🔬 Join us for a Seminar hosted by the CU Anschutz Shared Resource Genomics Core. Explore a cost-effective approach to whole genome sequencing (WGS) with genome-wide DNA methylation detection using Watchmaker Genomics’ TAPS+ library preparation workflow and Complete Genomics’ DNBSEQ-T7 sequencing platform. Agenda: 🎤TAPS+ Methylation WGS Library Preparation Watchmaker Genomics 🎤Cost-Effective TAPS+ Methylation WGS Sequencing on DNBSEQ-T7 Jim George, Technical Specialist, Complete Genomics 🎤TAPS+ WGS Data Showcase, Workflow Logistics, and Pricing Sky Lee, PhD, CU Anschutz Shared Resource 📆 Wednesday, November 18 ⏰ 12:00 PM - 1:00 PM MST 📍 Room 8105, CU Anschutz Research Complex 2 👉Register Here na2.hubs.ly/H08Q71b0 #Genomics #CompleteGenomics #DNBSEQ

🔬 Join Cleveland Clinic and Complete Genomics to celebrate the launch of Stereo-seq spatial transcriptomics services for FFPE and frozen tissue samples. Offered through Cleveland Clinic’s Discovery Laboratory, Computational Oncology Platform, and Translational and Correlative Services (TCS), these cost-effective, end-to-end solutions support researchers across Cleveland Clinic, Case Western Reserve University, University Hospitals, MetroHealth, and biotech and pharmaceutical collaborators. Explore applications in research and clinical trials, with expert support from experimental design through data analysis. Talks: 🎤Histology, tissue imaging, library prep, QC and sequencing Vartika Srivastava, PhD Cleveland Clinic Foundation 🎤Multiple sclerosis fresh frozen spinal cord analysis Ivan Juric, PhD, Cleveland Clinic Foundation 🎤Fresh fozen and FFPE brain tumor analysis Atefeh Bagheri, PhD, Cleveland Clinic Foundation 📆 Tuesday, November 17 ⏰ 1:00 PM - 3:00 PM ET 📍 Room NC1-202, Cleveland Clinic Main Campus 👉Register Here: na2.hubs.ly/H08Q6J60 #Genomics #CompleteGenomics #DNBSEQ

⏳ Last call for the Scavenger Hunt at ASHG 2026! Complete your hunt and stop by Complete Genomics at Booth 807 before you go! 🧬 Take a closer look at DNBSEQ-T7+ and connect with our team about your next human genetics study. From cohort size and coverage goals to sequencing throughput and workflow flexibility, bring your questions for one more scientific conversation. Learn more: na2.hubs.ly/H08zMCd0 na2.hubs.ly/H08zMCf0 Thanks for making us part of your ASHG experience! #ASHG2026 #CompleteGenomics #DNBSEQ #HumanGenetics

⏰ Last chance to catch our booth talks at ASHG 2026! We start in one hour. Join Complete Genomics at Booth 807 for our final booth presentations: 🎤 Tomohiro Takano (Genomelink) The Human Genome: Ready to Read 🎤 Angelica Olcott (Bio-Rad) Enhancing single-cell transcriptomics sensitivity with DNBSEQ-T1+ and the Bio-Rad ddSEQ 3′ RNA-Seq Kit. 📅 Today, Friday, October 23 | 10–11 AM 📍 Booth 807 Catch the talks, explore our scientific posters, and bring your sequencing questions to our team. See you there! #ASHG2026 #CompleteGenomics #DNBSEQ #SingleCell #Genomics

📸 Thursday highlights from Booth 807 at ASHG 2026! A big thank you to our Industry Workshop speakers, Christopher Douville, Alexander Kaplun, and Michael Snyder, for sharing their valuable insights on cancer detection, comprehensive whole-genome sequencing, and longitudinal multi-omics. We also thank our booth presentation speakers and everyone who stopped by the Complete Genomics booth yesterday! 🎤 Radoje Drmanac (Complete Genomics) explored the possibilities enabled by longer sequencing reads with CoolMPS 600. 🎤 Haodong Chen (Sentieon) shared insights into variant calling using DNAscope Pangenome and CoolMPS SE600 reads. The conversation continues today at Booth 807! Stop by to explore our scientific posters, meet our team, and discuss sequencing and analysis approaches for your research. #ASHG2026 #CompleteGenomics #CoolMPS600 #Genomics #VariantCalling

