<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yun H</submitter><funding>South Korean Government</funding><pagination>2320</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12566482</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(10)</volume><pubmed_abstract>Microbial forensics involves analyzing biological evidence to evaluate weaponized microorganisms or their toxins. This study aimed to detect and type &lt;i>Yersinia pestis&lt;/i> from four simulated forensic samples-human plasma diluted in phosphate-buffered saline (#24-2), tomato juice (#24-5), grape juice (#24-8), and a surgical mask (#24-10). Notably, samples #24-10 may have contained live bacteria other than &lt;i>Y. pestis&lt;/i>. A real-time polymerase chain reaction confirmed the presence of &lt;i>Y. pestis&lt;/i> in all samples; however, whole-genome sequencing (WGS) coverage of the &lt;i>Y. pestis&lt;/i> chromosome ranged from 0.46% to 97.1%, largely due to host DNA interference and low abundance. To address these limitations and enable strain-level identification, we designed a hybridization-based targe</pubmed_abstract><journal>Microorganisms</journal><pubmed_title>Typing of &amp;lt;i&amp;gt;Yersinia pestis&amp;lt;/i&amp;gt; in Challenging Forensic Samples Through Targeted Next-Generation Sequencing of Multilocus Variable Number Tandem Repeat Regions.</pubmed_title><pmcid>PMC12566482</pmcid><funding_grant_id>912A01201</funding_grant_id><pubmed_authors>Song DH</pubmed_authors><pubmed_authors>Yun H</pubmed_authors><pubmed_authors>Lee SH</pubmed_authors><pubmed_authors>Gu SH</pubmed_authors><pubmed_authors>Lim SH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Typing of &amp;lt;i&amp;gt;Yersinia pestis&amp;lt;/i&amp;gt; in Challenging Forensic Samples Through Targeted Next-Generation Sequencing of Multilocus Variable Number Tandem Repeat Regions.</name><description>Microbial forensics involves analyzing biological evidence to evaluate weaponized microorganisms or their toxins. This study aimed to detect and type &lt;i>Yersinia pestis&lt;/i> from four simulated forensic samples-human plasma diluted in phosphate-buffered saline (#24-2), tomato juice (#24-5), grape juice (#24-8), and a surgical mask (#24-10). Notably, samples #24-10 may have contained live bacteria other than &lt;i>Y. pestis&lt;/i>. A real-time polymerase chain reaction confirmed the presence of &lt;i>Y. pestis&lt;/i> in all samples; however, whole-genome sequencing (WGS) coverage of the &lt;i>Y. pestis&lt;/i> chromosome ranged from 0.46% to 97.1%, largely due to host DNA interference and low abundance. To address these limitations and enable strain-level identification, we designed a hybridization-based targe</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-05-15T03:16:33.533Z</modification><creation>2026-05-15T03:11:49.556Z</creation></dates><accession>S-EPMC12566482</accession><cross_references><pubmed>41156780</pubmed><doi>10.3390/microorganisms13102320</doi></cross_references></HashMap>