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. 2017 May 31;14(2):1526–1530. doi: 10.3892/ol.2017.6283

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Copyright: © Shen et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 1. — Organization of the training and validation datasets. Based on specific criteria, two datasets of OCS microarray data were selected from the Gene Expression Omnibus. Each dataset included data from OCS and normal ovarian tissue. OC, ovarian cancer; SBOC, ovarian borderline carcinoma specimens; SNO, normal ovary specimens; SC, ovarian serous carcinoma specimens; OCS, ovarian carcinoma specimens.