| Literature DB >> 25751143 |
Michael B Clark1, Tim R Mercer2, Giovanni Bussotti3, Tommaso Leonardi3, Katelin R Haynes4, Joanna Crawford5, Marion E Brunck6, Kim-Anh Lê Cao7, Gethin P Thomas4, Wendy Y Chen2, Ryan J Taft8, Lars K Nielsen6, Anton J Enright3, John S Mattick2, Marcel E Dinger2.
Abstract
We compared quantitative RT-PCR (qRT-PCR), RNA-seq and capture sequencing (CaptureSeq) in terms of their ability to assemble and quantify long noncoding RNAs and novel coding exons across 20 human tissues. CaptureSeq was superior for the detection and quantification of genes with low expression, showed little technical variation and accurately measured differential expression. This approach expands and refines previous annotations and simultaneously generates an expression atlas.Entities:
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Year: 2015 PMID: 25751143 DOI: 10.1038/nmeth.3321
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547