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High-throughput RNA interference screening using pooled shRNA libraries and next generation sequencing

机译:使用汇集的shRNA库和下一代测序进行高通量RNA干扰筛选

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RNA interference (RNAi) screening is a state-of-the-art technology that enables the dissection of biological processes and disease-related phenotypes. The commercial availability of genome-wide, short hairpin RNA (shRNA) libraries has fueled interest in this area but the generation and analysis of these complex data remain a challenge. Here, we describe complete experimental protocols and novel open source computational methodologies, shALIGN and shRNAseq, that allow RNAi screens to be rapidly deconvoluted using next generation sequencing. Our computational pipeline offers efficient screen analysis and the flexibility and scalability to quickly incorporate future developments in shRNA library technology.
机译:RNA干扰(RNAi)筛查是一种最先进的技术,可以解剖生物学过程和与疾病相关的表型。全基因组的短发夹RNA(shRNA)文库的商业可用性已经引起了人们对该领域的兴趣,但是如何生成和分析这些复杂的数据仍然是一个挑战。在这里,我们描述了完整的实验方案和新颖的开放源代码计算方法shALIGN和shRNAseq,可使用下一代测序技术对RNAi屏幕进行快速解卷积。我们的计算流水线提供了有效的屏幕分析以及灵活性和可扩展性,可快速整合shRNA库技术的未来发展。

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