Journal
Acta Neuropathologica Communications
Publication Date
7-14-2020
Volume
8
Issue
1
First Page
107
Document Type
Open Access Publication
DOI
10.1186/s40478-020-00980-z
Rights and Permissions
Torre, M., Vasudevaraja, V., Serrano, J. et al. Molecular and clinicopathologic features of gliomas harboring NTRK fusions. acta neuropathol commun 8, 107 (2020). doi.org/10.1186/s40478-020-00980-z This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
Recommended Citation
Torre, Matthew; Dahiya, Sonika; and et al, "Molecular and clinicopathologic features of gliomas harboring NTRK fusions." Acta Neuropathologica Communications. 8, 1. 107 (2020).
https://digitalcommons.wustl.edu/open_access_pubs/11870
Supplemental figure 1. Unsupervised principal component analysis (PCA) of methylation profiles of NTRK-fused gliomas demonstrates that no homogenous groups form when correlated with (a) NTRK gene involved, (b) patient age, or (c) histologic grade.
40478_2020_980_MOESM2_ESM.zip (25 kB)
Supplemental tables. (1) methods for each case; (2) single nucleotide variants and copy number variants encountered in each case; (3) legend for the methylation reports and t-sne plots corresponding to each case.