🧬 Highlights from our ASHG 2026 Industry Workshop! From cancer detection to personalized health monitoring, our speakers shared three complementary perspectives on precision genomics: 🔹 Christopher Douville (Johns Hopkins School of Medicine) Integrating genomic alterations and DNA fragmentation patterns to study cancer, including liquid biopsy approaches using blood and cerebrospinal fluid. 🔹 Alexander Kaplun (Variantyx) Clinical validation of DNBSEQ-T7+ for comprehensive whole-genome sequencing across diverse variant types, including structural variants and short tandem repeats. 🔹 Michael Snyder (Stanford University) Tracking one individual’s molecular landscape over 14 years, combining genomic, RNA, and protein profiling to study changes associated with infection, inflammation, and metabolic health. Thank you to our speakers for sharing their research and insights! Continue the conversation with Complete Genomics at Booth 807 to discuss sequencing and analysis approaches for your next study. #ASHG2026 #CompleteGenomics #DNBSEQ #PrecisionMedicine #Multiomics

🧀🧬 Power up your ASHG afternoon with Snack & SNPs! Join Complete Genomics at Booth 807 for a cheese-and-fruit plate and a chat about your research. From sequencing workflows to variant analysis, bring your questions and connect with our team over a snack. 📅 Thursday, October 22 | 4:15–6:15 PM 📍 Booth 807 | Exhibit & Poster Hall Full ASHG Agenda: na2.hubs.ly/H08xK1Z0 Stop by for a bite and let’s talk genomics! #ASHG2026 #CompleteGenomics #DNBSEQ #Genomics

⏰ Our Thursday booth talks start in one hour! Join us at Booth 807 to explore longer sequencing reads and pangenome-informed variant analysis: 🎤 Radoje Drmanac (Complete Genomics) Discover new possibilities with CoolMPS 600 and longer sequencing reads. 🎤 Haodong Chen (Sentieon) Explore variant calling with DNAscope Pangenome and CoolMPS SE600 reads. 📅 Today, Thursday, October 22 | 4:30–5:30 PM 📍 Booth 807 Full ASHG Agenda: na2.hubs.ly/H08xJZR0 Meet the speakers, bring your questions, and join the conversation! #ASHG2026 #CompleteGenomics #DNBSEQ #Genomics #VariantCalling

🐶 Save a little room in your ASHG bag for a plush puppy! Visit Complete Genomics at Booth 807, complete our quick survey, and take home a cuddly conference companion as our thank-you. Stay for a conversation about your research, explore our scientific posters, and discover sequencing solutions for your next study. Come talk genomics and leave with a little puppy love! Plush puppies available while supplies last. Full ASHG Agenda: na2.hubs.ly/H08xJWm0 #ASHG2026 #CompleteGenomics #DNBSEQ #Genomics

⏰ Our ASHG 2026 Industry Workshop starts in one hour! Join Complete Genomics for insights into liquid biopsy, clinical whole-genome sequencing, and longitudinal multiomics for personalized medicine, featuring: 🎤 Christopher Douville (Johns Hopkins School of Medicine) 🎤 Alexander Kaplun (Variantyx) 🎤 Michael Snyder (Stanford University) 📅 Today, Thursday, October 22 | 12:15–1:15 PM 📍 Room 514BC, Level 2 Full ASHG Agenda: na2.hubs.ly/H08xJW60 Bring your research questions and join us. See you there! #ASHG2026 #CompleteGenomics #DNBSEQ #PrecisionMedicine #Genomics

