Complete Genomics is excited to be part of ASHG 2026 in Montréal, connecting with the human genetics community and sharing advances in sequencing and genomic analysis! We’re bringing together experts in human genetics, sequencing, and AI-driven analysis for our CoLab, industry workshop, and booth presentations: 🧬 CoLab | October 21 Hear from Andrew Carroll, Google AI, on pangenome-informed, AI-driven variant calling. 🧬 Industry Workshop | October 22 Join Christopher Douville, Johns Hopkins School of Medicine; Alexander Kaplun, Variantyx; and Michael Snyder, Stanford University, for insights into liquid biopsy, clinical whole-genome sequencing, and longitudinal multiomics for personalized medicine. 🎤 Booth Presentations | October 21–23 Explore genomic analysis and interpretation with Ronjon Nag, Superbio AI; Radoje Drmanac, Complete Genomics; Haodong Chen, Sentieon; Tomohiro Takano, Genomelink; Angelica Olcott, Bio-Rad; and Gary Burnett, NVIDIA. 🧀 Snack & SNPs | October 22, 4:15–6:15 PM See full Agenda here: na2.hubs.ly/H08nqk_0 Stop by Booth 807 for a chat and a cheese-and-fruit plate. Complete our booth survey to take home a plush puppy! Bring your research questions, meet our team, and discover sequencing solutions for your next study. See you at Booth 807!

We’re heading to MWACD 2026! 🧬 Complete Genomics is proud to be a Silver Sponsor of this year’s Midwest Association of Core Directors Annual Meeting, taking place October 19–20 at the University of Notre Dame. Join us to connect with the Complete Genomics team and learn how DNBSEQ™ and Stereo-seq™ technologies can help core facilities expand sequencing and spatial biology capabilities across a wide range of research applications. 📅 October 19–20, 2026 🧬 Table 26 📍 University of Notre Dame | Notre Dame, IN We look forward to seeing you there! #MWACD2026 #Genomics #CoreFacilities #Sequencing #SpatialBiology #DNBSEQ #StereoSeq #CompleteGenomics

We’re excited to sponsor and attend the 43rd Annual Symposium on Nonhuman Primate Models for AIDS, taking place October 20–23, 2026, in San Antonio, Texas. Hosted by the Southwest National Primate Research Center, this symposium brings together more than 250 leading scientists, veterinarians, investigators, and trainees to share the latest advances in HIV/AIDS research using nonhuman primate models. Topics will span HIV intervention, treatment, prevention, potential cures, and research on related coinfections. If you’re attending, be sure to connect with the Complete Genomics team while you’re there. We look forward to meeting researchers from across the field and learning more about the work advancing infectious disease and HIV research. 📍 The Westin Riverwalk | San Antonio, TX 📅 October 20–23, 2026 👉Register Here: na2.hubs.ly/H07VR6Z0 #Genomics #CompleteGenomics #DNBSEQ #HIVResearch #AIDSResearch #InfectiousDisease #NonhumanPrimates #NHPResearch

⏰ 24 hours to go. Pancreatic ductal adenocarcinoma remains one of the most challenging cancers to study and treat, in part because its biology is shaped by a highly complex tumor microenvironment. Tomorrow, Yuan Sui, PhD, from the Hunter Lab at the Salk Institute will share how his team is investigating the OSM-OSMR signaling axis to better understand how tumor, stromal, and immune programs are organized and altered in PDAC. The webinar will highlight how Stereo-seq spatial transcriptomics, multiplexed imaging, and ex vivo tumor models can be integrated to connect signaling activity with spatially resolved changes across the tumor microenvironment. 📅 Tomorrow, September 15 ⏰ 10:00 AM PT | 1:00 PM ET Register now to join us live: na2.hubs.ly/H07Ph_R0

Pancreatic cancer progression is closely tied to the cellular and molecular programs within its tumor microenvironment, making spatial context critical for understanding where therapeutic opportunities may emerge. On September 15, join Yuan Sui, PhD, from the Hunter Lab at the Salk Institute for a closer look at the OSM-OSMR signaling axis in PDAC and how perturbing this pathway can reshape the tumor microenvironment. The webinar will highlight how Stereo-seq spatial transcriptomics, multiplexed imaging, and ex vivo human tumor models can be combined to characterize: 🔬 Stromal remodeling across the tumor landscape 🧬 Spatially distinct tumor-cell responses 🛡️ Immune-suppressive programs and macrophage states 🎯 Changes induced by OSM stimulation and OSM-neutralizing treatment 📅 September 15 ⏰ 10:00 AM PT | 1:00 PM ET Register to explore how spatial biology can connect signaling mechanisms with potential therapeutic targets in pancreatic cancer: na2.hubs.ly/H07KST-0

