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Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing
We present the bottleneck sequencing system (BotSeqS), a next-generation sequencing method that simultaneously quantifies rare somatic point mutations across the mitochondrial and nuclear genomes. BotSeqS combines molecular barcoding with a simple dilution step immediately before library amplificati...
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| 發表在: | Proc Natl Acad Sci U S A |
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| Main Authors: | , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
National Academy of Sciences
2016
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5024639/ https://ncbi.nlm.nih.gov/pubmed/27528664 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1607794113 |
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