JP2019510473A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2019510473A5 JP2019510473A5 JP2018539370A JP2018539370A JP2019510473A5 JP 2019510473 A5 JP2019510473 A5 JP 2019510473A5 JP 2018539370 A JP2018539370 A JP 2018539370A JP 2018539370 A JP2018539370 A JP 2018539370A JP 2019510473 A5 JP2019510473 A5 JP 2019510473A5
- Authority
- JP
- Japan
- Prior art keywords
- subject
- colorectal cancer
- risk
- single nucleotide
- linkage disequilibrium
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000034 method Methods 0.000 claims 28
- 206010009944 Colon cancer Diseases 0.000 claims 23
- 208000001333 Colorectal Neoplasms Diseases 0.000 claims 23
- 239000002773 nucleotide Substances 0.000 claims 16
- 125000003729 nucleotide group Chemical group 0.000 claims 16
- 238000012502 risk assessment Methods 0.000 claims 10
- 230000002068 genetic effect Effects 0.000 claims 8
- 102000054765 polymorphisms of proteins Human genes 0.000 claims 8
- 238000012216 screening Methods 0.000 claims 7
- 238000002052 colonoscopy Methods 0.000 claims 4
- 102000039446 nucleic acids Human genes 0.000 claims 4
- 108020004707 nucleic acids Proteins 0.000 claims 4
- 150000007523 nucleic acids Chemical class 0.000 claims 4
- 238000002579 sigmoidoscopy Methods 0.000 claims 4
- 239000012472 biological sample Substances 0.000 claims 2
- 238000003500 gene array Methods 0.000 claims 2
- 238000009534 blood test Methods 0.000 claims 1
- 238000002405 diagnostic procedure Methods 0.000 claims 1
- 230000002550 fecal effect Effects 0.000 claims 1
- 239000000523 sample Substances 0.000 claims 1
- 230000000392 somatic effect Effects 0.000 claims 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2022048257A JP2022104934A (ja) | 2016-01-28 | 2022-03-24 | 結腸直腸癌発症のリスクを評価するための方法 |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2016900254A AU2016900254A0 (en) | 2016-01-28 | Methods for assessing risk of developing colorectal cancer | |
| AU2016900254 | 2016-01-28 | ||
| AU2016903246A AU2016903246A0 (en) | 2016-08-16 | Methods for assessing risk of developing colorectal cancer | |
| AU2016903246 | 2016-08-16 | ||
| PCT/AU2017/050066 WO2017127893A1 (en) | 2016-01-28 | 2017-01-27 | Methods for assessing risk of developing colorectal cancer |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2022048257A Division JP2022104934A (ja) | 2016-01-28 | 2022-03-24 | 結腸直腸癌発症のリスクを評価するための方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2019510473A JP2019510473A (ja) | 2019-04-18 |
| JP2019510473A5 true JP2019510473A5 (instruction) | 2020-03-05 |
| JP7126704B2 JP7126704B2 (ja) | 2022-08-29 |
Family
ID=59396853
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018539370A Active JP7126704B2 (ja) | 2016-01-28 | 2017-01-27 | 結腸直腸癌発症のリスクを評価するための方法 |
| JP2022048257A Withdrawn JP2022104934A (ja) | 2016-01-28 | 2022-03-24 | 結腸直腸癌発症のリスクを評価するための方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2022048257A Withdrawn JP2022104934A (ja) | 2016-01-28 | 2022-03-24 | 結腸直腸癌発症のリスクを評価するための方法 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US11773448B2 (instruction) |
| EP (1) | EP3408412B1 (instruction) |
| JP (2) | JP7126704B2 (instruction) |
| KR (1) | KR20180123480A (instruction) |
| CN (1) | CN109072308A (instruction) |
| AU (1) | AU2017212152B2 (instruction) |
| CA (1) | CA3012783A1 (instruction) |
| ES (1) | ES2976360T3 (instruction) |
| IL (1) | IL260777B (instruction) |
| MX (1) | MX2018009254A (instruction) |
| SG (1) | SG11201806432PA (instruction) |
