Abstract
This chapter reports a library preparation protocol for efficient high-throughput sequencing of double-stranded RNA viruses. The protocol consists of four main steps, viz., enzyme treatment, precipitation using lithium chloride, full-length amplification of cDNAs, and tailing adapters for high-throughput sequencing. This protocol will be useful for all double-stranded RNA viruses and for all of the high-throughput sequencing platforms.
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Dolgova, A.S., Safonova, M.V., Dedkov, V.G. (2020). Universal Library Preparation Protocol for Efficient High-Throughput Sequencing of Double-Stranded RNA Viruses. In: Astakhova, K., Bukhari, S. (eds) Nucleic Acid Detection and Structural Investigations. Methods in Molecular Biology, vol 2063. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-0138-9_14
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DOI: https://doi.org/10.1007/978-1-0716-0138-9_14
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Publisher Name: Humana, New York, NY
Print ISBN: 978-1-0716-0137-2
Online ISBN: 978-1-0716-0138-9
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