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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Detalles Bibliográficos
Autores principales: Hansen, Marcus Celik, Nederby, Line, Roug, Anne, Villesen, Palle, Kjeldsen, Eigil, Nyvold, Charlotte Guldborg, Hokland, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Biochemistry, Genetics and Molecular Biology
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

Internet

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

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