This report was created using the Covidex vr version() software for subtyping of genome sequences.
Covidex can be accessed online at http://covidex.unlu.edu.ar/.
Covidex was built using RShiny by Marco Cacciabue and Pablo Aguilera.
If you use Covidex please consider citing the following preprint: https://www.biorxiv.org/content/10.1101/2020.08.21.261347v1
For more information please visit Covidex download site(https://sourceforge.net/projects/covidex/).
Run was performed by user r input$user on r Sys.Date().
Input file r input$file[1,1] from which r as.character(length(data_reactive()$data_out$label)) sequences were selected for analysis.
The following table lists the sequences under analysis and the corresponding classification results.
# The `params` object is available in the document. col<-brewer.pal(5,"Blues") col2<-brewer.pal(5,"Reds") table<-table() datatable(table,selection = 'single', extensions = 'Buttons', options = list( columnDefs = list(list(targets = c(8,9,10,12,14), visible = FALSE)), dom = 'Bfrtip', lengthMenu = list(c(5, 15, -1), c('5', '15', 'All')), pageLength = 15, buttons = list('copy', 'print', list( extend = 'collection', buttons = list( list(extend = 'csv', filename = paste(input$file[1,1],"covidex_results"),sep=""), list(extend = 'excel', filename = paste(input$file[1,1],"covidex_results"),sep=""), list(extend = 'pdf', filename = paste(input$file[1,1],"covidex_results"),sep="")), text = 'Download' ) ) ))%>% formatStyle("Rambaut","FLAG", backgroundColor = styleEqual(c(0, 1), c(col[1], col[3])))%>% formatStyle("Length","Length_QC", backgroundColor = styleEqual(c(0, 1), c(col2[3], col2[1])))%>% formatStyle("N","N_QC", backgroundColor = styleEqual(c(0, 1), c(col2[3], col2[1])))
r as.character((sum(data_reactive()$data_out$VOC==TRUE))) of the r as.character(length(data_reactive()$data_out$label)) sequences in the analysis were labeled as putative VOC variants. In this sense, the following pie chart shows the percentage of VOC variants detected (true=VOC, false=non-VOC).
# The `params` object is available in the document. table<-table() data<-data.frame(Rambaut=table$Rambaut,VOC=table$VOC) plot_ly(data,labels = ~VOC,type = 'pie') if (sum(data$VOC)>0){ data<-data[data$VOC==TRUE,] plot_ly(data,labels = ~Rambaut,type = 'pie') }
r as.character((sum(data_reactive()$data_out$VOI==TRUE))) of the r as.character(length(data_reactive()$data_out$label)) sequences in the analysis were labeled as putative VOI variants. In this sense, the following pie chart shows the percentage of VOI variants detected (true=VOI, false=non-VOI).
# The `params` object is available in the document. table<-table() data<-data.frame(Rambaut=table$Rambaut,VOI=table$VOI) plot_ly(data,labels = ~VOI,type = 'pie') if (sum(data$VOI)>0){ data<-data[data$VOI==TRUE,] plot_ly(data,labels = ~Rambaut,type = 'pie',marker = list(colors = c('#FF7F0E', '#1F77B4'))) }
Variants of concern (VOC) and variants of Interest (VOI) are defined accorded to https://www.cdc.gov/coronavirus/2019-ncov/cases-updates/variant-surveillance/variant-info.html
# The `params` object is available in the document. model_data<-model_table() datatable(model_data)
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