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.
xGen NGS—made for you.
Unsure of what products are available? Or, perhaps you’d like guidance on which products are compatible? If so, try our xGen NGS Solutions Builder Tool today.
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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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For genotyping applications, what is the recommended minimum sequencing coverage per assay?
We recommend a minimum of 20 reads to accurately call genotypes in diploid species with heterozygosity (i.e., 50% allele frequencies).
For polyploid species or somatic mutations with lower allele frequencies, your minimum coverage may need to be higher.