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Genome-wide segregation of single nucleotide and structural variants into single cancer cells
BACKGROUND: Single-cell genome sequencing provides high-resolution details of the clonal genomic modifications that occur during cancer initiation, progression, and ongoing evolution as patients undergo treatment. One limitation of current single-cell sequencing strategies is a suboptimal capacity t...
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| Publicado no: | BMC Genomics |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5702214/ https://ncbi.nlm.nih.gov/pubmed/29178827 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-017-4286-1 |
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