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. 2022 Jul 16;19:28. doi: 10.1186/s12014-022-09366-w

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© The Author(s) 2022

Open AccessThis 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.

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Fig. 2 — Qualitative characteristics of the PRM assay. a All PRM transitions for target peptides were compared with their corresponding spectral library transitions. Each color bar represents one transition ion and its relative intensity among the others. The dot product (dotp) annotated above the bar graph is the normalized dot product of the light transition peak areas with the corresponding intensity in the library. b Relative quantification of target peptides in sera specimens of 13 SFTS patients and two normal subjects. The values were calculated based on each heavy peptide (1 pmol) peak area. The red bar denoted ELAYEGLDPALIIK peptides and blue bar denoted GILGPDGVPSR peptides. N.D.*Not detected