Application note
Reliable NGS-based aneuploidy analysis in trophectoderm research samples with Embgenix PGT-A and DNBSEQ sequencing platforms
Preimplantation Genetic Testing for Aneuploidy (PGT-A) is a process to identify potential chromosomal abnormalities in trophectoderm (TE) samples. Now with demonstrated compatibility on DNBSEQ sequencing platforms, the Embgenix PGT-A Kit (RUO) has been optimized for NGS-based detection of copy number variants (CNVs) in genomic DNA (gDNA) or human embryo TE research samples.
This application note investigates the compatibility of the Embgenix PGT-A Kit with DNBSEQ sequencing platforms. Read the app note for data demonstrating how this kit seamlessly integrated into the sequencing workflows to generate accurate data for CNV analysis.
More NGS-based profiling resources
Product information
The Embgenix PGT-A kit workflow has been optimized for detection of copy number variation (CNV) from gDNA or trophectoderm samples for multiple platforms.
Explore Embgenix PGT-A data
Learn how fast and accurate automated calling of aneuploidy makes the Embgenix PGT-A Kit a simple and scalable solution for any lab.
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