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Computational analysis of splicing errors and mutations in human transcripts
BACKGROUND: Most retained introns found in human cDNAs generated by high-throughput sequencing projects seem to result from underspliced transcripts, and thus they capture intermediate steps of pre-mRNA splicing. On the other hand, mutations in splice sites cause exon skipping of the respective exon...
Tallennettuna:
| Päätekijät: | , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2008
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2234086/ https://ncbi.nlm.nih.gov/pubmed/18194514 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-9-13 |
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