Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

The advent of next generation sequencing technologies has opened new possibilities in the analysis of human disease. In this review we present the main next-generation sequencing technologies, with their major contributions and possible applications to the study of the genetic etiology of complex diseases.

Original publication

DOI

10.1016/j.jneuroim.2011.12.017

Type

Journal article

Journal

Journal of neuroimmunology

Publication Date

07/2012

Volume

248

Pages

10 - 22

Addresses

Centre de Recherche du Centre Hospitalier Universitaire Sainte-Justine, Université de Montréal, Montréal, Québec, Canada. ferrancasalslopez@gmail.com

Keywords

Humans, Genetic Diseases, Inborn, Genetic Predisposition to Disease, Chromosome Mapping, Sequence Analysis, DNA, Genotyping Techniques