Description Usage Details Source References Examples
Pathways and genesets used by pathprint for R. norvegicus arrays, referenced by Entrez Gene ID
1 |
Gene sets were inferred by homology from the human genesets,
pathprint.Hs.gs
,
using the HomoloGene database, www.ncbi.nlm.nih.gov/homologene
O. Hofmann
Sayers et al. Database resources of the National Center for Biotechnology
Information. Nucleic Acids Research (2011) vol. 39 (Database issue) pp. D38-51
Altschuler, G. M., O. Hofmann, I. Kalatskaya, R. Payne, S. J. Ho Sui,
U. Saxena, A. V. Krivtsov, S. A. Armstrong, T. Cai, L. Stein
and W. A. Hide (2013). "Pathprinting: An integrative approach to understand the
functional basis of disease." Genome Med 5(7): 68.
1 2 | data("pathprint.Rn.gs")
pathprint.Rn.gs[grep("ZN175_7728", names(pathprint.Rn.gs))]
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