| Literature DB >> 21431681 |
Valérie Gausson1, Maria-Carla Saleh.
Abstract
At the current rate of technological progress, high-throughput sequencing of nucleic acids has become a commodity. These techniques are perfectly suitable for viral small RNAs sequencing and contribute to the understanding of many aspects of virus biology in the context of host-pathogen interaction. However, the generation of high quality data is still an issue and the preparation of small RNAs libraries that accurately reflect the viral siRNAs in the sample remains a challenge. In this chapter we describe how to clone and sequence libraries of viral small RNAs from infected insect samples (mosquito, drosophilidae, insect-derived cell lines).Mesh:
Substances:
Year: 2011 PMID: 21431681 DOI: 10.1007/978-1-61779-037-9_6
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745