SINGLE-CELL ATAC-SEQ

While traditional, bulk assay for transposase-accessible chromatin sequencing (ATAC-Seq) offers valuable insights into genome-wide epigenetic regulation, cells in heterogeneous populations are combined into a single transposition reaction – obscuring key chromatin signatures. Utilizing microfluidics and molecular barcoding, single-cell ATAC-Seq (scATAC-Seq) investigates chromatin accessibility in hundreds to thousands of individual nuclei from a single sample, enabling regulatory motif discovery and offering a deeper understanding of gene regulation. For a single-cell multi-omic approach, scATAC-Seq and scRNA-Seq can be combined through an integrated data analysis framework to uncover novel biological features.

GENEWIZ’s scATAC-Seq utilizes the latest technology on the market: the 10x Genomics® Chromium™ and Illumina® NovaSeq™. As an early adopter of these platforms, our optimized workflows — including pre-submission cryopreservation and post-submission dead cell removal — maximize project flexibility, speed, and data accuracy while eliminating costly overhead and ramp-up time to expedite your research.

scATAC-SEQ WORKFLOW

  • STEP 1.
    DEAD CELL REMOVAL

    If viability and cell count are low, dead cells are removed using a magnetic bead-based approach to enrich live cells. ​

  • STEP 2.
    CELL PARTITIONING

    Cells and barcoded beads are isolated in droplets using the 10x Genomics Chromium and tagmented. ​

  • STEP 3.
    LIBRARY PREPARATION

    Unique barcodes for each individual cell are added to DNA prior to library preparation. ​

  • STEP 4.
    SEQUENCING

    Barcoded libraries are pooled and sequenced on the Illumina NovaSeq​ for high-throughput characterization.

  • STEP 5.
    BIOINFORMATICS DATA ANALYSIS

    Visualize results through interactive software and receive custom analysis.

scATAC-SEQ: EPIGENOMIC INSIGHTS AT THE CELLULAR LEVEL

  • Cell Cluster and Classification

    Identify and classify diverse cell types in heterogenous cell populations.​

  • Trajectory Inference

    Discover states for lineage and development tracing to understand mechanisms of cell fate.

  • Regulatory Variation

    Detect altered gene regulation and/or novel enhancers in rare cells and sub-populations.

  • Chromatin Accessibility

    Reveal subpopulation-specific regulation, enabling prediction of cell type-specific, cis-regulatory networks.

FEATURES & BENEFITS

  • Superior Data Quality
    Exceeding manufacturer’s benchmarks​

  • Real-Time Project Updates
    Through our online system

  • Ph.D.-Level Support
    At every step

  • Proprietary cell freezing method maintains cell viability during storage and transit.

  • Dead cell removal protocol improves data quality, especially for samples with suboptimal viability.

  • Early adopter of the 10x Genomics Chromium with optimized workflows that maximize project flexibility, speed, and data accuracy.

  • Highest-throughput sequencing platforms, including the Illumina NovaSeq, provide cost-effective sequencing solutions.

  • Flexible starting materials accepted including cell pellets with as few as 10,000 viable cells and frozen tissue; isolated nuclei are not required.

  • Samples accepted at different stages of the 10x workflow including cells, Gel Beads in Emulsion (GEMs), or 10x barcoded cDNA libraries for maximum workflow flexibility.

View more reasons to choose GENEWIZ

SINGLE-CELL MULTI-OMICS

Integrate scRNA-Seq and scATAC-Seq data analysis frameworks to quantify how chromatin structure influences the regulation of gene expression. Download our poster about single-cell multi-omic profiling of cryopreserved tissue to learn more.

Figure: Frozen cells undergo GENEWIZ’s proprietary dead cell removal protocol. Viable cells are sorted, followed by nuclei and RNA extraction, and are subjected to scATAC-Seq and scRNA-Seq, respectively. Integrative data analysis of chromatin accessibility and gene expression for the same cell types can be used for confirming cell identity annotation by UMAP projections. The gene activity matrix derived from counts in gene body and promoter regions determines putative cell types.

SINGLE-CELL MULTI-OMICS BENEFITS

  • Streamlined experimental design with sample splitting to reduce variability between assays.

  • Integrated data analysis provides greater insight into gene regulation and enables more complete sample characterization.

  • Reduced cost and faster results from combined workflows compared to separate analyses.

  • Customized and extensive bioinformatic solutions with interactive, hands-on analysis and publication-ready images.

  • Poster: Highly Multiplexed Single-Cell Transcriptome and Epigenome Profiling of Cryopreserved Tissue Enables Multi-omic Tissue Characterization in Clinical Settings

    Single-cell analysis typically relies upon immediate processing of fresh tissue, presenting limitations for translational and clinical applications. Learn how GENEWIZ’s robust cryopreservation workflow for downstream processing enabled high-quality, single-cell transcriptomic and epigenomic analysis of translational and clinical samples by coupling scATAC-Seq and scRNA-Seq. 

  • Tech Note: Add More Life to Your Data: Optimizing Single-Cell RNA-Seq with Dead Cell Removal

    Obtaining samples with high cell viability can be difficult for many experiments but is necessary for success on the 10x Genomics Chromium platform. This tech note describes how GENEWIZ scientists used optimized single-cell workflows, including dead cell removal, to overcome low viability and generate high-quality sequencing data.

NGS PLATFORMS

GENEWIZ is a certified service provider for Illumina and Life Technology NGS platforms. For information on our NGS platforms as well as recommended configurations of your projects, please visit the NGS Platforms page. GENEWIZ does not guarantee data output or quality for sequencing-only projects.

How To Order


Email | Phone (1-877-GENEWIZ (436-3949), Ext. 1)