For a given chip or a given set of genes, it computes the mapping from probes to PubMed id.
The package name of the chip for which the incidence matrix should be computed.
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).
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