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SCONCE2: jointly inferring single cell copy number profiles and tumor evolutionary distances
BACKGROUND: Single cell whole genome tumor sequencing can yield novel insights into the evolutionary history of somatic copy number alterations. Existing single cell copy number calling methods do not explicitly model the shared evolutionary process of multiple cells, and generally analyze cells ind...
Autores principales: | Hui, Sandra, Nielsen, Rasmus |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9392257/ https://www.ncbi.nlm.nih.gov/pubmed/35986254 http://dx.doi.org/10.1186/s12859-022-04890-w |
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