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1. (WO2019043015) METHOD TO CONFIRM VARIANTS IN NGS PANEL TESTING BY SNP GENOTYPING
국제사무국에 기록된 최신 서지정보    정보 제출

공개번호: WO/2019/043015 국제출원번호: PCT/EP2018/073150
공개일: 07.03.2019 국제출원일: 28.08.2018
IPC:
C12Q 1/68 (2018.01)
C SECTION C — 화학; 야금
12
생화학; 맥주; 주정; 포도주; 식초; 미생물학; 효소학; 돌연변이 또는 유전자공학
Q
효소 또는 미생물을 함유한 측정 또는 시험방법; 그것을 위한 조성물 또는 시험지; 그 조성물을 조제하는 방법; 미생물학적 또는 효소학적 방법에 있어서의 상태응답 제어
1
효소 또는 미생물을 함유한 측정 또는 시험방법; 그것을 위한 조성물; 그 조성물의 제조방법
68
핵산을 함유한 것
출원인:
ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS [FR/FR]; 3, avenue Victoria 75004 PARIS, FR
발명자:
CAZENEUVE, Cécile; FR
NOEL, Sandrine; FR
대리인:
REGIMBEAU; REGIMBEAU 20, rue de Chazelles 75847 PARIS CEDEX 17, FR
우선권 정보:
17306106.029.08.2017EP
발명의 명칭: (EN) METHOD TO CONFIRM VARIANTS IN NGS PANEL TESTING BY SNP GENOTYPING
(FR) PROCÉDÉ DE CONFIRMATION DE VARIANTES DANS UN TEST DE PANEL DE NGS PAR GÉNOTYPAGE SNP
요약서:
(EN) The present invention belongs to the field of methods to validate genotyping results obtained by Next-Generation Sequencing (NGS) for a series of patients, to detect sample mix-ups and prevent misdiagnosis. In particular, the present invention relates to a method to validate Next-generation sequencing (NGS) genotyping results of a panel of genes tested in a series of at least 2 patients characterized in that said validation is provided by SNP profiling assay,adapted for allele-specific multiplex PCR, allowing accurate validation of NGS data by sample pairing. The present invention also relates to a kit comprising PCR multiplex reagents and/or NGS oligonucleotide probes or primers designed to capture or amplify sequences comprising a combination of at least 8 SNPs and its use for validating NGS genotyping results.
(FR) La présente invention concerne le domaine des procédés de validation des résultats de génotypage obtenus par séquençage de nouvelle génération (NGS) pour une série de patients, pour détecter des mélanges d'échantillons et empêcher un mauvais diagnostic. La présente invention concerne en particulier un procédé de validation de résultats de génotypage par séquençage de nouvelle génération (NGS) d'un panel de gènes testés dans une série d'au moins 2 patients, caractérisé en ce que ladite validation est fournie par un test de profilage SNP, adapté à la PCR multiplex spécifique des allèles, permettant une validation précise des données de NGS par appariement d'échantillons. La présente invention concerne également un kit comprenant des réactifs de PCR multiplex et/ou des sondes oligonucléotidiques de NGS ou des amorces conçues pour capturer ou amplifier des séquences comprenant une combinaison d'au moins 8 SNP et son utilisation pour valider des résultats de génotypage par NGS.
지정국: AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JO, JP, KE, KG, KH, KN, KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW
아프리카지역 지식재산권기구(ARIPO) (BW, GH, GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW)
유라시아 특허청 (AM, AZ, BY, KG, KZ, RU, TJ, TM)
유럽 특허청(EPO) (AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR)
African Intellectual Property Organization (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, KM, ML, MR, NE, SN, TD, TG)
공개언어: 영어 (EN)
출원언어: 영어 (EN)