🔬 Join us for a Lunch & Learn at the University of Illinois, Chicago, hosted by the Biological Graduate Student Association (BGSA). Discover how Stereo-seq and scalable DNBSEQ sequencing are advancing spatial biology across diverse tissues and organisms. This presentation will explore high-resolution spatial transcriptomics workflows, single-cell and multi-omics applications, and real-world research examples spanning development, neuroscience, and the tumor microenvironment. Talks: 🎤Unlocking Spatial Biology Across Organisms Through Stereo-seq and Scalable Sequencing Jim George Technical Specialist Complete Genomics 🎤Introduction to the Biology Graduate Student Association Fariha Islam Treasurer BGSA 📆 Tuesday, September 15 ⏰ 12:00 PM - 1:00 PM CDT 📍 4300 Seminar Room, MBRB-4th Floor 👉Register Here: na2.hubs.ly/H07FpSH0 #Genomics #CompleteGenomics #DNBSEQ

Complete Genomics and the Center for Microbiome Innovation (CMI) at UC San Diego are making high-resolution spatial transcriptomics more accessible with the Stereo-seq service promotion. CMI is offering an end-to-end workflow designed to help researchers generate spatial transcriptomics data with greater flexibility and less setup burden. With Stereo-seq, researchers can capture unbiased, whole-transcriptome data at single-cell resolution while preserving spatial context within tissue. Key benefits include: 🔬 Flexible sample compatibility, including fresh-frozen, PFA-fixed, and FFPE 📐 Multiple tissue and capture-area sizes 🧪 Scalable study design for pilot and larger projects 🧬 Study planning tailored to your research goals A practical way to move from sample to spatial insight, with support to design the right study from the start. Learn more: na2.hubs.ly/H07Bz1h0

Pancreatic ductal adenocarcinoma (PDAC) is characterized by a dense, immunosuppressive tumor microenvironment that can limit effective anti-tumor responses and complicate treatment. In our upcoming webinar, Yuan Sui, PhD, from the Hunter Lab at the Salk Institute, will present research investigating the OSM-OSMR signaling axis and its role in shaping tumor, stromal, and immune interactions in PDAC, using human PDAC tissue, ex vivo tumor slice cultures, multiplexed imaging, and Stereo-seq spatial transcriptomics to uncover spatial changes associated with stromal remodeling, immune suppression, and tumor-cell responses. 📅 September 15 ⏰ 10:00 AM PT | 1:00 PM ET Register to join live or receive the on-demand recording: na2.hubs.ly/H07zvJJ0

What drives immune suppression within the pancreatic tumor microenvironment? Join our upcoming webinar featuring Yuan Sui from the Hunter Lab at the Salk Institute, as he explores how OSM-OSMR signaling, multiplexed imaging, and Stereo-seq spatial transcriptomics can reveal tumor-stroma-immune interactions within the pancreatic ductal adenocarcinoma microenvironment. What you’ll learn: • The role of OSM-OSMR signaling in tumor-stroma-immune communication • The effects of OSM stimulation and OSM-neutralizing antibody treatment • Spatial insights into stromal remodeling, immune suppression, and tumor-cell responses 📅 Tuesday, September 15 ⏰ 10:00 AM PT | 1:00 PM ET Register to join us live or receive the on-demand webinar: na2.hubs.ly/H07sRQX0

Lauren Selig, entrepreneur, investor and award-winning film producer, will join the Complete Genomics Board of Directors upon closing of the company's pending acquisition by Swiss Rockets AG. completegenomics.com/complet… #Genomics #LifeSciences #PrecisionMedicine

🧠 Your brain runs on ~86 billion neurons and trillions of connections, and understanding how they change in disease is one of the hardest problems in modern biology. From Alzheimer's and Parkinson's to glioblastoma and rare neurological conditions, researchers are turning to genomics and spatial biology to reveal the genetic and cellular mechanisms that drive disease, and to find where new diagnostics and therapies might begin. The challenge is seeing both the sequence and the spatial context. High-quality sequencing shows what's changing; spatial transcriptomics shows where, and which cell types are interacting to make it happen. At Complete Genomics, our DNBSEQ™ platforms deliver high-quality genomic and transcriptomic data, while Stereo-seq™ lets researchers visualize gene expression within intact tissue at high resolution. Together they help scientists explore the complexity of the brain with greater depth and precision. On #WorldBrainDay, we recognize the researchers advancing neuroscience and the discoveries moving us toward better diagnostics, treatments, and brain health for future generations. For neuro researchers: which readout is the bigger bottleneck in your work right now, sequencing depth or spatial resolution? #Neuroscience #SpatialBiology

