IHNATOVÁ, Ivana, Vlad POPOVICI a Eva BUDINSKÁ. A critical comparison of topology-based pathway analysis methods. Plos one. San Francisco: Public Library Science, 2018, roč. 13, č. 1, s. 1-24. ISSN 1932-6203. Dostupné z: https://dx.doi.org/10.1371/journal.pone.0191154.
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Základní údaje
Originální název A critical comparison of topology-based pathway analysis methods
Autoři IHNATOVÁ, Ivana (703 Slovensko, domácí), Vlad POPOVICI (642 Rumunsko, domácí) a Eva BUDINSKÁ (703 Slovensko, garant, domácí).
Vydání Plos one, San Francisco, Public Library Science, 2018, 1932-6203.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 10700 1.7 Other natural sciences
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 2.776
Kód RIV RIV/00216224:14310/18:00102453
Organizační jednotka Přírodovědecká fakulta
Doi http://dx.doi.org/10.1371/journal.pone.0191154
UT WoS 000423416600042
Klíčová slova anglicky topology-based pathway analysis; gene-set enrichment analysis; pathway analysis; microarrays; RNA-seq
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Michaela Hylsová, Ph.D., učo 211937. Změněno: 6. 12. 2018 20:40.
Anotace
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.
Návaznosti
EF15_003/0000469, projekt VaVNázev: Cetocoen Plus
LM2015085, projekt VaVNázev: CERIT Scientific Cloud (Akronym: CERIT-SC)
Investor: Ministerstvo školství, mládeže a tělovýchovy ČR, CERIT Scientific Cloud
602901, interní kód MUNázev: 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 (Akronym: MErCuRIC)
Investor: Evropská unie, 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, Spolupráce
VytisknoutZobrazeno: 24. 8. 2024 10:29