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A survey of software for genome-wide discovery of differential splicing in RNA-Seq data

机译:用于全基因组发现RNA-Seq数据中差异剪接的软件的调查

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Alternative splicing is a major contributor to cellular diversity. Therefore the identification and quantification of differentially spliced transcripts in genome-wide transcript analysis is an important consideration. Here, I review the software available for analysis of RNA-Seq data for differential splicing and discuss intrinsic challenges for differential splicing analyses. Three approaches to differential splicing analysis are described, along with their associated software implementations, their strengths, limitations, and caveats. Suggestions for future work include more extensive experimental validation to assess accuracy of the software predictions and consensus formats for outputs that would facilitate visualizations, data exchange, and downstream analyses.
机译:选择性剪接是细胞多样性的主要贡献者。因此,全基因组转录本分析中差异剪接转录本的鉴定和定量是重要的考虑因素。在这里,我回顾了可用于差异剪接的RNA-Seq数据分析的软件,并讨论了差异剪接分析的内在挑战。描述了三种差分拼接分析方法,以及它们的相关软件实现,优势,局限性和警告。未来工作的建议包括进行更广泛的实验验证,以评估软件预测的准确性以及输出的共识格式,这将有助于可视化,数据交换和下游分析。

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