EP 2102651 A4 20101117 - GENETIC ANALYSIS SYSTEMS AND METHODS
Title (en)
GENETIC ANALYSIS SYSTEMS AND METHODS
Title (de)
GENANALYSESYSTEME UND -VERFAHREN
Title (fr)
PROCÉDÉS ET SYSTÈMES D'ANALYSE GÉNÉTIQUE
Publication
Application
Priority
- US 2007086138 W 20071130
- US 86806606 P 20061130
- US 95112307 P 20070720
- US 78167907 A 20070723
- US 97219807 P 20070913
- US 98562207 P 20071105
- US 98968507 P 20071121
Abstract (en)
[origin: GB2444410A] A method or system for assessing phenotypes, such as a disease or a susceptibility to a disease, of an individual's genomic information, such as single nucleotide polymorphisms (SNPs), comprises comparing a genomic profile of the individual with a database of genotype/phenotype correlations. reporting the results back to the individual, updating the database with newly discovered correlations and/or new genomic data and reporting the revised correlations back to the individual. Multiple genetic markers, together with other information, are combined to produce a Genetic Composite Index (GCI) score. An on-line portals comprising a website allows individuals to access and analyse the information. Methods for determining predisposition to, in particular, Alzheimer's Disease, colorectal cancer, osteoarthritis or exfoliation glaucoma, based on specific SNP markers, are provided.
IPC 8 full level
G06F 19/00 (2011.01); C12Q 1/68 (2006.01); G01N 33/48 (2006.01); G06F 17/30 (2006.01); G16B 20/10 (2019.01); G16B 20/20 (2019.01); G16B 20/40 (2019.01); G16B 50/30 (2019.01)
CPC (source: CN EP GB KR US)
C12Q 1/6827 (2013.01 - GB); C12Q 1/6837 (2013.01 - GB); C12Q 1/6883 (2013.01 - CN EP GB KR); C12Q 1/6886 (2013.01 - CN EP KR); G01N 33/48 (2013.01 - KR); G16B 20/00 (2019.02 - EP GB KR); G16B 20/10 (2019.02 - CN EP GB US); G16B 20/20 (2019.02 - CN EP GB US); G16B 20/40 (2019.02 - CN EP GB US); G16B 50/00 (2019.02 - KR); G16B 50/30 (2019.02 - CN EP GB US); C12Q 2600/156 (2013.01 - CN EP KR); C12Q 2600/172 (2013.01 - CN EP KR); G16B 50/00 (2019.02 - EP); Y02A 90/10 (2018.01 - EP)
Citation (search report)
- [XI] US 2005214811 A1 20050929 - MARGULIES DAVID M [US], et al
- [Y] WO 0126029 A2 20010412 - ORCHID BIOSCIENCES INC [US]
- [Y] HAMOSH A ET AL: "Online Mendelian Inheritance in Man (OMIM).", HUMAN MUTATION 2000 LNKD- PUBMED:10612823, vol. 15, no. 1, 2000, pages 57 - 61, XP002603004, ISSN: 1059-7794
Citation (examination)
- CATHRYN LEWIS: "Genetic association studies: Design, analysis and interpretation", BRIEFINGS IN BIOINFORMATICS, vol. 3, no. 2, 1 June 2002 (2002-06-01), pages 146 - 153, XP055094751
- HAMOSH A ET AL: "Online Mendelian Inheritance in Man (OMIM)", HUMAN MUTATION, JOHN WILEY & SONS, INC, US, vol. 15, no. 1, 1 January 2000 (2000-01-01), pages 57 - 61, XP002603004, ISSN: 1059-7794
Designated contracting state (EPC)
AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR
DOCDB simple family (publication)
GB 0723512 D0 20080109; GB 2444410 A 20080604; GB 2444410 B 20110824; AU 2007325021 A1 20080605; AU 2007325021 B2 20130509; CA 2671267 A1 20080605; CN 103642902 A 20140319; CN 103642902 B 20160120; EP 2102651 A2 20090923; EP 2102651 A4 20101117; HK 1139737 A1 20100924; JP 2010522537 A 20100708; JP 2014140387 A 20140807; KR 20090105921 A 20091007; TW 200847056 A 20081201; TW I363309 B 20120501; WO 2008067551 A2 20080605; WO 2008067551 A3 20081211
DOCDB simple family (application)
GB 0723512 A 20071130; AU 2007325021 A 20071130; CA 2671267 A 20071130; CN 201310565723 A 20071130; EP 07854875 A 20071130; HK 10106416 A 20100630; JP 2009539519 A 20071130; JP 2014102062 A 20140516; KR 20097013756 A 20071130; TW 96145856 A 20071130; US 2007086138 W 20071130