Arima Genomics, Inc.

Scalable Single-cell Workflow for Multiomic Analyses of Chromatin Interactions, Accessibility, Gene Expression and Cell Surface Proteins to Unravel Mechanisms of Cellular Diversity - Scalable Single-cell Workflow for Multiomic Analyses of Chromatin Interactions, Accessibility, Gene Expression and Cell Surface Proteins to Unravel Mechanisms of Cellular Diversity Arima Genomics Project Summary/abstract All Cells in the Human Body Carry the Same Dna Sequence and Yet Individual Cells Are Highly Diverse in Identity, Morphology, Proliferation, and Function, Leading to Enormous Heterogeneity in the Context of Tissues, Organs, and Organisms. Individual Cells Achieve This Diversity via Unique Gene Regulatory Programs – Where in, Unique Sets of Regulatory Elements (RES) Precisely Instruct Each Cell Which Genes to Express and When. Mapping Such Gene Regulatory Programs Are Central to Molecular Biology and Genomics, as Mis-regulation Is a Major Cause of Disease – Mapping Not Only Helps in Diagnosis But Also Enables Therapies That Can Intervene and Correct Mis-regulation. Single Cell Atac Sequencing (SCATAC) Has Emerged as the Popular Mapping Assay to Delineate Res Unique to Each Cell. When Scatac Is Performed Alongside Single Cell Rna Sequencing (scrna), the Researcher Has Access to Both Res and Gene Expression, Allowing Them to Obtain Unprecedented Insight Into the Gene Regulatory Programs of Living Cells. There Is Only One Problem – There Are Often Multiple Res in the Neighborhood of a Gene and Without the Ability to Link Specific Res to Its Target Genes, a Mechanistic View of Gene Regulation Is Lacking, Limiting Our Ability to Enable Precise Diagnosis and Drug Discovery Programs. High Throughput Chromatin Interaction Capture Assay and Sequencing (HIC) Presents a Three-dimensional View of the Genome, Often Informing the Missing Link Between Re and Their Target Genes. Indeed, Several Kols – E.g., DR. Tomi Pastinen Calls Scatac, Scrna and Schic as the “trifecta of Modalities” That Can Truly Delineate Gene Regulatory Programs of Individual Cells (see DR. Pastinen’s Letter and 30+ Additional Letters of Support). Recognizing the Value, Several Academic Labs Have Developed Schic Protocols, Which Has Already Unraveled Incredibly Detailed Mechanistic Insights of Gene Regulation of Complex Microenvironments Including Breast Cancer, Prostate Cancer, Hippocampus – Several of These Studies Are Discussed in This Application. Despite the Enthusiasm Around Schic Data, Adoption Has Been Restricted to a Few Labs Because of (1) Severe Experimental Inefficiencies That Result in Exorbitant Costs (upwards of $20,000 Per Sample), and (2) Because Current Schic Protocols Involve Complex Plate- or Combinatorial Indexing Workflows That Are Challenging to Setup and Execute. via a Self-funded PHASE-1 Program, We Tackled Problem (1) to Drastically Improve Efficiency of Schic and Consequently, Drive Costs Down From Earlier $10 Per Cell, to <$2 Per Cell, Details of Which Are Discussed Both in Research and Commercial Plans. We Then Used Our Rigorous Product Development Expertise to Translate the Resultant Schic Chemistry Into Kits That Were Extensively Validated by Multiple Kols (see Letters From Joe Ecker, Longzhi Tan and Others). Upon Validation, These Kols Have Become Customers Using Arima’s Schic, Referred to as A-schic Kits, in Their Single Cell Workflows Instead of the Inefficient Former Academic Protocols. Webinars and Conference Presentations From These Early Adopters Created a Ripple in the Community and in a Span of Few Months, We Have Sold >1,000 Reactions of A-schic Kits to Tens of Academic Labs (despite No Marketing Activity From Arima), Who Have Embedded Our Kits Within Both the Plate- and Combinatorial Indexing Single Cell Workflows. the Scope of PHASE-2 Program Is to Tackle Problem (2) to Enable Widespread Adoption. in Particular, We Propose to Build Off the A-schic Chemistry Toward What We Refer to as the SC3DGR Chemistry That Is Performed Upstream of 10X Genomics (10XG) Chromium – I.e., the Output of SC3DGR Kit Will Be an Input Into the 10X Atac (FLAVOR1) or 10X Multiome (FLAVOR2) Kits, to Concurrently Capture Schic and Scatac (FLAVOR1), or, Schic, Scatac and Scrna (FLAVOR2), Respectively. Such a Chemistry Will Not Only Solve the Ease to Use Problem (2) Given Its Combability With the Market Leader 10XG, But Importantly, It Will Enable Multiomic Analyses of the “trifecta” From the Same Individual Cell Concurrently, Thus Enabling Cell Perturbation, Characterization and Screening Use-cases for Precision Mapping, Diagnosis, and Therapy. Once the SC3DGR Chemistry Is Finalized, We Translate It Into Robust Kits, to Be Validated by 14 Kols (see Letters of Support) Across Academia and Pharma (abbvie, Astrazeneca & Genentech). for Arima, the Chemistry, the Informatics, the Easy End-to-end Workflows, the Overall Workflow Cost, the Kol-based Go-to-market Strategy – All Play Major Factors in a Seamless Commercialization Process of This Leapfrog Technology for Delineating Gene Regulation Programs of Individual Cells.