Research rapid test PG-Seq™

geneticgenomic DNAcell

The PG-Seq™ Rapid kit v2 has been developed to analyze picogram quantities of DNA (single/multi-cells or low template DNA) from an embryo biopsy for preimplantation genetic testing. The PG-Seq™ Rapid kit v2 utilizes whole genome amplification (WGA) and next generation sequencing (NGS) technology to accurately screen all 24 chromosomes for whole chromosome aneuploidy and sub-chromosomal abnormalities. This PGT solution is compatible with Illumina® and Element Biosciences® sequencing platforms. Overview Fast PGT-A prep: 3 hours from cell lysis to NGS ready Updated, streamlined, simple PGT protocol From DNA to data, the PG-Seq™ Rapid kit v2 includes all reagents required for cell lysis, whole genome amplification, indexing along with the PG-Find™ analysis software for automatic calling of aneuploidy and copy number variants used in PGS (preimplantation genetic screening). Now you can schedule a one-on-one 30-minute online demonstration with our experts to cover everything you need to know about the PG-Seq™ Rapid protocol and data analysis with PG-Find. Please choose a timeframe that suits you best and we will provide you a Microsoft Teams personal link to join when the time comes. We look forward to speaking with you. Accurate Copy Number Detection Extensively tested using over 100 cell lines and genomic DNA samples with known ploidy. Tested from whole chromosome aneuploidies down to segmental aberrations 7Mb in size with 30pg of genomic DNA or 5 cell fibroblast samples, representative of a trophectoderm biopsy. See PG-Seq™ Rapid kit v2 app note for more information.