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Harness the Power of More

Multiple Omes + High Quality Data + 

Less than 1 Cent per Cell

Maximize Your Single Cell Insights

The power of multiomics makes your single cell research future proof turning a single experiment into insights about the many omes of each cell. With our complete solution you can now get more omes. More quality data. And more breakthroughs. All at less than 1 cent per cell.*

 

It's time to harness the power of more.
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One Source, More Omes

Leave no cell behind and maximize insights about each single cell with coverage of DNA, RNA and Protein.

Less than 1 Cent per Cell

Gather more information, for less, with minimal cost per cell.

 

No Capital Instrument Expense

Get the high reproducibility and throughput of an instrument, without the usual price tag.

Simple and Free Data Analysis

Turn complex data into actionable insights with just a few clicks. Our high dimensional data analysis software requires no expertise and no coding.

The Only Complete Single-Cell Multiomics Solution

High data quality + high throughput + millions of cells, all in one solution.

 

Complete BD Solutions

 

 

 

The BD Difference

 

Features**10x GenomicsBDParse Biosciences or Scale Biosciences
High capital expenditure
Yes 

No

N/A
Sample loss
Clogging and wetting failures

None

Poor retrieval due to multiple pipetting steps
Hands-on time
Moderate

Moderate

High
Multiomics assays offered by same vendor
DNA (Epigenomics), RNA

DNA (Epigenomics), RNA, Protein

RNA
Inter-user variability
Low, except for clogging and wetting failures

Low to none

Potentially high, due to multiple pipetting steps
Fragile samples and granulocytes
Poor

Good capture and recovery

Poor
Long-term stopping point during the workflow
<4 weeks

1 year after cell capture on beads

<6months
Partial use consumables
No

Yes

No
Multiplet rate
High

Moderate

Low

 

Generate

Fast track your single cell research without compromise

The BD Rhapsody™ HT Xpress System eliminates the need for expensive capital equipment or hours of pipetting into 96-well plates—providing reproducible, high-quality data, at less than 1 cent per cell.


With no capital expense, the cartridge-based system gives you the high-throughput you need to conduct million cell studies.

 
Analyze
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Analyze

Go from sequencer to t-SNE plots with ease—for free
  • With no coding and no bioinformaticians needed, our free data analysis software finally makes uncovering insights simple and easy. You’ll also get access to our team of experts if you ever need additional support.

  • BD Rhapsody Sequence Analysis Pipeline: Simply load data from your sequencer and get ready-to-read, deconvoluted outputs.

  • BD Cellismo Data Visualization Tool: Turn your data into insightful visualizations with our newest secondary analysis software, launching in February, 2025.
 
Analyze
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Latest News

At BD, we are here to provide comprehensive applications and bioinformatics support for your single-cell experiments. Please contact us if you need support with your experimental workflow or data analysis needs.

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      Read our latest eBook to discover how single cell multiomics, the BD Rhapsody™ System, and cell sorting can help you gain important insights into cancer immunology.

      Download e-Book
       
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      The BD Rhapsody single-cell platform has been instrumental in advancing our translational research projects in inflammatory bowel disease (IBD) at Stanford. With the BD Rhapsody platform, we have been successful in robustly capturing traditionally difficult to isolate cell types (e.g. neutrophils) from intestinal biopsies. The platform has also enabled us to multiplex a large number of samples, capture significantly more cells, and perform advanced analyses combining whole transcriptomics with paired TCR and BCR sequencing.

      The BD Rhapsody single-cell platform has been instrumental in advancing our translational research projects in inflammatory bowel disease (IBD) at Stanford. With the BD Rhapsody platform, we have been successful in robustly capturing traditionally difficult to isolate cell types (e.g. neutrophils) from intestinal biopsies. The platform has also enabled us to multiplex a large number of samples, capture significantly more cells, and perform advanced analyses combining whole transcriptomics with paired TCR and BCR sequencing.

      John Gubatan, MD
      Stanford University School of Medicine
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      Schedule a Meeting


      Want to learn more about our solution? Contact us now to connect with our Multiomics Specialists.

       

       

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      *1 cent per cell calculation includes instruments and reagents, but is not inclusive of sequencing costs. 
      ** As of December, 2024
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      For Research Use Only. Not for use in diagnostic or therapeutic procedures.