| WO (1) | WO2017127893A1 (instruction) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7101143B2 (ja) * | 2019-04-23 | 2022-07-14 | ジェネシスヘルスケア株式会社 | 大腸がんのリスクを判定する方法 |
| CN111057767A (zh) * | 2020-01-19 | 2020-04-24 | 北京市第一中西医结合医院 | 一种中国人胃肠道肿瘤风险相关的位于mlh1基因的snp位点及其应用 |
| CN111739642A (zh) * | 2020-06-23 | 2020-10-02 | 杭州和壹医学检验所有限公司 | 一种结直肠癌风险预测方法、系统、计算机设备及可读存储介质 |
| CN112029852B (zh) * | 2020-09-24 | 2023-12-05 | 吉林大学 | ONFH易感相关TNF-α、GREM1、TGF-β、CR2基因SNP检测物质 |
| CN114672556A (zh) * | 2020-12-25 | 2022-06-28 | 上海善准生物科技有限公司 | 结直肠癌分子分型及生存风险基因群及诊断产品和应用 |
| CN114334142A (zh) * | 2021-07-02 | 2022-04-12 | 中山大学肿瘤防治中心（中山大学附属肿瘤医院、中山大学肿瘤研究所） | 一种用于结直肠癌发病风险预测的snp位点组合、发病风险预测模型及系统 |
| CN115786501B (zh) * | 2022-07-02 | 2023-06-16 | 武汉大学 | 一种与结直肠癌早期筛查和辅助诊断相关的增强子功能位点及其应用 |
| WO2024138243A1 (en) * | 2022-12-27 | 2024-07-04 | Genetic Technologies Limited | Colorectal cancer risk assessment |
| CN116949179A (zh) * | 2023-07-04 | 2023-10-27 | 中国医学科学院北京协和医院 | 结直肠肿瘤多基因遗传风险评分系统、存储介质和电子设备 |
| CN118658626A (zh) * | 2024-08-19 | 2024-09-17 | 杭州和壹基因科技有限公司 | 一种基于机器学习的消化系统肿瘤的筛查方法及系统 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54147035A (en) | 1978-05-10 | 1979-11-16 | Minolta Camera Co Ltd | Tessar type photographic lens placed behind aperture |
| US4240608A (en) | 1979-11-02 | 1980-12-23 | Acf Industries, Incorporated | Controlled float seat arrangement for expanding gate valves |
| US5210015A (en) | 1990-08-06 | 1993-05-11 | Hoffman-La Roche Inc. | Homogeneous assay system using the nuclease activity of a nucleic acid polymerase |
| CA2257109C (en) | 1996-06-04 | 2009-10-06 | University Of Utah Research Foundation | Monitoring hybridization during pcr |
| US6174170B1 (en) | 1997-10-21 | 2001-01-16 | Sony Corporation | Display of text symbols associated with audio data reproducible from a recording disc |
| AU785425B2 (en) | 2001-03-30 | 2007-05-17 | Genetic Technologies Limited | Methods of genomic analysis |
| US6898531B2 (en) | 2001-09-05 | 2005-05-24 | Perlegen Sciences, Inc. | Algorithms for selection of primer pairs |
| WO2003021259A1 (en) | 2001-09-05 | 2003-03-13 | Perlegen Sciences, Inc. | Selection of primer pairs |
| US20040023237A1 (en) | 2001-11-26 | 2004-02-05 | Perelegen Sciences Inc. | Methods for genomic analysis |
| US6897025B2 (en) | 2002-01-07 | 2005-05-24 | Perlegen Sciences, Inc. | Genetic analysis systems and methods |
| US20050019787A1 (en) | 2003-04-03 | 2005-01-27 | Perlegen Sciences, Inc., A Delaware Corporation | Apparatus and methods for analyzing and characterizing nucleic acid sequences |
| US20040241657A1 (en) | 2003-05-28 | 2004-12-02 | Perlegen Sciences, Inc. | Liver related disease compositions and methods |
| US7127355B2 (en) | 2004-03-05 | 2006-10-24 | Perlegen Sciences, Inc. | Methods for genetic analysis |
| KR101206029B1 (ko) * | 2005-04-01 | 2012-11-28 | 삼성전자주식회사 | 대장암 진단용 다중 ｓｎｐ, 그를 포함하는 마이크로어레이및 키트 및 그를 이용한 대장암 진단 방법 |
| CA2721313A1 (en) * | 2008-04-10 | 2009-10-15 | Genenews Corporation | Method and apparatus for determining a probability of colorectal cancer in a subject |
| CN102876791B (zh) * | 2012-09-21 | 2015-09-02 | 湖北维达健基因技术有限公司 | 一种用于肛肠疾病患病风险评估基因芯片、制备方法及其试剂盒 |
| EP3207161A4 (en) * | 2014-10-14 | 2018-09-12 | Wake Forest University Health Sciences | Methods and compositions for correlating genetic markers with cancer risk |
| US10609708B1 (en) | 2017-06-27 | 2020-03-31 | Sprint Spectrum L.P. | Use of TDD special subframe for transmission of small quantity of data |
-
2017
- 2017-01-27 SG SG11201806432PA patent/SG11201806432PA/en unknown
- 2017-01-27 EP EP17743495.8A patent/EP3408412B1/en active Active
