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. 2016 Jul 12;44(18):e145. doi: 10.1093/nar/gkw629

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© The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 1. — Long-read sequencing data and validation strategy. (A) Percentages of consensus full-length isoforms mapped to cellular or EBV genomes. (B) Length distribution of consensus full-length isoforms mapped to cellular or EBV genomes. Blue boxes represent second and third quartiles, horizontal black lines indicate mean. (C) Distribution of proportion of annotated transcripts, by length, that are represented by full-length sequenced isoforms. (D) Strategy for data integration to validate full-length sequenced transcripts. (E) Example validated cellular transcripts.