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Potential viral proteins identified from this study were aligned with their corresponding homologs of reference negative-sense RNA viruses using MAFFT version 7 and employing the E-INS-i algorithm (Katoh and Standley, 2013).
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The unique regional health delivery systems and policies may have influenced participants' responses; however, many findings of this study are aligned with literature published from other practice settings.
Outcome data extracted from the studies were aligned with the analytic framework, to answer specific research questions.
The gene sequences analyzed in the present study were aligned with the MUSCLE software [39].
The study was aligned with the Consolidated Criteria for Reporting Qualitative Research COREQQ) [ 22].
PDZ sequences obtained from these databases were aligned with MUSLCE 3.6 to filter redundant entries.
Protein sequences from each family were aligned with MAFFT.
The 6a sequences from Liuhzou were aligned with other 6a sequences randomly selected from the Genebank.
The sequences from the remaining datasets were aligned with ClustalX as above, with no sites excluded.
Copies of 23S rRNA genes from each remaining genome were aligned with Clustalw [15].
Dromedary MERS-CoV full genomes obtained in this study (GenBank accession nos. KJ650295 KJ650297) were aligned with human MERS-CoV genomes retrieved from GenBank.
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