CAMP4 Therapeutics’ Post

The use of AI (artificial intelligence) in one of the most exciting international event within a panel discussion featuring experts ( Lisa Vincent, PhD, FACMGG, CGMB, MB(ASCP) from Natera - USA, Ana Krivokuca from Genetic Counseling Institute - Serbia and me - Atil Bisgin ) in the field of clinical genomics. The challanges and opportunities in the future of diagnostic testing as well as the limitations of using AI-driven approaches to exome and genome sequencing workflows were featured. #clinicalgenomics #genomics #ai #artificialintelligence #genetictesting #qiagen #diagnostics #wholeexomesequencing #wholegenomesequencing #expertopinion

🌟 Unlock the Potential of Genomic Data! 🌟 HackBio's Advanced Genomics course covers the use of TCGA datasets to advance precision medicine. Discover how to tailor treatments based on individual genetic profiles and improve patient outcomes. https://buff.ly/4e4fvBq Be part of the genomic revolution. #Genomics #TCGA #PrecisionMedicine #HackBio

With the ability to read any length of DNA or RNA, short to ultra-long, nanopore sequencing captures more genomic variation — including structural variation and methylation — so you can get the context and clarity you need, every time. Hear from the researcher gaining the most comprehensive view of genetic diseases, revealing more biology than ever to transform human health. What you’re missing matters. #WYMM Discover what you've been missing: https://bit.ly/4aZKY5n

With the ability to read any length of DNA or RNA, short to ultra-long, nanopore sequencing captures more genomic variation — including structural variation and methylation — so you can get the context and clarity you need, every time. Hear from the researchers gaining the most comprehensive view of genetic diseases, revealing more biology than ever, to transform human health. What you’re missing matters. #WYMM Discover what you've been missing: https://bit.ly/3uJB4p1

💫 Transforming genome tertiary analysis! We are excited to announce that GenomeArc HORIZON™ profiles comprehensive short tandem repeats (STR) from insertion. GenomeArc HORIZON™ automation provides unprecedented insights into short tandem repeat expansions from the most complex genome insertions. 💫Our platform uniquely features the decomposition of STR from insertions, enabling clinical genetic diagnosis. ✨ For more about GenomeArc HORIZON™: https://lnkd.in/dFdgNzXS ✨ Please request a demo: https://lnkd.in/dQpCct4V #genomics #rarediseases #tandemRepeat

At #Davos 2024, the spotlight on Genomic & Genetic Medicine unveiled transformative insights, from redefining health systems to influencing care delivery, the intersection of genetics and healthcare promises a paradigm shift in patient-centric approaches. @ftlive

In support of #rarediseaseday, Stephen Kingsmore willing posed with me in my zebra stripes at Rady Children's Institute for Genomic Medicine! Every single day Dr. Kingsmore and all my other colleagues work to make ultra-rapid whole genome sequencing testing available for every patient who might benefit. For us, it's our mission to try to take some of the burden off the moms and dads of those little kiddos who tenaciously strive to find answers and get help for their kids. I can't imagine what they go through. #raredisease #rarediseaseday #wholegenomesequencing #genetictesting #geneticdisease

Unlocking the DNA code: Your top questions on genome sequencing, answered! 🧬 From understanding its meaning to navigating its applications, here's a dive into the world of genomic analysis. Let's explore the fascinating realm of genetics together! Visit: www.mediomixdb.com #Mediomix #GenomeSequencing #ScienceFAQs

Structural variants (SVs) are a major source of genetic diversity in the human genome. Accurate genotyping of these variants using short-read data is essential for the progression of genetic research. GGTyper, a novel tool, addresses this need by generating genotype-specific probability distributions from aligned read pairs and enabling genotyping of complex SVs. https://lnkd.in/g-T9urve

Since the discovery of the DNA double helix in 1953, scientists have been working to learn more about the role of genetics in driving diseases. Now, 70 years later, UK Biobank has unveiled new data from whole genome sequencing of its half a million volunteer participants. Approved researchers around the globe will be able to access an unprecedented amount of genomic information that can potentially drive the discovery of new diagnostics and targeted treatments for more patients. We’re proud to have been a part of the consortium that supported this landmark victory for the scientific community. Learn more about how this unprecedented dataset is helping to advance innovation and drive progress toward precision medicine – and about other major milestones in genetics research that have helped us get here: https://bit.ly/48gNWkH #Gentics #DataScience #Data #Innovation #PrecisionMedicine #500KGenomes