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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...
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| Publicat a: | MethodsX |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4487347/ https://ncbi.nlm.nih.gov/pubmed/26150983 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mex.2015.03.003 |
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