Tuesday, February 13, 2018 8:08:03 PM
Hardly. Ariana's KEM which stands for "Knowledge Extraction Management, is one of the fastest medical AI platforms in the business. The technology originated from the laboratory of Professor Jean Sallantin, of the Artificial Intelligence Group at the CNRS (Centre National de Recherche Scientifique) in Montpellier, France. I am familiar with the AIG, and most of their AI platforms are a dual combo of high-powered CPU's (for software and processing power) from Intel and Titan-X GPU chips from Nvidia (which powers the actual data-mining and bio-marker relevance). Heck, I wouldn't be surprised id this year, they may even be running Nvidia Xavier Architecture and Intels FPGA Platform (most AI Platforms are updated with new chip Architecture, as it becomes available, ever 12-14 months on average). Your claim of 6-8 months is probably closer to 6-8 days.
Obviously, the FDA is so impressed with Ariania, that the FDA choose Ariana do ALL THEIR DNA SEQUENCING AND BIO-MARKER WORK
8 years ago and still on-going.
“We are looking forward to this collaboration to help the agency systematically analyze all equivalent signatures combining both genomic and phenotypic data, thus increasing chances of selecting the best biomarker signature,” comments Federico Goodsaid, Ph.D., FDA’s associate director for operations in genomics at the Center for Drug Evaluation and Research’s Office of Clinical Pharmacology.
https://www.genengnews.com/gen-news-highlights/fda-selects-ariana-s-kem-platform-for-biomarker-signature-validation/81243886
-Fireman
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