Mark Terndrup
@terndrupmark
Supporting the implementation of personalised medicine in the Danish healthcare system. Clinical Account Manager, Danish Health Regions @illumina
ID: 2149855025
23-10-2013 18:23:01
674 Tweet
86 Followers
362 Following
A recent peer-reviewed paper from From the Labs at Baylor College of Medicine in Nature Biotechnology highlights the comprehensiveness, accuracy, and scalability of Illumina DRAGEN germline algorithms. Its targeted callers show far fewer false negatives and false positive results versus eight others, and we want
Dylan Mooijman, PhD and his team at Single Cell Discoveries revolutionized the way they work with the help of the NovaSeq X, taking on projects with millions of cells in a single experiment for their customers. Learn how the NovaSeq X is enabling multiomic experiments of the future:
Today on Bloomberg TV, our CEO Jacob Thaysen discussed the company’s transformation and how our strategy is driving the advances that our customers need—from reducing the cost of sequencing, to unlocking multiomic insights, and accelerating AI and informatics solutions. View the
Single-cell sequencing was a niche academic field a decade ago, and it took the global community years to process a million cells. Now with the high-throughput power of the NovaSeq X, the team at Single Cell Discoveries can do it in a weekend. CEO Mauro Muraro and his team share how
We’re hosting a session on the Main Stage The Festival of Genomics & Biodata – join us for “The Rare Disease Multiomics Programme at Genomic England” 30th January at 9.30am #FoG2025
In 2025, #informatics will be key to unlocking NGS potential. Our Head of Global Software and Informatics Rami Mehio explains in Genetic Engineering & Biotechnology News how data organization, advanced algorithms and AI models will drive the next wave of genomics breakthroughs. Read here: bit.ly/3EjDrTG
Meet Shane Liddelow 🍊, a neuroscientist at NYU Langone Health who is using the new Illumina Single Cell 3’ Prep to investigate a challenging target: astrocytes. With the flexibility of our new technology, the team can sequence 2,000 cells just as easily as 200,000—and it allows them
We're expanding our multiomics portfolio with game-changing spatial technology that delivers cellular resolution and breadth of coverage – without the compromise. Read Julianna LeMieux PhD’s article in Genetic Engineering & Biotechnology News's of how we're making spatial biology more accessible: bit.ly/41rt3Bx
Today, we unveiled PromoterAI, a groundbreaking algorithm that, for the first time at scale, accurately deciphers pathogenic regulatory genetic variants in the noncoding regions of the human genome. In a study published today in Science Magazine, researchers report a 6% increase