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DOI: 10.3791/59901-v
Please note that some of the translations on this page are AI generated. Click here for the English version.
This article presents a detailed protocol for isolating small RNAs and enriching microRNAs for high-throughput sequencing. It also outlines the processing of sequence reads and alignment to microRNAs using open-source bioinformatics tools.
在这里,我们描述了一个分步策略,用于隔离小型RNA、丰富微RNA和为高通量测序准备样本。然后,我们介绍如何使用开源工具处理序列读取并将其与微RNA对齐。
我们开发了一种定义、可重复和长期的协议,用于小型RNA测序和使用开源生物信息学工具分析规范化读取。我们战略的主要优点是,它通过凝胶纯化准确收集微RNA,无论微RNA如何收集,生物信息学分析都可以应用。微RNA的高通量测序可以揭示对疾病机制、微RNA处理以及提供小型RNA的基因治疗方法的准确定量。
确保在无 RNase 的环境中工作,并在整个过程中将所有RNA产品保持在冰上。可视化凝胶切割步骤将有助于查看者识别下游应用所需的产品的正确尺寸。对于三种原生适配器连接,将 11 微升 RNA 与 1.5 微升 ATP 无 ATP 10X T4RNA 连接酶反应缓冲液、1 微升聚乙烯二醇和 0.5 微升三个原成链接器。
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