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Data Analysis
FREQUENTLY ASKED QUESTIONS
What is the difference between scaling and normalization when I scale or normalize my data to all genes on the array?
How can the Mismatch probe cell have a higher intensity than its complementary Perfect Match probe cell?
How important is it to evaluate the value of the Scaling Factor between different arrays?
What does high background mean?
Why can't I analyze data files stored on a CD?
How can the mismatch probe cell have a higher intensity than its corresponding perfect match probe cell?
Which is greater, sample or assay variability?
Can I run Affymetrix software on Windows XP?