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<SDOBI lang="en"><B000><eptags><B001EP>ATBECHDEDKESFRGBGRITLILUNLSEMCPTIESILTLVFIROMKCYALTRBGCZEEHUPLSK..HRIS..MTNORS..SM..................</B001EP><B005EP>J</B005EP><B007EP>BDM Ver 0.1.67 (18 Oct 2017) -  2999001/0</B007EP></eptags></B000><B100><B110>2772549</B110><B120><B121>CORRECTED EUROPEAN PATENT SPECIFICATION</B121></B120><B130>B8</B130><B132EP>B1</B132EP><B140><date>20190911</date></B140><B150><B151>W1</B151><B153>73</B153><B155><B1551>de</B1551><B1552>Bibliographie</B1552><B1551>en</B1551><B1552>Bibliography</B1552><B1551>fr</B1551><B1552>Bibliographie</B1552></B155></B150><B190>EP</B190></B100><B200><B210>11878559.1</B210><B220><date>20111231</date></B220><B240><B241><date>20140530</date></B241><B242><date>20170629</date></B242></B240><B250>zh</B250><B251EP>en</B251EP><B260>en</B260></B200><B400><B405><date>20190911</date><bnum>201937</bnum></B405><B430><date>20140903</date><bnum>201436</bnum></B430><B450><date>20190731</date><bnum>201931</bnum></B450><B452EP><date>20190221</date></B452EP><B480><date>20190911</date><bnum>201937</bnum></B480></B400><B500><B510EP><classification-ipcr sequence="1"><text>C12Q   1/6869      20180101AFI20190212BHEP        </text></classification-ipcr><classification-ipcr sequence="2"><text>C12Q   1/6809      20180101ALI20190212BHEP        </text></classification-ipcr><classification-ipcr sequence="3"><text>G16B  30/00        20190101ALI20190212BHEP        </text></classification-ipcr></B510EP><B540><B541>de</B541><B542>VERFAHREN ZUM NACHWEIS VON GENETISCHEN VARIATIONEN</B542><B541>en</B541><B542>METHOD FOR DETECTING GENETIC VARIATION</B542><B541>fr</B541><B542>PROCÉDÉ DE DÉTECTION D'UNE VARIATION GÉNÉTIQUE</B542></B540><B560><B561><text>WO-A1-2010/042716</text></B561><B561><text>WO-A1-2010/054284</text></B561><B561><text>WO-A1-2010/057132</text></B561><B561><text>WO-A1-2010/075459</text></B561><B561><text>WO-A2-2010/001419</text></B561><B561><text>CN-A- 101 555 528</text></B561><B562><text>S. YOON ET AL: "Sensitive and accurate detection of copy number variants using read depth of coverage", GENOME RESEARCH, vol. 19, no. 9, 5 August 2009 (2009-08-05) , pages 1586-1592, XP055167321, ISSN: 1088-9051, DOI: 10.1101/gr.092981.109</text></B562><B562><text>ERIC Z. CHEN ET AL: "Noninvasive Prenatal Diagnosis of Fetal Trisomy 18 and Trisomy 13 by Maternal Plasma DNA Sequencing", PLOS ONE, vol. 6, no. 7, 6 July 2011 (2011-07-06), page e21791, XP055024137, DOI: 10.1371/journal.pone.0021791</text></B562><B562><text>Anonymous: "Resampling (statistics) - Wikipedia, the free encyclopedia", , 29 December 2011 (2011-12-29), XP055168025, Retrieved from the Internet: URL:http://en.wikipedia.org/w/index.php?ti tle=Resampling_(statistics)&amp;oldid=46831285 8 [retrieved on 2015-02-06]</text></B562><B562><text>Daisuke Komura ET AL: "Noise reduction from genotyping microarrays using probe level information", In silico biology, 1 January 2006 (2006-01-01), pages 79-92, XP055168063, Netherlands Retrieved from the Internet: URL:http://www.ncbi.nlm.nih.gov/pubmed/167 89916 [retrieved on 2015-02-06]</text></B562><B565EP><date>20150216</date></B565EP></B560></B500><B700><B720><B721><snm>CHEN, Shengpei</snm><adr><str>Main Building
Beishan Industrial Zone
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Yantian District</str><city>Shenzhen
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Yantian District</str><city>Shenzhen
Guangdong 518083</city><ctry>CN</ctry></adr></B721><B721><snm>WANG, Jian</snm><adr><str>Main Building
Beishan Industrial Zone
Yantian District</str><city>Shenzhen
Guangdong 518083</city><ctry>CN</ctry></adr></B721><B721><snm>WANG, Jun</snm><adr><str>Main Building
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Yantian District</str><city>Shenzhen
Guangdong 518083</city><ctry>CN</ctry></adr></B721></B720><B730><B731><snm>BGI Genomics Co., Ltd.</snm><iid>101834224</iid><irf>RAW/P216813EP</irf><adr><str>21 Hongan 3rd Street 
BGI Park Building 7 Floor 7-14 
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