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Discovering chimeric transcripts in paired-end RNA-seq data by using EricScript

机译:使用EricScript在配对末端RNA-seq数据中发现嵌合转录本

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Motivation: The discovery of novel gene fusions can lead to a better comprehension of cancer progression and development. The emergence of deep sequencing of trancriptome, known as RNA-seq, has opened many opportunities for the identification of this class of genomic alterations, leading to the discovery of novel chimeric transcripts in melanomas, breast cancers and lymphomas. Nowadays, few computational approaches have been developed for the detection of chimeric transcripts. Although all of these computational methods show good sensitivity, much work remains to reduce the huge number of false-positive calls that arises from this analysis. Results: We proposed a novel computational framework, named chimEric tranScript detection algorithm (EricScript), for the identification of gene fusion products in paired-end RNA-seq data. Our simulation study on synthetic data demonstrates that EricScript enables to achieve higher sensitivity and specificity than existing methods with noticeably lower running times. We also applied our method to publicly available RNA-seq tumour datasets, and we showed its capability in rediscovering known gene fusions.
机译:动机:新型基因融合的发现可以更好地理解癌症的进展和发展。转录组的深度测序(称为RNA-seq)的出现为鉴定这类基因组改变打开了许多机会,从而导致在黑色素瘤,乳腺癌和淋巴瘤中发现了新的嵌合转录本。如今,很少有计算方法可用于检测嵌合转录本。尽管所有这些计算方法都显示出良好的敏感性,但是要减少此分析产生的大量假阳性呼叫,仍有大量工作要做。结果:我们提出了一种新的计算框架,称为chimEric tranScript检测算法(EricScript),用于识别双末端RNA-seq数据中的基因融合产物。我们对合成数据的仿真研究表明,与现有方法相比,EricScript可以实现更高的灵敏度和特异性,并且运行时间明显缩短。我们还将我们的方法应用于可公开获得的RNA-seq肿瘤数据集,并且我们展示了其重新发现已知基因融合体的能力。

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