<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Canier L</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>To achieve the goal of malaria elimination in low transmission areas such as in Cambodia, new, inexpensive, high-throughput diagnostic tools for identifying very low parasite densities in asymptomatic carriers are required. This will enable a switch from passive to active malaria case detection in the field.&lt;h4>Methods&lt;/h4>DNA extraction and real-time PCR assays were implemented in an "in-house" designed mobile laboratory allowing implementation of a robust, sensitive and rapid malaria diagnostic strategy in the field. This tool was employed in a survey organized in the context of the MalaResT project (NCT01663831).&lt;h4>Results&lt;/h4>The real-time PCR screening and species identification assays were performed in the mobile laboratory between October and November 2012, in Ra</pubmed_abstract><journal>Malaria journal</journal><pagination>405</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3829804</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>An innovative tool for moving malaria PCR detection of parasite reservoir into the field.</pubmed_title><pmcid>PMC3829804</pmcid><pubmed_authors>Uk S</pubmed_authors><pubmed_authors>Sokny M</pubmed_authors><pubmed_authors>Durnez L</pubmed_authors><pubmed_authors>Canier L</pubmed_authors><pubmed_authors>Masse-Navette P</pubmed_authors><pubmed_authors>Sluydts V</pubmed_authors><pubmed_authors>Loch K</pubmed_authors><pubmed_authors>Menard D</pubmed_authors><pubmed_authors>Heng S</pubmed_authors><pubmed_authors>Eam R</pubmed_authors><pubmed_authors>Chuor CM</pubmed_authors><pubmed_authors>Coosemans M</pubmed_authors><pubmed_authors>Tho S</pubmed_authors><pubmed_authors>Dourng D</pubmed_authors><pubmed_authors>Gryseels C</pubmed_authors><pubmed_authors>Van Roey K</pubmed_authors><pubmed_authors>Chy S</pubmed_authors><pubmed_authors>Khim N</pubmed_authors><pubmed_authors>Deubel V</pubmed_authors><pubmed_authors>Thavrin B</pubmed_authors><pubmed_authors>Kim S</pubmed_authors><pubmed_authors>Khean C</pubmed_authors><pubmed_authors>Siv S</pubmed_authors><pubmed_authors>Ken M</pubmed_authors><pubmed_authors>Grietens KP</pubmed_authors><pubmed_authors>Lim H</pubmed_authors></additional><is_claimable>false</is_claimable><name>An innovative tool for moving malaria PCR detection of parasite reservoir into the field.</name><description>&lt;h4>Background&lt;/h4>To achieve the goal of malaria elimination in low transmission areas such as in Cambodia, new, inexpensive, high-throughput diagnostic tools for identifying very low parasite densities in asymptomatic carriers are required. This will enable a switch from passive to active malaria case detection in the field.&lt;h4>Methods&lt;/h4>DNA extraction and real-time PCR assays were implemented in an "in-house" designed mobile laboratory allowing implementation of a robust, sensitive and rapid malaria diagnostic strategy in the field. This tool was employed in a survey organized in the context of the MalaResT project (NCT01663831).&lt;h4>Results&lt;/h4>The real-time PCR screening and species identification assays were performed in the mobile laboratory between October and November 2012, in Ra</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Nov</publication><modification>2026-07-15T05:23:43.733Z</modification><creation>2026-06-30T03:22:59.072Z</creation></dates><accession>S-EPMC3829804</accession><cross_references><pubmed>24206649</pubmed><doi>10.1186/1475-2875-12-405</doi></cross_references></HashMap>