Targeted variant detection using unaligned RNA-Seq reads

Mutations identified in acute myeloid leukemia patients are useful for prognosis and for selecting targeted therapies. Detection of such mutations using next-generation sequencing data requires a computationally intensive read mapping step followed by several variant calling methods. Targeted mutati...

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Detalles Bibliográficos
Autores principales: Audemard, Eric Olivier, Gendron, Patrick, Feghaly, Albert, Lavallée, Vincent-Philippe, Hébert, Josée, Sauvageau, Guy, Lemieux, Sébastien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Life Science Alliance LLC 2019
Materias:
Methods
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6701478/
https://www.ncbi.nlm.nih.gov/pubmed/31427380
http://dx.doi.org/10.26508/lsa.201900336

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6701478/
https://www.ncbi.nlm.nih.gov/pubmed/31427380
http://dx.doi.org/10.26508/lsa.201900336

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