Germline Panels

Next generation sequencing (NGS) panels specifically designed for accurate cytogenetics analysis.

Conventional methods for assessing chromosomal abnormalities associated with germline disorders require multiple tests from FISH and karyotyping, to MLPA and microarrays. Our NGS solutions consolidate these workflows, combining the analysis of SNVs, INDELs and CNVs, into a single assay, saving you time and resources. 

Germline genetics panels

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Cell3 Target: Whole Exome Enrichment

Optimize your sequencing efficiency with our Cell3 Target: Whole Exome Enrichment panel.

By capturing 33 Mb of highly-conserved protein-coding regions and 99% of ClinVar variants, you can focus on the most relevant genomic content while reducing sequencing costs.

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Cell3 Direct: Fetal RhD Genotyping

The first 'direct from plasma' non-invasive prenatal test for fetal Rhesus D (RhD) genotyping. With no cffDNA extraction required, Cell3 Direct reduces costs and saves time in fetal Rhesus D diagnosis. Targeting sequences specific for exons 5, 7 and 10 of the RhD gene, this kit can distinguish between RhD positive, negative and Psi genotypes in cffDNA.

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Cell3 Target: Nexome

Maximize your coverage of clinically relevant targets in coding, and non-coding regions. with our Cell3 Target: Nexome panel.

Validate and run one workflow for all variants including SNVs, INDELs and CNVs in a single, clinical-grade assay with this enhanced whole exome panel.  No matter how challenging, Cell3 Target: Nexome is validated with all DNA types (gDNA, FFPE DNA, cfDNA (cffDNA)).  

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GALEAS HereditaryPlus

A comprehensive hereditary cancer test with tailored bioinformatics offering a viable option for reducing MLPA.

An expertly curated NGS panel design with coverage of 146 genes with known associations in inherited cancer, GALEAS HereditaryPlus offers full coverage of the UK National Genomics Test Directory and compliant with ESMO/AMP guidelines.







Panel Design Tool

Are you ready to find out more about our Germline genetic products?