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Optimizing sparse sequencing of single cells for highly multiplex copy number profiling
Genome-wide analysis at the level of single cells has recently emerged as a powerful tool to dissect genome heterogeneity in cancer, neurobiology, and development. To be truly transformative, single-cell approaches must affordably accommodate large numbers of single cells. This is feasible in the ca...
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| Udgivet i: | Genome Res |
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| Main Authors: | , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Cold Spring Harbor Laboratory Press
2015
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4417119/ https://ncbi.nlm.nih.gov/pubmed/25858951 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.188060.114 |
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