A general method to eliminate laboratory induced recombinants during massive, parallel sequencing of cDNA library.
Waugh,C, Cromer,D, Grimm,A, Chopra,A, Mallal,S, Davenport,M and Mak,J 2015, A general method to eliminate laboratory induced recombinants during massive, parallel sequencing of cDNA library., Virology Journal, vol. 12, no. 1, pp. 55, doi: 10.1186/s12985-015-0280-x.
Massive, parallel sequencing is a potent tool for dissecting the regulation of biological processes by revealing the dynamics of the cellular RNA profile under different conditions. Similarly, massive, parallel sequencing can be used to reveal the complexity of viral quasispecies that are often found in the RNA virus infected host. However, the production of cDNA libraries for next-generation sequencing (NGS) necessitates the reverse transcription of RNA into cDNA and the amplification of the cDNA template using PCR, which may introduce artefact in the form of phantom nucleic acids species that can bias the composition and interpretation of original RNA profiles.
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Every reasonable effort has been made to ensure that permission has been obtained for items included in DRO. If you believe that your rights have been infringed by this repository, please contact drosupport@deakin.edu.au.