The impressive work by the @Illumina #DRAGEN team to integrate in the NovaSeq X, the numbers do the talking - accurate, fast, efficient, sustainable and easy to use!

Field Applications Scientist role open in Mumbai, India. Work with a great team to support customers using Illumina technology. Very fulfilling role. Check out the link. #genomics #scientist #NovaSeq #NextSeq #infinium bit.ly/3FnRSn0

A huge step by the UK Biobank and its partners for the #500KGenomes project in unlocking the power of the genome; 500k WGS sequenced on Illumina NovaSeq6k, analyzed on #DRAGEN and aggregated using Illumina Connected Analytics #iCA ow.ly/qsyy50QcJ7w

An awesome bioRxiv from a few of my colleagues on data analysis speed, accuracy and previously tricky medically relevant genes using #DRAGEN. Not such a black box! Daniel Cameron Shyamal Mehtalia Rami mehio #genomics #variants Illumina biorxiv.org/content/10.110…

A highly accurate framework to simultaneous assess all genome #variants (SNV, indels, STR, SV & CNV) at scale: #DRAGEN Illumina. Amazing work Severine C. Sairam Behera James H. Rami mehio Shyamal Mehtalia many more! biorxiv.org/content/10.110… BCM HGSC #Bioinformatics #Genomics

Can't decide how to spend afternoon @ #PAG31? Come to the Illumina workshop, Palm 5-6, from 4-6pm. I'll be chatting about our adventures with the DRAGEN at 16:35. We have some exiting news. Here is background of who we are, video created by @Illumina youtube.com/watch?v=eecnhl…

Pioneering Genomic Progress: An Interview with Rami Mehio, Illumina's Software and Informatics Expert | Rami mehio Illumina news-medical.net/news/20240115/…

Latest job opening Illumina. Manager of the Bioinformatics Sales Specialist team. Some great people and great products including #DRAGEN. Based in Australia or Singapore. Apply online. #genomics bit.ly/3SSKwyn

High-homology regions are notoriously difficult to analyze, but #DRAGEN has targeted callers for specific genetic conditions to help locate their genetic origins. Learn about three of them. illumina.com/company/news-c…

Why does .25% difference matter?  When it leads to increased accuracy and a significant reduction in False Positives and False Negatives for your data analysis, it matters. Make every percent count with DRAGEN. ilmn.ly/DRAGEN bit.ly/3xJ6QDO

Introducing #DRAGEN v4.3! The latest update leverages advancements in multigenome mapping, machine learning, and variant calling in segmental duplication regions, enabling a more comprehensive coverage of the genome. For more on the latest capabilities: bit.ly/4aWwMcN

Hello!

And see this big little sequencer in action, youtu.be/t096wwuLHqY?si…

Comprehensive genome analysis and variant detection at scale using DRAGEN go.nature.com/4eXQRT1

As part of @Illumina complete workflows, #DRAGEN pushes what’s possible in secondary analysis by providing a comprehensive, highly accurate and scalable genome with industry-leading innovations. Read peer reviewed publication from Nature to learn more.​ nature.com/articles/s4158…

Today’s Illumina Innovation talk in Sydney has to be fast, accurate and interpretable…. #DRAGEN Rami mehio Shyamal Mehtalia Daniel Cameron

It's the final day in the exhibit hall at #AMPath24! This is your last chance to drop by booth #1107 to experience our DRAGEN and @Illumina Connected Insights demo station. 🔬