Frequently Asked Questions

How does OpenCure’s AI technology work?

Our open source technology comes in the form of our bioinformatics toolkit which helps independent, government, and private researchers create meaningful and impactful CRISPR-Cas9 training sets for use in cancer research.

What are the benefits of using OpenCure’s AI services?

Our open source software exists under the Apache V2 License and we have a firm commitment to ensuring that effective cancer drugs can not be price gouged by massive corporate entities who get patents before others. Cancer treatments should follow a steadily decreasing plot similar to whole genome sequencing which was once $100 Million dollars for a single human genome. It is now around $150 USD.

How can I get started with OpenCure’s AI services?

Fill out our contact form on the main page and we will reach out when we begin beta testing of CPT-9, in the meantime you can start creating your .jsonl fine tuning data for specific types of cancer you may have sequences for.

Which reference genomes & data do you use for research?

We use NIH’s GRCh38 and also Tumor / Normal data derived from genomedata.org