http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3283653-A1

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filingDate 2016-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_24db7ac55bded75f2db2c41dcfde5a7c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8dfce6c256ba759cd169bbf17ae81054
publicationDate 2018-02-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-3283653-A1
titleOfInvention Methods, systems and processes of identifying genetic variation in highly similar genes
abstract Provided herein are novel methods, systems, and processes for mapping sequence reads to a modified reference genome and determining the presence or absence of a genetic variation, or the likelihood thereof, in a gene of interest in a subject. Provided herein are methods and compositions for analyzing a sample obtained from a subject. In some aspects provided herein is a computer-implemented method for determining a likelihood of a presence or absence of a genetic variation in a gene of interest for a subject. In some aspects provided herein is a non-transitory computer-readable storage medium with an executable program stored thereon.
priorityDate 2015-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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