<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>24</volume><submitter>Lamien-Meda A</submitter><pubmed_abstract>High Resolution Melting (HRM) analysis is a post-PCR analysis method used for identifying genetic variation in nucleic acid sequences. These data are presenting the identity of the 33 samples used for a qPCR-HRM and a nested snapback methods validation. In addition we are presenting the high resolution melting profiles of &lt;i>P. ovale curtisi&lt;/i> (Poc) and &lt;i>P. ovale wallikeri&lt;/i> (Pow) in the following conditions: after a direct qPCR run and after a nested snapback run. The qPCR-HRM of artificial mixture of Poc and Pow plasmids (200 copies/μl, each) at different proportions are showing the melting pattern of co-infections with both species. The sequencing methodology of the c&lt;i>lpc&lt;/i> gene fragment of 12 randomly selected samples is described and their likeness to published sequences is </pubmed_abstract><journal>Data in brief</journal><pagination>103937</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6502744</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Data on High Resolution Melting (HRM) and phylogenetic analysis of &lt;i>P. ovale wallikeri&lt;/i> and &lt;i>P. ovale curtisi&lt;/i>.</pubmed_title><pmcid>PMC6502744</pmcid><pubmed_authors>Lamien-Meda A</pubmed_authors><pubmed_authors>Noedl H</pubmed_authors><pubmed_authors>Fuehrer HP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Data on High Resolution Melting (HRM) and phylogenetic analysis of &lt;i>P. ovale wallikeri&lt;/i> and &lt;i>P. ovale curtisi&lt;/i>.</name><description>High Resolution Melting (HRM) analysis is a post-PCR analysis method used for identifying genetic variation in nucleic acid sequences. These data are presenting the identity of the 33 samples used for a qPCR-HRM and a nested snapback methods validation. In addition we are presenting the high resolution melting profiles of &lt;i>P. ovale curtisi&lt;/i> (Poc) and &lt;i>P. ovale wallikeri&lt;/i> (Pow) in the following conditions: after a direct qPCR run and after a nested snapback run. The qPCR-HRM of artificial mixture of Poc and Pow plasmids (200 copies/μl, each) at different proportions are showing the melting pattern of co-infections with both species. The sequencing methodology of the c&lt;i>lpc&lt;/i> gene fragment of 12 randomly selected samples is described and their likeness to published sequences is </description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jun</publication><modification>2026-05-07T13:46:54.826Z</modification><creation>2026-04-07T22:47:32.794Z</creation></dates><accession>S-EPMC6502744</accession><cross_references><pubmed>31080854</pubmed><doi>10.1016/j.dib.2019.103937</doi></cross_references></HashMap>