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Integrative pipeline for profiling DNA copy number and inferring tumor phylogeny
SUMMARY: Copy number variation is an important and abundant source of variation in the human genome, which has been associated with a number of diseases, especially cancer. Massively parallel next-generation sequencing allows copy number profiling with fine resolution. Such efforts, however, have me...
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| 出版年: | Bioinformatics |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6248831/ https://ncbi.nlm.nih.gov/pubmed/29415173 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bty057 |
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