Reproductive health
Embgenix kits leverage PicoPLEX whole genome amplification and patented library prep technology to enable NGS-based analysis of chromosomal copy number variations (CNVs) in various sample types. The protocols for these kits have been simplified to reduce time to results while minimizing handling errors and background. Provided with the kits is proprietary cloud-based analysis software for streamlined processing of sequencing data and reporting of results.
Embgenix product FAQs
Please refer to our FAQs page for additional information about Embgenix kits and analysis software.
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