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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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| Publicat a: | Oncogene |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group UK
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7892346/ https://ncbi.nlm.nih.gov/pubmed/33420369 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41388-020-01614-3 |
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