BRB-seq cloud
Demultiplexing, alignment and gene counts at the click of a button.
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From 5 mins to 20 mins depending on file size
Upload raw read1 and read2.fastq files
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Upload sample info in .xls format
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Select genome of interest
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From 20 min to 24 hours depending on .fastq and genome size
Launch platform
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Download results
- Gene count matrix
- UMI count matrix
- PDF QC report file with individual sample info:
- Number of raw reads/sample
- Alignment stats
- Number of detected genes
- UMI duplication levels
Products & Services
Our BRB-seq and DRUG-seq kits make it possible to process up to 384 RNA samples in one single tube, which helps reduce technical variation, turnaround times and costs. Experience sample to sequencing-ready library in one day.
Our BRB-seq and DRUG-seq services deliver raw sequencing data (fastq files), gene count matrices and analysis report files. A cost-efficient option suitable for projects of all sizes.
