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全长长链非编码 RNA 的捕获长读测序(CLS)注释。

Annotation of Full-Length Long Noncoding RNAs with Capture Long-Read Sequencing (CLS).

机构信息

Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Catalonia, Spain.

Institute of Bioorganic Chemistry Polish Academy of Sciences, Poznan, Poland.

出版信息

Methods Mol Biol. 2021;2254:133-159. doi: 10.1007/978-1-0716-1158-6_9.

Abstract

Metazoan genomes produce thousands of long-noncoding RNAs (lncRNAs), of which just a small fraction have been well characterized. Understanding their biological functions requires accurate annotations, or maps of the precise location and structure of genes and transcripts in the genome. Current lncRNA annotations are limited by compromises between quality and size, with many gene models being fragmentary or uncatalogued. To overcome this, the GENCODE consortium has developed RNA capture long-read sequencing (CLS), an approach combining targeted RNA capture with third-generation long-read sequencing. CLS provides accurate annotations at high-throughput rates. It eliminates the need for noisy transcriptome assembly from short reads, and requires minimal manual curation. The full-length transcript models produced are of quality comparable to present-day manually curated annotations. Here we describe a detailed CLS protocol, from probe design through long-read sequencing to creation of final annotations.

摘要

后生动物基因组产生数千种长非编码 RNA(lncRNA),其中只有一小部分得到了很好的描述。要了解它们的生物学功能,需要进行准确的注释,即基因组中基因和转录本的精确位置和结构图谱。目前的 lncRNA 注释受到质量和大小之间的权衡限制,许多基因模型都是不完整的或未被编目的。为了克服这一问题,GENCODE 联盟开发了 RNA 捕获长读测序 (CLS),这是一种结合靶向 RNA 捕获和第三代长读测序的方法。CLS 以高通量的速度提供准确的注释。它消除了对来自短读的嘈杂转录组组装的需求,并且需要最小的人工策管。生成的全长转录本模型的质量可与当今的人工策管注释相媲美。在这里,我们描述了一个详细的 CLS 方案,从探针设计到长读测序再到最终注释的创建。

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