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Update PFCdevApp.qmd

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  1. PFCdevApp.qmd +20 -5
PFCdevApp.qmd CHANGED
@@ -55,7 +55,11 @@ 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
@@ -224,10 +228,21 @@ output$gene_plot <- renderPlot({
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  output$vln_plot <- renderPlot({
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- VlnPlot(seu(), 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
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+
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+
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+
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+ , 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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  output$vln_plot <- renderPlot({
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+ FeaturePlot(
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+ seu(),
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+ features = input$gene,
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+ reduction = 'umap',
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+ split.by = "orig.ident",
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+ ncol=4,
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+ order = T,
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+ pt.size = 0.5
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+ ) &
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+ theme_bw(base_size = 15) &
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+ theme(panel.grid = element_blank(), plot.title = element_text(hjust = 0.5),
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+ strip.text = element_text(size = 20, face = "bold"),
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+ legend.position = c(0.1,0.25)) &
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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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