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. 2014 Aug 9;7:49. doi: 10.1186/1755-8794-7-49

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Copyright © 2014 Wang et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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A overview of phenotypes, functions and RNA-seq quality control of CIK_IL-15and CIK_IL-2. (A) Flow cytometric and statistical analysis of the proportion of CD3⁺CD56⁺ CIK cells. Numbers indicate the percentage of each subset. (B) Cell proliferation capacity assay of CIK_IL-15 and CIK_IL-2 based on automatic cell counting; (C) Detection of tumor cytotoxic effect of CIK_IL-15 and CIK_IL-2 against SPC-A-1 and BGC823; (D) Distribution of reads on chromosomes; (E) Percentage of mapped reads onto the regions of exons, introns, 5’-UTR, 3’-UTR, transcription start site (TSS), transcription end site (TES) and intergenic region.