Scale without the premium. Introducing VITARI™ 
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      Meet Element Biosciences at ASHG 2026

      EP_Header_ASHG2026_2400px (1)

      Human genetics at scale requires sequencing that doesn’t make you choose between quality, throughput, flexibility, and cost. At ASHG 2026, visit us at booth #1108 to explore how VITARI™ and AVITI24™ are enabling population genomics, rare disease research, complex variant analysis, and multiomic workflows.

      Posters

      Next‑Generation Multiplex Hybrid Capture and Sequencing Enabled by Workflow Integration and Enhanced Library Complexity
      Author: Sangwon Lee, Agilent

      Improved sequencing of difficult regions reduces variant calling errors
      Author: Meredith Ashby, Element Biosciences

      Targeted in situ SNP genotyping enables single-cell identity deconvolution for scalable human cell village studies
      Author: Andrew Boddicker, Element Biosciences

      Time-series single-cell multiomics on AVITI24 captures transcriptional morphological consequences of acutely depleting the neurodevelopmental gene SETD5 in hiPSCs
      Author: June Zhao, Element Biosciences

      Spatially Resolved Mapping of Intratumor Clonal Architecture in Human Tumors Using Direct In-Sample Sequencing
      Author: Ben Krajacich, Element Biosciences

      Scientific agenda

      CoLab Theater Presentation

      Title: Decoding Disease Mechanisms with Multimodal Cellular and Spatial Profiling
      Date: Wednesday, October 21, 2026
      Time: 1:00 PM – 1:30 PM
      Location: Exhibit Hall, CoLab Theater #2

      Speaker:

      Headshot_Abbey-Cutchin_1121-x-898-1_2025-04-17-183928_gdxj Abbey Cutchin
      Director, Product Management
      Element Biosciences

      Industry Education Session

      Title: From variant discovery to biological insights: NGS and multiomics workflows for understanding genetic disease
      Date: Wednesday, October 21, 2026
      Time: 3:00 PM – 4:00 PM
      Location: Meeting Room 514BC

      Learn how VITARI and Cytos are enabling cost-effective, high-throughput approaches to detecting and understanding the biological impact of genetic variants.

      • Presentation: Whole Genome Sequencing of Rare Disease Samples on VITARI
        Speaker: Mike Eberle, PhD., VP Computational Biology and Informatics, GeneDx

      • Presentation: Time-series single-cell multiomics on AVITI24 captures transcriptional and morphological consequences of acutely depleting the neurodevelopmental gene SETD5 in hiPSCs”
        Speaker: Prof Alon Goren, UCSD Institute for Genomic Medicine