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. 2016 May 25;6:26017. doi: 10.1038/srep26017

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Copyright © 2016, Macmillan Publishers Limited

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Whole genome sequencing of HTNV was performed by multiplex PCR-based NGS. The number and coverage of reads for HTNV tripartite genomes is shown. The reads were analyzed by reference matching mapping for HTNV 76-118 (L segment, NC005222; M segment, M14627; S segment, M14626). CLC Genomic Workbench version 7.5.2 was used. (a) ROKA13-8 (b) ROKA14-11 (c) US8A14-2 (d) US8A15-1.