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use the right gene means file and remove tsne data file
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inst/templates/SCOneSample.Rmd

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@@ -438,25 +438,12 @@ The iSEE shiny app can be accessed through this link [iSEE explorer](`r {lastPro
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##### Mean expression of every gene across the cells in each cluster
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[geneMeanPerCluster](gene_means_per_cluster.txt)
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##### Mean expression of every gene across all the cells
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[geneMeans](gene_means.txt)
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[geneMeans](gene_means.tsv)
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##### Positive markers of each cluster
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[posMarkers](pos_markers.tsv)
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```{r, results='asis', eval = param$all2allMarkers}
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cat("##### Differential expressed genes from clusters paired comparisons")
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cat("\n")
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cat("[all2allMarkers](all2allMarkers.tsv)")
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```
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##### Coordinates of every cell on the TSNE
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[tSNE](tSNE_data.tsv)
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##### The final Single Cell Experiment Object is [here](sce_h5)
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