-
Your selected country is
eu
- Change country/language
Old Browser
Your account has been put on hold due to inactivity. To re-activate, check your account information and make all necessary updates.
Looks like you're visiting us from {{countryName}}.
Would you like to remain on the current country site or be redirected to one based on your location?
live copy GB
Your account has been put on hold due to inactivity. To re-activate, check your account information and make all necessary updates.
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
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.
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.
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.
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.
For Research Use Only. Not for use in diagnostic or therapeutic procedures.
Report a Site Issue
This form is intended to help us improve our website experience. For other support, please visit our Contact Us page.