WO2024157222 - METHOD FOR IDENTIFYING GENETIC VARIANT IN AN EMBRYO
National phase entry is expected:
Publication Number
WO/2024/157222
Publication Date
02.08.2024
International Application No.
PCT/IB2024/050754
International Filing Date
26.01.2024
Title **
[English]
METHOD FOR IDENTIFYING GENETIC VARIANT IN AN EMBRYO
[French]
PROCÉDÉ D'IDENTIFICATION D'UN VARIANT GÉNÉTIQUE DANS UN EMBRYON
Applicants **
EMBRYOME INC.
Inventors
VENNER, Eric
BAINBRIDGE, Matthew
GRUSCHOW, Jeremy
Priority Data
63/441,291
26.01.2023
US
Application details
| Total Number of Claims/PCT | * |
| Number of Independent Claims | * |
| Number of Priorities | * |
| Number of Multi-Dependent Claims | * |
| Number of Drawings | * |
| Pages for Publication | * |
| Number of Pages with Drawings | * |
| Pages of Specification | * |
| * | |
| Number of Office Actions | * |
| * | |
International Searching Authority |
CIPO
* |
| Recordal of a Change of the Applicant's Name/Address |
Change of Applicant's Name and Address
* |
| Type of Assignment |
The Standard Agent's Assignment
* |
| Applicant's Legal Status |
Legal Entity
* |
| * | |
| * | |
| * | |
| * | |
| * | |
| Entry into National Phase under |
Chapter I
* |
| Patent Delivery |
Send the Letters Patent by Courier
* |
| 译文 |
|
* The data is based on automatic recognition. Please verify and amend if necessary.
** IP-Coster compiles data from publicly available sources. If this data includes your personal information, you can contact us to request its removal.
Quotation for National Phase entry
| Country | Stages | Total | |
|---|---|---|---|
| China | Filing, Examination, Granting | 3294 | |
| EPO | Filing, Examination, Granting | 29302 | |
| Japan | Filing, Examination, Granting | 3172 | |
| South Korea | Filing, Examination, Granting | 4317 | |
| USA | Filing, Examination, Granting | 10340 |
Total:
50,425
The term for entry into the National Phase has expired. This quotation is for informational purposes only
Contact Us
Abstract[English]
The present disclosure provides, in part, a method of identifying a genetic variant in an embryo. The method comprising: (a) obtaining two or more sources of analytes from the embryo; (b) analyzing the two or more sources of analytes to obtain genetic information of each source; (c) comparing the genetic information of each source against one or more reference genome using at least one variant caller, wherein the variant caller identifies variant(s) between each source and the reference genome; and (d) combining the variant(s) to identify a difference that is present only from the sources, wherein the difference is a genetic variant in the embryo.[French]
La présente divulgation propose, en partie, un procédé d'identification d'un variant génétique dans un embryon. Le procédé comprend : (a) l'obtention d'au moins deux sources d'analytes à partir de l'embryon; (b) l'analyse de ces sources d'analytes pour obtenir des informations génétiques de chaque source; (c) la comparaison des informations génétiques de chaque source par rapport à un ou plusieurs génomes de référence à l'aide d'au moins un appelant de variant, l'appelant de variant identifiant un ou plusieurs variants entre chaque source et le génome de référence; et (d) la combinaison du ou des variants pour identifier une différence qui est présente uniquement à partir des sources, la différence étant un variant génétique dans l'embryon..