EP3455760 - METHODS OF DETERMINING GENOMIC HEALTH RISK [Right-click to bookmark this link] | Status | The application is deemed to be withdrawn Status updated on 12.02.2021 Database last updated on 03.09.2024 | |
Former | Request for examination was made Status updated on 15.02.2019 | ||
Former | The international publication has been made Status updated on 17.11.2017 | Most recent event Tooltip | 12.02.2021 | Application deemed to be withdrawn | published on 17.03.2021 [2021/11] | Applicant(s) | For all designated states Human Longevity, Inc. 4570 Executive Dr. San Diego, CA 92121 / US | [2019/12] | Inventor(s) | 01 /
DI IULIO, Julia 4570 Executive Drive San Diego California 92121 / US | 02 /
TELENTI, Amalio 4570 Executive Drive San Diego California 92121 / US | [2019/12] | Representative(s) | Hutter, Anton, et al Venner Shipley LLP 5 Stirling House Stirling Road The Surrey Research Park Guildford GU2 7RF / GB | [N/P] |
Former [2019/12] | Hutter, Anton, et al Venner Shipley LLP 200 Aldersgate London EC1A 4HD / GB | Application number, filing date | 17796629.8 | 08.05.2017 | [2019/12] | WO2017US31559 | Priority number, date | US201662333653P | 09.05.2016 Original published format: US 201662333653 P | US201662410783P | 20.10.2016 Original published format: US 201662410783 P | [2019/12] | Filing language | EN | Procedural language | EN | Publication | Type: | A2 Application without search report | No.: | WO2017196728 | Date: | 16.11.2017 | Language: | EN | [2017/46] | Type: | A2 Application without search report | No.: | EP3455760 | Date: | 20.03.2019 | Language: | EN | The application published by WIPO in one of the EPO official languages on 16.11.2017 takes the place of the publication of the European patent application. | [2019/12] | Search report(s) | International search report - published on: | KR | 26.07.2018 | (Supplementary) European search report - dispatched on: | EP | 17.02.2020 | Classification | IPC: | C12Q1/6883, C12Q1/6886 | [2019/50] | CPC: |
G16B20/20 (EP,US);
C12Q1/6883 (EP,US);
C12Q1/6886 (EP,US);
G16B20/00 (EP,US);
G16B30/00 (EP,US);
G16B30/10 (EP,US);
C12Q1/6869 (EP);
C12Q2600/118 (US);
C12Q2600/156 (EP,US);
G16B20/40 (EP,US)
(-)
| C-Set: |
C12Q1/6869, C12Q2537/165 (EP,US)
|
Former IPC [2019/12] | G06F19/18, G06F19/22, G06F19/24, G06F19/26 | Designated contracting states | AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LI, LT, LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR [2019/12] | Title | German: | VERFAHREN ZUR BESTIMMUNG DES GENOMISCHEN GESUNDHEITSRISIKOS | [2019/12] | English: | METHODS OF DETERMINING GENOMIC HEALTH RISK | [2019/12] | French: | PROCÉDÉS DE DÉTERMINATION D'UN RISQUE POUR LA SANTÉ GÉNOMIQUE | [2019/12] | Entry into regional phase | 08.11.2018 | National basic fee paid | 08.11.2018 | Search fee paid | 08.11.2018 | Designation fee(s) paid | 08.11.2018 | Examination fee paid | Examination procedure | deleted | Date on which the examining division has become responsible | 08.11.2018 | Examination requested [2019/12] | 19.06.2019 | Amendment by applicant (claims and/or description) | 16.09.2020 | Application deemed to be withdrawn, date of legal effect [2021/11] | 15.10.2020 | Despatch of communication that the application is deemed to be withdrawn, reason: reply to the communication from the examining division not received in time [2021/11] | Fees paid | Renewal fee | 28.05.2019 | Renewal fee patent year 03 | Penalty fee | Additional fee for renewal fee | 31.05.2020 | 04   M06   Not yet paid |
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Responsibility for the accuracy, completeness or quality of the data displayed under the link provided lies entirely with the Unified Patent Court. | Documents cited: | Search | [XI]US2002142295 (BYWATER MARGARET [US], et al) [X] 1-3,5,8-11,13,15 * paragraphs [0013] - [0015] - [0037] - [0040] - [0046] - [0047] - [0095] , [0100] - [0101]; tables 1-2 * * figure 9 * * claims 1,10-11 * [I] 4,6,12; | [XI] - VARUN AGGARWALA ET AL, "An expanded sequence context model broadly explains variability in polymorphism levels across the human genome", NATURE GENETICS., NEW YORK, US, (20160215), vol. 48, no. 4, doi:10.1038/ng.3511, ISSN 