🧬 Longer reads bring more context to human genetics research. Discover CoolMPS 600 at ASHG 2026 and explore how longer sequencing reads can help improve mapping and characterize insertions and deletions in repetitive genomic regions. Visit Complete Genomics at Booth 807 to explore our scientific posters, discuss the data, and learn how CoolMPS 600 could support your sequencing workflows. Learn more: na2.hubs.ly/H08xJH20 Bring your research questions. Let’s explore what longer reads could reveal in your next study. #ASHG2026 #CompleteGenomics #CoolMPS600 #HumanGenetics #Genomics

📸 Wednesday highlights from our CoLab and Booth 807 at ASHG 2026! Thank you to everyone who stopped by our CoLab session and booth yesterday to share research questions, explore our scientific posters, and take a closer look at the DNBSEQ-T7+ sequencer. 🎤 Andrew Carroll (Google) presented 🎤 Gary Burnett (NVIDIA) on accelerating genomics analysis with NVIDIA Parabricks. Cheers to Jason Fenwick for joining us at the Booth! 🎤 Ronjon Nag (Superbio) presenting Talk to Your Genome. Thank you to all speakers for sharing their perspectives on genomic analysis and interpretation! Full ASHG agenda: na2.hubs.ly/H08xJnm0 The conversation continues today at Booth 807. Join us for more booth presentations, browse our posters, and discuss sequencing and analysis approaches for your next study. #ASHG2026 #CompleteGenomics #DNBSEQ #Genomics #AI

🧬 Complete Genomics is excited to bring you Thursday’s lineup at ASHG 2026! Join us Thursday, October 22, for scientific insights spanning cancer detection, clinical whole-genome sequencing, personalized medicine, and variant analysis. Industry Workshop | 12:15–1:15 PM 📍 Room 514BC, Level 2 🎤 Christopher Douville (Johns Hopkins School of Medicine): Genomic and liquid biopsy approaches to cancer detection. 🎤 Alexander Kaplun (Variantyx): Clinical whole-genome sequencing with DNBSEQ-T7+. 🎤 Michael Snyder (Stanford University): Longitudinal multiomics for personalized medicine. Booth Presentations | 4:30–5:30 PM 📍 Booth 807 🎤 Radoje Drmanac (Complete Genomics): Longer sequencing reads and new possibilities with CoolMPS 600. 🎤 Haodong Chen (Sentieon): Variant calling with DNAscope Pangenome and CoolMPS SE600 reads. 🧀 Snack & SNPs | 4:15–6:15 PM | Booth 807 Refuel with a cheese-and-fruit plate and talk genomics with our team! Full ASHG Agenda: na2.hubs.ly/H08xz9D0 Bring your research questions, explore our scientific posters, and join the conversation. #ASHG2026 #CompleteGenomics #DNBSEQ #PrecisionMedicine #Genomics

🧬 CoLab highlights from ASHG 2026! Thank you to Andrew Carroll for sharing how pangenome-informed analysis and AI can improve variant calling using DNBSEQ-T7+ and CoolMPS 600 sequencing data. Our CoLab session at ASHG 2026 showed how sequencing chemistry and informatics can work together to improve variant analysis. "Pangenome mapping with DeepVariant models trained on Complete Genomics' CoolMPS 600 chemistry brought errors on the T2T v5 GIAB truth set below 50,000 for HG002, a more than 50% accuracy improvement over linear pipelines, driven largely by how cleanly these reads resolve homopolymers and tandem repeats," said Andrew Carroll, PhD, product lead for genomics at Google Research. "And because the pipeline is open source and built for scale, any lab can use it.” Continue the conversation with Complete Genomics at Booth 807. Bring your questions about sequencing, variant analysis, and your next study! #ASHG2026 #CompleteGenomics #DNBSEQ #HumanGenetics #AIinGenomics

⏰ Our Wednesday booth talks start in one hour! Join Complete Genomics at Booth 807 for expert perspectives on AI and genomic analysis: 🎤 Gary Burnett (NVIDIA) Accelerating genomics analysis with NVIDIA Parabricks. 🎤 Ronjon Nag (Superbio) Talk to Your Genome. 📅 Today, Wednesday, October 21 | 3–4 PM 📍 Booth 807 Full ASHG Agenda: na2.hubs.ly/H08xblX0 Bring your research questions, meet the speakers, and join the conversation! #ASHG2026 #CompleteGenomics #Genomics #AI

