| pathprint.Dm.gs {pathprint} | R Documentation |
Pathways and genesets used by pathprint for D. melanogaster arrays, referenced by Entrez Gene ID
pathprint.Dm.gs
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.
data("pathprint.Dm.gs")
pathprint.Dm.gs[grep("ZN175_7728", names(pathprint.Dm.gs))]