发明名称 |
METHOD FOR CONSTRUCTING METHYLATED HIGH-THROUGHPUT SEQUENCING LIBRARY FOR WHOLE GENOME AND USE THEREOF |
摘要 |
Provided are a method for constructing a methylated high-throughput sequencing library for a whole genome and the use thereof. The method for constructing a methylated high-throughput sequencing library for a whole genome comprises: enzyme-digesting genome DNA with Msp I and a second restriction endonuclease; end-repairing the DNA fragments; adding base A at the 3' end of the DNA fragments that have been end-repaired; linking the DNA fragments with cohesive end A with a methylated linker; selecting fragments among the linking products with a methylated linker so as to obtain a target fragment; treating the target fragment with bisulfate so as to transform non-methylated cytosine in the target fragment to uracil; PCR amplifying the transformed target fragment; and isolating and purifying the amplification products. The amplification products constitute the methylated high-throughput sequencing library for the whole genome. The whole genome methylated high-throughput sequencing library of the genome DNA sample can be conveniently and effectively constructed using the method for constructing a methylated high-throughput sequencing library for a whole genome and the use thereof of the present invention. |
申请公布号 |
WO2013064066(A1) |
申请公布日期 |
2013.05.10 |
申请号 |
WO2012CN83821 |
申请日期 |
2012.10.31 |
申请人 |
BGI SHENZHEN CO., LIMITED;BGI SHENZHEN |
发明人 |
GAO, FEI;WANG, JUNWEN;XIA, YUDONG;WANG, JUN |
分类号 |
C40B50/06;C12M1/00;C12N9/22;C12Q1/68 |
主分类号 |
C40B50/06 |
代理机构 |
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代理人 |
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主权项 |
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地址 |
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