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Reproducibility of Illumina platform deep sequencing errors allows accurate determination of DNA barcodes in cells
BACKGROUND: Next generation sequencing (NGS) of amplified DNA is a powerful tool to describe genetic heterogeneity within cell populations that can both be used to investigate the clonal structure of cell populations and to perform genetic lineage tracing. For applications in which both abundant and...
Autores principales: | Beltman, Joost B., Urbanus, Jos, Velds, Arno, van Rooij, Nienke, Rohr, Jan C., Naik, Shalin H., Schumacher, Ton N. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818877/ https://www.ncbi.nlm.nih.gov/pubmed/27038897 http://dx.doi.org/10.1186/s12859-016-0999-4 |
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