The 10K Genes Project
Help us build a better future. Submit a sequence request for one of 10,000 useful genes that will be synthesized, cloned, and distributed completely free
How It Works
What You Can Expect
1. We hold all sequences until there are enough for a batch order from Twist Bioscience.
2. Synthesis via Twist Bioscience now takes ~3-4 weeks to complete, depending on sequence complexity.
3. Once we receive the newly synthesized DNA, it is processed in one of two ways:
A. If you have requested DNA that can be made into MoClo-compatible parts, we will clone and sequence verify the DNA before shipping clonal plasmid stock to you.
B. If you have requested DNA that cannot be made MoClo-compatible, we will ship an aliquot of the raw synthesized DNA, keeping other aliquots for any other people interested.
4. The process of cloning and validation takes an additional ~2 weeks.
5. The 10K Gene Project is still in beta, so please work with us to make this an efficient and productive community effort.
Frequently Asked Questions
How is this different from the iGEM registry?
There are two major differences between the 10K Genes Project and the iGEM registry: The scope of distribution and the distribution methodology. First, iGEM only distributes once a year to academics and non-profits, while 10K Genes distributes continuously to anyone, including academics, non-profits, companies, and even DIYbio hackers. Second, 10K Genes is also interested in increasing access to biological tools through alternative distribution methodologies, such as decentralized B. subtilis spore-based distribution sets, which may drastically lower costs in DNA production, distribution, and storage. Rather than being a purely central hub for DNA, we hope that in the future there will be nodes of decentralized distributors throughout the world.
What restriction sites do you add/remove? (MoClo parts only)
We remove all common Type IIS restriction enzyme sites from coding sequences. These include AarI, BsmBI, BbsI, BtgZI, BsaI, BfuAI, and SapI. For other parts, such as promoters and terminators, we strongly recommend removing BsaI, BsmBI, and SapI if possible.
Why do you remove restriction enzyme sites? (MoClo parts only)
In order to scale our cloning methods, we take advantage of GoldenGate assembly standardization, and in particular, the MoClo assembly method. We aim to make standardized open access libraries for every major organism in order to clone new synthetic DNA very quickly for any desired application. By doing this, we drastically lower costs and increase our assembly speed.
What about third party patent rights?
We are currently developing an online tool to enable the community to quickly check DNA sequences for potential third party patent claims. Our goal is to empower the community to design sequences for synthesis that are free of third party rights and that can be widely shared. Stay tuned for developments on this front…
Do you ship internationally?
We would like to support the international community, but will have to manage this on a case-by-case basis. Please contact us at email@example.com for more information.
What have you finished synthesizing?
We have completed synthesis of codon optimized versions of all the JCVI syn3.0 genes. If you are interested in any of those genes, please contact us at firstname.lastname@example.org
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