How is quality control of the data performed?

How is the Limit of Detection (LOD) estimated and how is this handled in the data analysis?

How do I convert my NPX-values into linearized data?

Where can I find a standard curve for the proteins I have run?

What is NPX Manager?

How should data from overlapping analytes/proteins be handled?

How is %CV calculated?

Why do some of your biomarkers have several Uniprot numbers?

How is it determined whether a sample has failed quality control because of operator error or due to some property of the sample?

I see that the same protein can be measured by more than one panel, are these the same assay?