GECT 2024 - The 5th Int'l Conference on Gene Editing and CRISPR Technologies (GECT 2024)

The 5th Int'l Conference on Gene Editing and CRISPR Technologies (GECT 2024)
Website：https://www.academicx.org/GECT2024/
Date：May 28-30, 2024
Venue：Kunming,China
The 5th Int'l Conference on Gene Editing and CRISPR Technologies (GECT 2024) will be held in Kunming, China, during May 28-30, 2024. 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 2024 will be a valuable and important platform for inspiring international and interdisciplinary exchange at the forefront of CGene Editing and CRISPR Technologies.
Attendance Methods
1. Full Paper submission
Submit full paper ( Regular Attendance + Paper Publication + Presentation )
You are invited to submit papers and participate in our academic exchange. One author will be invited to make an oral presentation and the paper will be published by peer-reviewed open access journal and submitted to CNKI and Google Scholar for indexing.
2.Abstract submission
Submit abstract ( Regular Attendance + Abstract + Presentation )
You are welcome to submit abstract for oral presentation or poster presentation.
3.Regular Attendance ( No Submission Required )
You're also welcome to attend our conference (without submitting full paper or abstract).
Publication and Presentation
Publication: All the accepted papers will be published by a peer-reviewed open access journal that can ensure the widest dissemination of your published work, for more information, please contact us (wsconf5-AT-163.com).
Index: CNKI and Google Scholar
Note: 1. 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.
2. Please click Template for Manuscripts (below the Registration button at the top left corner) to download the Full Paper template and prepare your article according to it. The full length of one paper is suggested to be 8-10 pages (within the template format with all tables, figures and references). If your paper is over 10 pages, you will be kindly requested to pay for extra pages fees.
3. The simple Abstract submission should include the title, contents, keywords, authors names, affiliations and emails. The length is suggested to be controlled within 1 page and no more than 2 pages.
4. You will receive the review results within 3-5 working days after submission. If you do not get any notification within the time limit, please contact us as soon as possible.
Contact Us
Email: wsconf5-AT-163.com
Whatsapp: 0086 13264702250
Tel: +86 132 6470 2250 (From Monday to Friday)
QQ: 1349406763
WeChat: 3025797047
Twitter: ConfPriii59781
Official Account: Academic Communications
Topics: The conference is soliciting state-of-the-art research papers in the following areas of interest:
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