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How is the Limit of Detection (LOD) estimated and how is this handled in the data analysis?
Should I dilute my samples before shipping them to Olink?
How many replicates of each sample are analyzed?
Why do the negative control and interplate control samples flag/not pass the quality control (QC)?
Why is the limit for a sample passing or failing the quality control set to +/- 0.3NPX of the plate median for Incubation control 2 and the detection control?
What is the maximum sample throughput for Olink Target?
Where can I find a standard curve for the proteins I have run?
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?
Why would a sample not pass quality control in only one out of several panels run?
Protein data points generated
Publications listed on website