This is a function to map a probe to annotated nucleotide sequence file.
You can read the probe file and map it to the origin position on the current genome sequence.
When there is position information on the genome, paste the probe feature to the corresponding genome position based on the position information of each probe.
If position information does not exist and only the base sequence of the probe is given, mapping is performed based on the homology of the probe base sequence.
Currently mappable probes belong to the following array makers.
This function can be executed with the following edition.
AE, DS, GT