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Detecting haplotype-specific transcript variation in long reads with FLAIR2
BACKGROUND: RNA-Seq has brought forth significant discoveries regarding aberrations in RNA processing, implicating these RNA variants in a variety of diseases. Aberrant splicing and single nucleotide variants in RNA have been demonstrated to alter transcript stability, localization, and function. In...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Cold Spring Harbor Laboratory
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312636/ https://www.ncbi.nlm.nih.gov/pubmed/37398362 http://dx.doi.org/10.1101/2023.06.09.544396 |