By leveraging BRB-seq, we not only provide to industrial and academic clients high quality RNA-seq data, but we also do so with the highest affordability and shortest turnaround times on the market.
The MERCURIUS ™ Blood BRB-seq service offers a convenient and streamlined solution for your blood transcriptomics projects. We have expertise with different types of RNA purification from blood samples and we have specialised in high-throughput RNA extraction from PaxGene tubes.
Customers can therefore either send us directly their blood samples or perform RNA extraction in-house and send us purified RNA samples. Upon samples reception, we always perform incoming QC before launching our Blood BRBseq pipeline. During the process, we always keep clients informed at defined checkpoint so that we can decide together how to best proceed to the next steps.
Next generation sequecing and data preprocessing (including alignment to the genome of choice) are part of our standard service as well. As a result, we provide our clients raw data, sequencing and alignment reports, and gene count matrices which can be used for downstream gene expression analysis.
Step 1
Step 2
(Nanodrop, Fragment Analyzer)
1 week
Step 3
2 days
Step 4
(Nanodrop and Fragment Analyzer)
1 week
Step 5
1 week
Step 6
Step 7
Number of samples:
96
Reads per sample in demo dataset:
10'000 reads
To have access to the deep-sequenced dataset (4.8M reads per sample) contact us.
Demo dataset file size:
57.7 MB
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