Abstract
Next-generation sequencing is a powerful method to interrogate the nucleotide composition for millions of DNA strands simultaneously. This technology can be utilized to profile microRNAs from multiple origins, such as tissues, cells, and body fluids. Next-generation sequencing is increasingly becoming a common and readily available technique for all laboratories. However, the bottleneck for next-generation sequencing is not within the laboratory but with the bioinformatics and data analysis of next-generation sequencing data. This chapter briefly describes the methods used to prepare samples for next-generation sequencing within the laboratory, before a deeper description of the methods used for data analysis.
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Acknowledgment
CS was in receipt of a Lions Medical Research Foundation Fellowship. This study was supported by the Lions Medical Research Foundation, UQ ECR Award, Royal Brisbane and Women’s Foundation, Diabetes Australia, and UQ-Ochsner Seed Grant. The ISO17025 accredited research facility was supported by grants from the Therapeutics Innovation Australia and the National Collaborative Research Infrastructure Strategy.
This review is supported partly by funding from the Lions Medical Research Foundation (LMRF), The University of Queensland, and Fondo Nacional de Desarrollo Científico y Tecnológico (FONDECYT 1170809), Chile.
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Guanzon, D., Iljas, J.D., Rice, G.E., Salomon, C. (2018). Using a Next-Generation Sequencing Approach to Profile MicroRNAs from Human Origin. In: Murthi, P., Vaillancourt, C. (eds) Preeclampsia . Methods in Molecular Biology, vol 1710. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-7498-6_16
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DOI: https://doi.org/10.1007/978-1-4939-7498-6_16
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