1061-4036, pages 349 - 355, XP055427377 [X] 1-3,8 * abstract * * page 349, column l, paragraph 1 * * page 350, column l, paragraph 1 * * page 353 * * figures 3-4 * [I] 4-7,9-15 DOI: http://dx.doi.org/10.1038/ng.3511 | [XI] - STURM RICHARD A ET AL, "A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color", AMERICAN JOURNAL OF HUMAN GENETICS, AMERICAN SOCIETY OF HUMAN GENETICS, CHICAGO, IL, US, (200802), vol. 82, no. 2, doi:10.1016/J.AJHG.2007.11.005, ISSN 0002-9297, pages 424 - 431, XP009100453 [X] 1-6,9-13 * abstract * * page 425, column r - page 426, column r, paragraph 2 * * page 427 - page 428, column l, paragraph 1 * * figures 2-3 * [I] 7,14 DOI: http://dx.doi.org/10.1016/j.ajhg.2007.11.005 | [I] - BO-YING BAO ET AL, "Genetic variants in ultraconserved regions associate with prostate cancer recurrence and survival", SCIENTIFIC REPORTS, (20160223), vol. 6, no. 1, doi:10.1038/srep22124, XP055638543 [I] 1-15 * abstract * DOI: http://dx.doi.org/10.1038/srep22124 | [IP] - Julia Di Iulio ET AL, bioRxiv, doi:10.1101/082362, (20161021), URL: https://www.biorxiv.org/content/biorxiv/early/2016/10/21/082362.full.pdf, (20191030), XP055637551 [IP] 1-15 * abstract * * page 3, paragraphs 2-3 * * page 4, paragraph last * * page 6, paragraph 3 - page 7, paragraph 1 * * page 8, paragraph 3 * DOI: http://dx.doi.org/10.1101/082362 | [AD] - IULIANA IONITA-LAZA ET AL, "A spectral approach integrating functional genomic annotations for coding and noncoding variants", NATURE GENETICS., NEW YORK, US, (20160104), vol. 48, no. 2, doi:10.1038/ng.3477, ISSN 1061-4036, pages 214 - 220, XP055637830 [AD] 1-15 * the whole document * DOI: http://dx.doi.org/10.1038/ng.3477 | [A] - JIA LI ET AL, "A Dual Model for Prioritizing Cancer Mutations in the Non-coding Genome Based on Germline and Somatic Events", PLOS COMPUTATIONAL BIOLOGY, (20151120), vol. 11, no. 11, doi:10.1371/journal.pcbi.1004583, page e1004583, XP055639341 [A] 1-15 * the whole document * DOI: http://dx.doi.org/10.1371/journal.pcbi.1004583 | [A] - KHURANA EKTA ET AL, "Role of non-coding sequence variants in cancer", NATURE REVIEWS: GENETICS, NATURE PUBLISHING GROUP, UNITED KINGDOM, (20160119), vol. 17, no. 2, doi:10.1038/NRG.2015.17, ISSN 1471-0064, pages 93 - 108, XP002773468 [A] 1-15 * the whole document * DOI: http://dx.doi.org/10.1038/nrg.2015.17 | [A] - B. J. WILLCOX ET AL, "FOXO3A genotype is strongly associated with human longevity", PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES, (20080916), vol. 105, no. 37, doi:10.1073/pnas.0801030105, ISSN 0027-8424, pages 13987 - 13992, XP055012050 [A] 1-15 * the whole document * DOI: http://dx.doi.org/10.1073/pnas.0801030105 | [T] - DI IULIO JULIA ET AL, "The human noncoding genome defined by genetic diversity", NATURE GENETICS, NATURE PUBLISHING GROUP, NEW YORK, US, vol. 50, no. 3, doi:10.1038/S41588-018-0062-7, ISSN 1061-4036, (20180226), pages 333 - 337, (20180226), XP036462462 [T] * the whole document * DOI: http://dx.doi.org/10.1038/s41588-018-0062-7 | [T] - JULIA DI IULIO, "Interpretation of the noncoding genome in medicine", PERSONALIZED MEDICINE, GB, (20181022), vol. 15, no. 6, doi:10.2217/pme-2018-0065, ISSN 1741-0541, pages 453 - 455, XP055637477 [T] * the whole document * DOI: http://dx.doi.org/10.2217/pme-2018-0065 | International search | [A]US2013332081 (REESE MARTIN G [US], et al) [A] 1-3, 20-27 * See the whole document. *; | [A]US2015066378 (ROBISON REID [US], et al) [A] 1-3, 20-27 * See abstract; and claims 1-8, 18-21. *; | [A]WO2015042496 (UNIVERSTIY OF WASHINGTON THROUGH ITS CT FOR COMMERCIALIZATION [US], et al) [A] 1-3, 20-27 * See abstract; and claims 1-7, 15-22. *; | [A]WO2015105771 (UNIV MICHIGAN [US]) [A] 1-3, 20-27 * See the whole document. *; | [A] - RITCHIE et al., "Computational approaches to interpreting genomic sequence variation", Genome Medicine, (20140000), vol. 6, no. 87, pages 1 - 11, XP 021208825 [A] 1-3, 20-27 * See the whole document. * | [PX] - TELENTI et al., "Deep sequencing of 10,000 human genomes", PNAS, (20161000), vol. 113, no. 42, pages 11901 - 11906, XP055506897 [PX] 1-3, 20-27 * See pages 11901-11902, 11905; and figures 2-3. * DOI: http://dx.doi.org/10.1073/pnas.1613365113 |