Extended Data Fig. 10: The transcriptome of MGs is shaped by the expression profiles from both neoplastic and non-neoplastic cells. | Nature

Extended Data Fig. 10: The transcriptome of MGs is shaped by the expression profiles from both neoplastic and non-neoplastic cells.

From: A clinically applicable integrative molecular classification of meningiomas

Extended Data Fig. 10

a, Bubble plot showing the expression of lineage specific markers for distinct cell types. b, Stacked barplot showing the relationship of samples to clusters. Samples are colored by patient of origin as in Fig. 4a. Barplot to the right shows the number of cells within each cluster. c, The top heatmap shows hierarchical clustering results of single cells by molecular group scores. Each cell was scored for the bulk signature of each molecular group and scores were compared to a permuted random gene set. Shown are cells with at least one score with FDR < 0.2. Scores were scaled such that the sum of all scores for each cell is equal to one. Below is a matched heatmap showing the number of genes detected for each MG signature in each cell. In a subset of cells, low scores are associated with low detection rate of genes (yellow and pink boxes). d, Stacked barplot showing the distribution of immune versus non-immune cells across molecular groups (left) and cycling versus non-cycling neoplastic cells across molecular groups (right) to clusters. Samples are colored by molecular group of tumor as in Fig. 4d. e, Barplot showing the total number of cells that are immune versus non-immune (left) and cycling versus non-cycling (right) by MG status of tumor of origin. f, Boxplots comparing the cell type composition of bulk RNA seq samples after deconvolution using single cell RNA-seq signatures. Pairwise comparisons in each boxplot are statistically significant (p < 0.05), unless explicitly stated otherwise (ns, not significant). g. Heatmap showing the expression of marker genes for single cell clusters (determined by CIBERSORTx) in bulk RNA seq data. Each column represents one tumor. Rows are designated marker genes for each cluster. Tumors were partitioned into 4 partitions by consensus k-means clustering with samples and gene sets clustered by hierarchical clustering using Pearson distance metric.

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