Description
The Embgenix PGT-A Kit (RUO) provides a complete solution for NGS-based detection of copy number variations (CNVs) from 3–10 trophectoderm (TE) research biopsy cells or genomic DNA equivalents. The kit employs PicoPLEX whole genome amplification (WGA) technology and a streamlined library prep methodology that can be completed in a single tube in about two hours, minimizing hands-on time and the likelihood of research sample processing errors. Sequencing libraries produced with the kit are broadly compatible with multiple platforms and provided unique dual indexes allow for multiplexing of up to 96 samples in a single sequencing run. Resulting data is analyzed using intuitive, cloud-based Embgenix Analysis Software (RUO), which employs a proprietary algorithm for CNV detection and provides an array of customizable features and reporting options.