Main menu

Discovering the missing variation: a long read sequencing study into the structural variation in two dairy breeds


Structural variants (SVs) play a substantial role in the evolution of species and have an impact on Mendelian and quantitative traits in mammals. However, SVs have been challenging to accurately identify and genotype at population scale using short-read sequencing. Long-read sequencing technologies are becoming competitively priced and can address several of the disadvantages of short-read for the discovery and genotyping of SVs. In this study, we ran a pilot population scale study to catalogue the SVs in a cohort of Holstein & Jersey cattle.

Download the PDF

Getting started

Buy a MinION starter pack Nanopore store Sequencing service providers Channel partners

Quick links

Intellectual property Cookie policy Corporate reporting Privacy policy Terms & conditions Accessibility

About Oxford Nanopore

Contact us News Media resources & contacts Investor centre Careers BSI 27001 accreditationBSI 90001 accreditationBSI mark of trust
Spanish flag