Pharmacogenomics products

Delivering compatible PCR solutions for Pharmacogenomics

SHARD DIAGNOSTICS™ Pharmacogenomics multiplex qPCR assays are designed for direct-on-sample testing from matrices such as blood, urine, saliva, and swabs, with no extraction required. Combined with rapid cycling conditions, they deliver gold-standard multiplex qPCR performance in a format compatible with point-of-care workflows, without compromising clinical output.

SHARD DIAGNOSTICS™ kit features

Each kit features lyophilized inhibitor-tolerant reagents that deliver consistent amplification even from challenging or impure samples, effectively eliminating performance variability caused by the sample. The universal chemistry supports all targets using a standardized cycling protocol, allowing multiple assays to run on the same 96-well plate. Quantified positive controls are included to standardise run performance across machines and provide quality control measures. 

Solutions not just kits

Universal cycling, common fluorophores and automation compatible for fast integration.

Complete kits

Quantified controls included as standard. Optional collection tubes provided.

Advanced performance

Extraction-free for RNA and DNA with high level multiplexing with rapid cycling.

Available globally

All reagents are lyophilized for field use or device integration with ambient shipping.

Pharmacogenomics Kits (qPCR)

BETA LAUNCH: DPYD SNP genotyping kit (extraction-free)

Product name: LyoMorph-Q DPYD direct-SNP kit
Product code (SKU): SD_PGX_00001
Format: qPCR - lyophilized and inhibitor-tolerant (standard). Also provided in liquid format.
Potential use cases / info: The shard-dx™ DPYD kit may allow for rapid detection of the four clinically recognised SNPs in under 1 hour. The assay requires the use of K2 EDTA tubes for blood collection or saliva can be used extraction-free with shard-dx™ recommended tubes that are provided with the kit as an option. The kit can also be utilised with extracted gDNA from blood, swab or saliva. Detection of DPYD SNPs may play a role in detecting potential toxicity to 5-FU chemotherapy for individuals.
Development status: Beta launch. Multiplex optimisation in finalisation.
Targets (Reaction 1 - allele 1):
- DPYD [c.1129-5923C>G] (FAM)
- DPYD [c.1679T>G] (HEX)
- DPYD [c.1905+1G>A] (ATTO 647)
- DPYD [c.2846A>T] (ATTO 590)
Targets (Reaction 2 - allele 2):
- DPYD [c.1129-5923 wild-type] (FAM)
- DPYD [c.1679 wild-type] (HEX)
- DPYD [c.1905+1 wild-type] (ATTO 647)
- DPYD [c.2846 wild-type] (ATTO 590)
Limit of Detection - copies (95%): ≤100 planned
Detection method: Probe
Sample type: gDNA, whole blood (direct), saliva (direct), swab (direct)
Reactions: 48
Shipping: Ambient
Number of mastermixes: 1
Number of reactions required per sample: 2
Positive control inclusion: Yes
Regulatory status: Research Use Only (RUO)
BETA launch program: Join the shard-dx™ beta access program to generate cutting-edge kits alongside us. Find out more on the launch programs definition section on each custom page and product page.

BETA LAUNCH: RNR1 SNP genotyping kit (extraction-free)

Product name: LyoMorph-Q RNR1 direct-SNP kit
Product code (SKU): SD_PGX_00002
Format: qPCR - lyophilized and inhibitor-tolerant (standard)
Potential use cases / info: The shard-dx™ RNR1 kit utilises saliva (direct) or plasma (direct) and requires the use of shard-dx™ collection tubes for saliva and K2 EDTA tubes for plasma processing. Detection of RNR1 SNPs may play a role in detecting potential ototoxicity to some antibiotics for individuals. Detection of the SNPs may be useful to determine parents hereditary risk of toxicity to some antibiotics as a screening tool. This test may be performed in a lab or is compatible with point-of-care by producing results in a rapid time frame without sample pre-processing in as few as 2 pipetting steps.
Development status: Beta launch. Multiplex optimisation in finalisation.
Targets (Reaction 1):
- RNR1 [m.1555A>G] (FAM)
- RNR1 [m.1494C>T] (FAM)
- RNR1 [m.1095T>C] (HEX)
- RNase P [internal control] (ATTO 647)
Total typical qPCR run time (machine-dependant): < 60 minutes
Limit of Detection - copies (95%): 200 copies - approximately 0.2 cells
Detection method: Probe
Sample type: direct saliva collected in shard-dx™ prescribed tubes or plasma
Reactions: 48
Shipping: Ambient
Number of mastermixes: 1
Number of reactions required per sample: 1
Positive control inclusion: Yes
Regulatory status: Research Use Only (RUO)
Beta-launch program: Join the shard-dx™ beta launch program to generate cutting-edge kits alongside us. Find out more on the launch programs definition section on each custom page and product page.

Didn't find your target or configuration? Try Custom.

Custom: OEM/White-label kits

License from us to gain an edge over the competition with industry-leading performance. Available in your branding.

Custom: Clinically focused applications

Your clinical application combined with our technology, completely custom with the option for extensive performance testing.

Custom: Academic collaborations

Collaborate with shard-dx™ to gain access to our innovative technology and support for rapid progression together.

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Launch Program Definitions

The shard-dx™ product launch pathway allows customers to access the technology earlier with exciting rewards.

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Contact Us

Location:

BioCity Nottingham, Pennyfoot Street, Nottingham, England, NG1 1GF

Email:

info@shard-dx.com


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SHARD DIAGNOSTICS™ and shard-dx™ are trademarks of SHARD DIAGNOSTICS LTD. All rights reserved.