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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...
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| Publicado no: | BMC Bioinformatics |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4818877/ https://ncbi.nlm.nih.gov/pubmed/27038897 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-016-0999-4 |
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