How will you use #SingleCell sequencing in your research? In this webinar hosted with Mission Bio and Illumina we’ll discuss Clonal Heterogeneity in Acute Lymphoblastic Leukemia with Dr Jan Cools, Gema Fuerte Hortigón, and Lei Tong. Register now: bddy.me/3BzYoDO

My brilliant colleague and friend @DaGenomics is presenting on cfRNA and it's not to miss.

Whole genome sequencing is a revolution in how we diagnose and treat our little ones. And it improves health equity. I'm so proud to be part of this event. If you're interested, come hear more tomorrow: eventregistration.illumina.com/TransformingPe…

We also recently entered a partnership with @SomaLogic to co-develop an end-to-end solution using the largest protein target set and the high-throughput capabilities of Illumina’s current and future next-generation #sequencing (NGS) platforms.

Infinity also enables 10x greater throughput with 90% less #DNA input than legacy long reads. We anticipate an early access launch for Infinity technology in the second half of the year.

We will reach the $100 genome. #TweetItIntoExistence

Infinity enables 10x greater throughput with 90% less DNA input than legacy long reads. Come to Rami Mehio’s plenary talk tomorrow to see initial data. #FoG2022 The Festival of Genomics & Biodata

Heading to #BioIT22 next week in Boston. Looking forward to seeing some familiar faces and meeting new folks in the informatics community! bit.ly/37NZnXa

📣Great webinar from Gary Schroth on Illumina new #Infinity long reads now available - link below 👇

Take a deep breath and read this thread of live lost to guns. And then turn your sadness into action. Moms Demand Action and Everytown are 2 ways, or call your state/federal officials. Change our gun policies NOW. #GunSense

Did you know Illumina announced new kits are coming to NextSeq™ 1000/2000 platforms later this year? Flexibility and scalability will be extended with the addition of the P1 100 cycle and 600 cycle kits. Learn more about the upcoming innovations here: illumina.com/destination/fu…

This is going to be so exciting! Illumina Announces Inaugural Illumina Genomics Forum with a Conversation with Former U.S. President Barack Obama prn.to/3cn0vD0

Illumina just released v4 of DRAGEN for mapping and calling variants with amazing accuracy & speed. Congrats Shyamal Mehtalia, Rami mehio and team for continual improvement. The below table shows the many informatics options available for Illumina data

If you haven't already, check out the amazing speakers at IGF in two weeks, and then register to see me there! illuminagenomicsforum.com

This morning at the Illumina Genomics Forum, we unveiled our fastest, most cost-efficient sequencing machine yet – the NovaSeq X series. This technology will slash the cost to $200 per human genome and provide a readout at twice the speed. WIRED feature: wired.com/story/the-era-…

Highly anticipated, unlike anything else at #AGBT23, I revealed the novel sequencing methodology behind Illumina Complete Long Reads. Land-marked technology at the single molecule scale generates highly accurate long reads & eliminates pain points, cost and complexity.

Such a privilege and SO FUN to be with the Illumina team as Susan Tousi rang the closing bell at the NASDAQ.

Yes, that is 2.41 Tb of Q40+ data on a NovaSeq X flow cell! Can't wait to see how the community will leverage this unrivalled combination of accuracy and throughput. Illumina

Only two days until our user group meeting in Boston. I hope to see you there! eventregistration.illumina.com/gvydr8?refid=E…