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Update PFCdevApp.qmd

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  1. PFCdevApp.qmd +16 -18
PFCdevApp.qmd CHANGED
@@ -55,7 +55,7 @@ Spatial data
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  </p>
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  <p style="font-size: 20px; text-align: justify;">
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- We collected the whole brain stereo-seq datasets of P1 and Adult mice from [(Han et al., Neuron, 2025)](https://doi.org/10.1016/j.neuron.2025.02.015 , extracted and analyzed the PFC brain region. Users can browse the following content through the spatial page:
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  </p>
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  - Spatial Clustering: Select different cell subtypes to view their spatial distribution
@@ -198,6 +198,21 @@ output$cluster_plot <- renderPlot({
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  guides(color = guide_legend(ncol = 1, override.aes = list(size = 3)))
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  })
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  output$gene_plot <- renderPlot({
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  if (input$dataset=="Neurons"){
@@ -221,23 +236,6 @@ output$gene_plot <- renderPlot({
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  coord_fixed() &
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  scale_color_gradientn(colours = c("lightblue3", "lightblue", "white", "red", "red4"), limits=c(0,2), breaks=c(0,2), na.value = "red4")
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  })
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-
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-
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- output$vln_plot <- renderPlot({
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- if (input$dataset=="Neurons"){
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- seu3 <- subset(seu.downsample, cells = colnames(seu.downsample)[seu.downsample$MainType %in% c("Excitatory", "Inhibitory")])
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- }else{
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- seu3 <- seu.downsample
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- }
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- seu3@meta.data[,input$celltype] <- factor(
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- seu3@meta.data[,input$celltype],
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- levels = names(col_cluster[[input$celltype]])
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- )
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- VlnPlot(seu3, features = input$gene, group.by = input$celltype,
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- col = col_cluster[[input$celltype]]) +
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- NoLegend() +
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- labs(x="")
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- })
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  ```
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  </p>
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  <p style="font-size: 20px; text-align: justify;">
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+ We collected the whole brain stereo-seq datasets of P1 and Adult mice from [(Han et al., Neuron, 2025)](https://doi.org/10.1016/j.neuron.2025.02.015, extracted and analyzed the PFC brain region. Users can browse the following content through the spatial page:
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  </p>
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  - Spatial Clustering: Select different cell subtypes to view their spatial distribution
 
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  guides(color = guide_legend(ncol = 1, override.aes = list(size = 3)))
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  })
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+ output$vln_plot <- renderPlot({
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+ if (input$dataset=="Neurons"){
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+ seu3 <- subset(seu.downsample, cells = colnames(seu.downsample)[seu.downsample$MainType %in% c("Excitatory", "Inhibitory")])
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+ }else{
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+ seu3 <- seu.downsample
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+ }
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+ seu3@meta.data[,input$celltype] <- factor(
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+ seu3@meta.data[,input$celltype],
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+ levels = names(col_cluster[[input$celltype]])
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+ )
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+ VlnPlot(seu3, features = input$gene, group.by = input$celltype,
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+ col = col_cluster[[input$celltype]]) +
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+ NoLegend() +
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+ labs(x="")
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+ })
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  output$gene_plot <- renderPlot({
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  if (input$dataset=="Neurons"){
 
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  coord_fixed() &
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  scale_color_gradientn(colours = c("lightblue3", "lightblue", "white", "red", "red4"), limits=c(0,2), breaks=c(0,2), na.value = "red4")
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  })
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
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  ```
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