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Novel scripts for improved annotation and selection of variants from whole exome sequencing in cancer research
Sequencing the exome is quickly becoming the preferred method for discovering disease-inducing mutations. While obtaining data sets is a straightforward procedure, the subsequent analysis and interpretation of the data is a limiting step for clinical applications. Thus, while the initial mutation an...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2015
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487347/ https://www.ncbi.nlm.nih.gov/pubmed/26150983 http://dx.doi.org/10.1016/j.mex.2015.03.003 |