FFPE-seq service
Massively multiplexed full-length total RNA-seq for heavily degraded samples.
Step 1
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Step 4
2 days
Step 5
(Qubit, Fragment analyzer, shallow sequencing)
1 week
Step 6
1 week
Step 7
Step 8
Read more about the FFPE-seq on our blog.
Genome browser view of the RNA-seq reads mapped to several human genes, using different library preparation protocols. The FFPE-seq shows comparable coverage as the NEB Ultra II, while the BRB-seq protocol is limited only to the 3' end genomic region.
Gene body coverage from FFPE-seq, BRB-seq, and NEB Ultra II. The FFPE-seq shows a similar coverage profile as the NEB Ultra II. By contrast, BRB-seq reads preferentially mapped to the 3'end.
We recommend that each sample contains 500ng of total RNA to guarantee high-quality data.
The service is validated with the purified RNA samples from various source and RIN values ranging from 1 to 10.
We normally recommend sequencing between 10-20 million reads for each sample.
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.
Optionally, we can include differential gene expression analysis.
Explore the latest, relevant publications in the industry to learn more about our technologies.
Book a one-on-one call with one of our RNA experts to discover how we can assist your next project.
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