http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2020370120-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6806
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filingDate 2018-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_944476db05f18370983a50d3907341fc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_737a8fe32d29e1ff12920d008ec4792c
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publicationDate 2020-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2020370120-A1
titleOfInvention Reference material for non-invasive prenatal testing and manufacturing method thereof
abstract The invention relates to a method for preparing a simulated maternal cfDNA component for non-invasive prenatal testing, using a DNA fragmentation factor to digest a nucleus for simulating a maternal sample cell line, so as to obtain a simulated maternal cfDNA (short nucleic acid fragment) component. The reference material for non-invasive prenatal testing prepared by mixing different chromosome aneuploid cfDNA fragments with the normal chromosome number cfDNA fragments obtained by the present invention provides a method for manufacturing a reference material for internal quality control and external quality assessment. This method of making a reference material by mixing chromosome aneuploid cfDNA fragments and normal chromosome number cfDNA fragments produced with different enzyme digestions is the first case in the art. This method can also be used to make a series of mixed cfDNA sample reference materials for other noninvasive testing.
priorityDate 2018-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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