1. Evaluation of commercially available RNA amplification kits for RNA sequencing using very low input amounts of total RNA.
- Author
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Shanker, Savita, Paulson, Ariel, Edenberg, Howard J, Peak, Allison, Perera, Anoja, Alekseyev, Yuriy O, Beckloff, Nicholas, Bivens, Nathan J, Donnelly, Robert, Gillaspy, Allison F, Grove, Deborah, Gu, Weikuan, Jafari, Nadereh, Kerley-Hamilton, Joanna S, Lyons, Robert H, Tepper, Clifford, and Nicolet, Charles M
- Subjects
Biological Sciences ,Bioinformatics and Computational Biology ,Genetics ,Biotechnology ,Human Genome ,Animals ,Base Sequence ,DNA ,Complementary ,Humans ,Limit of Detection ,Mice ,Nucleic Acid Amplification Techniques ,Polyadenylation ,RNA ,Rats ,Reference Standards ,Sequence Analysis ,RNA ,cDNA synthesis kits ,polyA ,ribodepletion ,Technology ,Medical and Health Sciences ,Biological sciences - Abstract
This article includes supplemental data. Please visit http://www.fasebj.org to obtain this information.Multiple recent publications on RNA sequencing (RNA-seq) have demonstrated the power of next-generation sequencing technologies in whole-transcriptome analysis. Vendor-specific protocols used for RNA library construction often require at least 100 ng total RNA. However, under certain conditions, much less RNA is available for library construction. In these cases, effective transcriptome profiling requires amplification of subnanogram amounts of RNA. Several commercial RNA amplification kits are available for amplification prior to library construction for next-generation sequencing, but these kits have not been comprehensively field evaluated for accuracy and performance of RNA-seq for picogram amounts of RNA. To address this, 4 types of amplification kits were tested with 3 different concentrations, from 5 ng to 50 pg, of a commercially available RNA. Kits were tested at multiple sites to assess reproducibility and ease of use. The human total reference RNA used was spiked with a control pool of RNA molecules in order to further evaluate quantitative recovery of input material. Additional control data sets were generated from libraries constructed following polyA selection or ribosomal depletion using established kits and protocols. cDNA was collected from the different sites, and libraries were synthesized at a single site using established protocols. Sequencing runs were carried out on the Illumina platform. Numerous metrics were compared among the kits and dilutions used. Overall, no single kit appeared to meet all the challenges of small input material. However, it is encouraging that excellent data can be recovered with even the 50 pg input total RNA.
- Published
- 2015