Each cancer type from TCGA was analyzed to identify subtypes from the RNA-seq samples with unsupervised clustering. Samples from each clusters can be submitted to TargetRanger for analysis. Information about each cluster is provided near each interactive UMAP plot.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.
Top cell-surface targets for each subtype. Rows are tumor subtypes determined by the Leiden algorithm. Columns are the top significant (adjusted p-value < .01) targets identified by TargetRanger, sorted by frequency across subtypes and filtered for targets identified using the ARCHS4, GTEx, and Tabula Sapiens atlases as backgrounds.