🧬 Come see us at the BVS Vendor Show at MIT! Stop by our table to learn how our DNBSEQ sequencing platforms and Stereo-seq spatial transcriptomics technology are helping researchers generate high-quality genomic and spatial data to advance discoveries across cancer research, single-cell biology, multi-omics, and beyond. Whether you're exploring new sequencing solutions or looking to expand your spatial biology capabilities, our team will be available to answer your questions and discuss how Complete Genomics can support your research. 📅 Thursday, July 16 ⏰ 11am - 1pm EDT 📍 MIT Biology Building 68, Cambridge, MA 👉Register Here: (na2.hubs.ly/H06Bd4V0) DNBSEQ Technology: na2.hubs.ly/H06BdnC0 Stereo-seq Technology: na2.hubs.ly/H06Bfm_0 #CompleteGenomics #DNBSEQ #StereoSeq #SpatialTranscriptomics #Genomics #NGS #Sequencing #SpatialBiology #LifeSciences #CancerResearch #SingleCell #MIT #CambridgeBiotech

🔬 Join us for the next seminar in the 2026 UC San Diego Center for Microbiome Innovation (CMI) Microbiome Seminar Series. We will explore how cutting-edge spatial transcriptomics is advancing our understanding of cancer biology, tumor heterogeneity, and the complex interactions within the tumor microenvironment. This seminar is ideal for researchers working in cancer biology, tumor microenvironment research, spatial biology, immunology, metabolism, and translational medicine. Talks: 🎤Spatial Transcriptomics Reveals Site-Specific Cellular Heterogeneity Across Bladder Tumor Regions Andy Bartko - Executive Director, Center for Microbiome Innovation (CMI) 🎤Cracking the Shield: A New Target Against Pancreatic Cancer Targeting the OSM-OSMR Signaling Axis to Reprogram the Tumor Microenvironment and Overcome Immune Suppression in Pancreatic Cancer Yuan Sui - Post Doctoral Fellow, Salk Institute 📆 Wednesday, July 15 ⏰ 1:00 PM - 3:00 PM PDT 📍 Comer Commons at Moores Cancer Center, La Jolla, CA 👉Register Here: na2.hubs.ly/H06vjjc0 Start Your Spatial Transcriptomics Project with CMI: The Center for Microbiome Innovation (CMI) at UC San Diego is holding a promotion for end-to-end spatial transcriptomics services, from sample block to FASTQ generation.  Learn how you can get your samples processed for as little as $3k per sample. 🧬Learn More Here: na2.hubs.ly/H06vqmy0 #Microbiome #SpatialTranscriptomics #SpatialBiology #CancerResearch #TumorMicroenvironment #PrecisionOncology #Immunology #TranslationalMedicine #PancreaticCancer #BladderCancer #LifeScience #Genomics #CompleteGenomics #UCSD #CMI

Happy Fourth of July from Complete Genomics! Today we celebrate the birth of our nation and the values of freedom, unity, and opportunity that bring us together. Whether you're spending the day with family, friends, or enjoying your favorite Fourth of July traditions, we hope your holiday is filled with laughter, great food, and spectacular fireworks. From all of us at Complete Genomics, thank you for being part of our community. Wishing you a safe, happy, and memorable Independence Day! #FourthOfJuly #IndependenceDay #HappyFourth #USA #CelebrateFreedom #StarsAndStripes #SummerCelebration #CompleteGenomics #Genomics

Today is World Microbiome Day — a reminder that the smallest organisms can have an outsized impact on human health, agriculture, ecosystems, and the planet. Microbiome research is helping scientists better understand how microbial communities influence disease, nutrition, environmental resilience, soil health, and more. Turning microbial complexity into biological insight requires sequencing technologies that can scale across sample types, study sizes, and research questions. At Complete Genomics, we’re proud to support researchers advancing microbiome science with high-quality, accessible sequencing solutions for applications such as 16S sequencing, metagenomics, and microbial genomics. Today, we celebrate the researchers uncovering the hidden microbial networks that shape life around us. Explore our microbiology solutions: na2.hubs.ly/H06lcGg0 #WorldMicrobiomeDay #Microbiome #MicrobiomeResearch #DNSBEQ #genomics #LifeSciences #ScientificCommunity #UCSDCMI #CompleteGenomicsmmunity #CompleteGenomics

AI is changing how scientists work with large-scale genomics data. Join us for a webinar introducing Locus by na2.hubs.ly/H06j3hc0, an AI-powered computational biology collaborator with a plain English interface. Featuring a showcase from Biniam Feleke at Complete Genomics. 📅 June 29 ⏰ 10 AM PT / 1 PM ET / 6 PM UK Register: na2.hubs.ly/H06j3Bx0 In case you missed our webinar, The Future of Data-Driven Genomics, featuring experts from Google and NVIDIA, you can watch it on demand here: na2.hubs.ly/H06j3gj0 #Genomics #BioAI #ComputationalBiology #AIinScience

Today, Complete Genomics celebrates Juneteenth, a day that honors freedom, resilience and progress. On June 19, 1865, enslaved people in Galveston, Texas, finally learned of their freedom, more than two years after the Emancipation Proclamation. Juneteenth is a time to reflect, celebrate and honor the enduring spirit of freedom. Happy Juneteenth. #Juneteenth #FreedomDay #CelebrateFreedom #Inclusion #LifeSciences #Genomics #CompleteGenomics

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