- 2017-01-27 IL IL260777A patent/IL260777B/en unknown
- 2017-01-27 CA CA3012783A patent/CA3012783A1/en active Pending
- 2017-01-27 JP JP2018539370A patent/JP7126704B2/ja active Active
- 2017-01-27 MX MX2018009254A patent/MX2018009254A/es unknown
- 2017-01-27 WO PCT/AU2017/050066 patent/WO2017127893A1/en not_active Application Discontinuation
- 2017-01-27 AU AU2017212152A patent/AU2017212152B2/en active Active
- 2017-01-27 KR KR1020187024547A patent/KR20180123480A/ko not_active Ceased
- 2017-01-27 US US16/074,032 patent/US11773448B2/en active Active
- 2017-01-27 CN CN201780021329.8A patent/CN109072308A/zh active Pending
- 2017-01-27 ES ES17743495T patent/ES2976360T3/es active Active
-
2022
- 2022-03-24 JP JP2022048257A patent/JP2022104934A/ja not_active Withdrawn
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2019510473A5 (instruction) | ||
| JP7689557B2 (ja) | 相同組換え欠損を推定するための統合された機械学習フレームワーク | |
| LaDuca et al. | Exome sequencing covers> 98% of mutations identified on targeted next generation sequencing panels | |
| Dubois et al. | Multiple common variants for celiac disease influencing immune gene expression | |
| Festen et al. | A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease | |
| Valette et al. | Melanocortin-4 receptor mutations and polymorphisms do not affect weight loss after bariatric surgery | |
| Oey et al. | Genetic and epigenetic variation among inbred mouse littermates: identification of inter-individual differentially methylated regions | |
| Perot et al. | Microarray-based sketches of the HERV transcriptome landscape | |
| Yagil et al. | Identification of hypertension-related genes through an integrated genomic-transcriptomic approach | |
| Debrand et al. | A non-invasive droplet digital PCR (ddPCR) assay to detect paternal CFTR mutations in the cell-free fetal DNA (cffDNA) of three pregnancies at risk of cystic fibrosis via compound heterozygosity | |
| JP2019531048A (ja) | 無細胞核酸の多重解像度分析のための方法 | |
| Yamazaki et al. | Positive association of genetic variants in the upstream region of NKX2-3 with Crohn’s disease in Japanese patients | |
| Carapito et al. | On the genetics of the Silk Route: association analysis of HLA, IL10, and IL23R-IL12RB2 regions with Behçet’s disease in an Iranian population | |
| Huang et al. | Genome-wide association study on chicken carcass traits using sequence data imputed from SNP array | |
| KR20190119859A (ko) | 알츠하이머성 치매가 발병될 가능성 평가방법 | |
| Helfer-Hungerbuehler et al. | GAPDH pseudogenes and the quantification of feline genomic DNA equivalents | |
| He et al. | East Asian-specific and cross-ancestry genome-wide meta-analyses provide mechanistic insights into peptic ulcer disease | |
| Wang et al. | CARD15 gene polymorphisms are associated with tuberculosis susceptibility in Chinese Holstein cows | |
| Mistry et al. | Exome sequencing of 75 individuals from multiply affected coeliac families and large scale resequencing follow up | |
| Yang et al. | The next generation of complex lung genetic studies | |
| Hagiwara et al. | Homozygosity mapping on homozygosity haplotype analysis to detect recessive disease-causing genes from a small number of unrelated, outbred patients | |
| Bonifazi et al. | A long PCR-based molecular protocol for detecting normal and expanded ZNF9 alleles in myotonic dystrophy type 2 | |
| Choi et al. | Genome-wide association study of coronary artery calcification in asymptomatic Korean populations | |
| Salomon et al. | GWASeq: targeted re-sequencing follow up to GWAS | |
| CN110914453B (zh) | 动脉粥样硬化性心血管疾病的生物标志物 |