Comprehensive characterisation of intronic mis-splicing mutations in human cancers

Previous studies studying mis-splicing mutations were based on exome data and thus our current knowledge is largely limited to exons and the canonical splice sites. To comprehensively characterise intronic mis-splicing mutations, we analysed 1134 pan-cancer whole genomes and transcriptomes together...

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Detalles Bibliográficos
Autores principales: Jung, Hyunchul, Lee, Kang Seon, Choi, Jung Kyoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7892346/
https://www.ncbi.nlm.nih.gov/pubmed/33420369
http://dx.doi.org/10.1038/s41388-020-01614-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7892346/
https://www.ncbi.nlm.nih.gov/pubmed/33420369
http://dx.doi.org/10.1038/s41388-020-01614-3

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