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. 2022 Nov 14;9:699. doi: 10.1038/s41597-022-01825-1

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© The Author(s) 2022

Open Access 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 2 — Coverage of generated omics datasets. (a) Shows the sequencing coverage of epigenomic and transcriptomic data. Each data point represents a single sample for which the amount of raw sequencing reads was depicted. (b) Shows the coverage of proteomic data through the amount of confident PSM, confident peptides and confident proteins. Each data point represents a single sample.