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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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Detalhes bibliográficos
Publicado no:Nucleic Acids Res
Main Authors: Song, Li, Sabunciyan, Sarven, Florea, Liliana
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2016
Assuntos:
Acesso em linha: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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