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Accurate identification of single nucleotide variants in whole genome amplified single cells

Genome-wide, DNA mutation analysis in single cells is prone to artifacts associated with cell lysis and whole genome amplification. Here we addressed these issues by developing Single-Cell Multiple Displacement Amplification (SCMDA) and the single-cell variant caller, SCcaller. Validated by comparin...

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Detalles Bibliográficos
Autores principales: Dong, Xiao, Zhang, Lei, Milholland, Brandon, Lee, Moonsook, Maslov, Alexander Y., Wang, Tao, Vijg, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408311/
https://www.ncbi.nlm.nih.gov/pubmed/28319112
http://dx.doi.org/10.1038/nmeth.4227
Descripción
Sumario:Genome-wide, DNA mutation analysis in single cells is prone to artifacts associated with cell lysis and whole genome amplification. Here we addressed these issues by developing Single-Cell Multiple Displacement Amplification (SCMDA) and the single-cell variant caller, SCcaller. Validated by comparing SCMDA-amplified single cells with unamplified clones from the same population, the procedure provides a firm foundation for standardizing somatic mutation analysis in single-cell genomics.