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Single-cell genomic variation induced by mutational processes in cancer
How cell-to-cell copy number alterations that underpin genomic instability(1) in human cancers drive genomic and phenotypic variation, and consequently the evolution of cancer(2), remains understudied. Here, by applying scaled single-cell whole-genome sequencing(3) to wild-type, TP53-deficient and T...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9712114/ https://www.ncbi.nlm.nih.gov/pubmed/36289342 http://dx.doi.org/10.1038/s41586-022-05249-0 |