Diagnostics Learning Zone

The best place to learn about NGS and qPCR. At YouSeq we are aware that our field is a large, complex subject. We’re determined to simplify it.

We built our learning zone as a place with high quality, easy to understand materials.

So where do you want to start?


The basics of NGS and qPCR.

How do our qPCR custom panels work?

If you are developing a LDT our custom panels make it fast and easy

Why and when to adjust your qPCR baseline manually

Download our free beginner's guide to Next Generation Sequencing

How does a Covid19 qPCR test work?

What is 16S NGS sequencing and why is it so important?

The basics of all NGS workflows

NGS adapters and indexes

NGS Bioinformatics and Data Analysis

NGS Whole genome, Exome or targeted sequencing

NGS Library Prep methods

BBC Article - What does personalised medicine mean for you?

Bit of an expert

Learn more about NGS and qPCR with some more detail.

Why are we so excited about 16S and NGS?

Illumina Sequencing by Synthesis (SBS) explained

Ion Torrent™ next-gen sequencing technology

Genomics and Personalised Medicine

New study challenges standard for validating DNA sequencing results

What's happening?

Find out what’s new in the world of YouSeq.

Vacancy - Verification Scientist

Vacancy - Quality Assurance Associate

STI qPCR Panels

UTI qPCR Panels

MonkeyPox qPCR Product Guide

Custom qPCR Panels to Build your Lab Developed Test

Tetra White Paper

Introducing Our Revolutionary qPCR MasterMix - Tetra

Celebrating National DNA Day with our Head of Operations

NGS Career Opportunities at YouSeq

International Day of Women and Girls in Science

YouSeq Announces 100 qPCR Kit Launch

YouSeq embraces Nanopore sequencing for Covid19 surveillance

Worldwide qPCR and NGS solutions

We are now ISO13485 compliant: Interview with Jim Wicks, Founder and CEO

Announcing our first CE-IVD Marked kit

The University of Oxford is happy to be using our 16S kit!

YouSeq lays the first foundations in its quest to make a difference to the world we live in

Your questions answered

There are disadvantages to nearly all other methods for library quantification. Typical alternative methods include Qubit® (spectrophotometry) or Bioanalyser®/Tapestation® (electrophoresis). Neither of these methods are for suited to high-throughput of samples, requiring laborious and error-prone manual liquid handling. Furthermore they both measure total nucleic acid concentration which is not an accurate measure of sequence-ready library. Our qPCR kit is highly specific in identifying sequence-ready library only. In addition both of these methods lack sensitivity compared to qPCR and are typically more expensive.
Inaccurate liquid handling is the most common reason for variability. We are happy to give guidance on good pipetting technique and good laboratory practice. Even simple things like ensuring that all standards are thoroughly vortexed to ensure they are correctly resuspended will help to ensure good data quality.
Upon receipt, store the kit at -20°C. When stored and handled correctly, the kit components will remain perfect for at least six months from the date of receipt. All components of the kit – are stable for more than 20 freeze/thaw cycles.
Using 4 points instead of (for example) 6 saves previous wells on every plate that you run. The primers in the kit are highly efficient ~100%. We have demonstrated (during our kit development process) that the kit works over a wide dynamic range. Therefore, it is fair to extrapolate the 4 point standard curve in both directions and still deliver highly accurate results for samples that may fall out side of the range of the standard curve.
The One 16S NGS kit is compatible with all Illumina platforms. We use iSeq and MiSeq instruments in our lab and they work perfectly.
We supply everything that is required for the library preparation side of the workflow. We would expect the customer to have the usual molecular laboratory tools available to them.
A collection of DNA or cDNA fragments prepared for sequencing by a performing a series of enzymatic steps. These steps are commonly referred to as the Library Preparation.
- Single-End Read (SE), which provides sequence from only one end of the DNA insert - Paired-End Read (PE), which provides sequence from both ends of a DNA insert - Mate Pair Read (ME), Similar to paired-end but both reads come from a single strand of DNA
The number of times a nucleotide is sequenced. The deeper the read depth, the higher degrees of confidence in the base calls.
Due to the targeting regions being amplified using PCR, YouSeq’s kits work with as little as 5 ng of purified genomic DNA.
PhiX is a ready-made DNA library. It’s useful as a positive control to check all is working well with your sequencing run. It also adds “complexity” which is useful. DNA sequencers don’t like to sequence multiple identical libraries at the same time so adding PhiX mixes things up a bit and helps your sequencer perform better.
The ability to insert the correct base during a PCR cycle. Therefore, having a high fidelity master mix would mean having a low error base incorporation rate and higher quality libraries
The number of bases sequenced by your sequencer as a continuous length.
Our kits are platform agnostic, and we have a generic protocol which will run on all platforms capable of reading the fluorophores included in the kit.
If the kit you are looking for is not currently in our catalogue, we can certainly custom develop this for you. Please get in contact with us to discuss this further.
Our Endogenous control targets a human gene to confirm that a successful sample was taken. Our Internal extraction control is an exogenous target. It is spiked into the lysis buffer before extraction. This enables users to determine the success of the extraction step.
All YouSeq products have an expiry date of 1 year from the date of shipping when stored at -20C.
No, the positive controls supplied with our kits are synthetic versions of the amplicons built into a single stranded DNA oligo. They are then carefully calibrated to a known copy number and stabilised.
All our multiplex qPCR kits are designed for qualitative detection of the targets.
We don't supply extraction kits. However, all our qPCR kits will work with any industry leading extraction kit available to them that derives high quality DNA/RNA.
The detection profile of our assays are described in the specificity section of the relevant handbook. If this section does not list any specific species names, it should be assumed that all species in the genus are detected.

Any questions?

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What's new?

Just a few of the latest products we’re proud of...

RNaseP Endogenous Control

DNA Internal Control

RNA Internal Control

NGS Library Quantification Kit