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How is the NPX value calculated in Explore?
What is the Negative Control composed of and how is it used in the data analysis in Olink Explore?
Are there any stopping points during the Explore experiment? Which steps?
What is the main difference between proteomics sequencing using Olink technology compared with traditional DNA sequencing?
How long is the Explore reagents shelf life-time?
What sample types can be used with Olink Explore?
Can customers compare and combine Explore runs with Target 96 or other historical Target 96 studies?
Can customers compare and combine different Explore runs with each other or with other historical Explore studies?
How many samples are needed for an Explore study to provide sufficient power in order to find signification protein signatures? Will power differ between Target 96 and Explore?
What are internal controls and how are they used in the data analysis?