Benefits
Custom-developed panels
Users communicate their targets of interest, and we will develop ad-hoc detection panels.
Up to
100
targets
Experimentally validated panels for differential expression analysis.
Minimal sequencing cost
By only sequencing the targets, sequencing costs are drastically decreased.
What we do
MERCURIUS ™
Targeted BRB-seq service
The MERCURIUS™ Targeted BRB-seq service offers the most comprehensive, high-throughput and cost-efficient solution for targeted gene expression analysis projects.
As part of the Targeted BRB-seq service, clients share their genes of interest with us, we develop a corresponding custom detection panel and validate it directly on their purified RNA samples.
Once the validation is complete, we will inform the client that the dedicated service is correctly established and that we are ready to receive their test samples.
By combining the advantages of the targeted approach with the BRB-seq system, up to 100 different genes can be assessed across tens to thousands of samples in parallel, significantly reducing the time and costs associated with library preparation and sequencing.
As a result of our service, our clients receive raw sequencing data (fastq files), gene count matrices and analysis reports files.
Optional downstream differential gene expression analysis are also available upon request.
How does it work
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4 to 8 weeks
Alithea developes and validate the custom detection panel on customer's samples - Client Checkpoint
-
-
1 week
Incoming QC - Client Checkpoint
(Nanodrop, Ribogreen, Tapestation) -
2 days
MERCURIUS™ Targeted BRB-seq library prep for Illumina and AVITI
-
1 week
Library QC - Client Checkpoint
(Qubit, Fragment analyzer) -
1.5 weeks
Sequencing - Illumina / AVITI
-
1 week
Data analysis and reporting - Client Checkpoint
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Data
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Optional: Alithea performs Differential Gene Expression analysis
Performance
Improvement of target genes detection with Targeted BRB-seq
Enrichment of UMIs related to targeted genes
Targeted BRB-seq shows greater enrichment for targeted...
Relative enrichment of targeted genes between Targeted BRB-seq and BRB-seq
Improvement of target genes detection with Targeted BRB-seq
Enrichment of UMIs related to targeted genes
Targeted BRB-seq shows greater enrichment for targeted genes.
Relative enrichment of targeted genes between Targeted BRB-seq and BRB-seq
FAQs
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To guarantee high quality data, we normally request that each sample contains at least 200ng of total RNA in at least 10μl.
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In addition to total RNA amount, it is important that the samples contain RNA of high integrity (RIN > 6) and are devoid of contaminants (Nanodrop A260/A230 between 1.8 and 2.2).
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Targeted BRB-seq is a 3’-end RNA sequencing method that requires significantly less sequencing than standard BRB-seq to achieve accurate gene quantification. Therefore, we recommend sequencing 100 reads per target for each sample, which enables reliable detection of the targeted genes.
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As part of our standard service pipeline, we align the generated data to the genome of choice, provide a detailed report on the alignment and gene counting statistics and, finally, provide ready-to-use gene count matrices for downstream analysis.
Speak with our RNA sequencing experts
Need guidance or have questions about DRUG-seq and our service?
Easily book a call with our RNA-seq experts.