Ultima Genomics Provides Free Sequencing to Enhance Research

Ultima Genomics Launches Innovative Initiative for Researchers

Ultima Genomics, Inc., known for its advanced sequencing technology, has embarked on an exciting new initiative titled 'Count on Us.' Aiming to support the scientific community, the company will provide a staggering 3 trillion DNA sequencing reads at no cost to researchers.

Applications for Free Sequencing Reads Now Open

The free sequencing offer is open to researchers affiliated with academic, public, government, or other non-profit institutions. Each applicant has the chance to request a share of 3 trillion sequencing reads, which is roughly equivalent to 9,000 human genomes analyzed with 30x coverage. This initiative begins now and remains open for applications throughout the month.

Ultima Genomics believes in broadening access to genomic data, especially during times when research budgets are under strain. "With research budgets in flux and uncertainty facing many labs, we want scientists to know they can count on us to help keep their work moving forward," commented Gilad Almogy, founder and CEO of Ultima Genomics. This offer underscores their commitment to easing the financial burdens placed on researchers.

Eligibility Criteria and Application Process

Researchers wishing to participate must propose projects that require sequencing. Each selected project can receive between 10 billion and 100 billion reads, utilizing the latest UG 100™ sequencing platform. Candidates must also ensure their libraries are compatible and submit concise project proposals of up to 250 words. Projects facing significant challenges due to budget cuts will be prioritized.

What Researchers Need to Know

Projects must be submitted by new customers only, and each principal investigator (PI) or lab is limited to one application. All libraries should be sent in a single batch and received by the specified deadline. The sequencing data will be delivered using S3 buckets or GCP, conforming to standard analytical workflows. Given the anticipated high demand for this initiative, early submissions are encouraged to enhance the chances of award.

Supported Applications within the Initiative

Ultima Genomics supports a diverse range of applications, including:

• Single Cell Sequencing
• Proteomics
• Whole Genome Sequencing, including various methodologies such as PCR-free
• RNA Sequencing
• Spatial Transcriptomics

About Ultima Genomics

Ultima Genomics is dedicated to making transformative advancements in genetics more accessible. Their revolutionary sequencing architecture is designed to drive down costs and overcome the challenges posed by existing next-generation sequencing technologies. The company believes that overcoming barriers to genomic information is crucial for enabling groundbreaking scientific discoveries.

Their new sequencing architecture allows for unprecedented scalability, making it possible to tackle the complexities of biology and provide essential information for innovative research and healthcare advancements.

To learn more about Ultima Genomics and this initiative, you can visit their website and explore the vast possibilities within genomic research.

Frequently Asked Questions

What is the 'Count on Us' initiative by Ultima Genomics?

The 'Count on Us' initiative offers researchers 3 trillion free DNA sequencing reads aimed at enhancing research capabilities.

Who can apply for the free sequencing reads?

Researchers affiliated with academic, public, government, or non-profit institutions are eligible to apply for free sequencing reads.

How many reads can selected projects receive?

Eligible projects can receive between 10 billion and 100 billion DNA sequencing reads.

What is the deadline to submit applications?

Applications are accepted on a rolling basis, and submissions must be received by the specified date.

Is there a limit to the number of applications per institution?

Yes, only one application per principal investigator or lab is allowed.

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