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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://dirros.openscience.si/IzpisGradiva.php?id=30039"><dc:title>A novel digital PCR assay for detection and comprehensive characterization of Molluscum contagiosum virus genotypes MOCV1, MOCV2, and MOCV3 and recombinant lineages</dc:title><dc:creator>Zorec,	Tomaž Mark	(Avtor)
	</dc:creator><dc:creator>Skubic,	Lucijan	(Avtor)
	</dc:creator><dc:creator>Poljak,	Mario	(Avtor)
	</dc:creator><dc:subject>Molluscum contagiosum</dc:subject><dc:subject>Molluscum contagiosum virus</dc:subject><dc:subject>digital PCR</dc:subject><dc:subject>diversity screening</dc:subject><dc:subject>molecular diagnostics</dc:subject><dc:subject>sample prioritization triage</dc:subject><dc:description>Molluscum contagiosum virus (MOCV) is an important human pathogen causing a high disease burden worldwide. It is the last exclusively human-infecting poxvirus still circulating in its natural reservoir-a valuable model of poxviral evolution. Unfortunately, MOCV remains neglected, and little is known about its evolutionary history and circulating genomic variants, especially in non-privileged countries. The design weaknesses of available MOCV detection/genotyping assays surfaced with recent accumulation of abundant sequence information: all existing MOCV assays fail at accurate genotyping and capturing sub-genotype level diversity. Because complete MOCV genome characterization is an expensive and labor-intensive task, it makes sense to prioritize samples for whole-genome sequencing by diversity triage screening. To meet this demand, we developed a novel assay for accurate MOCV detection and genotyping, and comprehensive sub-genotype qualification to the level of phylogenetic groups (PGs). The assay included a novel set of oligonucleotide primers and probes, and it was implemented using digital polymerase chain reaction (dPCR). It offers sensitive, specific, and accurate detection, genotyping (MOCV1-MOCV3), and PG qualification (PG1-6) of MOCV DNA from clinical samples. The novel dPCR assay is suitable for MOCV diversity triage screening and prioritization of samples for complete MOCV genome characterization.</dc:description><dc:date>2024</dc:date><dc:date>2026-06-12 11:10:51</dc:date><dc:type>Neznano</dc:type><dc:identifier>30039</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
