发明名称 |
GENOME-WIDE SCREENING FOR SNPS AND MUTATIONS RELATED TO DISEASE CONDITIONS |
摘要 |
The present invention provides a genome-wide methodology for identifying single nucleotide polymorphisms and mutations related to disease conditions, such as cancer. Specifically, the invention provides methods for detecting genome-wide mutations by successively amplifying sequence differences between two sample populations.
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申请公布号 |
WO2008016879(A9) |
申请公布日期 |
2009.05.07 |
申请号 |
WO2007US74742 |
申请日期 |
2007.07.30 |
申请人 |
DEUTSCHES KREBSFORSCHUNGSZENTRUM;HOHEISEL, JOERG;ANGENENDT, PHILIPP |
发明人 |
HOHEISEL, JOERG;ANGENENDT, PHILIPP |
分类号 |
C12Q1/68 |
主分类号 |
C12Q1/68 |
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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