT-PCR). CANEapp adapts to any server architecture by effectively using available resources and thus handles large amounts of data efficiently. CANEapp performance has been experimentally validated on various biological datasets. CANEapp is available free of charge at http://psychiatry.med.miami.edu/research/laboratory-of-translational-rna-genomics/CANE-app . We believe that CANEapp will serve both biologists with no computational experience and bioinformaticians as a simple, timesaving but accurate and powerful tool to analyze large RNA-seq datasets and will provide foundations for future development of integrated and automated high-throughput genomics data analysis tools. Due to its inherently standardized pipeline and combination of automated analysis and platform-independence, CANEapp is an ideal for large-scale collaborative RNA-seq projects between different institutions and research groups.

X Demographics

X Demographics

The data shown below were collected from the profiles of 8 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 71 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 5 7%
Germany 1 1%
Chile 1 1%
Switzerland 1 1%
United Kingdom 1 1%
Luxembourg 1 1%
Unknown 61 86%

Demographic breakdown

Readers by professional status Count As %
Researcher 22 31%
Student > Ph. D. Student 12 17%
Student > Doctoral Student 11 15%
Student > Master 6 8%
Student > Postgraduate 4 6%
Other 10 14%
Unknown 6 8%
Readers by discipline Count As %
Agricultural and Biological Sciences 27 38%
Biochemistry, Genetics and Molecular Biology 13 18%
Computer Science 12 17%
Engineering 4 6%
Environmental Science 2 3%
Other 4 6%
Unknown 9 13%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 5. 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 06 June 2016.
All research outputs
#6,714,896
of 24,406,515 outputs
Outputs from BMC Genomics
#2,750
of 10,975 outputs
Outputs of similar age
#103,032
of 404,868 outputs
Outputs of similar age from BMC Genomics
#62
of 254 outputs
Altmetric has tracked 24,406,515 research outputs across all sources so far. This one has received more attention than most of these and is in the 72nd percentile.
So far Altmetric has tracked 10,975 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 74% 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 404,868 tracked outputs that were published within six weeks on either side of this one in any source. This one has gotten more attention than average, scoring higher than 74% of its contemporaries.
We're also able to compare this research output to 254 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 74% of its contemporaries.