Overview

The BD Rhapsody^™ Assay for Transposase-Accessible Chromatin assay (ATAC-seq) enables you to either reproducibly generate standalone open chromatin profiling data or perform a multiomic analysis of open chromatin accessibility and transcriptome of single cells in one experiment on the BD Rhapsody^™ Single-Cell Analysis System.

The BD Rhapsody^™ ATAC-Seq Assays enable you to either generate highly reproducible open chromatin profiling data from single cells or perform a multiomic analysis of open chromatin accessibility and transcriptome of single cells in one experiment using the BD Rhapsody^™ Single-Cell Analysis System.

Learn more from the BD Rhapsody^™ ATAC-Seq Assay Brochure.

Why Choose BD Rhapsody™ ATAC-Seq?

Features

Validated on the new BD Rhapsody™ Enhanced Cell Capture Beads V3, BD Rhapsody™ ATAC-Seq Assays generate consistent, high-quality data across different samples and users and a wide range of cell inputs. Key features include:

High sensitivity and specificity across different experimental conditions
Capable of accommodating a wide range of cell inputs
Integrated epigenomic and transcriptomic characterization on the same cells
Compatibility with Custom BD^® Nuclear Antibody-Oligonucleotide Conjugates

Unveil Epigenomic Heterogeneity with Great Precision

Sensitivity and specificity metrics for the BD Rhapsody™ Single-Cell ATAC-Seq Assay.

Uncover Ties Between Gene Regulation and Expression at the Single-cell Level

Sensitivity and specificity metrics for the BD Rhapsody™ Single-Cell Multiomic ATAC-Seq Assay.

Reproducible Results Across Different Samples and Studies

High reproducibility with BD Rhapsody™ ATAC-Seq Assays

Generate Consistent, High-quality Data Across a Wide Range of Cell Inputs

Robust performance across different cell input amounts.

Applications

More accurate and comprehensive picture of cellular identities with the BD Rhapsody™ Single-Cell Multiomic ATAC-Seq Assay

In this study, the BD Rhapsody™ Single-Cell Multiomic ATAC-Seq Assay was used to analyze 2,190 nuclei from human peripheral blood mononuclear cells (PBMCs). A joint whole transcriptome analysis (WTA) and ATAC-seq dimensionality reduction was performed by Uniform Manifold Approximation and Projection (UMAP) and cells were annotated as members of distinct cell types using the WTA data from a PBMC reference atlas.

Joint WTA ATAC-Seq Dimensionality Reduction

Enrichment of cell type-specific transcription factor motifs in PBMCs

The heat map shows normalized enrichment scores of cell type–specific transcription factor motifs. Motif scores were calculated using a binomial distribution, determining the relative enrichment of each motif in differentially accessible regions of a given cell type compared to GC-matched background regions. The scores were then normalized across cell types per motif on a 0–1 scale, where 0 indicates least enrichment and 1 indicates highest enrichment of each motif.

Cell Type Specific Transcription Factor Motif in PBMC

Comparison between single-cell ATAC-seq data and WTA data in PBMCs

A. Read density across each ATAC-seq cluster at the transcription start sites of cell type marker genes.

B. Violin plots showing cell type-specific gene expression in WTA data.

Single-Cell ATAC-Seq Data vs WTA Data in PBMCs

Concordance between gene expression and inferred gene activity score

This heatmap shows Pearson’s correlation coefficients between ATAC-seq gene activity scores and gene expression values in PBMCs, with each row representing a cell type in WTA data and each column a cell type in ATAC-seq data.