FAQ
Get answers to common questions. Filter by category or search for your specific question. If you cannot find what you are looking for, please contact Olink support, and we’ll reach out as soon as possible.
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| Category | Question | Answer |
|---|---|---|
How can I open the csv export in Excel? | ||
How to handle bimodal or multimodal assays in NPX Map v1.x? | ||
How to handle bimodal or multimodal assays in NPX Signature v2.x? | ||
How to handle longitudinal studies when the upgrade to NPX Signature v2.x is required? | ||
What is an alternative matrix? | ||
What formula is used to calculate intra-plate CV? | ||
What are the recommendations for data below LOD in downstream analysis? | ||
How should data below LLOQ or above ULOQ be used in downstream analysis? | ||
How do I interpret negative NPX values? | ||
How should data with quality control warnings be handled in downstream analysis? | ||
What tools are available to support downstream analysis of Olink data? | ||
How was bridging, normalization, etc. performed in the UKBB study? | ||
Can I compare and combine NPX data from different Olink products? | ||
What are the main differences between Olink Explore 384/3072 and Olink Explore HT? | ||
What software can be used to analyze Olink Reveal, Olink Explore HT and Olink Explore 3072/384? | ||
What are the requirements for Focus panel development? | ||
What is the lead time for Focus panel development? | ||
What is the minimum and maximum number of assays in Focus panel? | ||
I have more than 21 assays that I would like to include in Focus panel development. How can you help me? | ||
Is it possible to include proteins in a Focus panel that are not in Olink’s library? |