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CLASS2: accurate and efficient splice variant annotation from RNA-seq reads
Next generation sequencing of cellular RNA is making it possible to characterize genes and alternative splicing in unprecedented detail. However, designing bioinformatics tools to accurately capture splicing variation has proven difficult. Current programs can find major isoforms of a gene but miss...
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| Yayımlandı: | Nucleic Acids Res |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4889935/ https://ncbi.nlm.nih.gov/pubmed/26975657 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkw158 |
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