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Studying the consequences of somatic mutations in pre-malignant and cancerous tissues is challenging due to noise in single-cell transcriptome data and difficulty in identifying the clonal identity of single cells. We optimized TARGET-seq to develop TARGET-seq+, which combines RNA sequencing (RNA-seq), the analysis of cell surface protein expression, and genotyping in single cells with improved sensitivity. We describe the steps for cell isolation, the preparation of single-cell RNA-seq (scRNA-seq) and genotyping libraries, and sequencing. We also provide guidance on the analysis of single-cell genotyping, transcriptome pre-processing, and data integration. For complete details on the use and execution of this protocol, please refer to Jakobsen et al.1.

Original publication

DOI

10.1016/j.xpro.2025.103832

Type

Journal article

Journal

STAR Protoc

Publication Date

21/05/2025

Volume

6

Keywords

Flow Cytometry, Gene Expression, Genomics, Molecular Biology, RNA-seq, Sequencing, Single Cell, Stem Cells