[작성자:] Ashley Zhu
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Rare disease screening firm 3Billion closes $13M Series C financing
The Korean startup 3billion has officially closed its Series C funding by raising $13 million. They have raised a total of $30 million since its seed round in 2017. The recent Series C round was led by Wells Investment, JW Asset, Magna Investment, Yuanta Investment, Aventures Investment, Korea Investment & Securities, and Kakao Investment. 3billion…
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3B-EXOME updated!
3billion’s WES product, 3B-EXOME, has been upgraded.These enhancements will be effective for all samples arriving after May 1, 2023. What changed? Mitochondrial genome coverageWe have now included the entire mtDNA sequence evenly in our coverage. This enhancement has improved the accuracy of analysis for mtDNA variants. Increased RPGR gene coverageWe have complemented the RPGR gene coverage with the ORF15 exon…
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3billion aims for the global market by IPO
3billion, an AI-based rare disease genetic diagnosis startup, aims for the global market by IPO. 3billion has selected Korea Investment & Securities Co. as its representative organizer and is pushing for listing on KOSDAQ, a stock market, and the Korea Exchange trading board. Until now, 3billion has been targeting the global market by advancing AI…
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Accelerating Diagnosis of Rare Diseases in Malaysia
3billion recently held symposiums to accelerate the diagnosis of rare diseases in Malaysia. 3billion is a Korean biotechnology company that provides genetic testing services for diagnosing rare diseases. The tour’s purpose was to go beyond being a simple service provider and interacting more closely with our collaborators, whose purpose is the diagnosis of rare diseases.…
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Accelerating Diagnosis of Rare Diseases in Morocco
From Dec. 13-16, 3billion met many clients locally in Morocco. We presented to eight professors and students from various departments at University Hassan2 Hospital and discussed future research projects. We discussed the introduction of Gebra, a software service, with local distributor AskYourOmics. We promised to collaborate with the Moroccan Society of Pediatric Endocrinology. We will also create great opportunities…
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3billion CEO: “We diagnose 7,000 rare diseases at once using AI”
In an interview with Seoul Economic Daily, Changwon Keum, CEO of the genetic analysis technology startup 3billion said, “As AI can increase the efficiency of identifying rare diseases necessary for doctors’ final diagnoses, the demand for AI genetic diagnosis will increase.” Traditionally, it takes 20 to 40 hours for a doctor to interpret genetic variations…
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3billion Wins in CAGI6, a Global Artificial Intelligence Genome Interpretation Contest
In the 6th CAGI(Critical Assessment of Genome Interpretation) Challenges, a global artificial intelligence genomic interpretation contest, 3billion took first place by predicting the rare diseases of 79 patients within the data of The Hospital for Sick Children in Canada. 3billion’s AI model recorded 58%, showing a 16%p gap from the 2nd group with a score of 42%,…
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3billion Company Video: From 3 billion bases to 1 answer
3billion released a company video explaining why rare disease is so difficult to diagnose and how 3billion is solving them. Check out the video and learn about 3billion and its solutions.
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3billion announces Dr. Hane Lee of UCLA as Chief Clinical Geneticist
3billion has announced Dr. Hane Lee, a former UCLA professor of pathology/diagnostic medicine and human genetics, as ‘Chief Clinical Geneticist and Director of Clinical Genetic Laboratory’ overseeing the R&D for genetic diagnosis process to advance the interpretation of genetic mutation in rare diseases. Dr. Lee had been a professor at UCLA since 2011. Dr. Lee…
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Fabry disease: Interview with Dr. Ji-Hee Kim
3billion collaborates with pharmaceutical companies to help with personalized drug prescriptions. We will look into a few cases of patients who were diagnosed with Fabry disease in a diagnostic program for this disease operated through collaboration in 2022. The cases will be introduced through an interview with Professor Ji-Hee Kim who diagnosed Fabry disease. *This…