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Hybridization capture-based NGS panel tests enable comprehensive sequencing of entire genes, copy number variation (CNV) analysis, and fusion detection.
Using hybridization libraries, it is possible to analyze hundreds of genes simultaneously. These panels require substantial input material—more than 50 ng for FFPE samples and over 20 ng for plasma samples—and the library preparation process typically takes several days.
This approach is particularly recommended when the specific genetic variant or variants have not yet been identified.


If the service you are looking for is not listed, or you require specialist modification to an existing process, please do get in touch, and our team will build a bespoke offering with you.