Through evolution and innovation, the EmbryoMap solution has been analytically validated for detection of whole- and sub-chromosomal imbalances with highly reproducible copy-number, using cell line reference material and embryo biopsy samples
Samples are prepared for sequencing using the EmbryoMap Sample Prep Kit, sequenced on the Illumina MiSeq Sequencing System and data analysis and reporting performed using eMap software
Disclaimer: This product is labelled for Research Use Only – Not for use in diagnostic procedures.