Complete Genomics @CompleteGenomic

Complete Genomics has announced the appointment of Edward McMullen Jr. to its Board of Directors, further strengthening the company’s leadership in global business strategy, international relations and U.S. government affairs. McMullen served as U.S. ambassador to Switzerland and Liechtenstein from 2017 to 2021 and has more than three decades of experience spanning diplomacy, public policy, foreign direct investment, international business and government relations. He currently serves as senior policy advisor at Adams & Reese, where he advises clients on economic development, international investment, and cross-border business matters. McMullen’s appointment to the Complete Genomics Board of Directors is expected to become effective upon the closing of the pending acquisition of Complete Genomics by Swiss Rockets AG, including satisfaction of customary closing conditions.

What does it take to move from high-throughput sequencing to real-time genomic insight? That was the focus of our recent webinar and panel discussion with Complete Genomics, Google, and NVIDIA. The discussion highlighted that the next bottleneck in genomics is not just sequencing, but how quickly and reliably we can analyze, interpret, and validate the data. Three key takeaways stood out: · Real-time genomic analysis for the clinical setting is here! The next challenge is building a seamless end-to-end workflow that connects laboratories, bioinformatics, IT infrastructure, and clinical stakeholders. · Faster and cheaper AI/GPU based analysis without compromising accuracy. The cost for DNBSEQ-T7+ with  Google DeepVariant and NVIDIA Parabricks delivers highly accurate variant calling for only ~$0.75 per sample. · High-throughput sequencing and AI are transforming large-scale genomics, but robust validation remains essential. In case you missed our webinar yesterday, catch the on-demand version here: na2.hubs.ly/H0659w10 Learn more about DNBSEQ-T7+: na2.hubs.ly/H0659RD0 #Genomics #Bioinformatics #AI #PrecisionMedicine #DNBSEQ #Parabricks #CompleteGenomics #NVIDIA #Google

Starting in 1 hour: The Future of Data-Driven Genomics Join Complete Genomics, Google, and NVIDIA for a live webinar exploring how high-throughput sequencing, GPU-accelerated analysis, and AI-driven variant calling are enabling faster, more scalable genomics workflows. The session will include a panel discussion with Biniam Feleke, Andrew Carroll, and Gary Burnett on how to connect sequencing, accelerated compute, and AI-enabled analysis. ⏰ 10:00 AM PT | 1:00 PM ET Register here: na2.hubs.ly/H061YZX0 #Genomics #WholeGenomeSequencing #Bioinformatics #VariantCalling #AIinGenomics #GPUComputing #DeepVariant #NVIDIAParabricks #NGS

Happening tomorrow: The Future of Data-Driven Genomics Join Complete Genomics, Google, and NVIDIA for a webinar on how high-throughput sequencing, GPU-accelerated analysis, and AI-driven variant calling are helping researchers move from FASTQ files to accurate insights faster. The session will feature a live panel discussion with Biniam Feleke, Andrew Carroll, and Gary Burnett on how to connect sequencing, accelerated compute, and AI-enabled analysis to enable more scalable genomics workflows. 📅 Tuesday, June 9 ⏰ 10:00 AM PT | 1:00 PM ET Register here: na2.hubs.ly/H061jl00 #Genomics #WholeGenomeSequencing #Bioinformatics #VariantCalling #AIinGenomics #GPUComputing #DeepVariant #NVIDIAParabricks #NGS

As high-throughput sequencing continues to scale, the next major challenge is turning growing volumes of genomic data into accurate insights faster. Join Complete Genomics, Google, and NVIDIA for The Future of Data-Driven Genomics, a webinar exploring how high-throughput sequencing, GPU-accelerated analysis, and AI-driven variant calling are advancing modern genomics workflows. The webinar will feature a live panel discussion in which Biniam Feleke, Andrew Carroll, and Gary Burnett connect sequencing, accelerated compute, and AI-enabled analysis to enable faster, more scalable genomics. 📅 Tuesday, June 9 ⏰ 10:00 AM PT | 1:00 PM ET Register here: na2.hubs.ly/H05WSRB0 #Genomics #WholeGenomeSequencing #Bioinformatics #VariantCalling #AIinGenomics #GPUComputing #DeepVariant #NVIDIAParabricks #NGS

RNA modifications add an important regulatory layer beyond gene expression, with growing relevance in cancer biology, biomarker discovery, and disease stratification. Join our upcoming webinar, Beyond Gene Expression: Mapping RNA Modifications in Cancer, featuring: Wenchi Liao | Complete Genomics Wenchi will introduce how DNBSEQ technology and DNBSEQ-T1+ can support scalable transcriptomic profiling workflows, including high-depth sequencing applications for sensitive detection of RNA modifications and broader RNA-based research. Ananya Anmangandla | Alida Biosciences Ananya will discuss how the EpiPlex platform enables simultaneous profiling of m6A, inosine, and gene expression from low-input clinical samples, including blood, tissue, and FFPE. Her talk will highlight how RNA modification profiling can reveal differentially modified regions and pathway-level insights relevant to cancer research. 📅 Thursday, May 28 🕙 10:00 AM PT | 1:00 PM ET Register to learn how epitranscriptome profiling can expand cancer transcriptomics beyond expression analysis alone: na2.hubs.ly/H05Fr2v0 #Epitranscriptomics #RNAmodifications #CancerResearch #RNASeq #Transcriptomics #m6A #RNAEditing #CancerBiomarkers #DNBSEQ #NGS

