Unbiased identification and characterization of single CTC transcriptomes are aided by the unCTC process, which includes multiple techniques. Clustering of scRNA-seq profiles is a crucial part of this process. We describe a robust method for grouping single-cell transcriptomes in a meta-space that spans pathways and computes enrichment scores based on gene expression readouts. The log-transformed TPM (Transcripts Per Million) matrix/count associated with CTC transcriptomes is transformed into a matrix comprising pathway enrichment scores obtained using an R package, GSVA, for unsupervised clustering. Deep dictionary learning with k-means clustering cost (DDLK) is applied to these pathway scores. The K-means clustering cost is included in the deep dictionary learning (DDL) architecture by DDLK. With the use of Stouffer's Z-score, unCTC allows for the determination of a variety of canonical markers identifying malignant/epithelial/immune origins (Stouffer et al., 1949). In our opinion, gene-set-based techniques are effective in enhancing single-marker-based and inferred-CNV-based cell-group characterization.
Package details |
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Bioconductor views | CTC Clustering CopyNumberVariation SingleCell |
Maintainer | |
License | GPL-3 |
Version | 0.1.0 |
Package repository | View on GitHub |
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