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A review of somatic single nucleotide variant calling algorithms for next-generation sequencing data
Detection of somatic mutations holds great potential in cancer treatment and has been a very active research field in the past few years, especially since the breakthrough of the next-generation sequencing technology. A collection of variant calling pipelines have been developed with different under...
保存先:
| 出版年: | Comput Struct Biotechnol J |
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| 第一著者: | |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Research Network of Computational and Structural Biotechnology
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5852328/ https://ncbi.nlm.nih.gov/pubmed/29552334 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.csbj.2018.01.003 |
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