PMIDAmat | R Documentation |
For a given chip or a given set of genes, it computes the mapping from probes to PubMed id.
PMIDAmat(pkg, gene=NULL)
pkg |
The package name of the chip for which the incidence matrix should be computed. |
gene |
A character vector of interested probe set ids or NULL (default). |
Not much to say, just find which probes are associated with which PubMed ids and return the incidence matrix, with PubMed ids as rows and probes as columns.
To specify a set of probes to use, let the argument gene
to be
a vector of probe ids. Bt this way, the calculations are not
involved with non-interested genes/PubMed ids so that the whole
process could finish soon.
A matrix containing zero or one, depending on whether the probe (column) is associated with a PubMed id (row).
R. Gentleman
library("hgu95av2.db")
probe <- names(as.list(hgu95av2ACCNUM))
Amat <- PMIDAmat("hgu95av2", gene=sample(probe, 10))
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