http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2022364080-A1

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filingDate 2020-09-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2022-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2022364080-A1
titleOfInvention Methods for dna library generation to facilitate the detection and reporting of low frequency variants
abstract Methods are disclosed for adding adapters to fragmented nucleic acids for next generation sequencing, including providing numerical codes based on variable adapter molecular barcode lengths on both sides of the fragmented nucleic acids and identifying reads from the same fragment based on both barcodes. The methods and products allow for the amplification of the fragmented nucleic acids when there is a low yield of isolated fragmented nucleic acids and also for efficient and reliable detection of low-frequency mutations including in subpopulations of cells within a subject.
priorityDate 2019-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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