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Exon Array Design
FREQUENTLY ASKED QUESTIONS
How is this array design principle different from the GeneChip® Human Genome U133 type of arrays?
What is the length of each Probe Selection Region (PSR)?
What is the difference between a PSR and an Exon?
Are all PSRs represented by 4 probes?
Are there junction probes?
It seems that the probes may overlap heavily within a given PSR, how is this managed?
What type of alternative splicing events are you able to interrogate with this design?
On average, how many probes are used to represent a corresponding GeneChip® Human Genome U133 (HG-U133) Array probe set where there are 11 probe pairs?
Are all of the content sources taken into consideration to define the probe selection regions and how many of the PSRs are only supported by a single type of content?
If all sources are taken into consideration for the array design, will that result in over-fragmentation of the PSRs?
Which controls are included in the new array?
Will the probe and target sequences be made available?
What kinds of annotation will be available?
Can I use this Human Exon Array to detect the expression of microRNAs?
Are mitochondrial RNAs represented on this Human Exon Array?