💡Simple is not easy.
Despite the complexity of our AI architecture going up, we try hard to make it easy to understand
👉Here, we demonstrate that by using molecular data from real patients powered by Multimodal Machine Learning, it is possible to identify tumor vulnerabilities
👉The ARETEai is a custom-made, AI-driven platform developed by MNM Bioscience’s experts.
It is making communication easier between biologists, bioinformaticians and data scientists, which is pivotal for advancing drug target discovery and personalized medicine.
💡 We have just published exciting results in PLOS Genetics of our cooperation with the COVID-19 Host Genetics Initiative – a global scientific collaboration for COVID research.
🤝 Proud to be part of this global initiative: https://t.co/EXFnmDUHDw
Precision #AI is a fusion of #MachineLearning and biological #knowledge. Read the whole story by our VP of AI @MaciejPiernik on why and how we are building precision AI. 👇https://t.co/24c06czq3P
By using #AI and #genomic#data from real patients, we can pinpoint which patients will benefit from existing therapies, identify new therapeutic uses for drugs that are already available, and find new #drug targets.
👉Find out more about our technology: https://t.co/vDo7LOloaf
👉 Great opportunity to tell the story of how our #precisionAI is being integrated into cancer care.
We hope to see many of you!🤝
https://t.co/1lGuD4RrCO
#precisionAI#drugdevelopment
In MNM, we support the culture of sharing, which is why our latest software - the #NeKO ☁ component, will be released on an Open-Source Licence 💪
Great work @pa_piatkowski_ and @bokens01
👉 Find out more: https://t.co/wU5hssWy4k
#cloud#software#bigdata#mnmbioscience
Incredible data emphasizing the power of #genomic-based and #AI research presented at #ESMO2022 makes us extremely excited about the future of the fight against cancer.
👉Read more: https://t.co/KbCbnpxoGo
We are happy to announce that MNM will support a multi-site PROTECTAA TRIAL. Our #AI platform will be used to stratify breast #cancer patients for anthracycline treatment supported by novel cardioprotective #therapy.💪 More details soon! 🤞
More than twenty years after having the first sequenced human #genome, the price of such service had fallen from billions of dollars to just $1000. But that’s not enough! 💪
Find out more on our blog: https://t.co/bCziWxvG9t
We are more than happy to announce that our #research on “AUTOMATIC FEATURE EXTRACTION FROM WHOLE-GENOME DATA” has been published in the "Bioinformatics" 💪
Learn more: https://t.co/iJr6RYDdI3
Two fantastic papers published recently in #Nature only proved the importance of MNM’s focus on copy-number changes and structural variant signatures in #cancer#genomes 👌
👉 Find out more on our blog: https://t.co/7DIvskHjrp
Faster may mean better, especially in #science....
Nanopore sequencing enables rapid, cost-effective, and decentralized #WGS data analysis and has become a useful tool in #genomic surveillance initiatives across the globe.
Find out more from our blog:
https://t.co/hQu4J8EJ8w
We are very happy to announce that our abstract and related publication titled “Random similarity forests” has been accepted at this year’s European Conference on Machine Learning and Principles and Practice of Knowledge Discovery in Databases- @ECMLPKDD! 🥳🥳
A thoughtful 2021 review on role of somatic mutations in disease (not cancer). Supplementary table lists known examples to date. I bet the list will soon be longer with new tech for sensitive mutation detection
https://t.co/SNd8HcrszE