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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發表在:Genome Res
Main Authors: Baslan, Timour, Kendall, Jude, Ward, Brian, Cox, Hilary, Leotta, Anthony, Rodgers, Linda, Riggs, Michael, D'Italia, Sean, Sun, Guoli, Yong, Mao, Miskimen, Kristy, Gilmore, Hannah, Saborowski, Michael, Dimitrova, Nevenka, Krasnitz, Alexander, Harris, Lyndsay, Wigler, Michael, Hicks, James
格式: Artigo
語言:Inglês
出版: Cold Spring Harbor Laboratory Press 2015
主題:
Method
在線閱讀: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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