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publicationDate 2020-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2020112566-A1
titleOfInvention Personalized ctdna disease monitoring via representative dna sequencing
abstract Disclosed herein is a method of deriving a plurality of genetic variants from a homogenized input sample. Also disclosed herein are methods of identifying a plurality of genetic variants in a sample comprising: homogenizing one or more input samples to provide a homogenized sample; preparing genomic material isolated from the homogenized input sample for sequencing; and identifying the plurality of genetic variants within sequencing data derived after sequencing the prepared genomic material.
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priorityDate 2018-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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