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nGBS/ddRAD and Flex-Seq for smarter marker discovery and screening 

With normalised genotyping-by-sequencing (nGBS/ddRAD), you can discover novel SNP markers tailored to your species’ genome. And with our bundle offering, you can seamlessly transition to targeted genotyping with Flex-Seq, for high-throughput screening of those markers to maximise the value of your data. 

This dual-service approach helps you save time, reduce costs, increase efficiency and enhance the overall quality of your genotyping results. Critically, upfront marker discovery permits proper characterisation of your samples, generating up to hundreds of thousands of loci for further screening. Even a small GBS project can ensure a fully tailored set of SNPs for sub-selecting from, providing a well-defined set of markers ahead of a targeted genotyping strategy.  

Get 10% off Flex-Seq when you start an nGBS/ddRAD project *

Celebrating 10+ years of experience

We are proud to celebrate over a decade of experience delivering high-quality Genotyping-by-Sequencing (GBS) services. Over the years, we have worked on a wide range of species, both commonly and less commonly studied, supporting research in breeding and population genetics.  

applied shape dolphin nGBS

Our experience spans everything from trees such as Picea and Alba species, plants with large genomes such as Paris quadrifolia, to complex crop and forage species like Helianthus annuus, Humulus lupulus and Phleum pratense.   

We’ve also supported studies in ornamental plants (e.g., Tulipa), mammals (e.g., Cervus, Delphinus), as well as fungi, corals, and a variety of insect species including Bruchus rufimanus and Osmia bicornis.

No matter the organism, we tailor our approach to meet the unique challenges of each project. 

Start your nGBS/ddRAD project today and get 10% off your follow-up Flex-Seq project*

Why choose this approach? 

nGBS/ddRAD service  Flex-Seq service 
Identify new, high-quality SNP markers with restriction-enzyme based reduced representation sequencing. Enzymes are tailored to your species/varieties for genome-wide SNP discovery, incorporating a normalisation of repetitive regions for improved and cost-effective sequencing efficiency. Screen your selected markers with precision and scalability. 
Together  
A powerful duo for marker discovery and validation. 

 

Short videos

Additional resources

Flex-Seq
Flex-Seq
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nGBS/ddRAD
nGBS/ddRAD
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Original nGBS tech note 2016 
Frequently cited nGBS technical note from 2016 
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nGBS tech note
nGBS technical note
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*Terms and conditions: Any new nGBS/ddRAD projects continuing with the same species would qualify for the 10% follow-up Flex-Seq discount. The follow-up Flex-Seq project needs to be started within 1 year. Discount code “nGBS2Flex-Seq” needs to be used by the customer to receive the discount. This discount cannot be combined with any other offers or promotions. This promotion does not apply to distributors, bulk orders, custom part numbers (valid for sample preparations), standing orders or sequestered orders. No minimum purchase required. These terms and conditions are subject to change without notice. LGC Biosearch Technologies standard terms and conditions of sale apply: https://www.biosearchtech.com/terms-and-conditions. Offer void where prohibited, licensed or restricted by federal, state, provincial or local laws or regulation or agency/institutional policy.
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