SET OF HIGHLY SPECIFIC OLIGONUCLEOTIDE PRIMERS FOR DETECTING GENETIC VARIANTS BY HIGH-THROUGHPUT DNA SEQUENCING
2024-03-28
专利权人GENETICO GENETICS & REPRODUCTIVE MEDICIN (GENE-Non-standard)
申请日期2024-03-28
专利号RU2833429-C1
成果简介NOVELTY - Present invention refers to medicine, particularly to oncology and laboratory and medical genetics. Present invention is a set (panel) of primers for high-throughput sequencing of target gene regions AKT1, ALK, APC, BRAF, CDH1, CDKN2A, CTNNB1, DDR2, EGFR, EIF1AX, ERBB2, ERBB4, FGFR1, FGFR2, FGFR3, FOXL2, GNA11, GNAQ, GNAS, H3F3A, HIST1H3B, HIST1H3C, HNF1A, HRAS, IDH1, IDH2, KDR, KIT, KRAS, MAP2K1, MET, MLH1, NRAS, PDGFRA, PIK3CA, PTEN, RET, ROS1, SF3B1, SMAD4, SMARCB1, SMO, SRC, STK11, TERT, TP53, TSC1, VHL. Disclosed is the use of a kit for detecting clinically significant genetic variants (in particular, somatic mutations) in tumour tissue samples in order to clarify the diagnosis and prognosis of the oncological disease and in order to further adjust the treatment plan, including for the purpose of selecting the optimal anti-tumour targeted therapy. USE - Medicine. ADVANTAGE - Present invention provides higher quality and efficiency of molecular diagnostics of solid tumours. 3 cl, 2 tbl
IPC 分类号C12Q-001/68
国家俄罗斯
专业领域生物科学
语种英语
成果类型专利
文献类型科技成果
条目标识符http://119.78.100.226:8889/handle/3KE4DYBR/17495
专题中国科学院新疆生态与地理研究所
作者单位
GENETICO GENETICS & REPRODUCTIVE MEDICIN (GENE-Non-standard)
推荐引用方式
GB/T 7714
ISAEV A A,KHMELKOVA D N,MIRONOVA I V. SET OF HIGHLY SPECIFIC OLIGONUCLEOTIDE PRIMERS FOR DETECTING GENETIC VARIANTS BY HIGH-THROUGHPUT DNA SEQUENCING. RU2833429-C1[P]. 2024.
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