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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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| Vydáno v: | Nucleic Acids Res |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2016
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| Témata: | |
| On-line přístup: | 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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