IHNATOVÁ, Ivana, Vlad POPOVICI and Eva BUDINSKÁ. A critical comparison of topology-based pathway analysis methods. Plos one. San Francisco: Public Library Science, 2018, vol. 13, No 1, p. 1-24. ISSN 1932-6203. Available from: https://dx.doi.org/10.1371/journal.pone.0191154.
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Basic information
Original name A critical comparison of topology-based pathway analysis methods
Authors IHNATOVÁ, Ivana (703 Slovakia, belonging to the institution), Vlad POPOVICI (642 Romania, belonging to the institution) and Eva BUDINSKÁ (703 Slovakia, guarantor, belonging to the institution).
Edition Plos one, San Francisco, Public Library Science, 2018, 1932-6203.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10700 1.7 Other natural sciences
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 2.776
RIV identification code RIV/00216224:14310/18:00102453
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1371/journal.pone.0191154
UT WoS 000423416600042
Keywords in English topology-based pathway analysis; gene-set enrichment analysis; pathway analysis; microarrays; RNA-seq
Tags International impact, Reviewed
Changed by Changed by: Mgr. Michaela Hylsová, Ph.D., učo 211937. Changed: 6/12/2018 20:40.
Abstract
One of the aims of high-throughput gene/protein profiling experiments is the identification of biological processes altered between two or more conditions. Pathway analysis is an umbrella term for a multitude of computational approaches used for this purpose. While in the beginning pathway analysis relied on enrichment-based approaches, a newer generation of methods is now available, exploiting pathway topologies in addition to gene/protein expression levels. However, little effort has been invested in their critical assessment with respect to their performance in different experimental setups. Here, we assessed the performance of seven representative methods identifying differentially expressed pathways between two groups of interest based on gene expression data with prior knowledge of pathway topologies: SPIA, PRS, CePa, TAPPA, TopologyGSA, Clipper and DEGraph. We performed a number of controlled experiments that investigated their sensitivity to sample and pathway size, threshold-based filtering of differentially expressed genes, ability to detect target pathways, ability to exploit the topological information and the sensitivity to different preprocessing strategies. We also verified type I error rates and described the influence of overexpression of single genes, gene sets and topological motifs of various sizes on the detection of a pathway as differentially expressed. The results of our experiments demonstrate a wide variability of the tested methods. We provide a set of recommendations for an informed selection of the proper method for a given data analysis task.
Links
EF15_003/0000469, research and development projectName: Cetocoen Plus
LM2015085, research and development projectName: CERIT Scientific Cloud (Acronym: CERIT-SC)
Investor: Ministry of Education, Youth and Sports of the CR, CERIT Scientific Cloud
602901, interní kód MUName: MErCuRIC - A Phase Ib/II study of MEK1/2 inhibitor PD-­‐0325901 with cMET inhibitor PF-­‐02341066 in KRASMT and KRASWT (with aberrant c-­‐MET) Colorectal Cancer Patients (Acronym: MErCuRIC)
Investor: European Union, Cooperation
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