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Extract from the Register of European Patents

EP About this file: EP3810805

EP3810805 - METHOD FOR DETECTION AND QUANTIFICATION OF GENETIC ALTERATIONS [Right-click to bookmark this link]
StatusRequest for examination was made
Status updated on  26.03.2021
Database last updated on 26.07.2024
FormerThe international publication has been made
Status updated on  03.01.2020
Most recent event   Tooltip10.04.2024New entry: Renewal fee paid 
Applicant(s)For all designated states
Lucence Life Sciences Pte Ltd.
211 Henderson Road
04-02 211
Henderson Industrial Park
Singapore 159552 / SG
[2021/17]
Inventor(s)01 / CHOUDHURY, Yukti
c/o Lucence Life Sciences Pte. Ltd. 211 Henderson
Road, 04-02, 211 Henderson Industrial Park
Singapore 159552 / SG
02 / CHEN, Hao
c/o Lucence Life Sciences Pte. Ltd. 211 Henderson
Road, 04-02, 211 Henderson Industrial Park
Singapore 159552 / SG
03 / TAN, Min-Han
c/o Lucence Life Sciences Pte. Ltd. 211 Henderson
Road, 04-02, 211 Henderson Industrial Park
Singapore 159552 / SG
 [2021/17]
Representative(s)Boult Wade Tennant LLP
Salisbury Square House
8 Salisbury Square
London EC4Y 8AP / GB
[2021/17]
Application number, filing date19825310.625.06.2019
[2021/17]
WO2019SG50317
Priority number, dateSG20181005450Y25.06.2018         Original published format: SG10201805450Y
[2021/17]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report
No.:WO2020005159
Date:02.01.2020
Language:EN
[2020/01]
Type: A1 Application with search report 
No.:EP3810805
Date:28.04.2021
Language:EN
The application published by WIPO in one of the EPO official languages on 02.01.2020 takes the place of the publication of the European patent application.
[2021/17]
Search report(s)International search report - published on:SG02.01.2020
(Supplementary) European search report - dispatched on:EP23.02.2022
ClassificationIPC:C12Q1/6869, C12Q1/6855, C12Q1/6858
[2022/12]
CPC:
C12Q1/6858 (EP); C12Q1/6855 (EP); C12N9/1252 (EP)
C-Set:
C12Q1/6855, C12Q2537/159, C12Q2563/149, C12Q2563/179 (EP);
C12Q1/6858, C12Q2525/191, C12Q2537/159, C12Q2563/149, C12Q2563/179 (EP)
Former IPC [2021/17]C12Q1/6869
Designated contracting statesAL,   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 [2021/17]
TitleGerman:VERFAHREN ZUR DETEKTION UND QUANTIFIZIERUNG VON GENETISCHEN VERÄNDERUNGEN[2021/17]
English:METHOD FOR DETECTION AND QUANTIFICATION OF GENETIC ALTERATIONS[2021/17]
French:PROCÉDÉ DE DÉTECTION ET DE QUANTIFICATION DE MODIFICATIONS GÉNÉTIQUES[2021/17]
Entry into regional phase23.12.2020National basic fee paid 
23.12.2020Search fee paid 
23.12.2020Designation fee(s) paid 
23.12.2020Examination fee paid 
Examination procedure23.12.2020Examination requested  [2021/17]
06.09.2022Amendment by applicant (claims and/or description)
Fees paidRenewal fee
16.06.2021Renewal fee patent year 03
31.03.2022Renewal fee patent year 04
04.04.2023Renewal fee patent year 05
08.04.2024Renewal fee patent year 06
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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[Y]WO2011019964  (NUGEN TECHNOLOGIES INC [US], et al) [Y] 1-15* paragraphs [0105] - [0107] - [0114] - [0120] *;
 [Y]WO2014093330  (CLEARFORK BIOSCIENCE INC [US]) [Y] 1-15 * claims 1-104 * * figures 1,2,4,15,16,19,21,31,33,34,36 * * examples 5-13 *;
 [Y]WO2015039006  (GEN HOSPITAL CORP [US]) [Y] 1-15 * figures 1,10 * * paragraphs [0012] , [0021] , [0035] , [0038] , [0040] *;
 [Y]WO2018111835  (DANA FARBER CANCER INST INC [US]) [Y] 1-15 * claims 1-56 * * page 25 - page 28, paragraph 1 * * figures 1-6,12 * * page 16, paragraph 3 *;
 [Y]  - SCOTT R KENNEDY ET AL, "Detecting ultralow-frequency mutations by Duplex Sequencing", NATURE PROTOCOLS, GB, (20141009), vol. 9, no. 11, doi:10.1038/nprot.2014.170, ISSN 1754-2189, pages 2586 - 2606, XP055745195 [Y] 1-15 * the whole document *

DOI:   http://dx.doi.org/10.1038/nprot.2014.170
 [Y]  - QING WANG ET AL, "Targeted sequencing of both DNA strands barcoded and captured individually by RNA probes to identify genome-wide ultra-rare mutations", SCIENTIFIC REPORTS, (20170613), vol. 7, no. 1, doi:10.1038/s41598-017-03448-8, XP055551336 [Y] 1-15 * the whole document *

DOI:   http://dx.doi.org/10.1038/s41598-017-03448-8
International search[Y]WO2015200541  (BIO RAD LABORATORIES [US]) [Y] 31 AND 32 * Para. [0172] *;
 [YA]WO2016081798  (CHILDRENS MEDICAL CENTER [US]) [Y] 31 AND 32 * Whole document, in particular Fig. 1A & Para. [00246]-[00253] * [A] 1-30;
 [YA]  - HU J. et al., "Detecting DNA Double-Stranded Breaks in Mammalian Genomes by Linear Amplification-mediated High-Throughput Genomewide Translocation Sequencing (LAM-HTGTS", Nat Protoc, (20160500), vol. 11, no. 5, pages 853 - 871, XP055668234 [Y] 31 AND 32 * Whole document, in particular Fig. 1b & Experimental design * [A] 1-30

DOI:   http://dx.doi.org/10.1038/nprot.2016.043
 [Y]  - "TruSeq® DNA Library Prep Kits", Illumina, (20141117), URL: https://www.illumina.com/content/dam/illumina-marketing/documents/products/datasheets/datasheet_truseq_dna_sample_prep_kits.pdf, (20190826), XP055668241 [Y] 31 AND 32 * Fig. 2D; Innovative Library Preparation Chemistry *
The EPO accepts no responsibility for the accuracy of data originating from other authorities; in particular, it does not guarantee that it is complete, up to date or fit for specific purposes.