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Additional file 1 of UMPlex™: a targeted next-generation sequencing primer design workflow

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posted on 2025-07-06, 03:20 authored by Dachuan Lin, Xiaomin Zhang, Dan Wang, Tongyingzi Liu, Tong Li, Yingluan Zhang, Lihua Li, Yi Huang, Yongchao Guo, Renli Zhang, Xinchun Chen, Tiejian Feng
Supplementary Material 1: Extended Fig. 1. Amplification Efficiency of Culture Samples. A and B: The relationship between CT values and the number of reads associated with primers targeting Influenza A virus. C and D: The relationship between CT values and the number of reads associated with primers targeting S. aureus. To enhance clarity and facilitate comparison, the CT values have been rounded; the precise CT values are available in Supplemental Table 7 (Sheet 2). Extended Fig. 2. Comparison of the Highest Pathogenic Reads. This figure delineates a comparison of the highest counts of pathogenic reads identified by tNGS across two distinct cohorts: the ‘Influenza-Like Patient’ group and the ‘Asymptomatic Control’ group. The former includes patients with confirmed pathogens, while the latter functions as a control, offering essential insights into pathogen detection within these populations. Extended Fig. 3. Comparison of Pathogen Detection Proportions. This figure presents a comparative analysis of pathogen detection proportions in samples with confirmed pathogens (not including known pathogens) versus those identified in the healthy control group. A: The detection rates of fungi across different groups. B: Illustrates the detection rates of the three most prevalent viruses (excluding those that clearly cause influenza-like illnesses) among the groups. C: The detection rates of the three most common bacteria across the groups. D: The prevalence of Acinetobacter baumannii within the various cohorts. The corresponding actual reads can be found in Supplemental Table 11. Extended Fig. 4. Comparison of tNGS and mNGS. This figure contrasts the efficacy of tNGS and mNGS in the detection of pathogens. A: The number of positive samples for different pathogens as reported by both tNGS and mNGS. The vertical axis represents the sample count, while the horizontal axis denotes the respective etiologies. B: The diversity of pathogen types identified in each patient sample by tNGS and mNGS. C: The proportion of pathogen reads relative to the total data for both tNGS and mNGS. The actual read counts are available in Supplemental Table 13.

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Guang Dong Basic and Applied Basic Research Foundation

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