🐶 Meet your next desk buddy at ASHG 2026! Stop by Complete Genomics at Booth 807, complete our quick survey, and take home an adorable plush puppy as a thank-you. While you’re there, explore our scientific posters and chat with our team about your sequencing questions and next study. 📅 October 21–23 | Booth 807 Share your thoughts and give a plush puppy a new home! While supplies last. #ASHG2026 #CompleteGenomics #DNBSEQ #Genomics

🧬 Discover what the $100 genome could mean for your next study. Meet DNBSEQ-T7+ at ASHG 2026 and explore how lower sequencing costs can open possibilities for larger cohorts and broader whole-genome studies. With sequencing costs as low as approximately $100 per human genome and four independently controlled flow cells, DNBSEQ-T7+ brings scale and flexibility to WGS, single-cell, and spatial transcriptomics research. Visit Complete Genomics at Booth 807 to take a closer look at the sequencer and discuss your study design, workflow needs, and sequencing goals. Learn More: na2.hubs.ly/H08x5jD0 Bring your next genomics challenge. Let’s explore the possibilities together. #ASHG2026 #CompleteGenomics #DNBSEQ #WholeGenomeSequencing #Genomics

⏰ Our ASHG 2026 CoLab starts in one hour! Join Andrew Carroll (Google) to explore pangenome-informed, AI-driven variant calling with Google DeepVariant, using DNBSEQ-T7+ and CoolMPS 600 sequencing data. Hear how these approaches can improve variant-calling accuracy across challenging regions of the human genome. 📍 Theater 2, Exhibit Hall Join Complete Genomics for the session. See you there! Full ASHG 2026 Agenda: na2.hubs.ly/H08x5g60 #ASHG2026 #CompleteGenomics #DNBSEQ #HumanGenetics

🧬 Complete Genomics is excited to welcome you to Wednesday’s CoLab and booth presentations at ASHG 2026! Join us Wednesday, October 21, for expert perspectives on AI and genomic analysis. CoLab | 10:15–10:45 AM 📍 Theater 2, Exhibit Hall Hear from Andrew Carroll (Google) on pangenome-informed, AI-driven variant calling with Google DeepVariant, using DNBSEQ-T7+ and CoolMPS 600 sequencing data. Booth Presentations | 3–4 PM 📍 Booth 807 🎤 Gary Burnett (NVIDIA) Accelerating genomics analysis with NVIDIA Parabricks. 🎤 Ronjon Nag (Superbio) Talk to Your Genome. Between sessions, stop by Booth 807 to explore our scientific posters, take a closer look at the DNBSEQ-T7+ sequencer, and discuss your research questions with our team. Full Agenda: na2.hubs.ly/H08wkzv0 Bring your sequencing goals and join the conversation! #ASHG2026 #CompleteGenomics #DNBSEQ #HumanGenetics #AIinGenomics

🧬 Complete Genomics is excited to welcome you to Wednesday’s CoLab and booth presentations at ASHG 2026! Join us Wednesday, October 21, for expert perspectives on AI and genomic analysis. CoLab | 10:15–10:45 AM 📍 Theater 2, Exhibit Hall Hear from Andrew Carroll (Google) on pangenome-informed, AI-driven variant calling with Google DeepVariant, using DNBSEQ-T7+ and CoolMPS 600 sequencing data. Booth Presentations | 3–4 PM 📍 Booth 807 🎤 Gary Burnett (NVIDIA) Accelerating genomics analysis with NVIDIA Parabricks. 🎤 Ronjon Nag (Superbio) Talk to Your Genome. Between sessions, stop by Booth 807 to explore our scientific posters, take a closer look at the DNBSEQ-T7+ sequencer, and discuss your research questions with our team. Bring your sequencing goals and join the conversation! Full Agenda: na2.hubs.ly/H08w10d0 #ASHG2026 #CompleteGenomics #DNBSEQ #HumanGenetics #AIinGenomics