BRB-seq Technology
Our innovative Bulk RNA Barcoding sequencing technology revolutionizes RNA-seq by enabling massive sample multiplexing at a fraction of the cost
The Power of Multiplexing
BRB-seq is a novel approach to RNA sequencing that dramatically reduces costs and increases throughput by tagging individual RNA samples with unique barcodes at the earliest stage of library preparation.
This innovative approach allows for the processing of hundreds to thousands of samples simultaneously, making large-scale transcriptomic studies accessible to all researchers.
This approach was first described by Alpern and colleagues: BRB-seq: ultra-affordable high-throughput transcriptomics enabled by bulk RNA barcoding and sequencing.
- Process 10x more samples at the same cost
- Reduce library preparation time by 50%
- Maintain high data quality and sensitivity
- Scale experiments without scaling costs
- Integrate seamlessly with GenoLens platform
Optimized Barcode Primers
Individual RNA sample tagging at the earliest stage of library preparation, enabling massive multiplexing capabilities
Efficient Processing
Reduced reagent consumption, lower plastic waste, and minimized manual handling for faster turnaround times
High-throughput Compatibility
Streamlined workflows and efficient multiplexing that scales to thousands of samples with minimal cost increase
Frequently Asked Questions
Find answers to common questions about our sequencing services and the GenoLens platform