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The site is undergoing maintenance. Ordering can continue through fax and phone.
Sunday, August 16, 2026, 1:30 - 4:30 pm (CEST).
If you encounter problems while ordering. Please contact us at BDBCustomerService@bd.com
See MoreThe site is undergoing maintenance. Ordering can continue through fax and phone.
Sunday, August 16, 2026, 1:30 - 4:30 pm (CEST)
.If you encounter problems while ordering. Please contact us at BDBCustomerService@bd.com
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The BD OMICS-One™ WTA Next Assay redefines single-cell RNA-seq with breakthrough sensitivity and unbiased whole transcriptome profiling. Generate highly reproducible data on the BD Rhapsody™ Single-Cell Analysis System—whether running standalone RNA-seq workflows or integrating with CITE-seq, ATAC-seq or immune repertoire workflows. The new BD OMICS-One™ WTA Next Assay produces consistent, high-quality results across all multiomics applications with cell input ranges from 1,000 to 100,000 per lane on an 8-lane cartridge.
Download the BD OMICS-One™ WTA Next Assay Brochure>
To see how you can incorporate this new assay into your BD Rhapsody™ System workflows, visit our Protocols page.
The BD OMICS-One™ WTA Next Assay expands what’s possible—providing superior sensitivity, enhanced multiomics capabilities, greater flexibility, reliable scalability and impactful economic value. The assay also delivers best-in-class sensitivity to reveal rare transcripts and cellular complexity across all supported workflows, exceeding 10x Genomics’ Chromium GEM-X Single Cell 3' v4 Gene Expression Assay in key metrics.
3,000+ Genes per Cell
| Scalable Throughput
|
Multiomics Excellence
| Lower Cost per Sample
|
Flexible Sample Handling |
Performance
Head-to-head comparison of the BD OMICS-One™ WTA Next Assay versus the 10x Genomics Chromium GEM-X Single Cell 3' v4 Gene Expression Assay using matched PBMC samples from three donors processed under identical conditions.
Bar graphs show median UMIs (A) and median genes per cell (B) at 25,000 and 50,000 raw sequencing reads per cell. The BD OMICS-One™ WTA Next Assay achieves higher molecular and gene detection that becomes increasingly more pronounced as sequencing depth increases, demonstrating best-in-class sensitivity for single-cell RNA sequencing applications. Error bars represent standard deviation across three biological replicates.
Performance comparison of the new BD OMICS-One™ WTA Next Assay (WTA Next) versus the current BD Rhapsody™ Whole Transcriptome Analysis (WTA) Assay using previously frozen PBMC samples from three healthy matched donors processed in standalone WTA experiments.
(A) Median number of unique molecular identifiers (UMIs) per cell as a function of raw sequencing reads per cell, demonstrating a 120% increase in transcript detection with WTA Next at 50,000 reads per cell.
(B) Median number of genes detected per cell across varying sequencing depths, showing a 67% improvement with WTA Next at 50,000 reads per cell. Error bars represent standard deviation across three biological replicates. .WTA workflow: 20,000 cells targeted with ~16,000 recovered, subsampled to 4,000 for analysis. WTA Next workflow: 40,000 cells targeted with ~30,000 recovered, subsampled to 3,000 cells. All captures were performed on a BD Rhapsody™ 8-Lane Cartridge.
Gene recovery comparison between the current BD Rhapsody™ Whole Transcriptome Analysis (WTA) Assay and new BD OMICS-One™ WTA Next Assay (WTA Next) across different multiomics applications.
(A) Cell-based workflows using frozen PBMCs. Left: CITE-seq showing 38% increase in median genes per cell with WTA Next at ~23,000 reads per cell. Right: TCR/BCR-based assay demonstrating 81% improvement with WTA Next at ~22,700 reads per cell.
(B) Nuclei-based workflows using fresh PBMCs. Left: ATAC-seq showing 156% increase in median genes per cell with WTA Next at 25,000 reads per cell. Right: Multiplexed ATAC-seq demonstrating 126% improvement with WTA Next at 25,000 reads per cell. The BD OMICS-One™ WTA Next Assay delivers substantial performance gains across all supported multiomic combinations, either in single-cell or nuclei-based implementations.
Reproducibility assessment with two independent users processing the same frozen PBMC sample from one donor in separate experiments (with 30,000 cells).
(A) Bar graphs show nearly identical median UMIs (left) and median genes (right) per cell at 25,000 reads per cell, confirming consistent sensitivity across users.
(B) Gene expression correlation (R2 = 1.0) demonstrating exceptional inter-user reproducibility, confirming robust assay performance independent of operator variability. Consistent results across users ensure reliable data generation in multi-operator laboratories and collaborative research settings.
Applications
Identification and resolution of distinct immune cell populations in PBMC samples
Gene expression distributions across immune cell types
Immune profiling ability to resolve functional subpopulations within major cell types
Download our FAQ document if you have more in-depth questions>
For Research Use Only. Not for use in diagnostic or therapeutic procedures.