New study demonstrates up to 73% reduction in genome analysis errors using AI-trained models versus standard approaches completegenomics.com/new-study-demo… #Genomics #WholeGenomeSequencing #VariantCalling #AIinGenomics #DeepVariant #Pangenome #DNBSEQT7plus #NGS

Last day of #AGBT2026 🚀 Final chance to visit the Complete Genomics Palm Beach Suite — we’re here until 11:00 AM. See DNBSEQ-T1+ and DNBSEQ-T7+ up close, meet the team, and talk workflows, applications, and data. See you in the suite. #Genomics #DNBSEQ #Bioinformatics

In 1 hour at #AGBT2026 ⏳ Join our Bronze 2 Sponsor Workshop: 🕒 2:40–3:00 PM 📍 Plenary Ballroom (Floridian) 🎤 Clinical Oncology Applications of ctDNA Sequencing Yuxuan Wang (@Johns Hopkins) A focused 20-minute session on liquid biopsy & clinical genomics. #ctDNA #LiquidBiopsy #Oncology #Genomics

#AGBT2026 is in full swing 🚀 The Palm Beach Suite is buzzing. Come see DNBSEQ-T1+ and the new DNBSEQ-T7+ up close, meet the team, and talk workflows, clinical sequencing, and data needs. 🏁 Last chance to run the race challenge and claim the podium. #Genomics #DNBSEQ #Bioinformatics

🏎️ F1 Simulator Highlights + Last Chance to Race! 🥇 Huge congrats to yesterday’s fastest lap winner 👏 Missed your shot? Today the leaderboard resets — new day, new champion. 🏁 Stop by the Palm Beach Suite 👕 Win an exclusive Complete Genomics t-shirt Can you finish on top? #AGBT2026 #Genomics #DNBSEQ

🚀 The DNBSEQ-T7+ is redefining ultra-high-throughput genomics at scale. ⚡ 14+ Tb in 24 hrs 🧬 Up to 35,000 WGS/year 💲 ~$1/Gb — enabling the $100 genome • Extreme daily output • 4 independent flow cells • True economics at scale 📍 Visit us at AGBT (Palm Beach Suite). #AGBTGM2026 #Genomics #NGS #WholeGenomeSequencing #DNBSEQ #PrecisionMedicine

Day 2 at #AGBT2026 ☕🚀 Morning Presentations | 8:00–9:00 AM | Palm Beach Suite • CoolMPS 600 — accuracy + longer reads • Stereo-seq spatial transcriptomics • Disease microenvironments (Mayo Clinic) Plus: 🎤 ctDNA Workshop (2:40 PM) 🏁 Final day of F1 challenge Full agenda: completegenomics.com/events/agbt-ge… #Genomics #StereoSeq #ctDNA #DNBSEQ

🏁 Think you’ve got the fastest lap at #AGBTGM2026? We’re bringing F1 energy to the Palm Beach Suite. Jump into our F1 simulator. Set the fastest lap. Win an exclusive Complete Genomics F1 t-shirt. 👕 🥇 New day = new leaderboard = new winner. Stop by between sessions and take your shot. #AGBTGM2026 #Genomics #NGS #DNBSEQ #LifeSciences

🚀 The DNBSEQ-T7+ is redefining ultra-high-throughput genomics. ⚡ 14 Tb ⏱️ 24 hours 💲 $100 genome 🎯 Zero compromise A new scale of discovery starts now. Stay tuned. 👀 #Genomics #NGS #WholeGenomeSequencing #DNBSEQ #PrecisionMedicine #AGBTGM2026

AGBT 2026 starts today 🚀 Join us for Morning Presentations with Breakfast in our Palm Beach Suite ☕ 🕗 8:00–9:00 AM • Ultra-High-Throughput DNBSEQ-T7+ • Clinical WGS insights w/ Alexander Kaplun (@variantyx ) • AI for Genomics w/ @RonjonNag (@superbioai ) • DeepVariant updates w/ Kishwar Shafin (@Google ) Plus: 🏁 Drive to Succeed Challenge 🍸 Sponsor Social Full agenda: completegenomics.com/events/agbt-ge… If you're into clinical WGS, AI workflows, or variant calling, start your day with us. #AGBTGM2026 #Genomics #NGS #ClinicalGenomics #AIinGenomics #DNBSEQ

Today at #AGBTGM2026, Complete Genomics announced it is commencing shipments of the DNBSEQ-T7+ high-throughput sequencing platform. completegenomics.com/complete-genom… #AGBT2026 #AGBT #DNBSEQ #Genomics

AGBT 2026: Visit Complete Genomics Palm Beach Suite for Morning Presentations with Breakfast Tomorrow Feb 24 8–9am. Full Agenda: completegenomics.com/events/agbt-ge…

Complete Genomics has entered into a definitive agreement, subject to customary closing conditions and approval by MGI shareholders, under which it will be acquired by Swiss Rockets AG, a Switzerland-based life sciences group. The transaction will enable the scaling of the Complete Genomics innovation pipeline and diversification of manufacturing capacity. completegenomics.com/complete-genom… #AGBTGM2026 #AGBT #Genomics #DNBSEQ

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