Int'l Conference on Gene Editing and CRISPR Technologies (GECT 2022)

Int'l Conference on Gene Editing and CRISPR Technologies (GECT 2022) 

Conference Date: May 27-29, 2022
Conference Venue: Xi'an, China
Website: https://www.maymeeting.org/conference/GECT2022/
Online Registration System: https://www.maymeeting.org/RegistrationSubmission/default.aspx?ConferenceID=1479
Email: [email protected]

Int'l Conference on Gene Editing and CRISPR Technologies (GECT 2022) will be held in Xi'an, China, during May 27-29, 2022. The aim of GECT is to provide a stage for researchers, engineers, academicians as well as industrial professionals from all over the world to present their research results and development activities in Biomedicine, Clinical Application of Gene Editing, CRISPR Systems and CRISPR Technologies, Effective Delivery for Genes in Vitro, Gene Knock In and Genomic Screening, Genome Engineering and DNA repair, Single Base Editing, etc. GECT 2022 will be a valuable and important platform for inspiring international and interdisciplinary exchange at the forefront of CGene Editing and CRISPR Technologies. 

If you wish to serve the conference as an invited speaker, please send email to us with your CV. We'll contact with you asap.

Publication and Presentation

Publication: Open Access Journal，please contact us for detailed information
Index: CNKI and Google Scholar
Note: If you want to present your research results but do NOT wish to publish a paper, you may simply submit an Abstract to our Registration System.

Contact Us

Email: [email protected]
Tel: +86 132 6470 2250 (From Monday to Friday)
QQ: 1349406763 
WeChat: 3025797047
Official Account: Academic Communications

Attendance Methods

1.Submit full paper (Regular Attendance+Paper Publication+Presentation)
You are welcome to submit full paper, all the accepted papers will be published by Open access journal.
2. Submit abstract (Regular Attendance+Abstract+Presentation)
3. Regular Attendance (No Submission Required) 

Conference Topics

Biomedicine
Cas Genes and CRISPR Subtypes
Clinical Application of Gene Editing
CRISPR Biology
CRISPR Systems and CRISPR Technologies
CRISPR-Associated Systems
Delivery and specificity of CRISPR-based tools
Different Gene Delivery Systems
Disease Models
Effective Delivery for Genes in Vitro
Gene Drive
Gene Editing Technology and Gene Editing Efficiency
Gene Editing-Based Safety and Ethics
Gene Function
Gene Knock In and Genomic Screening
Gene Therapy
Genetic Vaccines
Genetics and Genomic Medicine
Genome Editing and Genome Regulation
Genome Engineering and DNA repair
In Situ Gene Editing
In Vitro Genetic Depletion
In Vivo Gene Editing
Locus Structure
Molecular Epigenetics
Nano-Therapy
Off-Target Effects
Optimizing Repair of CRISPR-Generated DNA Breaks
Programmable Gene Expression
Regulatory, Safety Aspects of Cell and Gene Therapy
Repeated Sequences
RNA Editing Technology
RNA Guided Nuclease for Genome Modifications
RNAi and Gene Therapy
RNAi based Screening Technologies
Single Base Editing
Spacer Acquisition, Biogenesis, and Interference
Targeted Gene Replacement
Vectors for Gene Therapy
Viral Gene Therapy