So the two datasets are on similar patterns and so the same IDs are present in both.
However, the signals vary by a factor of 10:
Pepper Ave Signal: 184
Huttmann Ave Signal: 1725
That makes averaging the data as presented impossible.
Could do some kind of standardization to try to average or could do separate averages for the two data sets.
Could try calibrating with some known proteins....
Ideas here:
some high expressing proteins (actin, et al)
some prognostic markers CD38
Zap-70
Some important functional molecules
p50
mcl-1
others....
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