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高通量 RNA 干扰筛选技术:使用汇集 shRNA 文库和下一代测序。

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

机构信息

The Breakthrough Breast Cancer Research Centre, The Institute of Cancer Research, 237 Fulham Road, London, SW3 6JB, UK.

出版信息

Genome Biol. 2011 Oct 21;12(10):R104. doi: 10.1186/gb-2011-12-10-r104.

Abstract

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.

摘要

RNA 干扰 (RNAi) 筛选是一种先进的技术,可用于剖析生物过程和与疾病相关的表型。全基因组短发夹 RNA (shRNA) 文库的商业可用性激发了人们对此领域的兴趣,但这些复杂数据的生成和分析仍然是一个挑战。在这里,我们描述了完整的实验方案和新颖的开源计算方法 shALIGN 和 shRNAseq,它们允许使用下一代测序技术快速解析 RNAi 筛选。我们的计算流程提供了高效的筛选分析,以及灵活性和可扩展性,可以快速整合 shRNA 文库技术的未来发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9199/3333774/55d9e35d8aee/gb-2011-12-10-r104-1.jpg

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