library(readr)
library(knitr)
library(DT)
library(dplyr)
Overview
Quality Control
Cells with mitochondrial counts above 5% and feature count below 200
were filtered out.
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Basic Stats
Summary Statistics
Table of Cell Counts Per Sample
Table of Cell Counts Per Cluster
Table of Cell Counts Per Cluster
Filtered
Initial UMAP Clustering
UMAP clusters with no QC or batch correction.
UMAPS
UMAP Colored by Transcript
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UMAP Colored by Sample
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UMAP Colored by Epithelium
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UMAP Colored by Spleen
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UMAP Colored by Pooled JLN
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UMAP Colored by Pooled Spleen
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Heatmap
Heatmap of Gene expression per cluster
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UMAP Clustering after QC
This section generates UMAP clustering after filtering out cells with
greater than 5% mitochondrial gene counts and less than 200
features.
UMAP Colored by Transcript
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UMAP Colored by Sample
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UMAP Colored by Epithelium
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UMAP Colored by Spleen
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UMAP Colored by Pooled JLN
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UMAP Colored by Pooled Spleen
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Heatmap
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UMAP Clustering after Batch Correction
This section generates UMAP clustering after filtering out cells with
greater than 5% mitochondrial gene counts and less than 200 features.
Batch correction is implemented with Harmony before clustering.
UMAP Colored by Transcript
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UMAP Colored by Sample
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UMAP Colored by Epithelium
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UMAP Colored by Spleen
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UMAP Colored by Pooled JLN
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UMAP Colored by Pooled Spleen
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Heatmap
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UMAP Clustering with CSP and scRNAseq data merged
This UMAP is the clustering after merging the CSP and scRNAseq data
using a weighted nearest neighbor algorithm.
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Feature Plots for scRNAseq data
Feature plots for the single cell RNAseq data, used to identify
T-cell clusters.
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Feature Plots for CSP data
Feature plots for the cell surface protien data, used to identify
TCR-Beta positive clusters.
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Differential Gene Expression
Below are the volcano plots and gene tables generated from DESEQ2
output using the merged scRNAseq and CSP data.
Volcano Plots
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Epithelium VS GreenSpleen
Epithelium VS JLN