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General FAQs
Lexogen NGS Services
QuantSeq
QuantSeq General
What is the difference between QuantSeq FWD and QuantSeq REV protocols?
Is QuantSeq suitable for preparation of libraries from degraded RNA or FFPE samples?
What positive control do you recommend to use ?
What are the most critical steps in the QuantSeq library generation ?
How long does it take to generate QuantSeq libraries ?
How many PCR cycles are needed to amplify QuantSeq libraries?
What level of multiplexing can be provided with QuantSeq? What barcoding (indexing) system do you use?
Which Dual Indexing Kits are compatible with QuantSeq?
What can I do if my libraries are undercycled ?
Are my libraries overcycled? If so, what should I do?
What does this peak above the upper marker of my library trace mean?
What is the typical fragment size for QuantSeq Libraries?
Why do I see a peak at ~ 200 bp in my libraries?
I see internal priming in my QuantSeq data. How can I prevent this?
What effect does Mycoplasma have on QuantSeq data analysis?
How can I analyze my QuantSeq data?
Where do I find the voucher code for free QuantSeq data analysis?
Do you have a list of publications featuring QuantSeq on plants?
QuantSeq FWD V2
QuantSeq REV V2
QuantSeq-Pool
QuantSeq-Flex
QuantSeq FFPE
QuantSeq UMI Module
Globin Block Modules for QuantSeq
BC1 Block Module for QuantSeq
QuantSeq Automation
CORALL
LUTHOR High Definition
Small RNA-Seq Library Prep Kit
miRVEL
SLAMseq
Data Analysis
12 nt Unique Dual Indexing
RiboCop
Poly(A) Selection
SPLIT
TraPR
RNA/DNA Defender
TeloPrime
SIRVs
Modules and Add-on Kits
Breadcrumbs
QuantSeq
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QuantSeq General
General FAQs relevant for all of the QuantSeq 3' mRNA-Seq family of products.
