Your product is now available from Integrated DNA Technologies.
Many of the Swift products you have grown to love are now part of our new complete portfolio, xGen™ NGS. Through this new partnership we are pleased to offer you comprehensive next generation sequencing solutions.
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Frequently asked questions
Our Scientific Applications Support team has assembled a list of frequently asked questions to help you find answers quickly. Filter using one or more categories to focus on specific topics, or use the search bar to perform a text search.
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What causes variation of read counts (CV > 10%) among libraries within Normalase™ pools?
There are several causes for this which may include:
Libraries not meeting the 6 nM or 12 nM minimum threshold in 20 µL library yield
Sequencer overloading and subsequent over-clustering resulting in low sequencing quality