Zymo-Seq RRBS Library Kit
Zymo-Seq RRBS Library Kit is an all-in-one RRBS library prep kit that generates NGS libraries with a simplified workflow for the classic method Reduced Representation Bisulfite Sequencing (RRBS). This all-in-one RRBS library prep kit allows for DNA methylation profiling at single-nucleotide resolution in CpG-rich regions of the genome. This Zymo-Seq RRBS Library Kit is the ideal RRBS library prep kit to generate libraries that…
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I would strongly recommend it to my colleagues.
Sequencing
The sequencing library construction kit is really friendly and easy to use. The protocol is clear. The quality of library DNA is higher.
Review Date: 15 Jun 2021 | Zymo Research
Great results.
Prostate cancer methylation
Is the rrbs kit that works best on our samples. The help from the technical team was also great.
Review Date: 25 May 2021 | Zymo Research
Great result and applicable.
Methylation in prostate biopses
We achieved great results with this kit, it's the only one that works with our samples. The technical support was also great.
Review Date: 20 May 2021 | Zymo Research
Overall, this kit is really useful and easy to follow.
Genomics and epigenomics
The protocol of this kit is pretty straightforward to use, even for beginners. The kit is designed well and simple to use. The efficiency is also higher, the only question I am not sure about is the step of size selection since there is no step for size selection. But I will do it on my own. Overall, it is really good, and I will strongly recommend it to my colleagues.
Review Date: 21 Mar 2021 | Zymo Research
Zymo-Seq RRBS Library Kit is an all-in-one RRBS library prep kit that generates NGS libraries with a simplified workflow for the classic method Reduced Representation Bisulfite Sequencing (RRBS). This all-in-one RRBS library prep kit allows for DNA methylation profiling at single-nucleotide resolution in CpG-rich regions of the genome. This Zymo-Seq RRBS Library Kit is the ideal RRBS library prep kit to generate libraries that cover a significant percent (≥70% if using human genomic DNA) of all CpG islands, promotors, and gene bodies while largely reduces the sequencing cost, making it ideal for high-throughput screening and comparison experiments.
