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. 2018 Jan 10;13(1):e0190264. doi: 10.1371/journal.pone.0190264

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© 2018 Patch et al

This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Fig 4 — A summary of the somatic variants identified in 3 mesothelioma patient samples (patient ID: 9869, 11202 and 11398) using different sequencing platforms. The number of somatic SNV (a) and indels (b) identified using the BGISEQ-500 and HiSeq X Ten platforms in each patient. The somatic SNV (c) and indels (d) which were only called in one platform fall into three categories: i) identified as somatic in the other platform but with low evidence; ii) identified in the other platform but predicted as a germline variant; or iii) not identified in the other platform.