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Co-mapping clonal and transcriptional heterogeneity in somatic evolution via GoT-Multi.

Cell genomics 2026 Vol.6(1) p. 101036

Pak M, Saurty-Seerunghen MS, Wise K, Abera TA, Lama C, Parghi N, Kang T, Sun X, Gao Q, Bao L, Roshal M, Allan JN, Furman RR, Martelotto LG, Nam AS

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Somatic evolution leads to clonal heterogeneity, which fuels cancer progression and therapy resistance.

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BibTeX ↓ RIS ↓
APA Pak M, Saurty-Seerunghen MS, et al. (2026). Co-mapping clonal and transcriptional heterogeneity in somatic evolution via GoT-Multi.. Cell genomics, 6(1), 101036. https://doi.org/10.1016/j.xgen.2025.101036
MLA Pak M, et al.. "Co-mapping clonal and transcriptional heterogeneity in somatic evolution via GoT-Multi.." Cell genomics, vol. 6, no. 1, 2026, pp. 101036.
PMID 41075791

Abstract

Somatic evolution leads to clonal heterogeneity, which fuels cancer progression and therapy resistance. To decipher the consequences of clonal heterogeneity, we require a method that deconvolutes complex clonal architectures and their downstream transcriptional states. We developed Genotyping of Transcriptomes for multiple targets and sample types (GoT-Multi), a high-throughput, formalin-fixed paraffin-embedded (FFPE) tissue-compatible single-cell multi-omics for co-detection of multiple somatic genotypes and whole transcriptomes. We developed an ensemble-based machine learning pipeline to optimize genotyping. We applied GoT-Multi to frozen or FFPE samples of Richter transformation, a progression of chronic lymphocytic leukemia to therapy-resistant large B cell lymphoma. GoT-Multi detected heterogeneous cancer cell states with genotypic data of 27 mutations, enabling clonal architecture reconstruction linked with their transcriptional programs. Distinct subclonal genotypes, including therapy-resistant mutations, converged on an inflammatory state. Other subclones displayed enhanced proliferation and/or MYC program. Thus, GoT-Multi revealed that distinct genotypic identities may converge on similar transcriptional states to mediate therapy resistance.

MeSH Terms

Humans; Clonal Evolution; Leukemia, Lymphocytic, Chronic, B-Cell; Mutation; Transcriptome; Single-Cell Analysis; Genetic Heterogeneity; Genotype; Machine Learning; Gene Expression Profiling