2008
DOI: 10.1002/jcla.20224
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Comparison between two PCR‐based bacterial identification methods through artificial neural network data analysis

Abstract: The 16S ribosomal ribonucleic acid (rRNA) and 16S-23S rRNA spacer region genes are commonly used as taxonomic and phylogenetic tools. In this study, two pairs of fluorescent-labeled primers for 16S rRNA genes and one pair of primers for 16S-23S rRNA spacer region genes were selected to amplify target sequences of 317 isolates from positive blood cultures. The polymerase chain reaction (PCR) products of both were then subjected to restriction fragment length polymorphism (RFLP) analysis by capillary electrophor… Show more

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Cited by 3 publications
(1 citation statement)
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“…For example, many microfluidic DEP devices are solely designed for cell sorting which could be followed by an identification method not carried out within the study . On the other hand, many identification methods, such as Raman spectroscopy , PCR , or FTIR , already assume a sample free of debris, making them ill‐equipped to handle environmental or clinical samples which are bound to have debris. Only few combined isolation and identification designs exist, of which many require labels such as Raman reporters or antibodies.…”
Section: Resultsmentioning
confidence: 99%
“…For example, many microfluidic DEP devices are solely designed for cell sorting which could be followed by an identification method not carried out within the study . On the other hand, many identification methods, such as Raman spectroscopy , PCR , or FTIR , already assume a sample free of debris, making them ill‐equipped to handle environmental or clinical samples which are bound to have debris. Only few combined isolation and identification designs exist, of which many require labels such as Raman reporters or antibodies.…”
Section: Resultsmentioning
confidence: 99%