Sample preparation for small RNA massive parallel sequencing.

Autor: Gommans WM; InteRNA Technologies BV, Utrecht, The Netherlands. gommans@interna-technologies.com, Berezikov E
Jazyk: angličtina
Zdroj: Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2012; Vol. 786, pp. 167-78.
DOI: 10.1007/978-1-61779-292-2_10
Abstrakt: High-throughput sequencing has allowed for a comprehensive small RNA (sRNA) expression analysis of numerous tissues in a diverse set of organisms. The computational analysis of the millions of generated sequencing reads has led to the discovery of novel miRNAs and other sRNA species, and resulted in a better understanding of the roles these sRNAs play in development and disease. This chapter describes the generation of sRNA deep-sequencing libraries for the Illumina massively parallel sequencing platform by using a cloning method that anneals specific RNA sequences to the 5'- and 3'-ends of the sRNA molecules.
Databáze: MEDLINE