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Molecular identification is the gold standard technique for the identification of corneal fungal pathogens.
Hair-trapping and molecular identification is a reliable method for reconstructing the spatial organization of lynx population.
Most of these bacteria were identified by molecular methodology and were absent using standard culture, especially in patients 1, 2, 3 and 6, which suggests that the molecular identification is clinically useful than culture techniques.
Currently, molecular identification is used to identify related/newer NTM species.
Worldwide, M. lentiflavum may be underreported and incorrectly identified as other, more familiar species, especially if access to molecular identification is limited.
Therefore, molecular identification is a helpful tool in resolving taxonomic problems in cases where the morphological "boundaries" among monogenean genera or species groups are ambiguous [ 27, 61, 62].
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The molecular identification was obtained 48 h after the sample was taken.
Morphological observation of strain CCG1 was performed and molecular identification was conducted through 18S rRNA.
Molecular identification was carried out by phylogenetic analysis following the 16S rRNA sequencing.
Because immature mermithids were not morphologically identifiable, a molecular identification was performed.
Molecular identification was performed for 90 isolates, and 64 (71.1%) larvae were identified as Trichinella spiralis and 25 (27.9%) as Trichinella britovi.
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