Re:Pair Genomics Inc. Website Revamp

Open
Re:Pair Genomics Inc.
Vaughan, Ontario, Canada
Operations Coordinator
Project
Academic experience
60 hours of work total
Participant
Anywhere
Intermediate level

Project scope

Categories
Project management Website development
Skills
teamwork information sciences genomics innovation wordpress web development
Details

Project Description:

Welcome to Re:Pair Genomics! We are thrilled to present an exciting opportunity for talented students to contribute to our innovative project, Website development.


Main Goal:

The primary objective of this project is to 1)Continue modifications and improvements to our current webside page; 2) Resolve any current issues we have with the website; 3) Develop a PRODUCTS page on the website with new scientific information.


We want students to not only understand the significance of their contributions but also feel confident that the project is manageable within a realistic timeframe of 60 hours, spread over 2-8 weeks.

Deliverables

During this project, students will work as a team to split the tasks. We will ask students to help modify the website with our updated content. Students will update our news section and refine the current placeholder webpages for product launch.


  • Students will be given access to the WordPress account to work on the website directly.
Mentorship
Hands-on support

Direct involvement in project tasks, offering guidance, and demonstrating techniques.

Tools and/or resources

Providing access to necessary tools, software, and resources required for project completion.

Supported causes

The global challenges this project addresses, aligning with the United Nations Sustainable Development Goals (SDGs). Learn more about all 17 SDGs here.

Good health and well-being

About the company

Company
Vaughan, Ontario, Canada
11 - 50 employees
Science, Technology
Representation
Minority-Owned Women-Owned Small Business Youth-Owned Immigrant-Owned

Re:Pair Genomics uses AI to design compact synthetic promoters, which are DNA sequences required for gene therapies to target specific cell types. Rather than spending six months to a year to design and validate promoters manually, our algorithm can produce designs ready for testing within a day.