Protocol for capturing a full transcriptome from single preimplantation embryos using So-Smart-seq.

IF 1.3 Q4 BIOCHEMICAL RESEARCH METHODS STAR Protocols Pub Date : 2025-01-04 DOI:10.1016/j.xpro.2024.103540
Chunyao Wei, Jeannie T Lee
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引用次数: 0

Abstract

Strand-optimized Smart-seq (So-Smart-seq) can capture a comprehensive transcriptome from low-input samples. This technique detects both polyadenylated and non-polyadenylated RNAs, inclusive of repetitive RNAs, while excluding highly abundant ribosomal RNAs. So-Smart-seq preserves strand information and minimizes 5' to 3' coverage bias. We describe steps for the analysis of single mouse preimplantation embryos, including embryo isolation, library preparation, ribosomal cDNA depletion, and initial data processing. The protocol may be adapted for other low-input samples and the detection of small RNAs of <200 nt. For complete details on the use and execution of this protocol, please refer to Wei et al.1.

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使用So-Smart-seq从单个着床前胚胎中捕获完整转录组的方案。
链优化Smart-seq (So-Smart-seq)可以从低输入样本中捕获全面的转录组。该技术检测聚腺苷化和非聚腺苷化rna,包括重复rna,同时排除高度丰富的核糖体rna。So-Smart-seq保留了链信息,并最大限度地减少了5‘到3’覆盖偏差。我们描述了单个小鼠着床前胚胎分析的步骤,包括胚胎分离、文库制备、核糖体cDNA缺失和初始数据处理。该方案可适用于其他低输入样本和1的小rna的检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
STAR Protocols
STAR Protocols Biochemistry, Genetics and Molecular Biology-General Biochemistry, Genetics and Molecular Biology
CiteScore
2.00
自引率
0.00%
发文量
789
审稿时长
10 weeks
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