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通过下一代测序进行哺乳动物 miRNA 的调理。

Mammalian miRNA curation through next-generation sequencing.

机构信息

Laboratory of RNA Molecular Biology, Howard Hughes Medical Institute, The Rockefeller University New York, NY, USA.

出版信息

Front Genet. 2013 Aug 2;4:145. doi: 10.3389/fgene.2013.00145. eCollection 2013.

Abstract

Characteristic small RNA biogenesis processing patterns are used for the discovery of novel microRNAs (miRNAs) from next-generation sequencing data. Here, we highlight and discuss key criteria for mammalian - specifically human - miRNA database curation based on small RNA sequencing data. Sequence reads obtained from small RNA cDNA libraries are aligned to reference genomic regions, and miRNA genes are revealed by their distinct read length and bimodal read frequency distribution, the predicted secondary structure of the deduced miRNA stem-loop precursor molecule, and, to a lesser degree, based on evolutionary conservation of small RNAs from other vertebrates. Properly curated miRNA databases are an important resource for investigators interested in miRNA biology, diagnostics, and therapeutics.

摘要

特征性小 RNA 生物发生加工模式可用于从下一代测序数据中发现新的 microRNAs (miRNAs)。在这里,我们重点讨论并说明了基于小 RNA 测序数据对哺乳动物(特别是人类)miRNA 数据库进行管理的关键标准。从小 RNA cDNA 文库获得的序列读取与参考基因组区域进行比对,通过其独特的读取长度和双峰读取频率分布、推断出的 miRNA 茎环前体分子的预测二级结构,以及在较小程度上基于其他脊椎动物的小 RNA 的进化保守性来揭示 miRNA 基因。经过适当管理的 miRNA 数据库是对 miRNA 生物学、诊断和治疗感兴趣的研究人员的重要资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d131/3731538/fed318896433/fgene-04-00145-g001.jpg

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