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Fig. 4 | Clinical and Translational Medicine

Fig. 4

From: Using single-cell multiple omics approaches to resolve tumor heterogeneity

Fig. 4

Single-cell multi-omics analysis workflow. a Multi-omic technologies can produce reads from the transcriptome (RNA-seq), the genome (exome sequencing), and/or the methylome, from the same cells. b Read alignments, quality control (QC), and specific processing steps create “feature expression” matrices, where cells are represented as vectors and genomic features (e.g. gene expression, methylation) represented as columns. c The different omic matrices can then be analyzed independently, for detecting cell subpopulations and ranking the genomic features etc. d Finally, multi-omics integration can be performed to identify coherent features from different omics that separate different subpopulations

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