TY - GEN
T1 - enRoute
T2 - 2nd IEEE Symposium on Biological Data Visualization, BioVis 2012
AU - Partl, Christian
AU - Lex, Alexander
AU - Streit, Marc
AU - Kalkofen, Denis
AU - Kashofer, Karl
AU - Schmalstieg, Dieter
PY - 2012/12/13
Y1 - 2012/12/13
N2 - Pathway maps are an important source of information when analyzing functional implications of experimental data on biological processes. However, associating large quantities of data with nodes on a pathway map and allowing in depth-analysis at the same time is a challenging task. While a wide variety of approaches for doing so exist, they either do not scale beyond a few experiments or fail to represent the pathway appropriately. To remedy this, we introduce enRoute, a new approach for interactively exploring experimental data along paths that are dynamically extracted from pathways. By showing an extracted path side-by-side with experimental data, enRoute can present large amounts of data for every pathway node. It can visualize hundreds of samples, dozens of experimental conditions, and even multiple datasets capturing different aspects of a node at the same time. Another important property of this approach is its conceptual compatibility with arbitrary forms of pathways. Most notably, enRoute works well with pathways that are manually created, as they are available in large, public pathway databases. We demonstrate enRoute with pathways from the well-established KEGG database and expression as well as copy number datasets from humans and mice with more than 1,000 experiments. We validate enRoute using case studies with domain experts, who used enRoute to explore data for glioblastoma multiforme in humans and a model of steatohepatitis in mice.
AB - Pathway maps are an important source of information when analyzing functional implications of experimental data on biological processes. However, associating large quantities of data with nodes on a pathway map and allowing in depth-analysis at the same time is a challenging task. While a wide variety of approaches for doing so exist, they either do not scale beyond a few experiments or fail to represent the pathway appropriately. To remedy this, we introduce enRoute, a new approach for interactively exploring experimental data along paths that are dynamically extracted from pathways. By showing an extracted path side-by-side with experimental data, enRoute can present large amounts of data for every pathway node. It can visualize hundreds of samples, dozens of experimental conditions, and even multiple datasets capturing different aspects of a node at the same time. Another important property of this approach is its conceptual compatibility with arbitrary forms of pathways. Most notably, enRoute works well with pathways that are manually created, as they are available in large, public pathway databases. We demonstrate enRoute with pathways from the well-established KEGG database and expression as well as copy number datasets from humans and mice with more than 1,000 experiments. We validate enRoute using case studies with domain experts, who used enRoute to explore data for glioblastoma multiforme in humans and a model of steatohepatitis in mice.
KW - biological processes
KW - cellular networks
KW - copy number variation
KW - expression data
KW - path extraction
KW - Pathway analysis
UR - http://www.scopus.com/inward/record.url?scp=84872237748&partnerID=8YFLogxK
U2 - 10.1109/BioVis.2012.6378600
DO - 10.1109/BioVis.2012.6378600
M3 - Conference contribution
AN - SCOPUS:84872237748
SN - 9781467347303
T3 - IEEE Symposium on Biological Data Visualization 2012, BioVis 2012 - Proceedings
SP - 107
EP - 114
BT - IEEE Symposium on Biological Data Visualization 2012, BioVis 2012 - Proceedings
PB - Institute of Electrical and Electronics Engineers
Y2 - 14 October 2012 through 19 October 2012
ER -