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egSEQ Targeted Panels

Elevate your genomics research to new heights with egSEQ Panels. Harnessing the power of hybridisation capture technology to capture a wide array of target sequences in your Next-Generation Sequencing (NGS) library. Our panels are meticulously designed to cover an extensive range of genomic variations, including Single Nucleotide Polymorphisms (SNPs), Insertions and Deletions (InDels), Copy Number Variations (CNVs), Structural Variations (SVs), gene fusions, and Microsatellite Instability (MSI).
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