High-throughput single-cell whole-genome amplification through centrifugal emulsification and eMDA

被引:34
作者
Fu, Yusi [1 ,2 ]
Zhang, Fangli [1 ,2 ]
Zhang, Xiannian [1 ,2 ]
Yin, Junlong [3 ,4 ]
Du, Meijie [3 ,4 ]
Jiang, Mengcheng [1 ,2 ]
Liu, Lu [1 ,2 ]
Li, Jie [3 ,4 ]
Huang, Yanyi [1 ,2 ]
Wang, Jianbin [3 ,4 ]
机构
[1] Peking Univ, Beijing Adv Innovat Ctr Genom ICG, Biomed Pioneering Innovat Ctr BIOPIC, Sch Life Sci,Coll Engn, Beijing 100871, Peoples R China
[2] Peking Univ, Peking Tsinghua Ctr Life Sci, Beijing 100871, Peoples R China
[3] Tsinghua Univ, Sch Life Sci, Beijing 100084, Peoples R China
[4] Tsinghua Univ, Tsinghua Peking Ctr Life Sci, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
COPY-NUMBER VARIATION; MOUSE EARLY EMBRYOS; RNA-SEQ; GENE-EXPRESSION; READ ALIGNMENT; DNA; POLYMERASE; GENERATION; EVOLUTION;
D O I
10.1038/s42003-019-0401-y
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Single-cell whole-genome sequencing (scWGS) is mainly used to probe intercellular genomic variations, focusing on the copy number variations or alterations and the single-nucleotide variations (SNVs) occurring within single cells. Single-cell whole-genome amplification (scWGA) needs to be applied before scWGS but is challenging due to the low copy number of DNA. Besides, many genomic variations are rare within a population of cells, so the throughput of currently available scWGA methods is far from satisfactory. Here, we integrate a one-step micro-capillary array (MiCA)-based centrifugal droplet generation technique with emulsion multiple displacement amplification (eMDA) and demonstrate a high-throughput scWGA method, MiCA-eMDA. MiCA-eMDA increases the single-run throughput of scWGA to a few dozen, and enables the assessment of copy number variations and alterations at 50-kb resolution. Downstream target enrichment further enables the detection of SNVs with 20% allele drop-out.
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页数:10
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