Data
- 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?