↓ Skip to main content

A Review of Pathway-Based Analysis Tools That Visualize Genetic Variants

Overview of attention for article published in Frontiers in Genetics, November 2017
Altmetric Badge

About this Attention Score

  • In the top 5% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (93rd percentile)
  • High Attention Score compared to outputs of the same age and source (95th percentile)

Mentioned by

twitter
62 X users

Citations

dimensions_citation
65 Dimensions

Readers on

mendeley
242 Mendeley
citeulike
1 CiteULike
You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output. Click here to find out more.
Title
A Review of Pathway-Based Analysis Tools That Visualize Genetic Variants
Published in
Frontiers in Genetics, November 2017
DOI 10.3389/fgene.2017.00174
Pubmed ID
Authors

Elisa Cirillo, Laurence D. Parnell, Chris T. Evelo

Abstract

Pathway analysis is a powerful method for data analysis in genomics, most often applied to gene expression analysis. It is also promising for single-nucleotide polymorphism (SNP) data analysis, such as genome-wide association study data, because it allows the interpretation of variants with respect to the biological processes in which the affected genes and proteins are involved. Such analyses support an interactive evaluation of the possible effects of variations on function, regulation or interaction of gene products. Current pathway analysis software often does not support data visualization of variants in pathways as an alternate method to interpret genetic association results, and specific statistical methods for pathway analysis of SNP data are not combined with these visualization features. In this review, we first describe the visualization options of the tools that were identified by a literature review, in order to provide insight for improvements in this developing field. Tool evaluation was performed using a computational epistatic dataset of gene-gene interactions for obesity risk. Next, we report the necessity to include in these tools statistical methods designed for the pathway-based analysis with SNP data, expressly aiming to define features for more comprehensive pathway-based analysis tools. We conclude by recognizing that pathway analysis of genetic variations data requires a sophisticated combination of the most useful and informative visual aspects of the various tools evaluated.

X Demographics

X Demographics

The data shown below were collected from the profiles of 62 X users who shared this research output. Click here to find out more about how the information was compiled.
As of 1 July 2024, you may notice a temporary increase in the numbers of X profiles with Unknown location. Click here to learn more.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 242 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 242 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 52 21%
Researcher 45 19%
Student > Master 29 12%
Student > Bachelor 17 7%
Other 13 5%
Other 31 13%
Unknown 55 23%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 59 24%
Agricultural and Biological Sciences 45 19%
Medicine and Dentistry 17 7%
Computer Science 16 7%
Pharmacology, Toxicology and Pharmaceutical Science 8 3%
Other 34 14%
Unknown 63 26%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 35. 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 23 July 2021.
All research outputs
#1,213,326
of 26,408,359 outputs
Outputs from Frontiers in Genetics
#205
of 13,962 outputs
Outputs of similar age
#24,049
of 347,059 outputs
Outputs of similar age from Frontiers in Genetics
#4
of 93 outputs
Altmetric has tracked 26,408,359 research outputs across all sources so far. Compared to these this one has done particularly well and is in the 95th percentile: it's in the top 5% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 13,962 research outputs from this source. They receive a mean Attention Score of 3.9. This one has done particularly well, scoring higher than 98% 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 347,059 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 93% of its contemporaries.
We're also able to compare this research output to 93 others from the same source and published within six weeks on either side of this one. This one has done particularly well, scoring higher than 95% of its contemporaries.