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Methods for copy number aberration detection from single-cell DNA-sequencing data
Copy number aberrations (CNAs), which are pathogenic copy number variations (CNVs), play an important role in the initiation and progression of cancer. Single-cell DNA-sequencing (scDNAseq) technologies produce data that is ideal for inferring CNAs. In this review, we review eight methods that have...
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| Publicado no: | Genome Biol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7433197/ https://ncbi.nlm.nih.gov/pubmed/32807205 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13059-020-02119-8 |
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