August 19, 2021  |  Whitepapers

Whitepaper: Structural variation in the human genome

Structural variation accounts for much of the variation among human genomes. Structural variants of all types are known to cause Mendelian disease and contribute to complex disease. Learn how long-read sequencing is enabling detection of the full spectrum of structural variants to advance the study of human disease, evolution and genetic diversity.

Download File

 

Talk with an expert

If you have a question, need to check the status of an order, or are interested in purchasing an instrument, we're here to help.