Abstract
Provided are methods directed to enriching nucleic acids in a biological sample. These methods, in some embodiments can discriminately enrich the abundance of low-copy nucleic acids relative to higher-copy nucleic acids. In some embodiments, the methods provided can enrich a low-copy number mutant allele associated with a disease state, thus allowing early detection and optimized treatment. In other embodiments, the methods can be used for detection of particular molecules, such as antigens, in a sample.
| Original language | English |
|---|---|
| Patent number | WO2019178346 |
| Priority date | 14/03/18 |
| Publication status | Published - 19 Sept 2019 |
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